|
  | CGH: 2
|
Schaefer IM, Martinez R, Enders C, Loertzer H, Bruck W, Rohde V, Fuzesi L, et al.
Molecular cytogenetics of malignant pheochromocytoma with cerebral metastasis.
Cancer Genet Cytogenet, 200(2) 2010, 194-97.
(PMID 20620607)
|
|
| CGH: 89
|
Kowalczyk JR, Babicz M, Gaworczyk A, Lejman M, Winnicka D, Styka B, et al.
Structural and numerical abnormalities resolved in one-step analysis: the most common chromosomal rearrangements detected by comparative genomic hybridization in childhood acute . . .
Cancer Genet Cytogenet, 200(2) 2010, 161-66.
(PMID 20620600)
|
|
| CGH: 63
|
Jin S, Sun C, Yu S, Wang Q, Wu W, Sun Y, Zhao W, and An T.
Chromosome DNA imbalances in human astrocytic tumors: A comparative genomic hybridization study of 63 Chinese patients.
Pathol Res Pract, 2010.
(PMID 20591577)
|
|
| CGH: 40
|
Chang YC, Yeh KT, Liu TC, and Chang JG.
Molecular cytogenetic characterization of esophageal cancer detected by comparative genomic hybridization.
J Clin Lab Anal, 24(3) 2010, 167-74.
(PMID 20486198)
|
|
 | CGH: 11
aCGH: 34
|
Korshunov A, Remke M, Werft W, Benner A, Ryzhova M, Witt H, Sturm D, Wittmann A, et al.
Adult and pediatric medulloblastomas are genetically distinct and require different algorithms for molecular risk stratification.
J Clin Oncol, 28(18) 2010, 3054-60.
(PMID 20479417)
|
|
| CGH: 29
|
Silva M, Veiga I, Ribeiro FR, Vieira J, Pinto C, Pinheiro M, Mesquita B, Santos C, et al.
Chromosome copy number changes carry prognostic information independent of KIT/PDGFRA point mutations in gastrointestinal stromal tumors.
BMC Med, 8 2010, 26.
(PMID 20470368)
|
|
| CGH: 23
|
Gutenberg A, Gerdes JS, Jung K, Sander B, Gunawan B, Bock HC, Liersch T, Brück W, et al.
High chromosomal instability in brain metastases of colorectal carcinoma.
Cancer Genet. Cytogenet, 198(1) 2010, 47-51.
(PMID 20303014)
|
|
| CGH: 26
|
Faria C, Miguens J, Antunes JL, Salgado D, Nunes S, Barroso C, Martins Mdo C, et al.
Pediatric brain tumors: genetics and clinical outcome.
J Neurosurg Pediatr, 5(3) 2010, 263-70.
(PMID 20192643)
|
|
| CGH: 23
|
Micci F, Haugom L, Ahlquist T, Andersen HK, Abeler VM, Davidson B, Trope CG, Lothe RA, et al.
Genomic aberrations in borderline ovarian tumors.
J Transl Med, 8 2010, 21.
(PMID 20184781)
|
|
 | CGH: 58
aCGH: 20
|
Brekke HR, Ribeiro FR, Kolberg M, Agesen TH, Lind GE, Eknaes M, Hall KS, et al.
Genomic Changes in Chromosomes 10, 16, and X in Malignant Peripheral Nerve Sheath Tumors Identify a High-Risk Patient Group.
J Clin Oncol, 2010.
(PMID 20159821)
|
|
| CGH: 1
aCGH: 1
|
Golas MM, Gunawan B, Raab BW, Fuzesi L, and Lange B.
Malignant transformation of an untreated congenital sacrococcygeal teratoma: a amplification at 8q and 12p detected by comparative genomic hybridization.
Cancer Genet Cytogenet, 197(1) 2010, 95-98.
(PMID 20113846)
|
|
| CGH: 43
|
Gumus-Akay G, Unal AE, Elhan AH, Bayar S, Karadayt K, Sunguroglu A, Kadikiran A, et al.
DNA copy number changes in gastric adenocarcinomas: high resolution-comparative genomic hybridization study in Turkey.
Arch Med Res, 40(7) 2009, 551-60.
(PMID 20082868)
|
|
| CGH: 4
aCGH: 12
|
Jarosova M, Urbankova H, Plachy R, Papajik T, Holzerova M, Balcarkova J, Pikalova Z, et al.
Gain of chromosome 2p in chronic lymphocytic leukemia: significant heterogeneity and a new recurrent dicentric rearrangement.
Leuk Lymphoma, 51(2) 2010, 304-13.
(PMID 20078324)
|
|
| CGH: 72
aCGH: 12
|
Matteucci C, Barba G, Varasano E, Vitale A, Mancini M, Testoni N, Cuneo A, et al.
Rescue of genomic information in adult acute lymphoblastic leukaemia (ALL) with normal/failed cytogenetics: a GIMEMA centralized biological study.
Br J Haematol, 2010.
(PMID 20067559)
|
|
| CGH: 57
|
Ward SJ, Karakoula K, Phipps KP, Harkness W, Hayward R, Thompson D, Jacques TS, et al.
Cytogenetic analysis of paediatric astrocytoma using comparative genomic hybridisation and fluorescence in-situ hybridisation.
J Neurooncol, 98(3) 2010, 305-18.
(PMID 20052518)
|
|
| CGH: 1
|
Jeibmann A, Hasselblatt M, Pfister S, Strater R, Brentrup A, Holling M, et al.
From glioblastoma to gangliocytoma: an unforeseen but welcome shift in biological behavior.
J Neurosurg Pediatr, 4(5) 2009, 475-78.
(PMID 19877783)
|
|
| CGH: 32
|
Micci F, Haugom L, Ahlquist T, Abeler VM, Trope CG, Lothe RA, et al.
Tumor spreading to the contralateral ovary in bilateral ovarian carcinoma is a late event in clonal evolution.
J Oncol, 2010 2010, 646340.
(PMID 19759843)
|
|
| CGH: 50
|
Gumus-Akay G, Elhan AH, Unal AE, Demirkazik A, Sunguroglu A, et al.
Effects of genomic imbalances on telomerase activity in gastric cancer: clues to telomerase regulation.
Oncol Res, 17(10) 2009, 455-62.
(PMID 19725225)
|
|
| CGH: 68
|
Bauer J, Kilic E, Vaarwater J, Bastian BC, Garbe C, and de Klein A.
Oncogenic GNAQ mutations are not correlated with disease-free survival in uveal melanoma.
Br J Cancer, 2009.
(PMID 19654573)
|
|
| CGH: 42
|
Grade M, Gaedcke J, Wangsa D, Varma S, Beckmann J, Liersch T, Hess C, Becker H, et al.
Chromosomal copy number changes of locally advanced rectal cancers treated with preoperative chemoradiotherapy.
Cancer Genet Cytogenet, 193(1) 2009, 19-28.
(PMID 19602460)
|
|
| CGH: 2
aCGH: 2
|
Balcarkova J, Urbankova H, Scudla V, Holzerova M, Bacovsky J, Indrak K, et al.
Gain of chromosome arm 1q in patients in relapse and progression of multiple myeloma.
Cancer Genet Cytogenet, 192(2) 2009, 68-72.
(PMID 19596256)
|
|
| CGH: 4
|
Schmid K, Oehl N, Wrba F, Pirker R, Pirker C, and Filipits M.
EGFR/KRAS/BRAF mutations in primary lung adenocarcinomas and corresponding locoregional lymph node metastases.
Clin Cancer Res, 15(14) 2009, 4554-60.
(PMID 19584155)
|
|
| CGH: 19
|
Verdorfer I, Fehr A, Bullerdiek J, Scholz N, Brunner A, Krugmann J, Hager M, Haufe H, et al.
Chromosomal imbalances, 11q21 rearrangement and MECT1-MAML2 fusion transcript in mucoepidermoid carcinomas of the salivary gland.
Oncol Rep, 22(2) 2009, 305-11.
(PMID 19578770)
|
|
| CGH: 41
|
Stratakis CA and Carney JA.
The triad of paragangliomas, gastric stromal tumours and pulmonary chondromas (Carney triad), and the dyad of paragangliomas and gastric stromal sarcomas (Carney-Stratakis syndrome): . . .
J Intern Med, 266(1) 2009, 43-52.
(PMID 19522824)
|
|
| CGH: 184
aCGH: 11
|
Leich E, Salaverria I, Bea S, Zettl A, Wright G, Moreno V, Gascoyne RD, Chan WC, et al.
Follicular lymphomas with and without translocation t(14;18) differ in gene expression profiles and genetic alterations.
Blood, 114(4) 2009, 826-34.
(PMID 19471018)
|
|
| CGH: 1
aCGH: 1
|
Chuang SS, Liao YL, Liou CP, Wiggins ML, Ye H, Du MQ, Isaacson PG, et al.
Chronic lymphocytic leukemia with paraimmunoblastic transformation - with comparative genomic hybridization and review of the literature.
Pathol Res Pract, 2009.
(PMID 19433347)
|
|
| CGH: 3
banding: 3 |
Fang Y, Elahi A, Denley RC, Rao PH, Brennan MF, and Jhanwar SC.
Molecular characterization of permanent cell lines from primary, metastatic and recurrent malignant peripheral nerve sheath tumors (MPNST) with underlying neurofibromatosis-1.
Anticancer Res, 29(4) 2009, 1255-62.
(PMID 19414372)
|
|
| CGH: 45
|
Bruchim I, Israeli O, Mahmud SM, Aviram-Goldring A, Rienstein S, Friedman E, et al.
Genetic alterations detected by comparative genomic hybridization and recurrence rate in epithelial ovarian carcinoma.
Cancer Genet Cytogenet, 190(2) 2009, 66-70.
(PMID 19380021)
|
|
| CGH: 97
|
Pathare S, Schaffer AA, Beerenwinkel N, and Mahimkar M.
Construction of oncogenetic tree models reveals multiple pathways of oral cancer progression.
Int J Cancer, 2009.
(PMID 19267402)
|
|
| CGH: 24
|
Takeno SS, Leal MF, Lisboa LC, Lipay MV, Khayat AS, Assumpcao PP, Burbano RR, et al.
Genomic alterations in diffuse-type gastric cancer as shown by high-resolution comparative genomic hybridization.
Cancer Genet Cytogenet, 190(1) 2009, 1-7.
(PMID 19264226)
|
|
| CGH: 78
|
Homayounfar K, Gunawan B, Cameron S, Haller F, Baumhoer D, Uecker S, Sander B, et al.
Pattern of chromosomal aberrations in primary liver cancers identified by comparative genomic hybridization.
Hum Pathol, 2009.
(PMID 19200581)
|
|
| CGH: 15
|
Keser I, Toraman AD, Ozbilim G, Guney K, and Luleci G.
DNA gains and losses of chromosome in laryngeal squamous cell carcinoma using comparative genomic hybridization.
Yonsei Med J, 49(6) 2008, 949-54.
(PMID 19108018)
|
|
| CGH: 38
|
Habermann JK, Doering J, Hautaniemi S, Roblick UJ, Bündgen NK, Nicorici D, et al.
The gene expression signature of genomic instability in breast cancer is an independent predictor of clinical outcome.
Int J Cancer, 124(7) 2009, 1552-64.
(PMID 19101988)
|
|
 | CGH: 8
aCGH: 23
|
Paulson KG, Lemos BD, Feng B, Jaimes N, Peñas PF, Bi X, Maher E, Cohen L, Leonard JH, et al.
Array-CGH Reveals Recurrent Genomic Changes in Merkel Cell Carcinoma Including Amplification of L-Myc.
J. Invest. Dermatol, 2008, .
(PMID 19020549)
|
|
| CGH: 40
|
Santos SC, Cavalli IJ, Ribeiro EM, Urban CA, Lima RS, Bleggi-Torres LF, Rone JD, et al.
Patterns of DNA copy number changes in sentinel lymph node breast cancer metastases.
Cytogenet Genome Res, 122(1) 2008, 16-21.
(PMID 18931481)
|
|
 | CGH: 117
aCGH: 4
|
Bauer VL, Braselmann H, Henke M, Mattern D, Walch A, Unger K, Baudis M, Lassmann S, et al.
Chromosomal changes characterize head and neck cancer with poor prognosis.
J. Mol. Med, 2008, .
(PMID 18810378)
|
|
| CGH: 56
|
Salaverria I, Zettl A, Bea S, Hartmann EM, Dave SS, Wright GW, Boerma EJ, Kluin PM, et al.
Chromosomal alterations detected by comparative genomic hybridization in subgroups of gene expression-defined Burkitts lymphoma.
Haematologica, 93(9) 2008, 1327-34.
(PMID 18698080)
|
|
| CGH: 53
aCGH: 3
|
Rao PH, Roberts D, Zhao YJ, Bell D, Harris CP, Weber RS, and El-Naggar AK.
Deletion of 1p32-p36 is the most frequent genetic change and poor prognostic marker in adenoid cystic carcinoma of the salivary glands.
Clin Cancer Res, 14(16) 2008, 5181-87.
(PMID 18698036)
|
|
| CGH: 2
|
Lee HJ, Choi J, and Kim KR.
Pulmonary benign metastasizing leiomyoma associated with intravenous leiomyomatosis of the uterus: clinical behavior and genomic changes supporting a transportation . . .
Int J Gynecol Pathol, 27(3) 2008, 340-45.
(PMID 18580311)
|
|
| CGH: 80
|
Jancarkova N, Krkavcova M, Janashia M, Freitag P, Duskova J, et al.
[Importance of chromosomal changes correlated to prognostic factors in ovarian and cervical malignant tumors].
Ceska Gynekol, 73(2) 2008, 79-86.
(PMID 18567425)
|
|
| CGH: 4
|
Speel EJ, van de Wouw AJ, Claessen SM, Haesevoets A, Hopman AH, van der Wurff AA, et al.
Molecular evidence for a clonal relationship between multiple lesions in patients with unknown primary adenocarcinoma.
Int J Cancer, 123(6) 2008, 1292-300.
(PMID 18561313)
|
|
| CGH: 7
|
Barba G, Matteucci C, Girolomoni G, Brandimarte L, Varasano E, Martelli MF, et al.
Comparative genomic hybridization identifies 17q11.2 approximately q12 duplication as an early event in cutaneous T-cell lymphomas.
Cancer Genet Cytogenet, 184(1) 2008, 48-51.
(PMID 18558289)
|
|
| CGH: 2
banding: 1 |
Faussillon M, Murakami I, Bichat M, Telvi L, Jeanpierre C, Nezelof C, Jaubert F, et al.
Molecular cytogenetic anomalies and phenotype alterations in a newly established cell line from Wilms tumor with diffuse anaplasia.
Cancer Genet Cytogenet, 184(1) 2008, 22-30.
(PMID 18558285)
|
|
| CGH: 1
|
Agaimy A, Pelz AF, Wieacker P, Roessner A, Wunsch PH, and Schneider-Stock R.
Gastrointestinal stromal tumors of the vermiform appendix: clinicopathologic, immunohistochemical, and molecular study of 2 cases with literature review.
Hum Pathol, 39(8) 2008, 1252-57.
(PMID 18547614)
|
|
| CGH: 1
aCGH: 1
|
Kowalska A, Brunner B, Bozsaky E, Chen QR, Stock C, Lorch T, Khan J, et al.
Sequence based high resolution chromosomal CGH.
Cytogenet Genome Res, 121(1) 2008, 1-6.
(PMID 18544918)
|
|
| CGH: 22
banding: 17 |
Gayrard N, Cacheux V, Iborra F, Mourad G, and Argiles A.
Cytogenetic studies of 24 renal epithelial tumors with von Hippel-Lindau and fragile histidine triad protein expression correlation.
Arch Pathol Lab Med, 132(6) 2008, 965-73.
(PMID 18517280)
|
|
| CGH: 1
|
Balogh Z, Deak L, and Sapi Z.
Malignant myoepithelioma of soft tissue: a case report with cytogenetic findings.
Cancer Genet Cytogenet, 183(2) 2008, 121-24.
(PMID 18503832)
|
|
| CGH: 14
|
Loncarevic I, Hering A, Posorski N, Linden T, Hoyer H, and Bucsky P.
Number of genomic imbalances correlates with the overall survival for adrenocortical cancer in childhood.
Pediatric blood & cancer, 2008, .
(PMID 18478573)
|
|
| CGH: 12
banding: 12 |
McGrattan P, Campbell S, Cuthbert R, Jones F, McMullin M, and Humphreys M.
Integration of conventional cytogenetics (G-banding), comparative genomic hybridization (CGH) and interphase fluorescence in situ hybridization (i-FISH) for the detection of genomic . . .
Journal of clinical pathology, 2008, .
(PMID 18474541)
|
|
| CGH: 71
|
Blenk S, Engelmann J, Pinkert S, Weniger M, Schultz J, Rosenwald A, et al.
Explorative data analysis of MCL reveals gene expression networks implicated in survival and prognosis supported by explorative CGH analysis.
BMC cancer, 8(1) 2008, 106.
(PMID 18416826)
|
|
| CGH: 13
aCGH: 13
|
Rassekh SR, Chan S, Harvard C, Dix D, Qiao Y, and Rajcan-Separovic E.
Screening for submicroscopic chromosomal rearrangements in Wilms tumor using whole-genome microarrays.
Cancer Genet Cytogenet, 182(2) 2008, 84-94.
(PMID 18406869)
|
|
| CGH: 19
|
Mangia A, Chiarappa P, Tommasi S, Chiriatti A, Petroni S, Schittulli F, et al.
Genetic heterogeneity by comparative genomic hybridization in BRCAx breast cancers.
Cancer Genet Cytogenet, 182(2) 2008, 75-83.
(PMID 18406868)
|
|
| CGH: 21
|
Bettendorf O, Schmidt H, Staebler A, Grobholz R, Heinecke A, Boecker W, Hertle L, et al.
Chromosomal imbalances, loss of heterozygosity, and immunohistochemical expression of TP53, RB1, and PTEN in intraductal cancer, intraepithelial neoplasia, and invasive adenocarcinoma of the . . .
Genes, chromosomes & cancer, 47(7) 2008, 565-72.
(PMID 18383208)
|
|
| CGH: 13
|
Prat E, Rey J, Camps J, Ponsa I, Lloreta J, Egozcue J, Gelabert A, Campillo M, et al.
Genomic Imbalances in Urothelial Cancer: Intratumor Heterogeneity Versus Multifocality.
Diagnostic molecular pathology : the American journal of surgical pathology, part B, 2008, .
(PMID 18382360)
|
|
| CGH: 3
|
Pardo J, Aisa G, Alava E, Sola JJ, Panizo A, Rodriguez-Spiteri N, Garcia JL, et al.
Primary mixed squamous carcinoma and osteosarcoma (carcinosarcomas) of the lung have a CGH mapping similar to primitive squamous carcinomas and osteosarcomas.
Diagn Mol Pathol, 17(3) 2008, 151-58.
(PMID 18382357)
|
|
| CGH: 3
|
Da Silva L, Parry S, Reid L, Keith P, Waddell N, Kossai M, Clarke C, Lakhani SR, et al.
Aberrant expression of E-cadherin in lobular carcinomas of the breast.
Am J Surg Pathol, 32(5) 2008, 773-83.
(PMID 18379416)
|
|
| CGH: 65
|
Al-Mulla F, Hagan S, Al-Ali W, Jacob SP, Behbehani AI, Bitar MS, Dallol A, et al.
Raf kinase inhibitor protein: mechanism of loss of expression and association with genomic instability.
J Clin Pathol, 61(4) 2008, 524-29.
(PMID 18375747)
|
|
| CGH: 61
aCGH: 22
|
Hoischen A, Ehrler M, Fassunke J, Simon M, Baudis M, Landwehr C, Radlwimmer B, et al.
Comprehensive characterization of genomic aberrations in gangliogliomas by CGH, array-based CGH and interphase FISH.
Brain Pathol, 18(3) 2008, 326-37.
(PMID 18371186)
|
|
| CGH: 1
|
Faria C, Miguens J, Antunes JL, Barroso C, Pimentel J, Martins Mdo C, Moura-Nunes V, et al.
Genetic alterations in a papillary glioneuronal tumor.
J Neurosurg Pediatrics, 1(1) 2008, 99-102.
(PMID 18352813)
|
|
| CGH: 67
|
Qin YR, Wang LD, Fan ZM, Kwong D, and Guan XY.
Comparative genomic hybridization analysis of genetic aberrations associated with development of esophageal squamous cell carcinoma in Henan, China.
World J Gastroenterol, 14(12) 2008, 1828-35.
(PMID 18350619)
|
|
| CGH: 6
|
Hahtola S, Burghart E, Jeskanen L, Karenko L, Abdel-Rahman WM, Polzer B, Kajanti M, et al.
Clinicopathological characterization and genomic aberrations in subcutaneous panniculitis-like T-cell lymphoma.
J Invest Dermatol, 128(9) 2008, 2304-09.
(PMID 18337827)
|
|
| CGH: 46
|
Mensink HW, Kilic E, Vaarwater J, Douben H, Paridaens D, and de Klein A.
Molecular cytogenetic analysis of archival uveal melanoma with known clinical outcome.
Cancer Genet Cytogenet, 181(2) 2008, 108-11.
(PMID 18295662)
|
|
| CGH: 3
banding: 3 |
Shen H, Zhu Y, Wu YJ, Qiu HR, and Shu YQ.
Genomic alterations in lung adenocarcinomas detected by multicolor fluorescence in situ hybridization and comparative genomic hybridization.
Cancer Genet Cytogenet, 181(2) 2008, 100-07.
(PMID 18295661)
|
|
| CGH: 25
|
Haruta M, Matsumoto Y, Izumi H, Watanabe N, Fukuzawa M, Matsuura S, et al.
Combined BubR1 protein down-regulation and RASSF1A hypermethylation in Wilms tumors with diverse cytogenetic changes.
Mol Carcinog, 2008.
(PMID 18286482)
|
|
| CGH: 74
|
Salaverria I, Beà S, Lopez-Guillermo A, Lespinet V, Pinyol M, Burkhardt B, Lamant L, et al.
Genomic profiling reveals different genetic aberrations in systemic ALK-positive and ALK-negative anaplastic large cell lymphomas.
British journal of haematology, 140(5) 2008, 516-26.
(PMID 18275429)
|
|
| CGH: 91
|
Junker K, van Oers JM, Zwarthoff EC, Kania I, Schubert J, and Hartmann A.
Fibroblast growth factor receptor 3 mutations in bladder tumors correlate with low frequency of chromosome alterations.
Neoplasia, 10(1) 2008, 1-7.
(PMID 18231634)
|
|
| CGH: 1
|
van Gils W, Kilic E, Bruggenwirth HT, Vaarwater J, Verbiest MM, Beverloo B, et al.
Regional deletion and amplification on chromosome 6 in a uveal melanoma case without abnormalities on chromosomes 1p, 3 and 8.
Melanoma Res, 18(1) 2008, 10-15.
(PMID 18227702)
|
|
| CGH: 51
|
Petri BJ, Speel EJ, Korpershoek E, Claessen SM, van Nederveen FH, Giesen V, et al.
Frequent loss of 17p, but no p53 mutations or protein overexpression in benign and malignant pheochromocytomas.
Mod Pathol, 2008.
(PMID 18223555)
|
|
| CGH: 126
|
Friedrich K, Weber T, Scheithauer J, Meyer W, Haroske G, Kunze KD, et al.
Chromosomal genotype in breast cancer progression: Comparison of primary and secondary manifestations.
Cell Oncol, 30(1) 2008, 39-50.
(PMID 18219109)
|
|
| CGH: 48
|
Hsu LI, Chiu AW, Pu YS, Wang YH, Huan SK, Hsiao CH, Hsieh FI, et al.
Comparative genomic hybridization study of arsenic-exposed and non-arsenic-exposed urinary transitional cell carcinoma.
Toxicol Appl Pharmacol, 2007.
(PMID 18201742)
|
|
| CGH: 30
|
Schipf A, Mayr D, Kirchner T, and Diebold J.
Molecular genetic aberrations of ovarian and uterine carcinosarcomas-a CGH and FISH study.
Virchows Arch, 2008.
(PMID 18193277)
|
|
| CGH: 26
banding: 33 |
Vranova V, Mentzlova D, Oltova A, Linkova V, Zezulkova D, Filkova H, Mendelova D, et al.
Efficacy of high-resolution comparative genomic hybridization (HR-CGH) in detection of chromosomal abnormalities in children with acute leukaemia.
Neoplasma, 55(1) 2008, 23-30.
(PMID 18190236)
|
|
| CGH: 36
|
Lv S, Niu Y, Wei L, Liu Q, Wang X, and Chen Y.
Chromosomal aberrations and genetic relations in benign, borderline and malignant phyllodes tumors of the breast: a comparative genomic hybridization study.
Breast Cancer Res Treat, 2008.
(PMID 18189161)
|
|
| CGH: 5
banding: 29 |
Micci F, Haugom L, Abeler VM, Trope CG, Danielsen HE, and Heim S.
Consistent numerical chromosome aberrations in thecofibromas of the ovary.
Virchows Arch, 2008.
(PMID 18188592)
|
|
| CGH: 38
|
Fernàndez V, Jares P, Salaverria I, Giné E, Beà S, Aymerich M, Colomer D, et al.
Gene expression profile and genomic changes in disease progression of early-stage chronic lymphocytic leukemia.
Haematologica, 93(1) 2008, 132-36.
(PMID 18166798)
|
|
| CGH: 10
aCGH: 26
|
Lindholm PM, Salmenkivi K, Vauhkonen H, Nicholson AG, Anttila S, Kinnula VL, et al.
Gene copy number analysis in malignant pleural mesothelioma using oligonucleotide array CGH.
Cytogenet Genome Res, 119(1-2) 2007, 46-52.
(PMID 18160781)
|
|
| CGH: 30
|
Huang KF, Lee WY, Huang SC, Lin YS, Kang CY, Liou CP, and Tzeng CC.
Chromosomal gain of 3q and loss of 11q often associated with nodal metastasis in early stage cervical squamous cell carcinoma.
J Formos Med Assoc, 106(11) 2007, 894-902.
(PMID 18063510)
|
|
| CGH: 72
|
McIntyre A, Summersgill B, Lu YJ, Missiaglia E, Kitazawa S, Oosterhuis JW, et al.
Genomic copy number and expression patterns in testicular germ cell tumours.
Br J Cancer, 97(12) 2007, 1707-12.
(PMID 18059402)
|
|
| CGH: 12
|
Blaeker H, Mechtersheimer G, Sutter C, Hertkorn C, Kern MA, Rieker RJ, Penzel R, et al.
Recurrent deletions at 6q in early age of onset non-HNPCC- and non-FAP-associated intestinal carcinomas. Evidence for a novel cancer susceptibility locus at 6q14-q22.
Genes Chromosomes Cancer, 47(2) 2007, 159-64.
(PMID 18008368)
|
|
| CGH: 4
aCGH: 4
|
Selvarajah S, Yoshimoto M, Maire G, Paderova J, Bayani J, Squire JA, et al.
Identification of cryptic microaberrations in osteosarcoma by high-definition oligonucleotide array comparative genomic hybridization.
Cancer Genet Cytogenet, 179(1) 2007, 52-61.
(PMID 17981215)
|
|
| CGH: 24
aCGH: 34
|
Jones A, Thirlwell C, Howarth K, Graham T, Chambers W, Segditsas S, Page K, et al.
Analysis of copy number changes suggests chromosomal instability in a minority of large colorectal adenomas.
J Pathol, 2007.
(PMID 17893889)
|
|
| CGH: 15
|
Berkhout M, Nagtegaal ID, Cornelissen SJ, Dekkers MM, van de Molengraft FJ, Peters WH, et al.
Chromosomal and methylation alterations in sporadic and familial adenomatous polyposis-related duodenal carcinomas.
Mod Pathol, 2007.
(PMID 17873900)
|
|
| CGH: 5
|
de Krijger RR, Claessen SM, van der Ham F, van Unnik AJ, Hulsbergen-van de Kaa CA, et al.
Gain of chromosome 8q is a frequent finding in pleuropulmonary blastoma.
Mod Pathol, 2007.
(PMID 17873899)
|
|
| CGH: 17
|
Rodrigues R, Roque L, Espadinha C, Pinto A, Domingues R, Dinis J, Catarino A, et al.
Comparative genomic hybridization, BRAF, RAS, RET, and oligo-array analysis in aneuploid papillary thyroid carcinomas.
Oncol Rep, 18(4) 2007, 917-26.
(PMID 17786355)
|
|
| CGH: 11
aCGH: 11
|
Kamradt J, Jung V, Wahrheit K, Tolosi L, Rahnenfuehrer J, Schilling M, Walker R, et al.
Detection of novel amplicons in prostate cancer by comprehensive genomic profiling of prostate cancer cell lines using oligonucleotide-based arrayCGH.
PLoS ONE, 2(1) 2007, e769.
(PMID 17712417)
|
|
| CGH: 2
|
Baumhoer D, Glatz K, Schulten HJ, Fuzesi L, Fricker R, Kettelhack C, Hasenboehler P, et al.
Myxoinflammatory fibroblastic sarcoma: investigations by comparative genomic hybridization of two cases and review of the literature.
Virchows Arch, 2007.
(PMID 17694321)
|
|
| CGH: 31
banding: 31 |
Martin CL, Reshmi SC, Ried T, Gottberg W, Wilson JW, Reddy JK, Khanna P, Johnson JT, et al.
Chromosomal imbalances in oral squamous cell carcinoma: Examination of 31 cell lines and review of the literature.
Oral Oncol, 2007.
(PMID 17681875)
|
|
| CGH: 24
|
Ying HC, Zhang SL, Jiang T, Ouyang L, and Lu J.
[Mechanisms of drug resistance in human ovarian carcinoma studied by comparative genomic hybridization].
Zhonghua Yi Xue Za Zhi, 87(15) 2007, 1009-12.
(PMID 17672960)
|
|
| CGH: 40
|
van den Broek GB, Wreesmann VB, van den Brekel MW, Rasch CR, Balm AJ, et al.
Genetic abnormalities associated with chemoradiation resistance of head and neck squamous cell carcinoma.
Clin Cancer Res, 13(15) 2007, 4386-91.
(PMID 17671120)
|
|
| CGH: 3
|
Di Tommaso L, Kuhn E, Kurrer M, Zettl A, Marx A, Muller-Hermelink HK, Roncalli M, et al.
Thymic Tumor With Adenoid Cystic Carcinomalike Features: A Clinicopathologic Study of 4 Cases.
Am J Surg Pathol, 31(8) 2007, 1161-67.
(PMID 17667537)
|
|
| CGH: 2
banding: 1 |
Nestler U, Schmidinger A, Schulz C, Huegens-Penzel M, Gamerdinger UA, Koehler A, et al.
Glioblastoma Simultaneously Present with Meningioma - Report of Three Cases.
Zentralbl Neurochir, 2007.
(PMID 17665342)
|
|
| CGH: 15
aCGH: 23
|
Ghazani AA, Arneson N, Warren K, Pintilie M, Bayani J, Squire JA, et al.
Genomic alterations in sporadic synchronous primary breast cancer using array and metaphase comparative genomic hybridization.
Neoplasia, 9(6) 2007, 511-20.
(PMID 17603634)
|
|
| CGH: 16
|
Prochazkova M, Chevret E, Mainhaguiet G, Sobotka J, Vergier B, Belaud-Rotureau MA, et al.
Common chromosomal abnormalities in mycosis fungoides transformation.
Genes Chromosomes Cancer, 46(9) 2007, 828-38.
(PMID 17584911)
|
|
| CGH: 147
|
Schleiermacher G, Michon J, Huon I, dEnghien CD, Klijanienko J, Brisse H, Ribeiro A, et al.
Chromosomal CGH identifies patients with a higher risk of relapse in neuroblastoma without MYCN amplification.
British journal of cancer, 97(2) 2007, 238-46.
(PMID 17579628)
|
|
| CGH: 13
|
Kino M, Suzuki H, Naya Y, Komiya A, Imamoto T, Ichikawa T, Tatsuno I, Ishida H, et al.
Comparative genomic hybridization reveals frequent losses of 1p and 3q in benign pheochromocytomas of Japanese patients.
Cancer Genet Cytogenet, 175(2)(2) 2007, 169-72.
(PMID 17556075)
|
|
| CGH: 22
|
Heinrich UR, Brieger J, Gosepath J, Wierzbicka M, Sokolov M, Roth Y, Szyfter W, et al.
Frequent chromosomal gains in recurrent juvenile nasopharyngeal angiofibroma.
Cancer Genet Cytogenet, 175(2) 2007, 138-43.
(PMID 17556070)
|
|
| CGH: 31
|
Yen C-C, Liang S-C, Jong Y-J, Chen Y-J, Lin C-H, Chen Y-M, Wu Y-C, Su W-C, Huang C-YF, Tseng S-W, and Whang-Peng J.
Chromosomal aberrations of malignant pleural effusions of lung adenocarcinoma: different cytogenetic changes are correlated with genders and smoking habits.
Lung cancer (Amsterdam, Netherlands), 57(3) 2007, 292-301.
(PMID 17553591)
|
|
| CGH: 19
aCGH: 9
|
Adesina AM, Nguyen Y, Mehta V, Takei H, Stangeby P, Crabtree S, Chintagumpala M, et al.
FOXG1 dysregulation is a frequent event in medulloblastoma.
J Neurooncol, 85(2) 2007, 111-22.
(PMID 17522785)
|
|
| CGH: 27
|
Ferrer A, Salaverria I, Bosch F, Villamor N, Rozman M, Bea S, Gine E, et al.
Leukemic involvement is a common feature in mantle cell lymphoma.
Cancer, 2007.
(PMID 17477385)
|
|
| CGH: 19
|
Balogh Z, Reiniger L, Deak L, Bodor C, Csomor J, Szepesi A, Gagyi E, Kopper L, et al.
IgV(H) gene mutation status and genomic imbalances in chronic lymphocytic leukaemia with increased prolymphocytes (CLL/PL).
Hematol Oncol, 2007.
(PMID 17410523)
|
|
| CGH: 1
banding: 1 |
Corral MD, Villa O, Alfaro EM, Alonso CN, Baro C, Felice MS, Rossi J, Sole F, et al.
Complex chromosome 8;21 translocation with associated hyperdiploidy in acute myeloid leukemia (FAB-M2).
Pediatr Blood Cancer, 2007.
(PMID 17405156)
|
|
| CGH: 41
|
Xie D, Wu HX, Liu YD, Zeng SD, and Lin F.
[The significance and characteristics of chromosomal abnormalities in patients with microsatellite and chromosome stable colorectal carcinoma].
Zhonghua Yi Xue Za Zhi, 87(1) 2007, 11-15.
(PMID 17403304)
|
|
| CGH: 37
|
Yakut T, Gutenberg A, Bekar A, Egeli U, Gunawan B, Ercan I, Tolunay S, Doygun M, et al.
Correlation of chromosomal imbalances by comparative genomic hybridization and expression of EGFR, PTEN, p53, and MIB-1 in diffuse gliomas.
Oncol Rep, 17(5) 2007, 1037-43.
(PMID 17390041)
|
|
| CGH: 68
|
Arslantas A, Artan S, Oner U, Muslumanoglu MH, Ozdemir M, Durmaz R, Arslantas D, et al.
Genomic alterations in low-grade, anaplastic astrocytomas and glioblastomas.
Pathol Oncol Res, 13(1) 2007, 39-46.
(PMID 17387387)
|
|
| CGH: 23
|
Zhu YQ, Zhu ZG, Liu BY, Chen XH, Yin HR, and Wang XH.
[Chromosomal alterations analyzed by comparative genomic hybridization in primary gastric carcinoma].
Zhonghua Wei Chang Wai Ke Za Zhi, 10(2) 2007, 160-64.
(PMID 17380459)
|
|
| CGH: 32
|
Park SC, Hwang UK, Ahn SH, Gong GY, and Yoon HS.
Genetic changes in bilateral breast cancer by comparative genomic hybridisation.
Clin Exp Med, 7(1) 2007, 1-5.
(PMID 17380298)
|
|
| CGH: 6
|
Takahashi S, Hirose Y, Ikeda E, Fukaya R, and Kawase T.
Chromosome arm 1q gain associated with good response to chemotherapy in a malignant glioma. Case report.
J Neurosurg, 106(3) 2007, 488-94.
(PMID 17367075)
|
|
| CGH: 20
|
De Angelis PM, Stokke T, Beigi M, Flatberg G, Enger M, Haug K, Aass HC, Schjolberg A, et al.
Chromosomal 20q gain in the DNA diploid component of aneuploid colorectal carcinomas.
Int J Cancer, 2007.
(PMID 17354231)
|
|
| CGH: 1
banding: 1 |
Pelz AF, Klawunde P, Skalej M, Wieacker P, Kirches E, Schneider T, et al.
Novel chromosomal aberrations in a recurrent malignant meningioma.
Cancer Genet Cytogenet, 174(1) 2007, 48-53.
(PMID 17350466)
|
|
| CGH: 35
|
Konkimalla VB, Suhas VL, Chandra NR, Gebhart E, and Efferth T.
Diagnosis and therapy of oral squamous cell carcinoma.
Expert Rev Anticancer Ther, 7(3) 2007, 317-29.
(PMID 17338652)
|
|
| CGH: 30
|
Lae M, Vincent-Salomon A, Savignoni A, Huon I, Freneaux P, Sigal-Zafrani B, Aurias A, et al.
Phyllodes tumors of the breast segregate in two groups according to genetic criteria.
Mod Pathol, 20(4) 2007, 435-44.
(PMID 17334353)
|
|
| CGH: 21
aCGH: 35
|
Assaemaeki R, Sarlomo-Rikala M, Lopez-Guerrero JA, Lasota J, Andersson LC, et al.
Array comparative genomic hybridization analysis of chromosomal imbalances and their target genes in gastrointestinal stromal tumors.
Genes Chromosomes Cancer, 46(6) 2007, 564-76.
(PMID 17330260)
|
|
| CGH: 9
aCGH: 9
banding: 9 |
Kuchinskaya E, Nordgren A, Heyman M, Schoumans J, Corcoran M, Staaf J, Borg A, et al.
Tiling-resolution array-CGH reveals the pattern of DNA copy number alterations in acute lymphoblastic leukemia with 21q amplification: the result of telomere dysfunction and . . .
Leukemia, 21(6) 2007, 1327-30.
(PMID 17315016)
|
|
| CGH: 16
|
Wu SS, Liu JF, and Wang MR.
[Analyzing chromosomal abnormality in primary esophageal cancer by comparative genomic hybridization].
Ai Zheng, 26(2) 2007, 132-36.
(PMID 17298740)
|
|
| CGH: 77
|
Salaverria I, Zettl A, Beà S, Moreno V, Valls J, Hartmann E, Ott G, Wright G, et al.
Specific secondary genetic alterations in mantle cell lymphoma provide prognostic information independent of the gene expression-based proliferation signature.
J Clin Oncol, 25(10) 2007, 1216-22.
(PMID 17296973)
|
|
| CGH: 70
|
Trost D, Ehrler M, Fimmers R, Felsberg J, Sabel MC, Kirsch L, Schramm J, Wiestler OD, et al.
Identification of genomic aberrations associated with shorter overall survival in patients with oligodendroglial tumors.
Int J Cancer, 120(11) 2007, 2368-76.
(PMID 17285580)
|
|
| CGH: 3
aCGH: 3
banding: 3 |
Meyer S, Fergusson WD, Whetton AD, Moreira-Leite F, Pepper SD, Miller C, Saunders EK, et al.
Amplification and translocation of 3q26 with overexpression of EVI1 in Fanconi anemia-derived childhood acute myeloid leukemia with biallelic FANCD1/BRCA2 disruption.
Genes Chromosomes Cancer, 46(4) 2007, 359-72.
(PMID 17243162)
|
|
| CGH: 33
|
Schleicher C, Poremba C, Wolters H, Schafer KL, Senninger N, et al.
Gain of Chromosome 8q: A Potential Prognostic Marker in Resectable Adenocarcinoma of the Pancreas?
Ann Surg Oncol, 2007.
(PMID 17235717)
|
|
| CGH: 22
|
Ware ML, Hirose Y, Scheithauer BW, Yeh RF, Mayo MC, Smith JS, Chang S, Cha S, et al.
Genetic aberrations in gliomatosis cerebri.
Neurosurgery, 60(1) 2007, 150-8; discussion 158.
(PMID 17228264)
|
|
| CGH: 203
|
Gunawan B, von Heydebreck A, Sander B, Schulten HJ, Haller F, Langer C, Armbrust T, et al.
An oncogenetic tree model in gastrointestinal stromal tumours (GISTs) identifies different pathways of cytogenetic evolution with prognostic implications.
J Pathol, 211(4) 2007, 463-70.
(PMID 17226762)
|
|
| CGH: 10
|
Rickert CH, Schwering EM, Siebers J, Hartmann C, von Deimling A, et al.
Chromosomal imbalances and NF2 mutational analysis in a series of 10 spinal nerve sheath myxomas.
Histopathology, 50(2) 2007, 252-57.
(PMID 17222254)
|
|
| CGH: 1
|
Schick B and Urbschat S.
Endonasal approach for frontobasal malignant nerve sheath tumor: a case report.
Kulak Burun Bogaz Ihtis Derg, 16(6) 2006, 269-72.
(PMID 17220660)
|
|
| CGH: 10
|
Yildiz-Sezer S, Verdorfer I, Schafer G, Rogatsch H, Bartsch G, et al.
Gain of chromosome X in prostatic atrophy detected by CGH and FISH analyses.
Prostate, 67(4) 2007, 433-38.
(PMID 17219381)
|
|
| CGH: 64
|
Karlsson E, Danielsson A, Delle U, Olsson B, Karlsson P, and Helou K.
Chromosomal changes associated with clinical outcome in lymph node-negative breast cancer.
Cancer Genet Cytogenet, 172(2) 2007, 139-46.
(PMID 17213022)
|
|
| CGH: 6
aCGH: 6
|
Carr J, Bown NP, Case MC, Hall AG, Lunec J, and Tweddle DA.
High-resolution analysis of allelic imbalance in neuroblastoma cell lines by single nucleotide polymorphism arrays.
Cancer Genet Cytogenet, 172(2) 2007, 127-38.
(PMID 17213021)
|
|
| CGH: 1
aCGH: 2
|
Rennstam K, Jonsson G, Tanner M, Bendahl PO, Staaf J, Kapanen AI, Karhu R, et al.
Cytogenetic characterization and gene expression profiling of the trastuzumab-resistant breast cancer cell line JIMT-1.
Cancer Genet Cytogenet, 172(2) 2007, 95-106.
(PMID 17213017)
|
|
| CGH: 32
|
Grade M, Hormann P, Becker S, Hummon AB, Wangsa D, Varma S, Simon R, Liersch T, et al.
Gene expression profiling reveals a massive, aneuploidy-dependent transcriptional deregulation and distinct differences between lymph node-negative and lymph node-positive colon . . .
Cancer Res, 67(1) 2007, 41-56.
(PMID 17210682)
|
|
| CGH: 18
|
Vranova V, Necesalova E, Kuglik P, Cejpek P, Pesakova M, Budinska E, Relichova J, et al.
Screening of genomic imbalances in glioblastoma multiforme using high-resolution comparative genomic hybridization.
Oncol Rep, 17(2) 2007, 457-64.
(PMID 17203188)
|
|
| CGH: 21
|
Ouyang L, Zhang SL, and Wang X.
[Genetic aberrations and human papillomavirus status in vulvar squamous cell carcinomas].
Zhonghua Fu Chan Ke Za Zhi, 41(10) 2006, 701-05.
(PMID 17199928)
|
|
| CGH: 1
aCGH: 1
banding: 1 |
Hallor KH, Heidenblad M, Brosjo O, Mandahl N, and Mertens F.
Tiling resolution array comparative genomic hybridization analysis of a fibrosarcoma of bone.
Cancer Genet Cytogenet, 172(1) 2007, 80-83.
(PMID 17175386)
|
|
| CGH: 58
|
Berglund M, Enblad G, Thunberg U, Amini RM, Sundstrom C, Roos G, Erlanson M, et al.
Genomic imbalances during transformation from follicular lymphoma to diffuse large B-cell lymphoma.
Mod Pathol, 20(1) 2007, 63-75.
(PMID 17170743)
|
|
| CGH: 36
|
Ghadimi BM, Grade M, Monkemeyer C, Kulle B, Gaedcke J, Gunawan B, Langer C, et al.
Distinct chromosomal profiles in metastasizing and non-metastasizing colorectal carcinomas.
Cell Oncol, 28(5-6) 2006, 273-81.
(PMID 17167180)
|
|
| CGH: 8
|
Aguilera NS, Chen J, Bijwaard KE, Director-Myska AE, Barekman CL, Millward C, et al.
Gene rearrangement and comparative genomic hybridization studies of classic Hodgkin lymphoma expressing T-cell antigens.
Arch Pathol Lab Med, 130(12) 2006, 1772-79.
(PMID 17149949)
|
|
| CGH: 13
aCGH: 13
|
Reis-Filho JS, Simpson PT, Turner NC, Lambros MB, Jones C, Mackay A, Grigoriadis A, et al.
FGFR1 emerges as a potential therapeutic target for lobular breast carcinomas.
Clin Cancer Res, 12(22) 2006, 6652-62.
(PMID 17121884)
|
|
| CGH: 29
|
Schick B, Wemmert S, Bechtel U, Nicolai P, Hofmann T, Golabek W, et al.
Comprehensive genomic analysis identifies MDM2 and AURKA as novel amplified genes in juvenile angiofibromas.
Head Neck, 2006.
(PMID 17120309)
|
|
| CGH: 28
|
Vaghefi P, Martin A, Prevot S, Charlotte F, Camilleri-Broet S, Barli E, Davi F, et al.
Genomic imbalances in AIDS-related lymphomas: relation with tumoral Epstein-Barr virus status.
AIDS, 20(18) 2006, 2285-91.
(PMID 17117014)
|
|
| CGH: 6
|
Nair P, Pan H, Stallings RL, and Gao SJ.
Recurrent genomic imbalances in primary effusion lymphomas.
Cancer Genet Cytogenet, 171(2) 2006, 119-21.
(PMID 17116491)
|
|
| CGH: 2
aCGH: 22
|
Modena P, Lualdi E, Facchinetti F, Veltman J, Reid JF, Minardi S, Janssen I, et al.
Identification of tumor-specific molecular signatures in intracranial ependymoma and association with clinical characteristics.
J Clin Oncol, 24(33) 2006, 5223-33.
(PMID 17114655)
|
|
| CGH: 14
|
Wild PJ, Giedl J, Stoehr R, Junker K, Boehm S, van Oers JM, Zwarthoff EC, Blaszyk H, et al.
Genomic aberrations are rare in urothelial neoplasms of patients 19 years or younger.
J Pathol, 211(1) 2007, 18-25.
(PMID 17072825)
|
|
| CGH: 68
|
Wang LD, Qin YR, Fan ZM, Kwong D, Guan XY, Tsao GS, Sham J, Li JL, et al.
Comparative genomic hybridization: comparison between esophageal squamous cell carcinoma and gastric cardia adenocarcinoma from a high-incidence area for both cancers in Henan, northern . . .
Dis Esophagus, 19(6) 2006, 459-67.
(PMID 17069589)
|
|
| CGH: 52
|
Habermann JK, Paulsen U, Roblick UJ, Upender MB, McShane LM, Korn EL, Wangsa D, et al.
Stage-specific alterations of the genome, transcriptome, and proteome during colorectal carcinogenesis.
Genes Chromosomes Cancer, 46(1) 2007, 10-26.
(PMID 17044061)
|
|
| CGH: 59
|
Cerveira N, Ribeiro FR, Peixoto A, Costa V, Henrique R, Jeronimo C, et al.
TMPRSS2-ERG gene fusion causing ERG overexpression precedes chromosome copy number changes in prostate carcinomas and paired HGPIN lesions.
Neoplasia, 8(10) 2006, 826-32.
(PMID 17032499)
|
|
| CGH: 158
|
Poon TC, Wong N, Lai PB, Rattray M, Johnson PJ, and Sung JJ.
A tumor progression model for hepatocellular carcinoma: bioinformatic analysis of genomic data.
Gastroenterology, 131(4) 2006, 1262-70.
(PMID 17030195)
|
|
| CGH: 1
|
Kuhnen C, Herter P, Leuschner I, Mentzel T, Druecke D, Jaworska M, et al.
Sclerosing pseudovascular rhabdomyosarcoma-immunohistochemical, ultrastructural, and genetic findings indicating a distinct subtype of rhabdomyosarcoma.
Virchows Arch, 449(5) 2006, 572-78.
(PMID 17016719)
|
|
| CGH: 10
|
Valladares A, Hernandez NG, Gomez FS, Curiel-Quezada E, Madrigal-Bujaidar E, et al.
Genetic expression profiles and chromosomal alterations in sporadic breast cancer in Mexican women.
Cancer Genet Cytogenet, 170(2) 2006, 147-51.
(PMID 17011986)
|
|
| CGH: 45
|
Yakut T, Schulten HJ, Demir A, Frank D, Danner B, Egeli U, Gebitekin C, Kahler E, et al.
Assessment of molecular events in squamous and non-squamous cell lung carcinoma.
Lung Cancer S, 54(3) 2006, 293-301.
(PMID 17011066)
|
|
| CGH: 98
|
Levan K, Partheen K, Osterberg L, Helou K, and Horvath G.
Chromosomal alterations in 98 endometrioid adenocarcinomas analyzed with comparative genomic hybridization.
Cytogenet Genome Res, 115(1) 2006, 16-22.
(PMID 16974079)
|
|
| CGH: 8
aCGH: 1
|
Yoshimoto M, Bayani J, Nuin PA, Silva NS, Cavalheiro S, Stavale JN, Andrade JA, et al.
Metaphase and array comparative genomic hybridization: unique copy number changes and gene amplification of medulloblastomas in South America.
Cancer Genet Cytogenet, 170(1) 2006, 40-47.
(PMID 16965953)
|
|
| CGH: 33
|
Helou K, Padilla-Nash H, Wangsa D, Karlsson E, Osterberg L, Karlsson P, Ried T, et al.
Comparative genome hybridization reveals specific genomic imbalances during the genesis from benign through borderline to malignant ovarian tumors.
Cancer Genet. Cytogenet, 170(1) 2006, 1-8.
(PMID 16965948)
|
|
| CGH: 25
|
Gebert C, Brinkschmidt C, Bielack S, Bernhardt T, Jurgens H, Bocker W, Winkelmann W, et al.
The potential of comparative genomic hybridization as a tool in the differential diagnosis of matrix-producing bone lesions.
Int J Surg Pathol, 14(3) 2006, 187-92.
(PMID 16959697)
|
|
| CGH: 27
|
Pyakurel P, Montag U, Castanos-Velez E, Kaaya E, Christensson B, Tonnies H, et al.
CGH of microdissected Kaposis sarcoma lesions reveals recurrent loss of chromosome Y in early and additional chromosomal changes in late tumour stages.
AIDS, 20(14) 2006, 1805-12.
(PMID 16954721)
|
|
| CGH: 14
|
Larramendy ML, Kaur S, Svarvar C, Bohling T, and Knuutila S.
Gene copy number profiling of soft-tissue leiomyosarcomas by array-comparative genomic hybridization.
Cancer Genet Cytogenet, 169(2) 2006, 94-101.
(PMID 16938566)
|
|
| CGH: 59
aCGH: 10
|
Weber RG, Hoischen A, Ehrler M, Zipper P, Kaulich K, Blaschke B, Becker AJ, et al.
Frequent loss of chromosome 9, homozygous CDKN2A/p14(ARF)/CDKN2B deletion and low TSC1 mRNA expression in pleomorphic xanthoastrocytomas.
Oncogene, 26(7) 2007, 1088-97.
(PMID 16909113)
|
|
| CGH: 11
aCGH: 10
banding: 20 |
Bosga-Bouwer AG, Kok K, Booman M, Boven L, van der Vlies P, van den Berg A, et al.
Array comparative genomic hybridization reveals a very high frequency of deletions of the long arm of chromosome 6 in testicular lymphoma.
Genes Chromosomes Cancer, 45(10) 2006, 976-81.
(PMID 16865685)
|
|
| CGH: 60
aCGH: 60
banding: 112 |
Rucker FG, Bullinger L, Schwaenen C, Lipka DB, Wessendorf S, Frohling S, Bentz M, et al.
Disclosure of candidate genes in acute myeloid leukemia with complex karyotypes using microarray-based molecular characterization.
J Clin Oncol, 24(24) 2006, 3887-94.
(PMID 16864856)
|
|
| CGH: 52
|
Stembalska A, Blin N, Ramsey D, and Sasiadek MM.
Three distinct regions of deletion on 13q in squamous cell carcinoma of the larynx.
Oncol Rep, 16(2) 2006, 417-21.
(PMID 16820925)
|
|
| CGH: 2
banding: 2 |
Ishiguro M, Iwasaki H, Takeshita M, Hirose Y, and Kaneko Y.
A cytogenetic analysis in two cases of malignant peripheral nerve sheath tumor showing hypodiploid karyotype.
Oncol Rep, 16(2) 2006, 225-32.
(PMID 16820897)
|
|
| CGH: 71
|
Ribeiro FR, Jeronimo C, Henrique R, Fonseca D, Oliveira J, Lothe RA, et al.
8q gain is an independent predictor of poor survival in diagnostic needle biopsies from prostate cancer suspects.
Clin Cancer Res, 12(13) 2006, 3961-70.
(PMID 16818693)
|
|
| CGH: 10
|
White JS, Becker RL, McLean IW, Director-Myska AE, and Nath J.
Molecular cytogenetic evaluation of 10 uveal melanoma cell lines.
Cancer Genet Cytogenet, 168(1) 2006, 11-21.
(PMID 16772116)
|
|
| CGH: 70
|
Noutomi Y, Oga A, Uchida K, Okafuji M, Ita M, Kawauchi S, Furuya T, Ueyama Y, et al.
Comparative genomic hybridization reveals genetic progression of oral squamous cell carcinoma from dysplasia via two different tumourigenic pathways.
J Pathol, 210(1) 2006, 67-74.
(PMID 16767698)
|
|
| CGH: 24
|
Noguera Salva R, Piqueras Franco M, Ruiz Sauri A, Llombart-Bosch A, Castel Sanchez V, et al.
[Genomic profile in high risk neuroblastoma by comparative genomic hybridization].
An Pediatr (Barc), 64(5) 2006, 449-56.
(PMID 16756886)
|
|
| CGH: 26
aCGH: 26
|
Mayr D, Kanitz V, Anderegg B, Luthardt B, Engel J, Lohrs U, Amann G, et al.
Analysis of gene amplification and prognostic markers in ovarian cancer using comparative genomic hybridization for microarrays and immunohistochemical analysis for tissue . . .
Am J Clin Pathol, 126(1) 2006, 101-09.
(PMID 16753589)
|
|
| CGH: 11
banding: 11 |
Uchida K, Oga A, Okafuji M, Mihara M, Kawauchi S, Furuya T, Chochi Y, Ueyama Y, et al.
Molecular cytogenetic analysis of oral squamous cell carcinomas by comparative genomic hybridization, spectral karyotyping, and fluorescence in situ hybridization.
Cancer Genet Cytogenet, 167(2) 2006, 109-16.
(PMID 16737909)
|
|
| CGH: 20
|
Osterberg L, Akeson M, Levan K, Partheen K, Zetterqvist BM, Brannstrom M, et al.
Genetic alterations of serous borderline tumors of the ovary compared to stage I serous ovarian carcinomas.
Cancer Genet Cytogenet, 167(2) 2006, 103-08.
(PMID 16737908)
|
|
| CGH: 169
|
Clausen OP, Aass HC, Beigi M, Purdie KJ, Proby CM, Brown VL, Mattingsdal M, Micci F, et al.
Are keratoacanthomas variants of squamous cell carcinomas? A comparison of chromosomal aberrations by comparative genomic hybridization.
J Invest Dermatol, 126(10) 2006, 2308-15.
(PMID 16728973)
|
|
| CGH: 17
aCGH: 17
banding: 17 |
Rucker FG, Sander S, Dohner K, Dohner H, Pollack JR, and Bullinger L.
Molecular profiling reveals myeloid leukemia cell lines to be faithful model systems characterized by distinct genomic aberrations.
Leukemia, 20(6) 2006, 994-1001.
(PMID 16721385)
|
|
| CGH: 4
|
Rickert CH and Hasselblatt M.
Cytogenetic features of ependymoblastomas.
Acta Neuropathol, 111(6) 2006, 559-62.
(PMID 16718352)
|
|
| CGH: 9
aCGH: 10
banding: 13 |
Strefford JC, van Delft FW, Robinson HM, Worley H, Yiannikouris O, Selzer R, et al.
Complex genomic alterations and gene expression in acute lymphoblastic leukemia with intrachromosomal amplification of chromosome 21.
Proc Natl Acad Sci U S A, 103(21) 2006, 8167-72.
(PMID 16702559)
|
|
| CGH: 51
|
Svarvar C, Larramendy ML, Blomqvist C, Gentile M, Koivisto-Korander R, Leminen A, et al.
Do DNA copy number changes differentiate uterine from non-uterine leiomyosarcomas and predict metastasis?
Mod Pathol, 19(8) 2006, 1068-82.
(PMID 16648866)
|
|
| CGH: 26
|
Tarkkanen M, Larramendy ML, Bohling T, Serra M, Hattinger CM, Kivioja A, Elomaa I, et al.
Malignant fibrous histiocytoma of bone: analysis of genomic imbalances by comparative genomic hybridisation and C-MYC expression by immunohistochemistry.
Eur J Cancer, 42(8) 2006, 1172-80.
(PMID 16630715)
|
|
| CGH: 2
aCGH: 1
banding: 18 |
La Starza R, Aventin A, Matteucci C, Crescenzi B, Romoli S, Testoni N, Pierini V, et al.
Genomic gain at 6p21: a new cryptic molecular rearrangement in secondary myelodysplastic syndrome and acute myeloid leukemia.
Leukemia, 20(6) 2006, 958-64.
(PMID 16617324)
|
|
| CGH: 5
aCGH: 5
banding: 5 |
Park SJ, Jeong SY, and Kim HJ.
Y chromosome loss and other genomic alterations in hepatocellular carcinoma cell lines analyzed by CGH and CGH array.
Cancer Genet Cytogenet, 166(1) 2006, 56-64.
(PMID 16616112)
|
|
| CGH: 19
|
Schneider DT, Zahn S, Sievers S, Alemazkour K, Reifenberger G, Wiestler OD, et al.
Molecular genetic analysis of central nervous system germ cell tumors with comparative genomic hybridization.
Mod Pathol, 19(6) 2006, 864-73.
(PMID 16607373)
|
|
| CGH: 6
|
Scattone A, Pennella A, Gentile M, Musti M, Nazzaro P, Buonadonna AL, Marzullo A, et al.
Comparative genomic hybridisation in malignant deciduoid mesothelioma.
J Clin Pathol, 59(7) 2006, 764-69.
(PMID 16569690)
|
|
| CGH: 22
aCGH: 13
|
Nakagawa Y, Numoto K, Yoshida A, Kunisada T, Ohata H, Takeda K, Wai D, Poremba C, et al.
Chromosomal and genetic imbalances in synovial sarcoma detected by conventional and microarray comparative genomic hybridization.
J Cancer Res Clin Oncol, 132(7) 2006, 444-50.
(PMID 16557383)
|
|
| CGH: 24
|
Burnworth B, Popp S, Stark HJ, Steinkraus V, Brocker EB, Hartschuh W, Birek C, et al.
Gain of 11q/cyclin D1 overexpression is an essential early step in skin cancer development and causes abnormal tissue organization and differentiation.
Oncogene, 25(32) 2006, 4399-412.
(PMID 16547504)
|
|
| CGH: 21
aCGH: 21
|
Wilting SM, Snijders PJ, Meijer GA, Ylstra B, van den Ijssel PR, Snijders AM, et al.
Increased gene copy numbers at chromosome 20q are frequent in both squamous cell carcinomas and adenocarcinomas of the cervix.
J Pathol, 209(2) 2006, 220-30.
(PMID 16538612)
|
|
| CGH: 1
|
Jung SJ, Chung JI, Park SH, Ayala AG, and Ro JY.
Thyroid follicular carcinoma-like tumor of kidney: a case report with morphologic, immunohistochemical, and genetic analysis.
Am J Surg Pathol, 30(3) 2006, 411-15.
(PMID 16538064)
|
|
| CGH: 61
aCGH: 10
|
Al-Mulla F, Behbehani AI, Bitar MS, Varadharaj G, and Going JJ.
Genetic profiling of stage I and II colorectal cancer may predict metastatic relapse.
Mod Pathol, 19(5) 2006, 648-58.
(PMID 16528379)
|
|
| CGH: 34
banding: 23 |
Watanabe N, Nakadate H, Haruta M, Sugawara W, Sasaki F, Tsunematsu Y, Kikuta A, et al.
Association of 11q loss, trisomy 12, and possible 16q loss with loss of imprinting of insulin-like growth factor-II in Wilms tumor.
Genes Chromosomes Cancer, 45(6) 2006, 592-601.
(PMID 16518847)
|
|
| CGH: 10
banding: 10 |
Karpova MB, Schoumans J, Blennow E, Ernberg I, Henter JI, Smirnov AF, Nordenskjold M, et al.
Combined spectral karyotyping, comparative genomic hybridization, and in vitro apoptyping of a panel of Burkitts lymphoma-derived B cell lines reveals an unexpected complexity of chromosomal . . .
Int J Oncol, 28(3) 2006, 605-17.
(PMID 16465364)
|
|
| CGH: 22
|
Ehrbrecht A, Muller U, Wolter M, Hoischen A, Koch A, Radlwimmer B, Actor B, et al.
Comprehensive genomic analysis of desmoplastic medulloblastomas: identification of novel amplified genes and separate evaluation of the different histological components.
J Pathol, 208(4) 2006, 554-63.
(PMID 16400626)
|
|
| CGH: 21
|
Grade M, Ghadimi BM, Varma S, Simon R, Wangsa D, Barenboim-Stapleton L, Liersch T, et al.
Aneuploidy-dependent massive deregulation of the cellular transcriptome and apparent divergence of the Wnt/beta-catenin signaling pathway in human rectal carcinomas.
Cancer Res, 66(1) 2006, 267-82.
(PMID 16397240)
|
|
| CGH: 7
|
Su M, Chin SF, Li XY, Edwards P, Caldas C, and Fitzgerald RC.
Comparative genomic hybridization of esophageal adenocarcinoma and squamous cell carcinoma cell lines.
Dis Esophagus, 19(1) 2006, 10-14.
(PMID 16364037)
|
|
| CGH: 63
|
Osterberg L, Levan K, Partheen K, Helou K, and Horvath G.
Cytogenetic analysis of carboplatin resistance in early-stage epithelial ovarian carcinoma.
Cancer Genet Cytogenet, 163(2) 2005, 144-50.
(PMID 16337857)
|
|
| CGH: 20
|
Inda MM, Perot C, Guillaud-Bataille M, Danglot G, Rey JA, Bello MJ, Fan X, et al.
Genetic heterogeneity in supratentorial and infratentorial primitive neuroectodermal tumours of the central nervous system.
Histopathology, 47(6) 2005, 631-37.
(PMID 16324202)
|
|
| CGH: 18
|
Gimenez S, Costa C, Espinet B, Sole F, Pujol RM, Puigdecanet E, Garcia-Moreno P, et al.
Comparative genomic hybridization analysis of cutaneous large B-cell lymphomas.
Exp Dermatol, 14(12) 2005, 883-90.
(PMID 16274455)
|
|
| CGH: 32
|
Yan W, Song L, Wei W, Li A, Liu J, and Fang Y.
Chromosomal abnormalities associated with neck nodal metastasis in nasopharyngeal carcinoma.
Tumour Biol, 26(6) 2005, 306-12.
(PMID 16254460)
|
|
| CGH: 41
|
Packeisen J, Nakachi K, Boecker W, Brandt B, and Buerger H.
Cytogenetic differences in breast cancer samples between German and Japanese patients.
J Clin Pathol, 58(10) 2005, 1101-03.
(PMID 16189159)
|
|
| CGH: 14
|
Knuuttila A, Jee KJ, Taskinen E, Wolff H, Knuutila S, and Anttila S.
Spindle cell tumours of the pleura: a clinical, histological and comparative genomic hybridization analysis of 14 cases.
Virchows Arch, 448(2) 2006, 135-41.
(PMID 16170537)
|
|
| CGH: 29
|
Juhasz A, Balazs M, Sziklay I, Rakosy Z, Treszl A, Repassy G, et al.
Chromosomal imbalances in laryngeal and hypopharyngeal cancers detected by comparative genomic hybridization.
Cytometry A, 67(2) 2005, 151-60.
(PMID 16163698)
|
|
| CGH: 154
|
Binh MB, Sastre-Garau X, Guillou L, de Pinieux G, Terrier P, Lagace R, Aurias A, et al.
MDM2 and CDK4 immunostainings are useful adjuncts in diagnosing well-differentiated and dedifferentiated liposarcoma subtypes: a comparative analysis of 559 soft tissue neoplasms with . . .
Am J Surg Pathol, 29(10) 2005, 1340-47.
(PMID 16160477)
|
|
| CGH: 30
|
Qin YR, Wang LD, Dora K, Guan XY, Zhuang ZH, Fan ZM, Deng W, et al.
[Genomic changes in primary lesion and lymph node metastases of esophageal squamous cell carcinoma].
Ai Zheng, 24(9) 2005, 1048-53.
(PMID 16159423)
|
|
| CGH: 3
aCGH: 3
|
Ness GO, Lybaek H, Arnes J, and Rodahl E.
Chromosomal imbalances in a recurrent solitary fibrous tumor of the orbit.
Cancer Genet Cytogenet, 162(1) 2005, 38-44.
(PMID 16157198)
|
|
| CGH: 9
banding: 11 |
Langdon JA, Lamont JM, Scott DK, Dyer S, Prebble E, Bown N, Grundy RG, Ellison DW, et al.
Combined genome-wide allelotyping and copy number analysis identify frequent genetic losses without copy number reduction in medulloblastoma.
Genes Chromosomes Cancer, 45(1) 2006, 47-60.
(PMID 16149064)
|
|
| CGH: 21
|
Chang MC, Chang YT, Tien YW, Sun CT, Wu MS, and Lin JT.
Distinct chromosomal aberrations of ampulla of Vater and pancreatic head cancers detected by laser capture microdissection and comparative genomic hybridization.
Oncol Rep, 14(4) 2005, 867-72.
(PMID 16142344)
|
|
| CGH: 46
|
Qin SL, Chen XJ, Xu X, Shou JZ, Bi XG, Ji L, Han YL, Cai Y, Wei F, Ma JH, Wu M, et al.
Detection of chromosomal alterations in bladder transitional cell carcinomas from Northern China by comparative genomic hybridization.
Cancer Lett, 238(2) 2006, 230-39.
(PMID 16125302)
|
|
| CGH: 11
|
Wong QW, Wong N, Lai PB, To KF, and Wong N.
Clonal relationship of tumor nodules in hepatocellular carcinoma: a hierarchical clustering analysis of comparative genomic hybridization data.
Hum Pathol, 36(8) 2005, 893-98.
(PMID 16112006)
|
|
| CGH: 29
|
Maize JCJ, McCalmont TH, Carlson JA, Busam KJ, Kutzner H, and Bastian BC.
Genomic analysis of blue nevi and related dermal melanocytic proliferations.
Am J Surg Pathol, 29(9) 2005, 1214-20.
(PMID 16096412)
|
|
| CGH: 13
|
Sebenik M, Ricci AJ, DiPasquale B, Mody K, Pytel P, Jee KJ, Knuutila S, et al.
Undifferentiated intimal sarcoma of large systemic blood vessels: report of 14 cases with immunohistochemical profile and review of the literature.
Am J Surg Pathol, 29(9) 2005, 1184-93.
(PMID 16096408)
|
|
| CGH: 34
|
Morohara K, Nakao K, Tajima Y, Nishino N, Yamazaki K, Kaetsu T, Suzuki S, Tsunoda A, et al.
Analysis by comparative genomic hybridization of gastric cancer with peritoneal dissemination and/or positive peritoneal cytology.
Cancer Genet Cytogenet, 161(1) 2005, 57-62.
(PMID 16080958)
|
|
| CGH: 1
|
Kawashima H, Ogose A, Gu W, Nishio J, Kudo N, Kondo N, Hotta T, Umezu H, Tohyama T, et al.
Establishment and characterization of a novel myxofibrosarcoma cell line.
Cancer Genet Cytogenet, 161(1) 2005, 28-35.
(PMID 16080955)
|
|
| CGH: 18
|
Hu J, Rao UN, Jasani S, Khanna V, Yaw K, and Surti U.
Loss of DNA copy number of 10q is associated with aggressive behavior of leiomyosarcomas: a comparative genomic hybridization study.
Cancer Genet Cytogenet, 161(1) 2005, 20-27.
(PMID 16080954)
|
|
| CGH: 255
|
Bea S, Zettl A, Wright G, Salaverria I, Jehn P, Moreno V, Burek C, Ott G, Puig X, et al.
Diffuse large B-cell lymphoma subgroups have distinct genetic profiles that influence tumor biology and improve gene-expression-based survival prediction.
Blood, 106(9) 2005, 3183-90.
(PMID 16046532)
|
|
| CGH: 42
|
Korinth D, Pacyna-Gengelbach M, Deutschmann N, Hattenberger S, Bockmuhl U, Dietel M, et al.
Chromosomal imbalances in wood dust-related adenocarcinomas of the inner nose and their associations with pathological parameters.
J Pathol, 207(2) 2005, 207-15.
(PMID 16041693)
|
|
| CGH: 35
|
Poirel HA, Bernheim A, Schneider A, Meddeb M, Choquet S, Leblond V, Charlotte F, et al.
Characteristic pattern of chromosomal imbalances in posttransplantation lymphoproliferative disorders: correlation with histopathological subcategories and EBV status.
Transplantation, 80(2) 2005, 176-84.
(PMID 16041261)
|
|
| CGH: 56
|
Hermsen M, Alonso Guervos M, Meijer G, van Diest P, Suarez Nieto C, Marcos CA, et al.
Chromosomal changes in relation to clinical outcome in larynx and pharynx squamous cell carcinoma.
Cell Oncol, 27(3) 2005, 191-98.
(PMID 16037640)
|
|
| CGH: 1
|
Kuhnen C, Herter P, Kasprzynski A, Vogt M, Jaworska M, and Johnen G.
[Myoepithelioma of soft tissue -- case report with clinicopathologic, ultrastructural, and cytogenetic findings].
Pathologe, 26(5) 2005, 331-37.
(PMID 16032388)
|
|
| CGH: 2
|
Simon F, Johnen G, Krismann M, and Muller KM.
Chromosomal alterations in early stages of malignant mesotheliomas.
Virchows Arch, 447(4) 2005, 762-67.
(PMID 16012846)
|
|
| CGH: 1
banding: 1 |
Nishio J, Iwasaki H, Nabeshima K, Ishiguro M, Naumann S, Isayama T, Naito M, et al.
Establishment of a new human epithelioid sarcoma cell line, FU-EPS-1: molecular cytogenetic characterization by use of spectral karyotyping and comparative genomic . . .
Int J Oncol, 27(2) 2005, 361-69.
(PMID 16010416)
|
|
| CGH: 22
banding: 36 |
Karst C, Heller A, Claussen U, Gebhart E, and Liehr T.
Detection of cryptic chromosomal aberrations in the in vitro non-proliferating cells of acute myeloid leukemia.
Int J Oncol, 27(2) 2005, 355-59.
(PMID 16010415)
|
|
| CGH: 35
|
Pan E, Pellarin M, Holmes E, Smirnov I, Misra A, Eberhart CG, Burger PC, Biegel JA, et al.
Isochromosome 17q is a negative prognostic factor in poor-risk childhood medulloblastoma patients.
Clin Cancer Res, 11(13) 2005, 4733-40.
(PMID 16000568)
|
|
| CGH: 60
|
Poeaim S, Rerkamnuaychoke B, Jesdapatarakul S, and Campiranon A.
Chromosome alterations in colorectal cancer in Thai patients.
Cancer Genet Cytogenet, 160(2) 2005, 152-59.
(PMID 15993271)
|
|
| CGH: 4
|
Tabernero MD, Espinosa AB, Maillo A, Sayagues JM, Alguero Mdel C, Lumbreras E, et al.
Characterization of chromosome 14 abnormalities by interphase in situ hybridization and comparative genomic hybridization in 124 meningiomas: correlation with clinical, histopathologic, and . . .
Am J Clin Pathol, 123(5) 2005, 744-51.
(PMID 15981814)
|
|
| CGH: 40
aCGH: 14
|
Tanami H, Tsuda H, Okabe S, Iwai T, Sugihara K, Imoto I, and Inazawa J.
Involvement of cyclin D3 in liver metastasis of colorectal cancer, revealed by genome-wide copy-number analysis.
Lab Invest, 85(9) 2005, 1118-29.
(PMID 15980885)
|
|
| CGH: 39
|
Yan W, Song L, Liang Q, and Fang Y.
Progression analysis of lung squamous cell carcinomas by comparative genomic hybridization.
Tumour Biol, 26(3) 2005, 158-64.
(PMID 15970651)
|
|
| CGH: 2
banding: 2 |
Brandal P, Busund LT, and Heim S.
Chromosome abnormalities in juxtaglomerular cell tumors.
Cancer, 104(3) 2005, 504-10.
(PMID 15968688)
|
|
| CGH: 41
|
Schlomm T, Gunawan B, Schulten HJ, Sander B, Thangavelu K, Graf N, Leuschner I, et al.
Effects of chemotherapy on the cytogenetic constitution of Wilms tumor.
Clin Cancer Res, 11(12) 2005, 4382-87.
(PMID 15958621)
|
|
| CGH: 3
aCGH: 2
|
Reis-Filho JS, Simpson PT, Jones C, Steele D, Mackay A, Iravani M, Fenwick K, et al.
Pleomorphic lobular carcinoma of the breast: role of comprehensive molecular pathology in characterization of an entity.
J Pathol, 207(1) 2005, 1-13.
(PMID 15957152)
|
|
| CGH: 6
|
Brandal P, Bjerkehagen B, Danielsen H, and Heim S.
Chromosome 7 abnormalities are common in chordomas.
Cancer Genet Cytogenet, 160(1) 2005, 15-21.
(PMID 15949565)
|
|
| CGH: 19
|
Rodahl E, Lybaek H, Arnes J, and Ness GO.
Chromosomal imbalances in some benign orbital tumours.
Acta Ophthalmol Scand, 83(3) 2005, 385-91.
(PMID 15948796)
|
|
| CGH: 2
|
Foster NA, Banerjee AK, Xian J, Roberts I, Pezzella F, Coleman N, Nicholson AG, et al.
Somatic genetic changes accompanying lung tumor development.
Genes Chromosomes Cancer, 44(1) 2005, 65-75.
(PMID 15937994)
|
|
| CGH: 1
|
Martinez R, Schackert HK, Kirsch M, Paulus W, Joos S, and Schackert G.
Comparative genetic analysis of metachronous anaplastic oligoastrocytomas with extended recurrence-free interval.
J Neurooncol, 72(2) 2005, 95-102.
(PMID 15925987)
|
|
| CGH: 19
|
Kasamatsu A, Endo Y, Uzawa K, Nakashima D, Koike H, Hashitani S, Numata T, Urade M, et al.
Identification of candidate genes associated with salivary adenoid cystic carcinomas using combined comparative genomic hybridization and oligonucleotide microarray . . .
Int J Biochem Cell Biol, 37(9) 2005, 1869-80.
(PMID 15908262)
|
|
| CGH: 9
|
Toida M, Balazs M, Treszl A, Rakosy Z, Kato K, Yamazaki Y, Matsui T, Suwa T, et al.
Analysis of ameloblastomas by comparative genomic hybridization and fluorescence in situ hybridization.
Cancer Genet Cytogenet, 159(2) 2005, 99-104.
(PMID 15899380)
|
|
| CGH: 81
|
Simpson PT, Gale T, Reis-Filho JS, Jones C, Parry S, Sloane JP, Hanby A, Pinder SE, et al.
Columnar cell lesions of the breast: the missing link in breast cancer progression? A morphological and molecular analysis.
Am J Surg Pathol, 29(6) 2005, 734-46.
(PMID 15897740)
|
|
| CGH: 10
|
Rieker RJ, Aulmann S, Penzel R, Schnabel PA, Blaeker H, Esposito I, Morresi-Hauf A, et al.
Chromosomal imbalances in sporadic neuroendocrine tumours of the thymus.
Cancer Lett, 223(1) 2005, 169-74.
(PMID 15890250)
|
|
| CGH: 14
aCGH: 70
|
Roerig P, Nessling M, Radlwimmer B, Joos S, Wrobel G, Schwaenen C, Reifenberger G, et al.
Molecular classification of human gliomas using matrix-based comparative genomic hybridization.
Int J Cancer, 117(1) 2005, 95-103.
(PMID 15880582)
|
|
| CGH: 67
|
Muslumanoglu HM, Oner U, Ozalp S, Acikalin MF, Yalcin OT, Ozdemir M, et al.
Genetic imbalances in endometrial hyperplasia and endometrioid carcinoma detected by comparative genomic hybridization.
Eur J Obstet Gynecol Reprod Biol, 120(1) 2005, 107-14.
(PMID 15866096)
|
|
| CGH: 12
|
Halbwedl I, Ullmann R, Kremser ML, Man YG, Isadi-Moud N, Lax S, Denk H, Popper HH, et al.
Chromosomal alterations in low-grade endometrial stromal sarcoma and undifferentiated endometrial sarcoma as detected by comparative genomic hybridization.
Gynecol Oncol, 97(2) 2005, 582-87.
(PMID 15863163)
|
|
| CGH: 4
|
Baumhoer D, Gunawan B, Becker H, and Fuzesi L.
Comparative genomic hybridization in four angiosarcomas of the female breast.
Gynecol Oncol, 97(2) 2005, 348-52.
(PMID 15863129)
|
|
| CGH: 27
|
Freier K, Flechtenmacher C, Walch A, Ohl S, Devens F, Burke B, Hassfeld S, Lichter P, et al.
Copy number gains on 22q13 in adenoid cystic carcinoma of the salivary gland revealed by comparative genomic hybridization and tissue microarray analysis.
Cancer Genet Cytogenet, 159(1) 2005, 89-95.
(PMID 15860365)
|
|
| CGH: 30
|
Kasahara K, Taguchi T, Yamasaki I, Kamada M, and Shuin T.
Genetic changes in localized prostate cancer of Japanese patients shown by comparative genomic hybridization.
Cancer Genet Cytogenet, 159(1) 2005, 84-88.
(PMID 15860364)
|
|
| CGH: 19
aCGH: 19
|
Strefford JC, Stasevich I, Lane TM, Lu YJ, Oliver T, and Young BD.
A combination of molecular cytogenetic analyses reveals complex genetic alterations in conventional renal cell carcinoma.
Cancer Genet Cytogenet, 159(1) 2005, 1-9.
(PMID 15860350)
|
|
| CGH: 18
|
Castro P, Eknaes M, Teixeira MR, Danielsen HE, Soares P, Lothe RA, et al.
Adenomas and follicular carcinomas of the thyroid display two major patterns of chromosomal changes.
J Pathol, 206(3) 2005, 305-11.
(PMID 15852498)
|
|
| CGH: 1
|
Kushima R, Vieth M, Mukaisho K, Sakai R, Okabe H, Hattori T, Neuhaus H, Borchard F, et al.
Pyloric gland adenoma arising in Barretts esophagus with mucin immunohistochemical and molecular cytogenetic evaluation.
Virchows Arch, 446(5) 2005, 537-41.
(PMID 15838649)
|
|
| CGH: 54
aCGH: 54
|
Misra A, Pellarin M, Nigro J, Smirnov I, Moore D, Lamborn KR, Pinkel D, Albertson DG, et al.
Array comparative genomic hybridization identifies genetic subgroups in grade 4 human astrocytoma.
Clin Cancer Res, 11(8) 2005, 2907-18.
(PMID 15837741)
|
|
| CGH: 25
|
Al-Assar O, Ul-Hassan A, Brown R, Wilson GA, Hammond DW, and Reilly JT.
Gains on 9p are common genomic aberrations in idiopathic myelofibrosis: a comparative genomic hybridization study.
Br J Haematol, 129(1) 2005, 66-71.
(PMID 15801957)
|
|
| CGH: 36
|
Lin YS, Eng HL, Jan YJ, Lee HS, Ho WL, Liou CP, Lee WY, and Tzeng CC.
Molecular cytogenetics of ovarian granulosa cell tumors by comparative genomic hybridization.
Gynecol Oncol, 97(1) 2005, 68-73.
(PMID 15790439)
|
|
| CGH: 20
|
Pang E, Hu Y, Chan KY, Lai PB, Squire JA, Macgregor PF, Beheshti B, Albert M, et al.
Karyotypic imbalances and differential gene expressions in the acquired doxorubicin resistance of hepatocellular carcinoma cells.
Lab Invest, 85(5) 2005, 664-74.
(PMID 15765123)
|
|
| CGH: 11
banding: 36 |
Molist R, Gerbault-Seureau M, Sastre-Garau X, Sigal-Zafrani B, Dutrillaux B, et al.
Ductal breast carcinoma develops through different patterns of chromosomal evolution.
Genes Chromosomes Cancer, 43(2) 2005, 147-54.
(PMID 15751042)
|
|
| CGH: 36
|
Jiang JK, Chen YJ, Lin CH, Yu IT, and Lin JK.
Genetic changes and clonality relationship between primary colorectal cancers and their pulmonary metastases--an analysis by comparative genomic hybridization.
Genes Chromosomes Cancer, 43(1) 2005, 25-36.
(PMID 15723340)
|
|
| CGH: 23
|
Rodriguez S, Khabir A, Keryer C, Perrot C, Drira M, Ghorbel A, Jlidi R, Bernheim A, et al.
Conventional and array-based comparative genomic hybridization analysis of nasopharyngeal carcinomas from the Mediterranean area.
Cancer Genet Cytogenet, 157(2) 2005, 140-47.
(PMID 15721635)
|
|
| CGH: 1
banding: 1 |
Barenboim-Stapleton L, Yang X, Tsokos M, Wigginton JM, Padilla-Nash H, Ried T, et al.
Pediatric pancreatoblastoma: histopathologic and cytogenetic characterization of tumor and derived cell line.
Cancer Genet Cytogenet, 157(2) 2005, 109-17.
(PMID 15721631)
|
|
| CGH: 132
|
van Beers EH, van Welsem T, Wessels LF, Li Y, Oldenburg RA, Devilee P, Cornelisse CJ, et al.
Comparative genomic hybridization profiles in human BRCA1 and BRCA2 breast tumors highlight differential sets of genomic aberrations.
Cancer Res, 65(3) 2005, 822-27.
(PMID 15705879)
|
|
| CGH: 18
|
Postma C, Hermsen MA, Coffa J, Baak JP, Mueller JD, Mueller E, Bethke B, Schouten JP, et al.
Chromosomal instability in flat adenomas and carcinomas of the colon.
J Pathol, 205(4) 2005, 514-21.
(PMID 15685687)
|
|
| CGH: 19
|
Uhm KO, Park YN, Lee JY, Yoon DS, and Park SH.
Chromosomal imbalances in Korean intrahepatic cholangiocarcinoma by comparative genomic hybridization.
Cancer Genet Cytogenet, 157(1) 2005, 37-41.
(PMID 15676145)
|
|
| CGH: 20
|
Namiki T, Yanagawa S, Izumo T, Ishikawa M, Tachibana M, Kawakami Y, Yokozeki H, et al.
Genomic alterations in primary cutaneous melanomas detected by metaphase comparative genomic hybridization with laser capture or manual microdissection: 6p gains may predict poor . . .
Cancer Genet Cytogenet, 157(1) 2005, 1-11.
(PMID 15676140)
|
|
| CGH: 9
aCGH: 9
banding: 9 |
Hermsen M, Snijders A, Guervos MA, Taenzer S, Koerner U, Baak J, Pinkel D, et al.
Centromeric chromosomal translocations show tissue-specific differences between squamous cell carcinomas and adenocarcinomas.
Oncogene, 24(9) 2005, 1571-79.
(PMID 15674345)
|
|
| CGH: 2
|
Verbeek W, Schulten HJ, Sperling M, Tiesmeier J, Stoop H, Dinjens W, Looijenga L, et al.
Rectal adenocarcinoma with choriocarcinomatous differentiation: clinical and genetic aspects.
Hum Pathol, 35(11) 2004, 1427-30.
(PMID 15668903)
|
|
| CGH: 2
|
Aulmann S, Schnabel PA, Helmchen B, Dienemann H, Drings P, Otto HF, et al.
Immunohistochemical and cytogenetic characterization of acantholytic squamous cell carcinoma of the breast.
Virchows Arch, 446(3) 2005, 305-09.
(PMID 15668805)
|
|
| CGH: 89
|
Richter H, Braselmann H, Hieber L, Thomas G, Bogdanova T, Tronko N, et al.
Chromosomal imbalances in post-chernobyl thyroid tumors.
Thyroid, 14(12) 2004, 1061-64.
(PMID 15650359)
|
|
| CGH: 1
|
Rosario F, Marques AR, Roque L, Rodrigues R, Ferreira TC, Limbert E, Sobrinho L, et al.
Metastatic follicular carcinoma associated with hyperthyroidism.
Clin Nucl Med, 30(2) 2005, 79-82.
(PMID 15647670)
|
|
| CGH: 37
banding: 8 |
Martinez-Ramirez A, Urioste M, Melchor L, Blesa D, Valle L, de Andres SA, Kok K, et al.
Analysis of myelodysplastic syndromes with complex karyotypes by high-resolution comparative genomic hybridization and subtelomeric CGH array.
Genes Chromosomes Cancer, 42(3) 2005, 287-98.
(PMID 15611930)
|
|
| CGH: 68
|
Qin YR, Wang LD, Kwong D, Guan XY, Zhuang ZH, Fan ZM, An JY, and Tsao G.
[Comparative genomic hybridization of esophageal squamous cell carcinoma and gastric cardia adenocarcinoma in high-incidence region of esophageal carcinoma, Linzhou . . .
Zhonghua Yi Xue Yi Chuan Xue Za Zhi, 21(6) 2004, 625-28.
(PMID 15583998)
|
|
| CGH: 23
|
Kleivi K, Teixeira MR, Eknaes M, Diep CB, Jakobsen KS, Hamelin R, et al.
Genome signatures of colon carcinoma cell lines.
Cancer Genet Cytogenet, 155(2) 2004, 119-31.
(PMID 15571797)
|
|
| CGH: 11
aCGH: 11
|
Tsuda H, Birrer MJ, Ito YM, Ohashi Y, Lin M, Lee C, Wong WH, Rao PH, Lau CC, et al.
Identification of DNA copy number changes in microdissected serous ovarian cancer tissue using a cDNA microarray platform.
Cancer Genet Cytogenet, 155(2) 2004, 97-107.
(PMID 15571795)
|
|
| CGH: 2
|
Serio G, Scattone A, Gentile M, Nazzaro P, Pennella A, Buonadonna AL, Pollice L, et al.
Familial pleural mesothelioma with environmental asbestos exposure: losses of DNA sequences by comparative genomic hybridization (CGH).
Histopathology, 45(6) 2004, 643-45.
(PMID 15569059)
|
|
| CGH: 14
aCGH: 14
|
Jiang F, Yin Z, Caraway NP, Li R, and Katz RL.
Genomic profiles in stage I primary non small cell lung cancer using comparative genomic hybridization analysis of cDNA microarrays.
Neoplasia, 6(5) 2004, 623-35.
(PMID 15548372)
|
|
| CGH: 45
|
Gronwald J, Jauch A, Cybulski C, Schoell B, Bohm-Steuer B, Lener M, Grabowska E, et al.
Comparison of genomic abnormalities between BRCAX and sporadic breast cancers studied by comparative genomic hybridization.
Int J Cancer, 114(2) 2005, 230-36.
(PMID 15540206)
|
|
| CGH: 22
aCGH: 22
|
Atiye J, Wolf M, Kaur S, Monni O, Bohling T, Kivioja A, Tas E, Serra M, Tarkkanen M, et al.
Gene amplifications in osteosarcoma-CGH microarray analysis.
Genes Chromosomes Cancer, 42(2) 2005, 158-63.
(PMID 15540165)
|
|
| CGH: 57
banding: 53 |
Tchinda J, Volpert S, Kropff M, Berdel WE, Kienast J, Meinhardt F, et al.
Frequent gains of the short arm of chromosome 9 in multiple myeloma with normal G-banded karyotype detected by comparative genomic hybridization.
Am J Clin Pathol, 122(6) 2004, 875-82.
(PMID 15539380)
|
|
| CGH: 16
aCGH: 16
|
Hirai Y, Utsugi K, Takeshima N, Kawamata Y, Furuta R, Kitagawa T, Kawaguchi T, et al.
Putative gene loci associated with carcinogenesis and metastasis of endocervical adenocarcinomas of uterus determined by conventional and array-based CGH.
Am J Obstet Gynecol, 191(4) 2004, 1173-82.
(PMID 15507938)
|
|
| CGH: 59
|
Zhang X, Karnan S, Tagawa H, Suzuki R, Tsuzuki S, Hosokawa Y, Morishima Y, et al.
Comparison of genetic aberrations in CD10+ diffused large B-cell lymphoma and follicular lymphoma by comparative genomic hybridization and tissue-fluorescence in situ . . .
Cancer Sci, 95(10) 2004, 809-14.
(PMID 15504248)
|
|
| CGH: 19
aCGH: 19
|
Nakahara Y, Shiraishi T, Okamoto H, Mineta T, Oishi T, Sasaki K, et al.
Detrended fluctuation analysis of genome-wide copy number profiles of glioblastomas using array-based comparative genomic hybridization.
Neuro-oncol, 6(4) 2004, 281-89.
(PMID 15494095)
|
|
| CGH: 1
|
Peters I, Brunner C, Urbschat S, and Schick B.
A case of nasal leiomyosarcoma: the first comparative genomic hybridization analysis.
Kulak Burun Bogaz Ihtis Derg, 11(4) 2003, 113-16.
(PMID 15493339)
|
|
| CGH: 11
aCGH: 11
|
McIntyre A, Summersgill B, Jafer O, Rodriguez S, Zafarana G, Oosterhuis JW, Gillis AJ, et al.
Defining minimum genomic regions of imbalance involved in testicular germ cell tumors of adolescents and adults through genome wide microarray analysis of cDNA clones.
Oncogene, 23(56) 2004, 9142-47.
(PMID 15489896)
|
|
| CGH: 29
|
Schulten HJ, Gunawan B, Enders C, Donhuijsen K, Emons G, and Fuzesi L.
Overrepresentation of 8q in carcinosarcomas and endometrial adenocarcinomas.
Am J Clin Pathol, 122(4) 2004, 546-51.
(PMID 15487452)
|
|
| CGH: 33
|
Lee JY, Park YN, Uhm KO, Park SY, and Park SH.
Genetic alterations in intrahepatic cholangiocarcinoma as revealed by degenerate oligonucleotide primed PCR-comparative genomic hybridization.
J Korean Med Sci, 19(5) 2004, 682-87.
(PMID 15483344)
|
|
| CGH: 8
|
Verdorfer I, Rogatsch H, Tzankov A, Steiner H, and Mikuz G.
Molecular cytogenetic analysis of human spermatocytic seminomas.
J Pathol, 204(3) 2004, 277-81.
(PMID 15476269)
|
|
| CGH: 5
|
Wullich B, Riedinger S, Brinck U, Stoeckle M, Kamradt J, Ketter R, et al.
Evidence for gains at 15q and 20q in brain metastases of prostate cancer.
Cancer Genet Cytogenet, 154(2) 2004, 119-23.
(PMID 15474146)
|
|
| CGH: 86
|
Jones C, Ford E, Gillett C, Ryder K, Merrett S, Reis-Filho JS, Fulford LG, Hanby A, et al.
Molecular cytogenetic identification of subgroups of grade III invasive ductal breast carcinomas with different clinical outcomes.
Clin Cancer Res, 10(18 Pt 1) 2004, 5988-97.
(PMID 15447982)
|
|
| CGH: 33
|
Teixeira MR, Ribeiro FR, Eknaes M, Waehre H, Stenwig AE, Giercksky KE, Heim S, et al.
Genomic analysis of prostate carcinoma specimens obtained via ultrasound-guided needle biopsy may be of use in preoperative decision-making.
Cancer, 101(8) 2004, 1786-93.
(PMID 15386312)
|
|
| CGH: 20
|
Cavalli LR, Cornelio DA, Lima RS, Urban CA, Rone JD, Cavalli IJ, et al.
Lack of DNA copy number alterations revealed with comparative genomic hybridization in fibroadenomas of the breast.
Cancer Genet Cytogenet, 153(2) 2004, 173-76.
(PMID 15350309)
|
|
| CGH: 66
|
Bea S, Colomo L, Lopez-Guillermo A, Salaverria I, Puig X, Pinyol M, Rives S, et al.
Clinicopathologic significance and prognostic value of chromosomal imbalances in diffuse large B-cell lymphomas.
J Clin Oncol, 22(17) 2004, 3498-506.
(PMID 15337798)
|
|
| CGH: 4
banding: 15 |
Krupp W, Geiger K, Schober R, Siegert G, and Froster UG.
Cytogenetic and molecular cytogenetic analyses in diffuse astrocytomas.
Cancer Genet Cytogenet, 153(1) 2004, 32-38.
(PMID 15325091)
|
|
| CGH: 127
banding: 29 |
Casas S, Aventin A, Fuentes F, Vallespi T, Granada I, Carrio A, et al.
Genetic diagnosis by comparative genomic hybridization in adult de novo acute myelocytic leukemia.
Cancer Genet Cytogenet, 153(1) 2004, 16-25.
(PMID 15325089)
|
|
| CGH: 21
|
Liu XP, Sato T, Oga A, Ikemoto K, Kawauchi S, Ikeda E, and Sasaki K.
Two subtypes of mucinous colorectal carcinoma characterized by laser scanning cytometry and comparative genomic hybridization.
Int J Oncol, 25(3) 2004, 615-21.
(PMID 15289862)
|
|
| CGH: 13
|
Ozaki T, Wai D, Schafer KL, Lindner N, Bocker W, Winkelmann W, Dockhorn-Dworniczak B, et al.
Comparative genomic hybridization in cartilaginous tumors.
Anticancer Res, 24(3a) 2004, 1721-25.
(PMID 15274346)
|
|
| CGH: 13
|
Pan CC, Jong YJ, and Chen YJ.
Comparative genomic hybridization analysis of thymic neuroendocrine tumors.
Mod Pathol, 18(3) 2005, 358-64.
(PMID 15272285)
|
|
| CGH: 102
|
Wiltshire RN, Herndon JEn, Lloyd A, Friedman HS, Bigner DD, Bigner SH, et al.
Comparative genomic hybridization analysis of astrocytomas: prognostic and diagnostic implications.
J Mol Diagn, 6(3) 2004, 166-79.
(PMID 15269292)
|
|
| CGH: 16
|
Valladares A, Salamanca F, Madrigal-Bujaidar E, and Arenas D.
Identification of chromosomal changes with comparative genomic hybridization in sporadic breast cancer in Mexican women.
Cancer Genet Cytogenet, 152(2) 2004, 163-66.
(PMID 15262439)
|
|
| CGH: 48
|
Park SY, Kim YH, In KH, Chun YH, and Park SH.
Chromosomal aberrations in Korean nonsmall cell lung carcinomas: degenerate oligonucleotide primed polymerase chain reaction comparative genomic hybridization studies.
Cancer Genet Cytogenet, 152(2) 2004, 153-57.
(PMID 15262437)
|
|
| CGH: 27
|
Matsuda K, Matsuyama H, Hara T, Yoshihiro S, Oga A, Kawauchi S, Furuya T, Izumi H, et al.
DNA sequence copy number aberrations in prostate cancers: a comparison of comparative genomic hybridization data between Japan and European countries.
Cancer Genet Cytogenet, 152(2) 2004, 119-23.
(PMID 15262429)
|
|
| CGH: 16
banding: 16 |
Barth TF, Muller S, Pawlita M, Siebert R, Rother JU, Mechtersheimer G, Kitinya J, et al.
Homogeneous immunophenotype and paucity of secondary genomic aberrations are distinctive features of endemic but not of sporadic Burkitts lymphoma and diffuse large B-cell lymphoma with MYC . . .
J Pathol, 203(4) 2004, 940-45.
(PMID 15258997)
|
|
| CGH: 8
aCGH: 8
|
Peng DF, Sugihara H, Mukaisho K, Ling ZQ, and Hattori T.
Genetic lineage of poorly differentiated gastric carcinoma with a tubular component analysed by comparative genomic hybridization.
J Pathol, 203(4) 2004, 884-95.
(PMID 15258990)
|
|
| CGH: 1
banding: 1 |
Shyu RY, Jiang SY, Jong YJ, Cheng KC, Lin CH, Yu JC, Wu MF, and Chang TM.
Establishment and characterization of a human gastric carcinoma cell line TMC-1.
Cells Tissues Organs, 177(1) 2004, 37-46.
(PMID 15237194)
|
|
| CGH: 19
aCGH: 19
|
Holzmann K, Kohlhammer H, Schwaenen C, Wessendorf S, Kestler HA, Schwoerer A, Rau B, et al.
Genomic DNA-chip hybridization reveals a higher incidence of genomic amplifications in pancreatic cancer than conventional comparative genomic hybridization and leads to the identification . . .
Cancer Res, 64(13) 2004, 4428-33.
(PMID 15231651)
|
|
| CGH: 10
|
Stallings RL, Carty P, McArdle L, Mullarkey M, McDermott M, OMeara A, Ryan E, et al.
Evolution of unbalanced gain of distal chromosome 2p in neuroblastoma.
Cytogenet Genome Res, 106(1) 2004, 49-54.
(PMID 15218241)
|
|
| CGH: 21
|
Bryndorf T, Kirchhoff M, Larsen J, Andreasson B, Bjerregaard B, Westh H, Rose H, et al.
The most common chromosome aberration detected by high-resolution comparative genomic hybridization in vulvar intraepithelial neoplasia is not seen in vulvar squamous cell . . .
Cytogenet Genome Res, 106(1) 2004, 43-48.
(PMID 15218240)
|
|
| CGH: 8
|
Molist R, Remvikos Y, Dutrillaux B, and Muleris M.
Characterization of a new cytogenetic subtype of ductal breast carcinomas.
Oncogene, 23(35) 2004, 5986-93.
(PMID 15208688)
|
|
| CGH: 20
|
Kallio JP, Mahlamaki EH, Helin H, Karhu R, Kellokumpu-Lehtinen P, et al.
Chromosomal gains and losses detected by comparative genomic hybridization and proliferation activity in renal cell carcinoma.
Scand J Urol Nephrol, 38(3) 2004, 225-30.
(PMID 15204376)
|
|
| CGH: 48
|
Shelley Hwang E, Nyante SJ, Yi Chen Y, Moore D, DeVries S, Korkola JE, Esserman LJ, et al.
Clonality of lobular carcinoma in situ and synchronous invasive lobular carcinoma.
Cancer, 100(12) 2004, 2562-72.
(PMID 15197797)
|
|
| CGH: 2
banding: 2 |
Tonon G, Gehlhaus KS, Yonescu R, Kaye FJ, and Kirsch IR.
Multiple reciprocal translocations in salivary gland mucoepidermoid carcinomas.
Cancer Genet Cytogenet, 152(1) 2004, 15-22.
(PMID 15193437)
|
|
| CGH: 98
|
Partheen K, Levan K, Osterberg L, Helou K, and Horvath G.
Analysis of cytogenetic alterations in stage III serous ovarian adenocarcinoma reveals a heterogeneous group regarding survival, surgical outcome, and substage.
Genes Chromosomes Cancer, 40(4) 2004, 342-48.
(PMID 15188458)
|
|
| CGH: 26
|
Hallermann C, Kaune KM, Siebert R, Vermeer MH, Tensen CP, Willemze R, Gunawan B, et al.
Chromosomal aberration patterns differ in subtypes of primary cutaneous B cell lymphomas.
J Invest Dermatol, 122(6) 2004, 1495-502.
(PMID 15175042)
|
|
| CGH: 8
|
Camps J, Morales C, Prat E, Ribas M, Capella G, Egozcue J, Peinado MA, et al.
Genetic evolution in colon cancer KM12 cells and metastatic derivates.
Int J Cancer, 110(6) 2004, 869-74.
(PMID 15170669)
|
|
| CGH: 5
aCGH: 5
|
Harvell JD, Kohler S, Zhu S, Hernandez-Boussard T, Pollack JR, et al.
High-resolution array-based comparative genomic hybridization for distinguishing paraffin-embedded Spitz nevi and melanomas.
Diagn Mol Pathol, 13(1) 2004, 22-25.
(PMID 15163005)
|
|
| CGH: 5
|
Gangnus R, Langer S, Breit E, Pantel K, and Speicher MR.
Genomic profiling of viable and proliferative micrometastatic cells from early-stage breast cancer patients.
Clin Cancer Res, 10(10) 2004, 3457-64.
(PMID 15161702)
|
|
| CGH: 102
|
Kimura Y, Noguchi T, Kawahara K, Kashima K, Daa T, and Yokoyama S.
Genetic alterations in 102 primary gastric cancers by comparative genomic hybridization: gain of 20q and loss of 18q are associated with tumor progression.
Mod Pathol, 17(11) 2004, 1328-37.
(PMID 15154013)
|
|
| CGH: 2
|
Cho NH, Kim S, Ha MJ, and Kim HJ.
Simultaneous heterogenotypic renal cell carcinoma: immunohistochemical and karyoptic analysis by comparative genomic hybridization.
Urol Int, 72(4) 2004, 344-48.
(PMID 15153736)
|
|
| CGH: 3
aCGH: 3
|
Wolf M, Mousses S, Hautaniemi S, Karhu R, Huusko P, Allinen M, Elkahloun A, Monni O, et al.
High-resolution analysis of gene copy number alterations in human prostate cancer using CGH on cDNA microarrays: impact of copy number on gene expression.
Neoplasia, 6(3) 2004, 240-47.
(PMID 15153336)
|
|
| CGH: 10
|
Hoefling C, Schmidt H, Meinhardt M, Lohse A, Taubert H, Fuessel S, Schmidt U, et al.
Comparative evaluation of microsatellite marker, AP-PCR and CGH studies in primary renal cell carcinoma.
Int J Mol Med, 13(6) 2004, 835-42.
(PMID 15138621)
|
|
| CGH: 19
aCGH: 19
|
Hashimoto K, Mori N, Tamesa T, Okada T, Kawauchi S, Oga A, Furuya T, Tangoku A, et al.
Analysis of DNA copy number aberrations in hepatitis C virus-associated hepatocellular carcinomas by conventional CGH and array CGH.
Mod Pathol, 17(6) 2004, 617-22.
(PMID 15133472)
|
|
| CGH: 69
|
Tai AL, Yan WS, Fang Y, Xie D, Sham JS, and Guan XY.
Recurrent chromosomal imbalances in nonsmall cell lung carcinoma: the association between 1q amplification and tumor recurrence.
Cancer, 100(9) 2004, 1918-27.
(PMID 15112273)
|
|
| CGH: 81
|
Zettl A, Rudiger T, Konrad MA, Chott A, Simonitsch-Klupp I, Sonnen R, et al.
Genomic profiling of peripheral T-cell lymphoma, unspecified, and anaplastic large T-cell lymphoma delineates novel recurrent chromosomal alterations.
Am J Pathol, 164(5) 2004, 1837-48.
(PMID 15111330)
|
|
| CGH: 52
|
Gunawan B, Schulten HJ, von Heydebreck A, Schmidt B, Enders C, Hoer J, Langer C, et al.
Site-independent prognostic value of chromosome 9q loss in primary gastrointestinal stromal tumours.
J Pathol, 202(4) 2004, 421-29.
(PMID 15095269)
|
|
| CGH: 53
aCGH: 53
|
Kohlhammer H, Schwaenen C, Wessendorf S, Holzmann K, Kestler HA, Kienle D, Barth TF, et al.
Genomic DNA-chip hybridization in t(11;14)-positive mantle cell lymphomas shows a high frequency of aberrations and allows a refined characterization of consensus . . .
Blood, 104(3) 2004, 795-801.
(PMID 15090459)
|
|
| CGH: 32
|
Fischer TC, Gellrich S, Muche JM, Sherev T, Audring H, Neitzel H, Walden P, Sterry W, et al.
Genomic aberrations and survival in cutaneous T cell lymphomas.
J Invest Dermatol, 122(3) 2004, 579-86.
(PMID 15086538)
|
|
| CGH: 11
aCGH: 11
|
Yano S, Matsuyama H, Matsuda K, Matsumoto H, Yoshihiro S, and Naito K.
Accuracy of an array comparative genomic hybridization (CGH) technique in detecting DNA copy number aberrations: comparison with conventional CGH and loss of heterozygosity analysis in . . .
Cancer Genet Cytogenet, 150(2) 2004, 122-27.
(PMID 15066319)
|
|
| CGH: 206
|
Korsching E, Packeisen J, Helms MW, Kersting C, Voss R, van Diest PJ, Brandt B, et al.
Deciphering a subgroup of breast carcinomas with putative progression of grade during carcinogenesis revealed by comparative genomic hybridisation (CGH) and immunohistochemistry.
Br J Cancer, 90(7) 2004, 1422-28.
(PMID 15054466)
|
|
| CGH: 1
|
Bergmann F, Hackert T, Mechtersheimer G, Penzel R, Blaker H, Berger I, Esposito I, et al.
Differential diagnosis of non-epithelial tumors of the pancreas: malignant non-epithelial pancreatic tumor with focal pigmentation.
Virchows Arch, 444(2) 2004, 190-93.
(PMID 15046038)
|
|
| CGH: 44
|
Junker K, Romics I, Szendroi A, Riesz P, Moravek P, Hindermann W, Winter R, et al.
Genetic profile of bone metastases in renal cell carcinoma.
Eur Urol, 45(3) 2004, 320-24.
(PMID 15036677)
|
|
| CGH: 83
|
Rao PH, Arias-Pulido H, Lu XY, Harris CP, Vargas H, Zhang FF, Narayan G, Schneider A, et al.
Chromosomal amplifications, 3q gain and deletions of 2q33-q37 are the frequent genetic changes in cervical carcinoma.
BMC Cancer, 4 2004, 5.
(PMID 15018632)
|
|
| CGH: 19
|
Larramendy ML, Koljonen V, Bohling T, Tukiainen E, and Knuutila S.
Recurrent DNA copy number changes revealed by comparative genomic hybridization in primary Merkel cell carcinomas.
Mod Pathol, 17(5) 2004, 561-67.
(PMID 15001998)
|
|
| CGH: 78
|
Mattfeldt T, Gottfried HW, Wolter H, Schmidt V, Kestler HA, and Mayer J.
Classification of prostatic carcinoma with artificial neural networks using comparative genomic hybridization and quantitative stereological data.
Pathol Res Pract, 199(12) 2003, 773-84.
(PMID 14989489)
|
|
| CGH: 56
|
Diep CB, Teixeira MR, Thorstensen L, Wiig JN, Eknaes M, Nesland JM, Giercksky KE, et al.
Genome characteristics of primary carcinomas, local recurrences, carcinomatoses, and liver metastases from colorectal cancer patients.
Mol Cancer, 3 2004, 6.
(PMID 14977426)
|
|
| CGH: 16
|
Hannen EJ, Macville MV, Wienk SM, Slootweg PJ, Manni JJ, Hanselaar AG, et al.
Different chromosomal imbalances in metastasized and nonmetastasized tongue carcinomas identified by comparative genomic hybridization.
Oral Oncol, 40(4) 2004, 364-71.
(PMID 14969815)
|
|
| CGH: 14
aCGH: 13
|
Tong CY, Hui AB, Yin XL, Pang JC, Zhu XL, Poon WS, and Ng HK.
Detection of oncogene amplifications in medulloblastomas by comparative genomic hybridization and array-based comparative genomic hybridization.
J Neurosurg, 100(2 Suppl Pediatrics) 2004, 187-93.
(PMID 14758948)
|
|
| CGH: 2
|
Terracciano LM, Tornillo L, Avoledo P, Von Schweinitz D, Kuhne T, et al.
Fibrolamellar hepatocellular carcinoma occurring 5 years after hepatocellular adenoma in a 14-year-old girl: a case report with comparative genomic hybridization . . .
Arch Pathol Lab Med, 128(2) 2004, 222-26.
(PMID 14736278)
|
|
| CGH: 19
|
Rodrigues RF, Roque L, Rosa-Santos J, Cid O, and Soares J.
Chromosomal imbalances associated with anaplastic transformation of follicular thyroid carcinomas.
Br J Cancer, 90(2) 2004, 492-96.
(PMID 14735198)
|
|
| CGH: 28
|
Chen Y, Tzeng CC, Liou CP, Chang MY, Li CF, and Lin CN.
Biological significance of chromosomal imbalance aberrations in gastrointestinal stromal tumors.
J Biomed Sci, 11(1) 2004, 65-71.
(PMID 14730211)
|
|
| CGH: 13
|
Henegariu O, Heerema NA, Thurston V, Jung SH, Pera M, and Vance GH.
Characterization of gains, losses, and regional amplification in testicular germ cell tumor cell lines by comparative genomic hybridization.
Cancer Genet Cytogenet, 148(1) 2004, 14-20.
(PMID 14697636)
|
|
| CGH: 16
|
Habermann JK, Hellman K, Freitag S, Heselmeyer-Haddad K, Hellstrom AC, Shah K, et al.
A recurrent gain of chromosome arm 3q in primary squamous carcinoma of the vagina.
Cancer Genet Cytogenet, 148(1) 2004, 7-13.
(PMID 14697635)
|
|
| CGH: 35
|
Gebhart E, Liehr T, Wolff E, Wiltfang J, Koscielny S, and Ries J.
Loss of 9p21 is embedded in a complex but consistent pattern of genomic imbalances in oral squamous cell carcinomas.
Cytogenet Genome Res, 101(2) 2003, 106-12.
(PMID 14610349)
|
|
| CGH: 70
|
Karnan S, Tagawa H, Suzuki R, Suguro M, Yamaguchi M, Okamoto M, Morishima Y, et al.
Analysis of chromosomal imbalances in de novo CD5-positive diffuse large-B-cell lymphoma detected by comparative genomic hybridization.
Genes Chromosomes Cancer, 39(1) 2004, 77-81.
(PMID 14603444)
|
|
| CGH: 25
banding: 30 |
Lau CC, Harris CP, Lu XY, Perlaky L, Gogineni S, Chintagumpala M, Hicks J, Johnson ME, et al.
Frequent amplification and rearrangement of chromosomal bands 6p12-p21 and 17p11.2 in osteosarcoma.
Genes Chromosomes Cancer, 39(1) 2004, 11-21.
(PMID 14603437)
|
|
| CGH: 69
aCGH: 10
|
Peng DF, Sugihara H, Mukaisho K, Tsubosa Y, and Hattori T.
Alterations of chromosomal copy number during progression of diffuse-type gastric carcinomas: metaphase- and array-based comparative genomic hybridization analyses of multiple samples from . . .
J Pathol, 201(3) 2003, 439-50.
(PMID 14595756)
|
|
| CGH: 13
banding: 1 |
Prochazkova M, Chevret E, Beylot-Barry M, Sobotka J, Vergier B, Delaunay M, Turmo M, et al.
Chromosomal imbalances: a hallmark of tumour relapse in primary cutaneous CD30+ T-cell lymphoma.
J Pathol, 201(3) 2003, 421-29.
(PMID 14595754)
|
|
| CGH: 28
|
Ullmann R, Bongiovanni M, Halbwedl I, Fraire AE, Cagle PT, Mori M, Papotti M, et al.
Is high-grade adenomatous hyperplasia an early bronchioloalveolar adenocarcinoma?
J Pathol, 201(3) 2003, 371-76.
(PMID 14595748)
|
|
| CGH: 20
|
Shiomi H, Sugihara H, Kamitani S, Tokugawa T, Tsubosa Y, Okada K, Tamura H, Tani T, et al.
Cytogenetic heterogeneity and progression of esophageal squamous cell carcinoma.
Cancer Genet Cytogenet, 147(1) 2003, 50-61.
(PMID 14580771)
|
|
| CGH: 8
banding: 6 |
Costa D, Queralt R, Aymerich M, Carrio A, Rozman M, Vallespi T, Colomer D, et al.
High levels of chromosomal imbalances in typical and small-cell variants of T-cell prolymphocytic leukemia.
Cancer Genet Cytogenet, 147(1) 2003, 36-43.
(PMID 14580769)
|
|
| CGH: 22
|
Kim GJ, Kim JO, Hong EK, Kim H, Chun YH, and Park SH.
Detection of genetic alterations in Korean ovarian carcinomas by degenerate oligonucleotide primed polymerase chain reaction-comparative genomic hybridization.
Cancer Genet Cytogenet, 147(1) 2003, 23-27.
(PMID 14580767)
|
|
| CGH: 19
|
Habermann JK, Upender MB, Roblick UJ, Kruger S, Freitag S, Blegen H, Bruch HP, et al.
Pronounced chromosomal instability and multiple gene amplifications characterize ulcerative colitis-associated colorectal carcinomas.
Cancer Genet Cytogenet, 147(1) 2003, 9-17.
(PMID 14580765)
|
|
| CGH: 39
|
Okamoto H, Yasui K, Zhao C, Arii S, and Inazawa J.
PTK2 and EIF3S3 genes may be amplification targets at 8q23-q24 and are associated with large hepatocellular carcinomas.
Hepatology, 38(5) 2003, 1242-49.
(PMID 14578863)
|
|
| CGH: 189
|
Bastian BC, Olshen AB, LeBoit PE, and Pinkel D.
Classifying melanocytic tumors based on DNA copy number changes.
Am J Pathol, 163(5) 2003, 1765-70.
(PMID 14578177)
|
|
| CGH: 6
banding: 5 |
Boonstra R, Bosga-Bouwer A, Mastik M, Haralambieva E, Conradie J, van den Berg E, et al.
Identification of chromosomal copy number changes associated with transformation of follicular lymphoma to diffuse large B-cell lymphoma.
Hum Pathol, 34(9) 2003, 915-23.
(PMID 14562288)
|
|
| CGH: 35
|
Terracciano LM, Bernasconi B, Ruck P, Stallmach T, Briner J, Sauter G, Moch H, et al.
Comparative genomic hybridization analysis of hepatoblastoma reveals high frequency of X-chromosome gains and similarities between epithelial and stromal components.
Hum Pathol, 34(9) 2003, 864-71.
(PMID 14562281)
|
|
| CGH: 17
banding: 32 |
da Silva Veiga LC, Bergamo NA, dos Reis PP, Kowalski LP, and Rogatto SR.
DNA gains at 8q23.2: a potential early marker in head and neck carcinomas.
Cancer Genet Cytogenet, 146(2) 2003, 110-15.
(PMID 14553944)
|
|
| CGH: 47
|
Tarafa G, Prat E, Risques RA, Gonzalez S, Camps J, Grau M, Guino E, Moreno V, et al.
Common genetic evolutionary pathways in familial adenomatous polyposis tumors.
Cancer Res, 63(18) 2003, 5731-37.
(PMID 14522893)
|
|
| CGH: 88
|
Weber-Mangal S, Sinn HP, Popp S, Klaes R, Emig R, Bentz M, Mansmann U, Bastert G, et al.
Breast cancer in young women (< or = 35 years): Genomic aberrations detected by comparative genomic hybridization.
Int J Cancer, 107(4) 2003, 583-92.
(PMID 14520696)
|
|
| CGH: 50
|
Johnen G, Krismann M, Jaworska M, and Muller KM.
[CGH findings in neuroendocrine tumours of the lung].
Pathologe, 24(4) 2003, 303-07.
(PMID 14513278)
|
|
| CGH: 46
banding: 58 |
Garcia JL, Hernandez JM, Gutierrez NC, Flores T, Gonzalez D, Calasanz MJ, et al.
Abnormalities on 1q and 7q are associated with poor outcome in sporadic Burkitts lymphoma. A cytogenetic and comparative genomic hybridization study.
Leukemia, 17(10) 2003, 2016-24.
(PMID 14513052)
|
|
| CGH: 48
|
Pirker C, Holzmann K, Spiegl-Kreinecker S, Elbling L, Thallinger C, Pehamberger H, et al.
Chromosomal imbalances in primary and metastatic melanomas: over-representation of essential telomerase genes.
Melanoma Res, 13(5) 2003, 483-92.
(PMID 14512790)
|
|
| CGH: 3
|
Terracciano LM, Glatz K, Mhawech P, Vasei M, Lehmann FS, Vecchione R, et al.
Hepatoid adenocarcinoma with liver metastasis mimicking hepatocellular carcinoma: an immunohistochemical and molecular study of eight cases.
Am J Surg Pathol, 27(10) 2003, 1302-12.
(PMID 14508391)
|
|
| CGH: 59
|
Li LS, Kim NG, Kim SH, Park C, Kim H, Kang HJ, Koh KH, Kim SN, Kim WH, Kim NK, et al.
Chromosomal imbalances in the colorectal carcinomas with microsatellite instability.
Am J Pathol, 163(4) 2003, 1429-36.
(PMID 14507650)
|
|
| CGH: 10
|
Blaker H, Scholten M, Sutter C, Otto HF, and Penzel R.
Somatic mutations in familial adenomatous polyps. Nuclear translocation of beta-catenin requires more than biallelic APC inactivation.
Am J Clin Pathol, 120(3) 2003, 418-23.
(PMID 14502807)
|
|
| CGH: 12
|
Cavalli LR, Urban CA, Dai D, de Assis S, Tavares DC, Rone JD, Bleggi-Torres LF, et al.
Genetic and epigenetic alterations in sentinel lymph nodes metastatic lesions compared to their corresponding primary breast tumors.
Cancer Genet Cytogenet, 146(1) 2003, 33-40.
(PMID 14499694)
|
|
| CGH: 68
|
Pang A, Ng IO, Fan ST, and Kwong YL.
Clinicopathologic significance of genetic alterations in hepatocellular carcinoma.
Cancer Genet Cytogenet, 146(1) 2003, 8-15.
(PMID 14499690)
|
|
| CGH: 12
banding: 1 |
Brandal P, Micci F, Bjerkehagen B, Eknaes M, Larramendy M, Lothe RA, Knuutila S, et al.
Molecular cytogenetic characterization of desmoid tumors.
Cancer Genet Cytogenet, 146(1) 2003, 1-7.
(PMID 14499689)
|
|
| CGH: 30
|
Schuster AE, Schneider DT, Fritsch MK, Grundy P, and Perlman EJ.
Genetic and genetic expression analyses of clear cell sarcoma of the kidney.
Lab Invest, 83(9) 2003, 1293-99.
(PMID 13679437)
|
|
| CGH: 46
|
Israeli O, Gotlieb WH, Friedman E, Goldman B, Ben-Baruch G, Aviram-Goldring A, et al.
Familial vs sporadic ovarian tumors: characteristic genomic alterations analyzed by CGH.
Gynecol Oncol, 90(3) 2003, 629-36.
(PMID 13678737)
|
|
| CGH: 22
|
Brunaud L, Zarnegar R, Wada N, Magrane G, Wong M, Duh QY, Davis O, et al.
Chromosomal aberrations by comparative genomic hybridization in thyroid tumors in patients with familial nonmedullary thyroid cancer.
Thyroid, 13(7) 2003, 621-29.
(PMID 12964966)
|
|
| CGH: 8
|
Yen CC, Chen YJ, Lu KH, Hsia JY, Chen JT, Hu CP, Chen PM, Liu JH, Chiou TJ, Wang WS, et al.
Genotypic analysis of esophageal squamous cell carcinoma by molecular cytogenetics and real-time quantitative polymerase chain reaction.
Int J Oncol, 23(4) 2003, 871-81.
(PMID 12963965)
|
|
| CGH: 16
|
Hostein I, Coindre JM, Derre J, Mariani O, Chibon F, and Aurias A.
Comparative genomic hybridization study of paraffin-embedded dedifferentiated liposarcoma fixed with Holland Bouins fluid.
Diagn Mol Pathol, 12(3) 2003, 166-73.
(PMID 12960699)
|
|
| CGH: 24
|
Robanus-Maandag EC, Bosch CA, Kristel PM, Hart AA, Faneyte IF, Nederlof PM, et al.
Association of C-MYC amplification with progression from the in situ to the invasive stage in C-MYC-amplified breast carcinomas.
J Pathol, 201(1) 2003, 75-82.
(PMID 12950019)
|
|
| CGH: 25
|
Dahlgren L, Mellin H, Wangsa D, Heselmeyer-Haddad K, Bjornestal L, Lindholm J, et al.
Comparative genomic hybridization analysis of tonsillar cancer reveals a different pattern of genomic imbalances in human papillomavirus-positive and -negative tumors.
Int J Cancer, 107(2) 2003, 244-49.
(PMID 12949801)
|
|
| CGH: 9
banding: 37 |
Micci F, Teixeira MR, Scheistroen M, Abeler VM, and Heim S.
Cytogenetic characterization of tumors of the vulva and vagina.
Genes Chromosomes Cancer, 38(2) 2003, 137-48.
(PMID 12939741)
|
|
| CGH: 20
|
Chui DT, Hammond D, Baird M, Shield L, Jackson R, and Jarrett RF.
Classical Hodgkin lymphoma is associated with frequent gains of 17q.
Genes Chromosomes Cancer, 38(2) 2003, 126-36.
(PMID 12939740)
|
|
| CGH: 9
|
Ottesen AM, Skakkebaek NE, Lundsteen C, Leffers H, Larsen J, et al.
High-resolution comparative genomic hybridization detects extra chromosome arm 12p material in most cases of carcinoma in situ adjacent to overt germ cell tumors, but not before the invasive . . .
Genes Chromosomes Cancer, 38(2) 2003, 117-25.
(PMID 12939739)
|
|
| CGH: 29
aCGH: 29
|
Schraml P, Schwerdtfeger G, Burkhalter F, Raggi A, Schmidt D, Ruffalo T, King W, et al.
Combined array comparative genomic hybridization and tissue microarray analysis suggest PAK1 at 11q13.5-q14 as a critical oncogene target in ovarian carcinoma.
Am J Pathol, 163(3) 2003, 985-92.
(PMID 12937139)
|
|
| CGH: 19
banding: 20 |
Jarosova M, Holzerova M, Mihal V, Lakoma I, Divoky V, Blazek B, Pospisilova D, et al.
Complex karyotypes in childhood acute lymphoblastic leukemia: cytogenetic and molecular cytogenetic study of 21 cases.
Cancer Genet Cytogenet, 145(2) 2003, 161-68.
(PMID 12935929)
|
|
| CGH: 11
|
Mao X, Onadim Z, Price EA, Child F, Lillington DM, Russell-Jones R, Young BD, et al.
Genomic alterations in blastic natural killer/extranodal natural killer-like T cell lymphoma with cutaneous involvement.
J Invest Dermatol, 121(3) 2003, 618-27.
(PMID 12925224)
|
|
| CGH: 28
|
Wang R, Titley JC, Lu YJ, Summersgill BM, Bridge JA, Fisher C, et al.
Loss of 13q14-q21 and gain of 5p14-pter in the progression of leiomyosarcoma.
Mod Pathol, 16(8) 2003, 778-85.
(PMID 12920222)
|
|
| CGH: 22
|
Dellas A, Torhorst J, Gaudenz R, Mihatsch MJ, and Moch H.
DNA copy number changes in cervical adenocarcinoma.
Clin Cancer Res, 9(8) 2003, 2985-91.
(PMID 12912946)
|
|
| CGH: 50
|
Leslie A, Pratt NR, Gillespie K, Sales M, Kernohan NM, Smith G, Wolf CR, Carey FA, et al.
Mutations of APC, K-ras, and p53 are associated with specific chromosomal aberrations in colorectal adenocarcinomas.
Cancer Res, 63(15) 2003, 4656-61.
(PMID 12907646)
|
|
| CGH: 10
|
Matteucci C, Galieni P, Leoncini L, Lazzi S, Lauria F, Polito E, Martelli MF, et al.
Typical genomic imbalances in primary MALT lymphoma of the orbit.
J Pathol, 200(5) 2003, 656-60.
(PMID 12898603)
|
|
| CGH: 7
|
Jensen RH, Tiirikainen M, You L, Ginzinger D, He B, Uematsu K, Xu Z, Treseler P, et al.
Genomic alterations in human mesothelioma including high resolution mapping of common regions of DNA loss in chromosome arm 6q.
Anticancer Res, 23(3B) 2003, 2281-89.
(PMID 12894504)
|
|
| CGH: 22
|
Osin P, Lu YJ, Stone J, Crook T, Houlston RS, Gasco M, Gusterson BA, et al.
Distinct genetic and epigenetic changes in medullary breast cancer.
Int J Surg Pathol, 11(3) 2003, 153-58.
(PMID 12894346)
|
|
| CGH: 53
|
Noguchi T, Kimura Y, Takeno S, Chujo M, Uchida Y, Mueller W, et al.
Chromosomal imbalance in esophageal squamous cell carcinoma: 3q gain correlates with tumor progression but not prognostic significance.
Oncol Rep, 10(5) 2003, 1393-400.
(PMID 12883713)
|
|
| CGH: 43
|
Wang Q, Wang B, Guan X, Gao H, Cheng H, Zhang Q, Huang C, Li P, et al.
Analysis of comparative genomic hybridization and loss of heterozygosity in 43 primary gastric carcinomas.
Chin Med J (Engl), 116(4) 2003, 517-23.
(PMID 12875714)
|
|
| CGH: 5
banding: 9 |
Dettori T, Frau DV, Lai ML, Mariotti S, Uccheddu A, Daniele GM, Tallini G, Faa G, et al.
Aneuploidy in oncocytic lesions of the thyroid gland: diffuse accumulation of mitochondria within the cell is associated with trisomy 7 and progressive numerical chromosomal . . .
Genes Chromosomes Cancer, 38(1) 2003, 22-31.
(PMID 12874783)
|
|
| CGH: 1
|
Miller CT, Aggarwal S, Lin TK, Dagenais SL, Contreras JI, Orringer MB, Glover TW, et al.
Amplification and overexpression of the dual-specificity tyrosine-(Y)-phosphorylation regulated kinase 2 (DYRK2) gene in esophageal and lung adenocarcinomas.
Cancer Res, 63(14) 2003, 4136-43.
(PMID 12874018)
|
|
| CGH: 27
|
Ashton KJ, Weinstein SR, Maguire DJ, and Griffiths LR.
Chromosomal aberrations in squamous cell carcinoma and solar keratoses revealed by comparative genomic hybridization.
Arch Dermatol, 139(7) 2003, 876-82.
(PMID 12873882)
|
|
| CGH: 52
|
Ottaggio L, Viaggi S, Zunino A, Zupo S, Rossi E, Spriano M, Abbondandolo A, et al.
Chromosome aberrations evaluated by comparative genomic hybridization in B-cell chronic lymphocytic leukemia: correlation with CD38 expression.
Haematologica, 88(7) 2003, 769-77.
(PMID 12857555)
|
|
| CGH: 8
|
Ramirez T, Thoma K, Taja-Chayeb L, Efferth T, Herrera LA, Halatsch ME, et al.
Specific patterns of DNA copy number gains and losses in eight new glioblastoma multiforme cell lines.
Int J Oncol, 23(2) 2003, 453-60.
(PMID 12851695)
|
|
| CGH: 79
|
Tremmel SC, Gotte K, Popp S, Weber S, Hormann K, Bartram CR, and Jauch A.
Intratumoral genomic heterogeneity in advanced head and neck cancer detected by comparative genomic hybridization.
Cancer Genet Cytogenet, 144(2) 2003, 165-74.
(PMID 12850380)
|
|
| CGH: 44
|
Brieger J, Jacob R, Riazimand HS, Essig E, Heinrich UR, Bittinger F, et al.
Chromosomal aberrations in premalignant and malignant squamous epithelium.
Cancer Genet Cytogenet, 144(2) 2003, 148-55.
(PMID 12850378)
|
|
| CGH: 26
|
He QJ, Zeng WF, Sham JS, Xie D, Yang XW, Lin HL, Zhan WH, Lin F, Zeng SD, Nie D, et al.
Recurrent genetic alterations in 26 colorectal carcinomas and 21 adenomas from Chinese patients.
Cancer Genet Cytogenet, 144(2) 2003, 112-18.
(PMID 12850373)
|
|
| CGH: 46
|
Liebisch P, Viardot A, Bassermann N, Wendl C, Roth K, Goldschmidt H, Einsele H, et al.
Value of comparative genomic hybridization and fluorescence in situ hybridization for molecular diagnostics in multiple myeloma.
Br J Haematol, 122(2) 2003, 193-201.
(PMID 12846886)
|
|
| CGH: 20
|
Arslantas A, Artan S, Oner U, Muslumanoglu H, Durmaz R, Cosan E, Atasoy MA, et al.
The importance of genomic copy number changes in the prognosis of glioblastoma multiforme.
Neurosurg Rev, 27(1) 2004, 58-64.
(PMID 12845540)
|
|
| CGH: 7
|
Welkoborsky HJ, Jacob R, Riazimand SH, Bernauer HS, and Mann WJ.
Molecular biologic characteristics of seven new cell lines of squamous cell carcinomas of the head and neck and comparison to fresh tumor tissue.
Oncology, 65(1) 2003, 60-71.
(PMID 12837984)
|
|
| CGH: 82
|
Richter H, Slezak P, Walch A, Werner M, Braselmann H, Jaramillo E, Ost A, Hirata I, et al.
Distinct chromosomal imbalances in nonpolypoid and polypoid colorectal adenomas indicate different genetic pathways in the development of colorectal neoplasms.
Am J Pathol, 163(1) 2003, 287-94.
(PMID 12819033)
|
|
| CGH: 60
|
Tay ST, Leong SH, Yu K, Aggarwal A, Tan SY, Lee CH, Wong K, Visvanathan J, Lim D, et al.
A combined comparative genomic hybridization and expression microarray analysis of gastric cancer reveals novel molecular subtypes.
Cancer Res, 63(12) 2003, 3309-16.
(PMID 12810664)
|
|
| CGH: 9
|
Amiel A, Atzmon H, Klein Z, Kidron D, Gaber E, Vassilyev O, Shalom-Paz E, Fishman A, et al.
Application of comparative genomic hybridization technique for detection of chromosomal aberrations in benign cystic teratoma.
Cancer Genet Cytogenet, 144(1) 2003, 73-75.
(PMID 12810260)
|
|
| CGH: 25
|
Vajdic CM, Hutchins AM, Kricker A, Aitken JF, Armstrong BK, Hayward NK, et al.
Chromosomal gains and losses in ocular melanoma detected by comparative genomic hybridization in an Australian population-based study.
Cancer Genet Cytogenet, 144(1) 2003, 12-17.
(PMID 12810250)
|
|
| CGH: 7
|
Rajcan-Separovic E, Maguire J, Loukianova T, Nisha M, and Kalousek D.
Loss of 1p and 7p in radiation-induced meningiomas identified by comparative genomic hybridization.
Cancer Genet Cytogenet, 144(1) 2003, 6-11.
(PMID 12810249)
|
|
| CGH: 83
|
Schmidt-Kittler O, Ragg T, Daskalakis A, Granzow M, Ahr A, Blankenstein TJ, et al.
From latent disseminated cells to overt metastasis: genetic analysis of systemic breast cancer progression.
Proc Natl Acad Sci U S A, 100(13) 2003, 7737-42.
(PMID 12808139)
|
|
| CGH: 40
|
van Dekken H, Alers JC, Damen IA, Vissers KJ, Krijtenburg PJ, Hoedemaeker RF, et al.
Genetic evaluation of localized prostate cancer in a cohort of forty patients: gain of distal 8q discriminates between progressors and nonprogressors.
Lab Invest, 83(6) 2003, 789-96.
(PMID 12808114)
|
|
| CGH: 8
|
Boonstra R, Koning A, Mastik M, van den Berg A, and Poppema S.
Analysis of chromosomal copy number changes and oncoprotein expression in primary central nervous system lymphomas: frequent loss of chromosome arm 6q.
Virchows Arch, 443(2) 2003, 164-69.
(PMID 12802586)
|
|
| CGH: 33
banding: 6 |
Karhu R, Tobin G, Thunberg U, Vilpo L, Sundstrom C, Knuutila S, Rosenquist R, et al.
More extensive genetic alterations in unmutated than in hypermutated cases of chronic lymphocytic leukemia.
Genes Chromosomes Cancer, 37(4) 2003, 417-20.
(PMID 12800154)
|
|
| CGH: 53
|
Alcock HE, Stephenson TJ, Royds JA, and Hammond DW.
Analysis of colorectal tumor progression by microdissection and comparative genomic hybridization.
Genes Chromosomes Cancer, 37(4) 2003, 369-80.
(PMID 12800148)
|
|
| CGH: 10
banding: 10 |
Gribble SM, Reid AG, Roberts I, Grace C, Green AR, and Nacheva EP.
Genomic imbalances in CML blast crisis: 8q24.12-q24.13 segment identified as a common region of over-representation.
Genes Chromosomes Cancer, 37(4) 2003, 346-58.
(PMID 12800146)
|
|
| CGH: 25
|
Varis A, van Rees B, Weterman M, Ristimaki A, Offerhaus J, and Knuutila S.
DNA copy number changes in young gastric cancer patients with special reference to chromosome 19.
Br J Cancer, 88(12) 2003, 1914-19.
(PMID 12799636)
|
|
| CGH: 20
|
Hu J, Khanna V, Jones MW, and Surti U.
Comparative study of primary and recurrent ovarian serous carcinomas: comparative genomic hybridization analysis with a potential application for prognosis.
Gynecol Oncol, 89(3) 2003, 369-75.
(PMID 12798697)
|
|
| CGH: 46
|
Junker K, Sanger J, Schmidt A, Hindermann W, Presselt N, Helfritzsch H, et al.
Genetic characterization of lung metastases in renal cell carcinoma.
Oncol Rep, 10(4) 2003, 1035-38.
(PMID 12792766)
|
|
| CGH: 184
|
Junker K, Weirich G, Amin MB, Moravek P, Hindermann W, and Schubert J.
Genetic subtyping of renal cell carcinoma by comparative genomic hybridization.
Recent Results Cancer Res, 162 2003, 169-75.
(PMID 12790331)
|
|
| CGH: 3
|
Wharton SB, Wardle C, Ironside JW, Wallace WH, Royds JA, and Hammond DW.
Comparative genomic hybridization and pathological findings in atypical teratoid/rhabdoid tumour of the central nervous system.
Neuropathol Appl Neurobiol, 29(3) 2003, 254-61.
(PMID 12787322)
|
|
| CGH: 37
|
Amiel A, Biton I, Yukla M, Gaber E, Fejgin MD, and Lishner M.
The effect of chlorambucil treatment on cytogenetic parameters in chronic lymphocytic leukemia patients.
Cancer Genet Cytogenet, 143(2) 2003, 113-19.
(PMID 12781444)
|
|
| CGH: 66
|
Blegen H, Will JS, Ghadimi BM, Nash HP, Zetterberg A, Auer G, et al.
DNA amplifications and aneuploidy, high proliferative activity and impaired cell cycle control characterize breast carcinomas with poor prognosis.
Anal Cell Pathol, 25(3) 2003, 103-14.
(PMID 12775914)
|
|
| CGH: 2
banding: 2 |
Knutsen T, Pack S, Petropavlovskaja M, Padilla-Nash H, Knight C, Mickley LA, Ried T, et al.
Cytogenetic, spectral karyotyping, fluorescence in situ hybridization, and comparative genomic hybridization characterization of two new secondary leukemia cell lines with 5q deletions, and . . .
Genes Chromosomes Cancer, 37(3) 2003, 270-81.
(PMID 12759925)
|
|
| CGH: 10
banding: 10 |
Pavlovich CP, Padilla-Nash H, Wangsa D, Nickerson ML, Matrosova V, Linehan WM, et al.
Patterns of aneuploidy in stage IV clear cell renal cell carcinoma revealed by comparative genomic hybridization and spectral karyotyping.
Genes Chromosomes Cancer, 37(3) 2003, 252-60.
(PMID 12759923)
|
|
| CGH: 92
|
Kristensen TD, Wesenberg F, Jonsson OG, Carlsen NT, Forestier E, Kirchhoff M, et al.
High-resolution comparative genomic hybridisation yields a high detection rate of chromosomal aberrations in childhood acute lymphoblastic leukaemia.
Eur J Haematol, 70(6) 2003, 363-72.
(PMID 12756018)
|
|
| CGH: 85
|
Afonso S, Santamaria I, Guinsburg ME, Gomez AO, Miranda JL, Jofre R, Menarguez J, et al.
Chromosomal aberrations, the consequence of refractory hyperparathyroidism: its relationship with biochemical parameters.
Kidney Int Suppl, (85) 2003, S32-8.
(PMID 12753262)
|
|
| CGH: 2
|
Schwerer MJ, Hemmer J, Kraft K, Maier H, Moller P, and Barth TF.
Endoreduplication in conjunction with tumor progression in an aneuploid laryngeal squamous cell carcinoma.
Virchows Arch, 443(1) 2003, 98-103.
(PMID 12750885)
|
|
| CGH: 50
|
Ghadimi BM, Grade M, Liersch T, Langer C, Siemer A, Fuzesi L, et al.
Gain of chromosome 8q23-24 is a predictive marker for lymph node positivity in colorectal cancer.
Clin Cancer Res, 9(5) 2003, 1808-14.
(PMID 12738738)
|
|
| CGH: 11
|
Ariza Cobos M, Llorente Pendas JL, Alvarez Marcos C, Baragano Rio L, et al.
[Genetic alterations in sinonasal adenocarcinoma in wood workers studies with comparative genomic hybridization].
Acta Otorrinolaringol Esp, 54(1) 2003, 23-30.
(PMID 12733317)
|
|
| CGH: 10
|
Miura D, Wada N, Chin K, Magrane GG, Wong M, Duh QY, and Clark OH.
Anaplastic thyroid cancer: cytogenetic patterns by comparative genomic hybridization.
Thyroid, 13(3) 2003, 283-90.
(PMID 12729478)
|
|
| CGH: 28
|
Penzel R, Hoegel J, Schmitz W, Blaeker H, Morresi-Hauf A, Aulmann S, Hecker E, et al.
Clusters of chromosomal imbalances in thymic epithelial tumours are associated with the WHO classification and the staging system according to Masaoka.
Int J Cancer, 105(4) 2003, 494-98.
(PMID 12712440)
|
|
| CGH: 2
|
Scheil S, Hagen S, Bruderlein S, Leuschner I, Behnisch W, and Moller P.
Two novel in vitro human hepatoblastoma models, HepU1 and HepU2, are highly characteristic of fetal-embryonal differentiation in hepatoblastoma.
Int J Cancer, 105(3) 2003, 347-52.
(PMID 12704668)
|
|
| CGH: 8
|
Amiel A, Kaufman Z, Goldstein E, Bruchim RB, Kidron D, Gaber E, et al.
Application of comparative genomic hybridization in search for genetic aberrations in fibroadenomas of the breast.
Cancer Genet Cytogenet, 142(2) 2003, 145-48.
(PMID 12699893)
|
|
| CGH: 58
|
Kim GJ, Cho SJ, Won NH, Sung JM, Kim H, Chun YH, and Park SH.
Genomic imbalances in Korean hepatocellular carcinoma.
Cancer Genet Cytogenet, 142(2) 2003, 129-33.
(PMID 12699889)
|
|
| CGH: 10
banding: 10 |
Weise A, Liehr T, Efferth T, Kuechler A, and Gebhart E.
Comparative M-FISH and CGH analyses in sensitive and drug-resistant human T-cell acute leukemia cell lines.
Cytogenet Genome Res, 98(2-3) 2002, 118-25.
(PMID 12697993)
|
|
| CGH: 23
aCGH: 5
|
Mao X, Orchard G, Lillington DM, Russell-Jones R, Young BD, and Whittaker S.
Genetic alterations in primary cutaneous CD30+ anaplastic large cell lymphoma.
Genes Chromosomes Cancer, 37(2) 2003, 176-85.
(PMID 12696066)
|
|
| CGH: 11
|
Ullmann R, Bongiovanni M, Halbwedl I, Petzmann S, Gogg-Kammerer M, Sapino A, et al.
Bronchiolar columnar cell dysplasia--genetic analysis of a novel preneoplastic lesion of peripheral lung.
Virchows Arch, 442(5) 2003, 429-36.
(PMID 12684770)
|
|
| CGH: 38
|
Marsh DJ, Theodosopoulos G, Martin-Schulte K, Richardson AL, Philips J, Roher HD, et al.
Genome-wide copy number imbalances identified in familial and sporadic medullary thyroid carcinoma.
J Clin Endocrinol Metab, 88(4) 2003, 1866-72.
(PMID 12679485)
|
|
| CGH: 7
|
van Dekken H, Wink J, Alers JC, de Man RA, IJzermans JN, and Zondervan PE.
Genetic evaluation of the dysplasia-carcinoma sequence in chronic viral liver disease: a detailed analysis of two cases and a review of the literature.
Acta Histochem, 105(1) 2003, 29-41.
(PMID 12666986)
|
|
| CGH: 30
|
Hirose Y, Aldape KD, Chang S, Lamborn K, Berger MS, and Feuerstein BG.
Grade II astrocytomas are subgrouped by chromosome aberrations.
Cancer Genet Cytogenet, 142(1) 2003, 1-7.
(PMID 12660025)
|
|
| CGH: 4
|
Hidalgo A, Monroy A, Arana RM, Taja L, Vazquez G, and Salcedo M.
Chromosomal imbalances in four new uterine cervix carcinoma derived cell lines.
BMC Cancer, 3 2003, 8.
(PMID 12659655)
|
|
| CGH: 4
|
Gellrich S, Wilks A, Lukowsky A, Wernicke M, Muller A, Marcus Muche J, Fischer T, et al.
T cell receptor-gamma gene analysis of CD30+ large atypical individual cells in CD30+ large primary cutaneous T cell lymphomas.
J Invest Dermatol, 120(4) 2003, 670-75.
(PMID 12648233)
|
|
| CGH: 15
|
Stallings RL, Howard J, Dunlop A, Mullarkey M, McDermott M, Breatnach F, et al.
Are gains of chromosomal regions 7q and 11p important abnormalities in neuroblastoma?
Cancer Genet Cytogenet, 140(2) 2003, 133-37.
(PMID 12645651)
|
|
| CGH: 18
|
Coindre JM, Mariani O, Chibon F, Mairal A, De Saint Aubain Somerhausen N, et al.
Most malignant fibrous histiocytomas developed in the retroperitoneum are dedifferentiated liposarcomas: a review of 25 cases initially diagnosed as malignant fibrous . . .
Mod Pathol, 16(3) 2003, 256-62.
(PMID 12640106)
|
|
| CGH: 22
|
Jee KJ, Gong G, Ahn SH, Park JM, and Knuutila S.
Gain in 1q is a common abnormality in phyllodes tumours of the breast.
Anal Cell Pathol, 25(2) 2003, 89-93.
(PMID 12632018)
|
|
| CGH: 1
|
Bernard MH, Sidhu S, Berger N, Peix JL, Marsh DJ, Robinson BG, Gaston V, Le Bouc Y, et al.
A case report in favor of a multistep adrenocortical tumorigenesis.
J Clin Endocrinol Metab, 88(3) 2003, 998-1001.
(PMID 12629075)
|
|
| CGH: 16
aCGH: 16
|
Wessendorf S, Schwaenen C, Kohlhammer H, Kienle D, Wrobel G, Barth TF, Nessling M, et al.
Hidden gene amplifications in aggressive B-cell non-Hodgkin lymphomas detected by microarray-based comparative genomic hybridization.
Oncogene, 22(9) 2003, 1425-29.
(PMID 12618769)
|
|
| CGH: 1
|
Scolozzi P, Lombardi T, Maire G, Pedeutour F, and Richter M.
Infiltrating intramuscular lipoma of the temporal muscle. A case report with molecular cytogenetic analysis.
Oral Oncol, 39(3) 2003, 316-22.
(PMID 12618207)
|
|
| CGH: 2
|
Takata M, Maruo K, Kageshita T, Ikeda S, Ono T, Shirasaki F, Takehara K, et al.
Two cases of unusual acral melanocytic tumors: illustration of molecular cytogenetics as a diagnostic tool.
Hum Pathol, 34(1) 2003, 89-92.
(PMID 12605371)
|
|
| CGH: 32
|
Wong MP, Fung LF, Wang E, Chow WS, Chiu SW, Lam WK, Ho KK, Ma ES, Wan TS, et al.
Chromosomal aberrations of primary lung adenocarcinomas in nonsmokers.
Cancer, 97(5) 2003, 1263-70.
(PMID 12599234)
|
|
| CGH: 20
aCGH: 20
|
Paris PL, Albertson DG, Alers JC, Andaya A, Carroll P, Fridlyand J, Jain AN, et al.
High-resolution analysis of paraffin-embedded and formalin-fixed prostate tumors using comparative genomic hybridization to genomic microarrays.
Am J Pathol, 162(3) 2003, 763-70.
(PMID 12598311)
|
|
| CGH: 16
|
Langer C, Gunawan B, Schuler P, Huber W, Fuzesi L, and Becker H.
Prognostic factors influencing surgical management and outcome of gastrointestinal stromal tumours.
Br J Surg, 90(3) 2003, 332-39.
(PMID 12594669)
|
|
| CGH: 118
|
Mattfeldt T, Wolter H, Trijic D, Gottfried HW, and Kestler HA.
Chromosomal regions in prostatic carcinomas studied by comparative genomic hybridization, hierarchical cluster analysis and self-organizing feature maps.
Anal Cell Pathol, 24(4-5) 2002, 167-79.
(PMID 12590153)
|
|
| CGH: 109
|
Chibon F, Mariani O, Mairal A, Derre J, Coindre JM, Terrier P, Lagace R, Sastre X, et al.
The use of clustering software for the classification of comparative genomic hybridization data. an analysis of 109 malignant fibrous histiocytomas.
Cancer Genet Cytogenet, 141(1) 2003, 75-78.
(PMID 12581902)
|
|
| CGH: 27
|
Schleiermacher G, Janoueix-Lerosey I, Combaret V, Derre J, Couturier J, Aurias A, et al.
Combined 24-color karyotyping and comparative genomic hybridization analysis indicates predominant rearrangements of early replicating chromosome regions in neuroblastoma.
Cancer Genet Cytogenet, 141(1) 2003, 32-42.
(PMID 12581896)
|
|
| CGH: 8
|
Kellner U, Jacobsen A, Kellner A, Mantke R, Roessner A, and Rocken C.
Comparative genomic hybridization. Synchronous occurrence of focal nodular hyperplasia and hepatocellular carcinoma in the same liver is not based on common chromosomal . . .
Am J Clin Pathol, 119(2) 2003, 265-71.
(PMID 12579998)
|
|
| CGH: 25
|
Ng IO, Guan XY, Poon RT, Fan ST, and Lee JM.
Determination of the molecular relationship between multiple tumour nodules in hepatocellular carcinoma differentiates multicentric origin from intrahepatic metastasis.
J Pathol, 199(3) 2003, 345-53.
(PMID 12579536)
|
|
| CGH: 16
|
Arslantas A, Artan S, Oner U, Durmaz R, Muslumanoglu H, Atasoy MA, Basaran N, et al.
Detection of chromosomal imbalances in spinal meningiomas by comparative genomic hybridization.
Neurol Med Chir (Tokyo), 43(1) 2003, 12-8; discussion 19.
(PMID 12568317)
|
|
| CGH: 45
|
Chu LW, Troncoso P, Johnston DA, and Liang JC.
Genetic markers useful for distinguishing between organ-confined and locally advanced prostate cancer.
Genes Chromosomes Cancer, 36(3) 2003, 303-12.
(PMID 12557230)
|
|
| CGH: 32
banding: 11 |
Roque L, Rodrigues R, Pinto A, Moura-Nunes V, and Soares J.
Chromosome imbalances in thyroid follicular neoplasms: a comparison between follicular adenomas and carcinomas.
Genes Chromosomes Cancer, 36(3) 2003, 292-302.
(PMID 12557229)
|
|
| CGH: 20
banding: 14 |
Mao X, Lillington DM, Czepulkowski B, Russell-Jones R, Young BD, et al.
Molecular cytogenetic characterization of Sezary syndrome.
Genes Chromosomes Cancer, 36(3) 2003, 250-60.
(PMID 12557225)
|
|
| CGH: 1
|
Yuan BZ, Zhou X, Zimonjic DB, Durkin ME, and Popescu NC.
Amplification and overexpression of the EMS 1 oncogene, a possible prognostic marker, in human hepatocellular carcinoma.
J Mol Diagn, 5(1) 2003, 48-53.
(PMID 12552080)
|
|
| CGH: 7
|
Gordon A, McManus A, Anderson J, Fisher C, Abe S, Nojima T, Pritchard-Jones K, et al.
Chromosomal imbalances in pleomorphic rhabdomyosarcomas and identification of the alveolar rhabdomyosarcoma-associated PAX3-FOXO1A fusion gene in one case.
Cancer Genet Cytogenet, 140(1) 2003, 73-77.
(PMID 12550764)
|
|
| CGH: 1
banding: 2 |
Matteucci C, La Starza R, Crescenzi B, Romoli S, Santoro A, Magrin S, Lauria F, et al.
Different mechanisms lead to a karyotypically identical t(20;21) in myelodysplastic syndrome and in acute myelocytic leukemia.
Cancer Genet Cytogenet, 140(1) 2003, 13-17.
(PMID 12550752)
|
|
| CGH: 4
|
Flordal E, Berglund M, Rosenquist R, Erlanson M, Enblad G, Roos G, Larsson C, et al.
Clonal development of a blastoid mantle cell lymphoma studied with comparative genomic hybridization.
Cancer Genet Cytogenet, 139(1) 2002, 38-43.
(PMID 12547156)
|
|
| CGH: 58
|
Chibon F, Mariani O, Derre J, Malinge S, Coindre JM, Guillou L, Lagace R, et al.
A subgroup of malignant fibrous histiocytomas is associated with genetic changes similar to those of well-differentiated liposarcomas.
Cancer Genet Cytogenet, 139(1) 2002, 24-29.
(PMID 12547153)
|
|
| CGH: 25
|
Hu J, Khanna V, Jones MM, and Surti U.
Genomic imbalances in ovarian borderline serous and mucinous tumors.
Cancer Genet Cytogenet, 139(1) 2002, 18-23.
(PMID 12547152)
|
|
| CGH: 9
|
Rienstein S, Adams EF, Pilzer D, Goldring AA, Goldman B, and Friedman E.
Comparative genomic hybridization analysis of craniopharyngiomas.
J Neurosurg, 98(1) 2003, 162-64.
(PMID 12546365)
|
|
| CGH: 24
|
Gogusev J, Murakami I, Doussau M, Telvi L, Stojkoski A, Lesavre P, et al.
Molecular cytogenetic aberrations in autosomal dominant polycystic kidney disease tissue.
J Am Soc Nephrol, 14(2) 2003, 359-66.
(PMID 12538736)
|
|
| CGH: 54
|
Weiss MM, Kuipers EJ, Hermsen MA, van Grieken NC, Offerhaus J, Baak JP, Meuwissen SG, et al.
Barretts adenocarcinomas resemble adenocarcinomas of the gastric cardia in terms of chromosomal copy number changes, but relate to squamous cell carcinomas of the distal oesophagus with . . .
J Pathol, 199(2) 2003, 157-65.
(PMID 12533828)
|
|
| CGH: 28
|
Jones C, Merrett S, Thomas VA, Barker TH, and Lakhani SR.
Comparative genomic hybridization analysis of bilateral hyperplasia of usual type of the breast.
J Pathol, 199(2) 2003, 152-56.
(PMID 12533827)
|
|
| CGH: 60
|
Ioannidis P, Mahaira L, Papadopoulou A, Teixeira MR, Heim S, Andersen JA, et al.
8q24 Copy number gains and expression of the c-myc mRNA stabilizing protein CRD-BP in primary breast carcinomas.
Int J Cancer, 104(1) 2003, 54-59.
(PMID 12532419)
|
|
| CGH: 15
banding: 28 |
Dalley CD, Neat MJ, Foot NJ, Burridge M, Byrne L, Amess JA, Rohatiner AZ, Lister A, et al.
Comparative genomic hybridization and multiplex-fluorescence in situ hybridization: an appraisal in elderly patients with acute myelogenous leukemia.
Hematol J, 3(6) 2002, 290-98.
(PMID 12522451)
|
|
| CGH: 17
|
Diep CB, Parada LA, Teixeira MR, Eknaes M, Nesland JM, Johansson B, et al.
Genetic profiling of colorectal cancer liver metastases by combined comparative genomic hybridization and G-banding analysis.
Genes Chromosomes Cancer, 36(2) 2003, 189-97.
(PMID 12508247)
|
|
| CGH: 14
|
van Dijk M, Sprenger S, Rombout P, Marres H, Kaanders J, Jeuken J, et al.
Distinct chromosomal aberrations in sinonasal mucosal melanoma as detected by comparative genomic hybridization.
Genes Chromosomes Cancer, 36(2) 2003, 151-58.
(PMID 12508243)
|
|
| CGH: 59
|
Tomioka N, Kobayashi H, Kageyama H, Ohira M, Nakamura Y, Sasaki F, Todo S, et al.
Chromosomes that show partial loss or gain in near-diploid tumors coincide with chromosomes that show whole loss or gain in near-triploid tumors: evidence suggesting the involvement of the . . .
Genes Chromosomes Cancer, 36(2) 2003, 139-50.
(PMID 12508242)
|
|
| CGH: 24
|
Lillington DM, Kingston JE, Coen PG, Price E, Hungerford J, Domizio P, Young BD, et al.
Comparative genomic hybridization of 49 primary retinoblastoma tumors identifies chromosomal regions associated with histopathology, progression, and patient outcome.
Genes Chromosomes Cancer, 36(2) 2003, 121-28.
(PMID 12508240)
|
|
| CGH: 1
banding: 1 |
Zuber MA, Krupp W, Holland H, and Froster UG.
Characterization of chromosomal aberrations in a case of glioblastoma multiforme combining cytogenetic and molecular cytogenetic techniques.
Cancer Genet Cytogenet, 138(2) 2002, 111-15.
(PMID 12505254)
|
|
| CGH: 32
|
Inda MM, Fan X, Munoz J, Perot C, Fauvet D, Danglot G, Palacio A, Madero P, Zazpe I, et al.
Chromosomal abnormalities in human glioblastomas: gain in chromosome 7p correlating with loss in chromosome 10q.
Mol Carcinog, 36(1) 2003, 6-14.
(PMID 12503074)
|
|
| CGH: 2
|
Heimberger AB, Wiltshire RN, Bronec R, McLendon RE, and Cummings TJ.
Biphasic malignant meningioma: a comparative genomic hybridization study.
Clin Neuropathol, 21(6) 2002, 258-64.
(PMID 12489674)
|
|
| CGH: 5
|
Sieber OM, Heinimann K, Gorman P, Lamlum H, Crabtree M, Simpson CA, Davies D, et al.
Analysis of chromosomal instability in human colorectal adenomas with two mutational hits at APC.
Proc Natl Acad Sci U S A, 99(26) 2002, 16910-15.
(PMID 12486240)
|
|
| CGH: 90
|
Clausen OP, Beigi M, Bolund L, Kolvraa S, Gjersvik PJ, Mork G, et al.
Keratoacanthomas frequently show chromosomal aberrations as assessed by comparative genomic hybridization.
J Invest Dermatol, 119(6) 2002, 1367-72.
(PMID 12485441)
|
|
| CGH: 9
|
Swartz MA, Karth J, Schneider DT, Rodriguez R, Beckwith JB, and Perlman EJ.
Renal medullary carcinoma: clinical, pathologic, immunohistochemical, and genetic analysis with pathogenetic implications.
Urology, 60(6) 2002, 1083-89.
(PMID 12475675)
|
|
| CGH: 20
|
Obermann EC, Junker K, Stoehr R, Dietmaier W, Zaak D, Schubert J, Hofstaedter F, et al.
Frequent genetic alterations in flat urothelial hyperplasias and concomitant papillary bladder cancer as detected by CGH, LOH, and FISH analyses.
J Pathol, 199(1) 2003, 50-57.
(PMID 12474226)
|
|
| CGH: 34
|
Climent J, Martinez-Climent JA, Blesa D, Garcia-Barchino MJ, Saez R, et al.
Genomic loss of 18p predicts an adverse clinical outcome in patients with high-risk breast cancer.
Clin Cancer Res, 8(12) 2002, 3863-69.
(PMID 12473601)
|
|
| CGH: 1
|
Kawauchi S, Hayatsu Y, Takahashi M, Furuya T, Oga A, Niwa S, et al.
Spindle-cell ameloblastic carcinoma: A case report with immunohistochemical, ultrastructural, and comparative genomic hybridization analyses.
Oncol Rep, 10(1) 2003, 31-34.
(PMID 12469140)
|
|
| CGH: 42
|
Dyer S, Prebble E, Davison V, Davies P, Ramani P, Ellison D, et al.
Genomic imbalances in pediatric intracranial ependymomas define clinically relevant groups.
Am J Pathol, 161(6) 2002, 2133-41.
(PMID 12466129)
|
|
| CGH: 6
|
Fujii H, Anbazhagan R, Bornman DM, Garrett ES, Perlman E, and Gabrielson E.
Mucinous cancers have fewer genomic alterations than more common classes of breast cancer.
Breast Cancer Res Treat, 76(3) 2002, 255-60.
(PMID 12462386)
|
|
| CGH: 70
|
Wessels LF, van Welsem T, Hart AA, vant Veer LJ, Reinders MJ, et al.
Molecular classification of breast carcinomas by comparative genomic hybridization: a specific somatic genetic profile for BRCA1 tumors.
Cancer Res, 62(23) 2002, 7110-17.
(PMID 12460933)
|
|
| CGH: 124
|
Viardot A, Moller P, Hogel J, Werner K, Mechtersheimer G, Ho AD, Ott G, Barth TF, et al.
Clinicopathologic correlations of genomic gains and losses in follicular lymphoma.
J Clin Oncol, 20(23) 2002, 4523-30.
(PMID 12454108)
|
|
| CGH: 39
|
Aubele M, Auer G, Braselmann H, Nahrig J, Zitzelsberger H, Quintanilla-Martinez L, et al.
Chromosomal imbalances are associated with metastasis-free survival in breast cancer patients.
Anal Cell Pathol, 24(2-3) 2002, 77-87.
(PMID 12446957)
|
|
| CGH: 40
|
Hislop RG, Pratt N, Stocks SC, Steel CM, Sales M, Goudie D, Robertson A, et al.
Karyotypic aberrations of chromosomes 16 and 17 are related to survival in patients with breast cancer.
Br J Surg, 89(12) 2002, 1581-86.
(PMID 12445070)
|
|
| CGH: 123
|
Moore LE, Smith AH, Eng C, Kalman D, DeVries S, Bhargava V, Chew K, Moore Dn, et al.
Arsenic-related chromosomal alterations in bladder cancer.
J Natl Cancer Inst, 94(22) 2002, 1688-96.
(PMID 12441324)
|
|
| CGH: 30
|
Croft J, Parry EM, Jenkins GJ, Doak SH, Baxter JN, Griffiths AP, Brown TH, et al.
Analysis of the premalignant stages of Barretts oesophagus through to adenocarcinoma by comparative genomic hybridization.
Eur J Gastroenterol Hepatol, 14(11) 2002, 1179-86.
(PMID 12439111)
|
|
| CGH: 8
|
Shing DC, Morley-Jacob CA, Roberts I, Nacheva E, and Coleman N.
Ewings tumour: novel recurrent chromosomal abnormalities demonstrated by molecular cytogenetic analysis of seven cell lines and one primary culture.
Cytogenet Genome Res, 97(1-2) 2002, 20-27.
(PMID 12438733)
|
|
| CGH: 22
banding: 22 |
Micci F, Teixeira MR, Bjerkehagen B, and Heim S.
Characterization of supernumerary rings and giant marker chromosomes in well-differentiated lipomatous tumors by a combination of G-banding, CGH, M-FISH, and chromosome- and locus-specific . . .
Cytogenet Genome Res, 97(1-2) 2002, 13-19.
(PMID 12438732)
|
|
| CGH: 30
|
Hungermann D, Roeser K, Buerger H, Jakel T, Loning T, and Herbst H.
Relative paucity of gross genetic alterations in myoepitheliomas and myoepithelial carcinomas of salivary glands.
J Pathol, 198(4) 2002, 487-94.
(PMID 12434418)
|
|
| CGH: 71
|
Singh B, Wreesmann VB, Pfister D, Poluri A, Shaha AR, Kraus D, Shah JP, et al.
Chromosomal aberrations in patients with head and neck squamous cell carcinoma do not vary based on severity of tobacco/alcohol exposure.
BMC Genet, 3 2002, 22.
(PMID 12431278)
|
|
| CGH: 31
|
Leung TH, Wong N, Lai PB, Chan A, To KF, Liew CT, Lau WY, and Johnson PJ.
Identification of four distinct regions of allelic imbalances on chromosome 1 by the combined comparative genomic hybridization and microsatellite analysis on hepatocellular . . .
Mod Pathol, 15(11) 2002, 1213-20.
(PMID 12429801)
|
|
| CGH: 6
|
Rakozy C, Schmahl GE, Bogner S, and Storkel S.
Low-grade tubular-mucinous renal neoplasms: morphologic, immunohistochemical, and genetic features.
Mod Pathol, 15(11) 2002, 1162-71.
(PMID 12429795)
|
|
| CGH: 3
|
Musti M, Cavone D, Aalto Y, Scattone A, Serio G, and Knuutila S.
A cluster of familial malignant mesothelioma with del(9p) as the sole chromosomal anomaly.
Cancer Genet Cytogenet, 138(1) 2002, 73-76.
(PMID 12419589)
|
|
| CGH: 25
|
Wei F, Ni J, Wu SS, Liu H, Xu X, Han YL, Cai Y, Zhang JW, Chen XJ, Pang H, Lu N, et al.
Cytogenetic studies of esophageal squamous cell carcinomas in the northern Chinese population by comparative genomic hybridization.
Cancer Genet Cytogenet, 138(1) 2002, 38-43.
(PMID 12419583)
|
|
| CGH: 63
|
Burton EC, Lamborn KR, Feuerstein BG, Prados M, Scott J, Forsyth P, Passe S, et al.
Genetic aberrations defined by comparative genomic hybridization distinguish long-term from typical survivors of glioblastoma.
Cancer Res, 62(21) 2002, 6205-10.
(PMID 12414648)
|
|
| CGH: 17
|
Franke S, Wlodarska I, Maes B, Vandenberghe P, Achten R, Hagemeijer A, et al.
Comparative genomic hybridization pattern distinguishes T-cell/histiocyte-rich B-cell lymphoma from nodular lymphocyte predominance Hodgkins lymphoma.
Am J Pathol, 161(5) 2002, 1861-67.
(PMID 12414532)
|
|
| CGH: 41
|
Zettl A, Ott G, Makulik A, Katzenberger T, Starostik P, Eichler T, Puppe B, Bentz M, et al.
Chromosomal gains at 9q characterize enteropathy-type T-cell lymphoma.
Am J Pathol, 161(5) 2002, 1635-45.
(PMID 12414511)
|
|
| CGH: 42
|
Wreesmann VB, Ghossein RA, Patel SG, Harris CP, Schnaser EA, Shaha AR, Tuttle RM, et al.
Genome-wide appraisal of thyroid cancer progression.
Am J Pathol, 161(5) 2002, 1549-56.
(PMID 12414503)
|
|
| CGH: 13
|
Gijtenbeek JM, Jacobs B, Sprenger SH, Eleveld MJ, van Kessel AG, Kros JM, Sciot R, et al.
Analysis of von hippel-lindau mutations with comparative genomic hybridization in sporadic and hereditary hemangioblastomas: possible genetic heterogeneity.
J Neurosurg, 97(4) 2002, 977-82.
(PMID 12405390)
|
|
| CGH: 47
|
Ozaki T, Schaefer KL, Wai D, Buerger H, Flege S, Lindner N, Kevric M, Diallo R, et al.
Genetic imbalances revealed by comparative genomic hybridization in osteosarcomas.
Int J Cancer, 102(4) 2002, 355-65.
(PMID 12402305)
|
|
| CGH: 13
|
Wong N, Li L, Tsang K, Lai PB, To KF, and Johnson PJ.
Frequent loss of chromosome 3p and hypermethylation of RASSF1A in cholangiocarcinoma.
J Hepatol, 37(5) 2002, 633-39.
(PMID 12399230)
|
|
| CGH: 6
|
Ashman JN, Brigham J, Cowen ME, Bahia H, Greenman J, Lind M, et al.
Chromosomal alterations in small cell lung cancer revealed by multicolour fluorescence in situ hybridization.
Int J Cancer, 102(3) 2002, 230-36.
(PMID 12397641)
|
|
| CGH: 20
|
Mahlamaki EH, Barlund M, Tanner M, Gorunova L, Hoglund M, Karhu R, et al.
Frequent amplification of 8q24, 11q, 17q, and 20q-specific genes in pancreatic cancer.
Genes Chromosomes Cancer, 35(4) 2002, 353-58.
(PMID 12378529)
|
|
| CGH: 16
|
Ozaki T, Schaefer KL, Wai D, Yokoyama R, Ahrens S, Diallo R, Hasegawa T, Shimoda T, et al.
Population-based genetic alterations in Ewings tumors from Japanese and European Caucasian patients.
Ann Oncol, 13(10) 2002, 1656-64.
(PMID 12377657)
|
|
| CGH: 9
|
Kasahara K, Taguchi T, Yamasaki I, Kamada M, Yuri K, and Shuin T.
Detection of genetic alterations in advanced prostate cancer by comparative genomic hybridization.
Cancer Genet Cytogenet, 137(1) 2002, 59-63.
(PMID 12377415)
|
|
| CGH: 10
banding: 8 |
Rigola MA, Casadevall C, Bernues M, Caballin MR, Fuster C, Gelabert A, Egozcue J, et al.
Analysis of kidney tumors by comparative genomic hybridization and conventional cytogenetics.
Cancer Genet Cytogenet, 137(1) 2002, 49-53.
(PMID 12377413)
|
|
| CGH: 21
|
Beheshti B, Vukovic B, Marrano P, Squire JA, and Park PC.
Resolution of genotypic heterogeneity in prostate tumors using polymerase chain reaction and comparative genomic hybridization on microdissected carcinoma and prostatic intraepithelial . . .
Cancer Genet Cytogenet, 137(1) 2002, 15-22.
(PMID 12377408)
|
|
| CGH: 22
|
Fan X, Aalto Y, Sanko SG, Knuutila S, Klatzmann D, and Castresana JS.
Genetic profile, PTEN mutation and therapeutic role of PTEN in glioblastomas.
Int J Oncol, 21(5) 2002, 1141-50.
(PMID 12370766)
|
|
| CGH: 9
|
Dwight T, Nelson AE, Theodosopoulos G, Richardson AL, Learoyd DL, Philips J, et al.
Independent genetic events associated with the development of multiple parathyroid tumors in patients with primary hyperparathyroidism.
Am J Pathol, 161(4) 2002, 1299-306.
(PMID 12368203)
|
|
| CGH: 30
|
Bastian BC, Xiong J, Frieden IJ, Williams ML, Chou P, Busam K, Pinkel D, et al.
Genetic changes in neoplasms arising in congenital melanocytic nevi: differences between nodular proliferations and melanomas.
Am J Pathol, 161(4) 2002, 1163-69.
(PMID 12368190)
|
|
| CGH: 41
|
Chujo M, Noguchi T, Miura T, Arinaga M, Uchida Y, and Tagawa Y.
Comparative genomic hybridization analysis detected frequent overrepresentation of chromosome 3q in squamous cell carcinoma of the lung.
Lung Cancer, 38(1) 2002, 23-29.
(PMID 12367789)
|
|
| CGH: 14
|
Morio T, Morimitsu Y, Hisaoka M, Makishima K, and Hashimoto H.
DNA copy number changes in carcinoma in pleomorphic adenoma of the salivary gland: a comparative genomic hybridization study.
Pathol Int, 52(8) 2002, 501-07.
(PMID 12366808)
|
|
| CGH: 28
|
Wada N, Duh QY, Miura D, Brunaud L, Wong MG, and Clark OH.
Chromosomal aberrations by comparative genomic hybridization in hurthle cell thyroid carcinomas are associated with tumor recurrence.
J Clin Endocrinol Metab, 87(10) 2002, 4595-601.
(PMID 12364440)
|
|
| CGH: 148
|
Hermsen M, Postma C, Baak J, Weiss M, Rapallo A, Sciutto A, Roemen G, Arends JW, et al.
Colorectal adenoma to carcinoma progression follows multiple pathways of chromosomal instability.
Gastroenterology, 123(4) 2002, 1109-19.
(PMID 12360473)
|
|
| CGH: 62
|
Wu CW, Chen GD, Fann CS, Lee AF, Chi CW, Liu JM, Weier U, and Chen JY.
Clinical implications of chromosomal abnormalities in gastric adenocarcinomas.
Genes Chromosomes Cancer, 35(3) 2002, 219-31.
(PMID 12353264)
|
|
| CGH: 3
|
Mhawech P, Kinkel K, Vlastos G, and Pelte MF.
Ovarian carcinomas in endometriosis: an immunohistochemical and comparative genomic hybridization study.
Int J Gynecol Pathol, 21(4) 2002, 401-06.
(PMID 12352189)
|
|
| CGH: 3
|
Toncheval DI, Atanassova SY, Gergov TD, Todorovska EG, Roeva IG, Georgiev TH, et al.
Genetic changes in uroepithelial tumors of patients with Balkan endemic nephropathy.
J Nephrol, 15(4) 2002, 387-93.
(PMID 12243368)
|
|
| CGH: 23
|
Grill J, Avet-Loiseau H, Lellouch-Tubiana A, Sevenet N, Terrier-Lacombe MJ, Venuat AM, et al.
Comparative genomic hybridization detects specific cytogenetic abnormalities in pediatric ependymomas and choroid plexus papillomas.
Cancer Genet Cytogenet, 136(2) 2002, 121-25.
(PMID 12237235)
|
|
| CGH: 24
|
Koga T, Iwasaki H, Ishiguro M, Matsuzaki A, and Kikuchi M.
Losses in chromosomes 17, 19, and 22q in neurofibromatosis type 1 and sporadic neurofibromas: a comparative genomic hybridization analysis.
Cancer Genet Cytogenet, 136(2) 2002, 113-20.
(PMID 12237234)
|
|
| CGH: 25
|
Lillington DM, Goff LK, Kingston JE, Onadim Z, Price E, Domizio P, et al.
High level amplification of N-MYC is not associated with adverse histology or outcome in primary retinoblastoma tumours.
Br J Cancer, 87(7) 2002, 779-82.
(PMID 12232763)
|
|
| CGH: 24
|
Kros JM, Zheng P, Dinjens WN, and Alers JC.
Genetic aberrations in gliomatosis cerebri support monoclonal tumorigenesis.
J Neuropathol Exp Neurol, 61(9) 2002, 806-14.
(PMID 12230327)
|
|
| CGH: 1
|
Nicolo M, Nicolo G, and Zingirian M.
Pleomorphic adenocarcinoma of the ciliary epithelium: a clinicopathological, immunohistochemical, ultrastructural, DNA-ploidy and comparative genomic hybridization analysis of an unusual . . .
Eur J Ophthalmol, 12(4) 2002, 319-23.
(PMID 12220004)
|
|
| CGH: 20
|
Chan WY, Liu Y, Li CY, Ng EK, Chow JH, Li KK, and Chung SC.
Recurrent genomic aberrations in gastric carcinomas associated with Helicobacter pylori and Epstein-Barr virus.
Diagn Mol Pathol, 11(3) 2002, 127-34.
(PMID 12218450)
|
|
| CGH: 20
|
Mayr D, Kaltz-Wittmer C, Arbogast S, Amann G, Aust DE, and Diebold J.
Characteristic pattern of genetic aberrations in ovarian granulosa cell tumors.
Mod Pathol, 15(9) 2002, 951-57.
(PMID 12218213)
|
|
| CGH: 59
|
Bea S, Lopez-Guillermo A, Ribas M, Puig X, Pinyol M, Carrio A, Zamora L, Soler F, et al.
Genetic imbalances in progressed B-cell chronic lymphocytic leukemia and transformed large-cell lymphoma (Richters syndrome).
Am J Pathol, 161(3) 2002, 957-68.
(PMID 12213724)
|
|
| CGH: 12
|
Squire JA, Bayani J, Luk C, Unwin L, Tokunaga J, MacMillan C, Irish J, Brown D, et al.
Molecular cytogenetic analysis of head and neck squamous cell carcinoma: By comparative genomic hybridization, spectral karyotyping, and expression array analysis.
Head Neck, 24(9) 2002, 874-87.
(PMID 12211052)
|
|
| CGH: 59
|
Mao X, Lillington D, Scarisbrick JJ, Mitchell T, Czepulkowski B, Russell-Jones R, et al.
Molecular cytogenetic analysis of cutaneous T-cell lymphomas: identification of common genetic alterations in Sezary syndrome and mycosis fungoides.
Br J Dermatol, 147(3) 2002, 464-75.
(PMID 12207585)
|
|
| CGH: 55
|
Schulz WA, Elo JP, Florl AR, Pennanen S, Santourlidis S, Engers R, Buchardt M, et al.
Genomewide DNA hypomethylation is associated with alterations on chromosome 8 in prostate carcinoma.
Genes Chromosomes Cancer, 35(1) 2002, 58-65.
(PMID 12203790)
|
|
| CGH: 41
aCGH: 4
|
Mao X, Lillington D, Child F, Russell-Jones R, Young B, and Whittaker S.
Comparative genomic hybridization analysis of primary cutaneous B-cell lymphomas: identification of common genomic alterations in disease pathogenesis.
Genes Chromosomes Cancer, 35(2) 2002, 144-55.
(PMID 12203778)
|
|
| CGH: 14
|
Chen Y-J, Chen P-J, Lee M-C, Yeh S-H, Hsu M-T, and Lin C-H.
Chromosomal analysis of hepatic adenoma and focal nodular hyperplasia by comparative genomic hybridization.
Genes, chromosomes & cancer, 35(2) 2002, 138-43.
(PMID 12203777)
|
|
| CGH: 22
|
Cheung ST, Chen X, Guan XY, Wong SY, Tai LS, Ng IO, So S, and Fan ST.
Identify metastasis-associated genes in hepatocellular carcinoma through clonality delineation for multinodular tumor.
Cancer Res, 62(16) 2002, 4711-21.
(PMID 12183430)
|
|
| CGH: 14
|
Nagel H, Schulten HJ, Gunawan B, Brinck U, and Fuzesi L.
The potential value of comparative genomic hybridization analysis in effusion-and fine needle aspiration cytology.
Mod Pathol, 15(8) 2002, 818-25.
(PMID 12181266)
|
|
| CGH: 54
|
Berglund M, Enblad G, Flordal E, Lui WO, Backlin C, Thunberg U, Sundstrom C, Roos G, et al.
Chromosomal imbalances in diffuse large B-cell lymphoma detected by comparative genomic hybridization.
Mod Pathol, 15(8) 2002, 807-16.
(PMID 12181265)
|
|
| CGH: 48
|
Wolter H, Trijic D, Gottfried HW, and Mattfeldt T.
Chromosomal changes in incidental prostatic carcinomas detected by comparative genomic hybridization.
Eur Urol, 41(3) 2002, 328-34.
(PMID 12180237)
|
|
| CGH: 30
|
Umayahara K, Numa F, Inokuma A, Sueoka K, Kawasaki K, Hirakawa H, Emoto T, et al.
Genetic alterations related to lymph node metastasis and peritoneal dissemination in epithelial ovarian cancers.
Oncol Rep, 9(5) 2002, 1115-19.
(PMID 12168082)
|
|
| CGH: 27
|
Nishio JN, Iwasaki H, Ohjimi Y, Ishiguro M, Koga T, Isayama T, Naito M, et al.
Gain of Xq detected by comparative genomic hybridization in elastofibroma.
Int J Mol Med, 10(3) 2002, 277-80.
(PMID 12165800)
|
|
| CGH: 3
|
Riazimand SH, Brieger J, Jacob R, Welkoborsky HJ, and Mann WJ.
Analysis of cytogenetic aberrations in esthesioneuroblastomas by comparative genomic hybridization.
Cancer Genet Cytogenet, 136(1) 2002, 53-57.
(PMID 12165452)
|
|
| CGH: 20
|
Jaaskelainen K, Jee KJ, Leivo I, Saloniemi I, Knuutila S, and Heikinheimo K.
Cell proliferation and chromosomal changes in human ameloblastoma.
Cancer Genet Cytogenet, 136(1) 2002, 31-37.
(PMID 12165448)
|
|
| CGH: 25
|
Arslantas A, Artan S, Oner U, Durmaz R, Muslumanoglu H, Atasoy MA, Basaran N, et al.
Comparative genomic hybridization analysis of genomic alterations in benign, atypical and anaplastic meningiomas.
Acta Neurol Belg, 102(2) 2002, 53-62.
(PMID 12161900)
|
|
| CGH: 3
|
Nomdedeu JF, Lasa A, Ubeda J, Saglio G, Bellido M, Casas S, Carnicer MJ, Aventin A, et al.
Interstitial deletions at the long arm of chromosome 13 may be as common as monosomies in multiple myeloma. A genotypic study.
Haematologica, 87(8) 2002, 828-35.
(PMID 12161359)
|
|
| CGH: 22
|
Ell SR, Ashman JE, Stafford ND, and Greenman J.
Global genetic differences in squamous cell carcinoma of the head and neck.
Laryngoscope, 112(6) 2002, 1094-99.
(PMID 12160280)
|
|
| CGH: 47
|
Hauptmann S, Denkert C, Koch I, Petersen S, Schluns K, Reles A, Dietel M, et al.
Genetic alterations in epithelial ovarian tumors analyzed by comparative genomic hybridization.
Hum Pathol, 33(6) 2002, 632-41.
(PMID 12152163)
|
|
| CGH: 16
|
Thor AD, Eng C, Devries S, Paterakos M, Watkin WG, Edgerton S, Moore DHn, Etzell J, et al.
Invasive micropapillary carcinoma of the breast is associated with chromosome 8 abnormalities detected by comparative genomic hybridization.
Hum Pathol, 33(6) 2002, 628-31.
(PMID 12152162)
|
|
| CGH: 15
|
Bauer AJ, Cavalli LR, Rone JD, Francis GL, Burch HB, Tuttle RM, Ringel MD, et al.
Evaluation of adult papillary thyroid carcinomas by comparative genomic hybridization and microsatellite instability analysis.
Cancer Genet Cytogenet, 135(2) 2002, 182-86.
(PMID 12127404)
|
|
| CGH: 20
|
Kujawski M, Rydzanicz M, Sarlomo-Rikala M, Gabriel A, and Szyfter K.
Chromosome alterations reflect clonal evolution in squamous cell carcinoma of the larynx.
Med Sci Monit, 8(7) 2002, BR279-82.
(PMID 12118191)
|
|
| CGH: 5
|
Debiec-Rychter M, Pauwels P, Lasota J, Franke S, De Vos R, De Wever I, Hagemeijer A, et al.
Complex genetic alterations in gastrointestinal stromal tumors with autonomic nerve differentiation.
Mod Pathol, 15(7) 2002, 692-98.
(PMID 12118105)
|
|
| CGH: 72
|
Krismann M, Muller KM, Jaworska M, and Johnen G.
Molecular cytogenetic differences between histological subtypes of malignant mesotheliomas: DNA cytometry and comparative genomic hybridization of 90 cases.
J Pathol, 197(3) 2002, 363-71.
(PMID 12115883)
|
|
| CGH: 23
|
Actor B, Cobbers JM, Buschges R, Wolter M, Knobbe CB, Lichter P, Reifenberger G, et al.
Comprehensive analysis of genomic alterations in gliosarcoma and its two tissue components.
Genes Chromosomes Cancer, 34(4) 2002, 416-27.
(PMID 12112531)
|
|
| CGH: 3
|
Kros JM, Delwel EJ, de Jong TH, Tanghe HL, van Run PR, Vissers K, et al.
Desmoplastic infantile astrocytoma and ganglioglioma: a search for genomic characteristics.
Acta Neuropathol (Berl), 104(2) 2002, 144-48.
(PMID 12111357)
|
|
| CGH: 32
|
Sidhu S, Marsh DJ, Theodosopoulos G, Philips J, Bambach CP, Campbell P, Magarey CJ, et al.
Comparative genomic hybridization analysis of adrenocortical tumors.
J Clin Endocrinol Metab, 87(7) 2002, 3467-74.
(PMID 12107267)
|
|
| CGH: 4
|
Orntoft TF, Thykjaer T, Waldman FM, Wolf H, and Celis JE.
Genome-wide study of gene copy numbers, transcripts, and protein levels in pairs of non-invasive and invasive human transitional cell carcinomas.
Mol Cell Proteomics, 1(1) 2002, 37-45.
(PMID 12096139)
|
|
| CGH: 7
|
Murakami I, Gogusev J, Fournet JC, Glorion C, and Jaubert F.
Detection of molecular cytogenetic aberrations in langerhans cell histiocytosis of bone.
Hum Pathol, 33(5) 2002, 555-60.
(PMID 12094383)
|
|
| CGH: 23
|
Summersgill B, Thornton P, Atkinson S, Matutes E, Shipley J, Catovsky D, Houlston RS, et al.
Chromosomal imbalances in familial chronic lymphocytic leukaemia: a comparative genomic hybridisation analysis.
Leukemia, 16(7) 2002, 1229-32.
(PMID 12094247)
|
|
| CGH: 50
|
Koga T, Iwasaki H, Ishiguro M, Matsuzaki A, and Kikuchi M.
Frequent genomic imbalances in chromosomes 17, 19, and 22q in peripheral nerve sheath tumours detected by comparative genomic hybridization analysis.
J Pathol, 197(1) 2002, 98-107.
(PMID 12081210)
|
|
| CGH: 28
|
Steiner T, Junker K, Burkhardt F, Braunsdorf A, Janitzky V, and Schubert J.
Gain in chromosome 8q correlates with early progression in hormonal treated prostate cancer.
Eur Urol, 41(2) 2002, 167-71.
(PMID 12074404)
|
|
| CGH: 5
aCGH: 5
|
Rosenberg C, Geelen E, IJszenga MJ, Pearson P, Tanke HJ, Dinjens WN, et al.
Spectrum of genetic changes in gastro-esophageal cancer cell lines determined by an integrated molecular cytogenetic approach.
Cancer Genet Cytogenet, 135(1) 2002, 35-41.
(PMID 12072201)
|
|
| CGH: 7
|
Kurihara Y, Ghazizadeh M, Bo H, Shimizu H, Kawanami O, Moriyama Y, et al.
Genome-wide screening of laser capture microdissected gastric signet-ring cell carcinomas.
J Nippon Med Sch, 69(3) 2002, 235-42.
(PMID 12068314)
|
|
| CGH: 29
banding: 12 |
Bayani J, Brenton JD, Macgregor PF, Beheshti B, Albert M, Nallainathan D, et al.
Parallel analysis of sporadic primary ovarian carcinomas by spectral karyotyping, comparative genomic hybridization, and expression microarrays.
Cancer Res, 62(12) 2002, 3466-76.
(PMID 12067990)
|
|
| CGH: 47
|
Helfritzsch H, Junker K, Bartel M, and Scheele J.
Differentiation of positive autofluorescence bronchoscopy findings by comparative genomic hybridization.
Oncol Rep, 9(4) 2002, 697-701.
(PMID 12066195)
|
|
| CGH: 35
|
Harada T, Okita K, Shiraishi K, Kusano N, Furuya T, Oga A, Kawauchi S, Kondoh S, et al.
Detection of genetic alterations in pancreatic cancers by comparative genomic hybridization coupled with tissue microdissection and degenerate oligonucleotide primed polymerase chain . . .
Oncology, 62(3) 2002, 251-58.
(PMID 12065873)
|
|
| CGH: 2
|
Tsao SW, Wang X, Liu Y, Cheung YC, Feng H, Zheng Z, Wong N, Yuen PW, Lo AK, Wong YC, et al.
Establishment of two immortalized nasopharyngeal epithelial cell lines using SV40 large T and HPV16E6/E7 viral oncogenes.
Biochim Biophys Acta, 1590(1-3) 2002, 150-58.
(PMID 12063178)
|
|
| CGH: 22
|
Chang J, Kim NG, Piao Z, Park C, Park KS, Paik YK, Lee WJ, Kim BR, et al.
Assessment of chromosomal losses and gains in hepatocellular carcinoma.
Cancer Lett, 182(2) 2002, 193-202.
(PMID 12048165)
|
|
| CGH: 70
|
Zudaire I, Odero MD, Caballero C, Valenti C, Martinez-Penuela JM, Isola J, et al.
Genomic imbalances detected by comparative genomic hybridization are prognostic markers in invasive ductal breast carcinomas.
Histopathology, 40(6) 2002, 547-55.
(PMID 12047766)
|
|
| CGH: 3
banding: 2 |
Ojopi EP, Cavalli LR, Cavalieri LM, Squire JA, and Rogatto SR.
Comparative genomic hybridization analysis of benign and invasive male breast neoplasms.
Cancer Genet Cytogenet, 134(2) 2002, 123-26.
(PMID 12034524)
|
|
| CGH: 62
|
Yasui K, Arii S, Zhao C, Imoto I, Ueda M, Nagai H, Emi M, and Inazawa J.
TFDP1, CUL4A, and CDC16 identified as targets for amplification at 13q34 in hepatocellular carcinomas.
Hepatology, 35(6) 2002, 1476-84.
(PMID 12029633)
|
|
| CGH: 20
|
Jeuken JW, Sprenger SH, Gilhuis J, Teepen HL, Grotenhuis AJ, and Wesseling P.
Correlation between localization, age, and chromosomal imbalances in ependymal tumours as detected by CGH.
J Pathol, 197(2) 2002, 238-44.
(PMID 12015749)
|
|
| CGH: 71
|
Lung JC, Chu JS, Yu JC, Yue CT, Lo YL, Shen CY, and Wu CW.
Aberrant expression of cell-cycle regulator cyclin D1 in breast cancer is related to chromosomal genomic instability.
Genes Chromosomes Cancer, 34(3) 2002, 276-84.
(PMID 12007188)
|
|
| CGH: 40
|
Dellas A, Torhorst J, Schultheiss E, Mihatsch MJ, and Moch H.
DNA sequence losses on chromosomes 11p and 18q are associated with clinical outcome in lymph node-negative ductal breast cancer.
Clin Cancer Res, 8(5) 2002, 1210-16.
(PMID 12006540)
|
|
| CGH: 26
|
Tornillo L, Carafa V, Sauter G, Moch H, Minola E, Gambacorta M, Vecchione R, et al.
Chromosomal alterations in hepatocellular nodules by comparative genomic hybridization: high-grade dysplastic nodules represent early stages of hepatocellular carcinoma.
Lab Invest, 82(5) 2002, 547-53.
(PMID 12003995)
|
|
| CGH: 2
|
Xue WC, Guan XY, Ngan HY, Shen DH, Khoo US, and Cheung AN.
Malignant placental site trophoblastic tumor: a cytogenetic study using comparative genomic hybridization and chromosome in situ hybridization.
Cancer, 94(8) 2002, 2288-94.
(PMID 12001129)
|
|
| CGH: 5
|
Yin XL, Hui AB, Pang JC, Poon WS, and Ng HK.
Genome-wide survey for chromosomal imbalances in ganglioglioma using comparative genomic hybridization.
Cancer Genet Cytogenet, 134(1) 2002, 71-76.
(PMID 11996800)
|
|
| CGH: 19
|
Hemmer S, Wasenius VM, Haglund C, Zhu Y, Knuutila S, Franssila K, et al.
Alterations in the suppressor gene PPP2R1B in parathyroid hyperplasias and adenomas.
Cancer Genetics and Cytogenetics, 134(1) 2002, 13-17.
(PMID 11996789)
|
|
| CGH: 21
|
Popp S, Waltering S, Herbst C, Moll I, and Boukamp P.
UV-B-type mutations and chromosomal imbalances indicate common pathways for the development of Merkel and skin squamous cell carcinomas.
Int J Cancer, 99(3) 2002, 352-60.
(PMID 11992403)
|
|
| CGH: 4
|
Weil RJ, Vortmeyer AO, Zhuang Z, Pack SD, Theodore N, Erickson RK, et al.
Clinical and molecular analysis of disseminated hemangioblastomatosis of the central nervous system in patients without von Hippel-Lindau disease. Report of four . . .
J Neurosurg, 96(4) 2002, 775-87.
(PMID 11990821)
|
|
| CGH: 15
|
Michiels EM, Weiss MM, Hoovers JM, Baak JP, Voute PA, Baas F, et al.
Genetic alterations in childhood medulloblastoma analyzed by comparative genomic hybridization.
J Pediatr Hematol Oncol S, 24(3) 2002, 205-10.
(PMID 11990307)
|
|
| CGH: 25
|
Dwight T, Kytola S, Teh BT, Theodosopoulos G, Richardson AL, Philips J, Twigg S, et al.
Genetic analysis of lithium-associated parathyroid tumors.
Eur J Endocrinol, 146(5) 2002, 619-27.
(PMID 11980616)
|
|
| CGH: 75
|
Huang Q, Yu GP, McCormick SA, Mo J, Datta B, Mahimkar M, Lazarus P, Schaffer AA, et al.
Genetic differences detected by comparative genomic hybridization in head and neck squamous cell carcinomas from different tumor sites: construction of oncogenetic trees for tumor . . .
Genes Chromosomes Cancer, 34(2) 2002, 224-33.
(PMID 11979556)
|
|
| CGH: 33
|
Kraggerud SM, Skotheim RI, Szymanska J, Eknaes M, Fossa SD, Stenwig AE, Peltomaki P, et al.
Genome profiles of familial/bilateral and sporadic testicular germ cell tumors.
Genes Chromosomes Cancer, 34(2) 2002, 168-74.
(PMID 11979550)
|
|
| CGH: 22
|
Harvell JD, Bastian BC, and LeBoit PE.
Persistent (recurrent) Spitz nevi: a histopathologic, immunohistochemical, and molecular pathologic study of 22 cases.
Am J Surg Pathol, 26(5) 2002, 654-61.
(PMID 11979096)
|
|
| CGH: 2
|
Mullarkey M, Breen CJ, McDermott M, OMeara A, and Stallings RL.
Genetic abnormalities in a pre and post-chemotherapy hepatoblastoma.
Cytogenet Cell Genet, 95(1-2) 2001, 9-11.
(PMID 11978962)
|
|
| CGH: 47
|
Lin SC, Chen YJ, Kao SY, Hsu MT, Lin CH, Yang SC, Liu TY, and Chang KW.
Chromosomal changes in betel-associated oral squamous cell carcinomas and their relationship to clinical parameters.
Oral Oncol, 38(3) 2002, 266-73.
(PMID 11978549)
|
|
| CGH: 54
|
Knosel T, Petersen S, Schwabe H, Schluns K, Stein U, Schlag PM, Dietel M, et al.
Incidence of chromosomal imbalances in advanced colorectal carcinomas and their metastases.
Virchows Arch, 440(2) 2002, 187-94.
(PMID 11964050)
|
|
| CGH: 86
|
Carter M, Nicholson J, Ross F, Crolla J, Allibone R, Balaji V, Perry R, Walker D, et al.
Genetic abnormalities detected in ependymomas by comparative genomic hybridisation.
Br J Cancer, 86(6) 2002, 929-39.
(PMID 11953826)
|
|
| CGH: 25
|
Lindstrom I, Nordling S, Nissen AM, Tammilehto L, Mattson K, et al.
DNA copy number changes in lung adenocarcinoma in younger patients.
Mod Pathol, 15(4) 2002, 372-78.
(PMID 11950910)
|
|
| CGH: 23
|
Rieker RJ, Joos S, Bartsch C, Willeke F, Schwarzbach M, Otano-Joos M, Ohl S, Hogel J, et al.
Distinct chromosomal imbalances in pleomorphic and in high-grade dedifferentiated liposarcomas.
Int J Cancer, 99(1) 2002, 68-73.
(PMID 11948494)
|
|
| CGH: 22
|
Lemeta S, Aalto Y, Niemela M, Jaaskelainen J, Sainio M, Kere J, Knuutila S, et al.
Recurrent DNA sequence copy losses on chromosomal arm 6q in capillary hemangioblastoma.
Cancer Genet Cytogenet, 133(2) 2002, 174-78.
(PMID 11943349)
|
|
| CGH: 35
|
Schneider DT, Schuster AE, Fritsch MK, Calaminus G, Gobel U, Harms D, Lauer S, et al.
Genetic analysis of mediastinal nonseminomatous germ cell tumors in children and adolescents.
Genes Chromosomes Cancer, 34(1) 2002, 115-25.
(PMID 11921289)
|
|
| CGH: 41
|
Schmidt H, Taubert H, Wurl P, Kappler M, Lange H, Bartel F, Bache M, Holzhausen HJ, et al.
Gains of 12q are the most frequent genomic imbalances in adult fibrosarcoma and are correlated with a poor outcome.
Genes Chromosomes Cancer, 34(1) 2002, 69-77.
(PMID 11921284)
|
|
| CGH: 43
|
Zhao J, Roth J, Bode-Lesniewska B, Pfaltz M, Heitz PU, and Komminoth P.
Combined comparative genomic hybridization and genomic microarray for detection of gene amplifications in pulmonary artery intimal sarcomas and adrenocortical tumors.
Genes Chromosomes Cancer, 34(1) 2002, 48-57.
(PMID 11921282)
|
|
| CGH: 4
|
Aldosari N, Wiltshire RN, Dutra A, Schrock E, McLendon RE, Friedman HS, Bigner DD, et al.
Comprehensive molecular cytogenetic investigation of chromosomal abnormalities in human medulloblastoma cell lines and xenograft.
Neuro Oncol, 4(2) 2002, 75-85.
(PMID 11916498)
|
|
| CGH: 14
|
Fadl-Elmula I, Kytola S, Leithy ME, Abdel-Hameed M, Mandahl N, Elagib A, Ibrahim M, et al.
Chromosomal aberrations in benign and malignant bilharzia-associated bladder lesions analyzed by comparative genomic hybridization.
BMC Cancer, 2 2002, 5.
(PMID 11914143)
|
|
| CGH: 7
|
Rickert CH and Paulus W.
Genetic characterisation of granular cell tumours.
Acta Neuropathol (Berl), 103(4) 2002, 309-12.
(PMID 11904749)
|
|
| CGH: 13
|
Izumi H, Hara T, Oga A, Matsuda K, Sato Y, Naito K, and Sasaki K.
High telomerase activity correlates with the stabilities of genome and DNA ploidy in renal cell carcinoma.
Neoplasia, 4(2) 2002, 103-11.
(PMID 11896565)
|
|
| CGH: 10
|
Jeuken JW, Sprenger SH, Vermeer H, Kappelle AC, Boerman RH, and Wesseling P.
Chromosomal imbalances in primary oligodendroglial tumors and their recurrences: clues about malignant progression detected using comparative genomic hybridization.
J Neurosurg, 96(3) 2002, 559-64.
(PMID 11892633)
|
|
| CGH: 49
|
Rickert CH, Wiestler OD, and Paulus W.
Chromosomal imbalances in choroid plexus tumors.
Am J Pathol, 160(3) 2002, 1105-13.
(PMID 11891207)
|
|
| CGH: 31
|
Sham JS, Tang TC, Fang Y, Sun L, Qin LX, Wu QL, Xie D, and Guan XY.
Recurrent chromosome alterations in primary ovarian carcinoma in Chinese women.
Cancer Genet Cytogenet, 133(1) 2002, 39-44.
(PMID 11890988)
|
|
| CGH: 3
|
Schick B, Brunner C, Praetorius M, Plinkert PK, and Urbschat S.
First evidence of genetic imbalances in angiofibromas.
Laryngoscope, 112(2) 2002, 397-401.
(PMID 11889404)
|
|
| CGH: 25
|
Wang PH, Shyong WY, Lin CH, Chen YJ, Li YF, Chao HT, and Yuan CC.
Analysis of genetic aberrations in uterine adenomyosis using comparative genomic hybridization.
Anal Quant Cytol Histol, 24(1) 2002, 1-6.
(PMID 11865944)
|
|
| CGH: 22
|
Platzer P, Upender MB, Wilson K, Willis J, Lutterbaugh J, Nosrati A, Willson JK, et al.
Silence of chromosomal amplifications in colon cancer.
Cancer Res, 62(4) 2002, 1134-38.
(PMID 11861394)
|
|
| CGH: 41
|
Kusano N, Okita K, Shirahashi H, Harada T, Shiraishi K, Oga A, Kawauchi S, Furuya T, et al.
Chromosomal imbalances detected by comparative genomic hybridization are associated with outcome of patients with hepatocellular carcinoma.
Cancer, 94(3) 2002, 746-51.
(PMID 11857308)
|
|
| CGH: 27
|
Yin XL, Pang JC, and Ng HK.
Identification of a region of homozygous deletion on 8p22-23.1 in medulloblastoma.
Oncogene, 21(9) 2002, 1461-68.
(PMID 11857089)
|
|
| CGH: 50
|
Wolter H, Gottfried HW, and Mattfeldt T.
Genetic changes in stage pT2N0 prostate cancer studied by comparative genomic hybridization.
BJU Int, 89(3) 2002, 310-16.
(PMID 11856117)
|
|
| CGH: 51
|
Lui WO, Chen J, Glasker S, Bender BU, Madura C, Khoo SK, Kort E, Larsson C, et al.
Selective loss of chromosome 11 in pheochromocytomas associated with the VHL syndrome.
Oncogene, 21(7) 2002, 1117-22.
(PMID 11850829)
|
|
| CGH: 24
|
Nishio J, Iwasaki H, Ohjimi Y, Ishiguro M, Isayama T, Naito M, Iwashita A, et al.
Overrepresentation of 17q22-qter and 22q13 in dermatofibrosarcoma protuberans but not in dermatofibroma: a comparative genomic hybridization study.
Cancer Genet Cytogenet, 132(2) 2002, 102-08.
(PMID 11850069)
|
|
| CGH: 35
|
Iehara T, Hamazaki M, and Sawada T.
Cytogenetic analysis of infantile neuroblastomas by comparative genomic hybridization.
Cancer Lett, 178(1) 2002, 83-89.
(PMID 11849745)
|
|
| CGH: 31
|
Allen JE, Hough RE, Goepel JR, Bottomley S, Wilson GA, Alcock HE, Baird M, Lorigan PC, et al.
Identification of novel regions of amplification and deletion within mantle cell lymphoma DNA by comparative genomic hybridization.
Br J Haematol, 116(2) 2002, 291-98.
(PMID 11841429)
|
|
| CGH: 51
|
Ueno T, Tangoku A, Yoshino S, Abe T, Toshimitsu H, Furuya T, Kawauchi S, Oga A, et al.
Gain of 5p15 detected by comparative genomic hybridization as an independent marker of poor prognosis in patients with esophageal squamous cell carcinoma.
Clin Cancer Res, 8(2) 2002, 526-33.
(PMID 11839673)
|
|
| CGH: 83
|
Junker K, Kania K, Fiedler W, Hartmann A, Schubert J, and Werner W.
Molecular genetic evaluation of fluorescence diagnosis in bladder cancer.
Int J Oncol, 20(3) 2002, 647-53.
(PMID 11836583)
|
|
| CGH: 14
|
Garcia JL, Tardio JC, Gutierrez NC, Gonzalez MB, Polo JR, Hernandez JM, et al.
Chromosomal imbalances identified by comparative genomic hybridization in sporadic parathyroid adenomas.
Eur J Endocrinol, 146(2) 2002, 209-13.
(PMID 11834430)
|
|
| CGH: 71
|
Harada T, Okita K, Shiraishi K, Kusano N, Kondoh S, Sasaki K.
Interglandular cytogenetic heterogeneity detected by comparative genomic hybridization in pancreatic cancer.
Cancer Res. 2002 Feb 1;62(3):835-9.
(PMID 11830540)
|
|
| CGH: 41
|
Joos S, Menz CK, Wrobel G, Siebert R, Gesk S, Ohl S, Mechtersheimer G, Trumper L, et al.
Classical Hodgkin lymphoma is characterized by recurrent copy number gains of the short arm of chromosome 2.
Blood, 99(4) 2002, 1381-87.
(PMID 11830490)
|
|
| CGH: 30
|
Staebler A, Heselmeyer-Haddad K, Bell K, Riopel M, Perlman E, Ried T, et al.
Micropapillary serous carcinoma of the ovary has distinct patterns of chromosomal imbalances by comparative genomic hybridization compared with atypical proliferative serous tumors and . . .
Hum Pathol, 33(1) 2002, 47-59.
(PMID 11823973)
|
|
| CGH: 10
|
Toraman AD, Keser I, Luleci G, Tunali N, and Gelen T.
Comparative genomic hybridization in ganglioneuroblastomas.
Cancer Genet Cytogenet, 132(1) 2002, 36-40.
(PMID 11801306)
|
|
| CGH: 7
|
Kamitani S, Sugihara H, Shiomi H, Tani T, and Hattori T.
Intratumoral regional variations in copy number of the chromosomal part revealed by microdissection and combined ploidy and comparative genomic hybridization analyses in esophageal squamous . . .
Cancer Genet Cytogenet, 132(1) 2002, 30-35.
(PMID 11801305)
|
|
| CGH: 3
|
Yin XL, Hui AB, Liong EC, Ding M, Chang AR, and Ng HK.
Genetic imbalances in pleomorphic xanthoastrocytoma detected by comparative genomic hybridization and literature review.
Cancer Genet Cytogenet, 132(1) 2002, 14-19.
(PMID 11801302)
|
|
| CGH: 4
|
Pang E, Wong N, Lai PB, To KF, Lau WY, and Johnson PJ.
Consistent chromosome 10 rearrangements in four newly established human hepatocellular carcinoma cell lines.
Genes Chromosomes Cancer, 33(2) 2002, 150-59.
(PMID 11793441)
|
|
| CGH: 17
|
Blaker H, von Herbay A, Penzel R, Gross S, and Otto HF.
Genetics of adenocarcinomas of the small intestine: frequent deletions at chromosome 18q and mutations of the SMAD4 gene.
Oncogene, 21(1) 2002, 158-64.
(PMID 11791187)
|
|
| CGH: 4
|
Obara K, Ghazizadeh M, Shimizu H, Arai R, Tenjin T, Suzuki S, Moriyama Y, et al.
Comparative genomic hybridization study of genetic changes associated with vindesine resistance in esophageal carcinoma.
Int J Oncol, 20(2) 2002, 255-60.
(PMID 11788885)
|
|
| CGH: 2
|
Mihic-Probst D, Zhao J, Saremaslani P, Baer A, Komminoth P, and Heitz PU.
Spitzoid malignant melanoma with lymph-node metastasis. Is a copy-number loss on chromosome 6q a marker of malignancy?
Virchows Arch, 439(6) 2001, 823-26.
(PMID 11787857)
|
|
| CGH: 17
|
Yan J, Fang Y, and Liang Q.
[Frequent chromosomal gain of 4q and loss of 1p in primary nasopharyngeal carcinoma].
Zhonghua Zhong Liu Za Zhi, 23(3) 2001, 208-10.
(PMID 11783087)
|
|
| CGH: 18
|
Ness GO, Lybaek H, Arnes J, and Rodahl E.
Chromosomal imbalances in lymphoid tumors of the orbit.
Invest Ophthalmol Vis Sci, 43(1) 2002, 9-14.
(PMID 11773006)
|
|
| CGH: 33
|
Eberhart CG, Kratz JE, Schuster A, Goldthwaite P, Cohen KJ, Perlman EJ, et al.
Comparative genomic hybridization detects an increased number of chromosomal alterations in large cell/anaplastic medulloblastomas.
Brain Pathol, 12(1) 2002, 36-44.
(PMID 11770900)
|
|
| CGH: 16
|
Rickert CH, Dockhorn-Dworniczak B, Busch G, Moskopp D, Albert FK, Rama B, et al.
Increased chromosomal imbalances in recurrent pituitary adenomas.
Acta Neuropathol (Berl), 102(6) 2001, 615-20.
(PMID 11761722)
|
|
| CGH: 46
|
Yen CC, Chen YJ, Chen JT, Hsia JY, Chen PM, Liu JH, Fan FS, Chiou TJ, Wang WS, et al.
Comparative genomic hybridization of esophageal squamous cell carcinoma: correlations between chromosomal aberrations and disease progression/prognosis.
Cancer, 92(11) 2001, 2769-77.
(PMID 11753950)
|
|
| CGH: 33
|
Rienstein S, Loven D, Israeli O, Ram Z, Rappaport ZH, Barkai G, Goldman B, et al.
Comparative genomic hybridization analysis of radiation-associated and sporadic meningiomas.
Cancer Genet Cytogenet, 131(2) 2001, 135-40.
(PMID 11750053)
|
|
| CGH: 83
|
Goeze A, Schluns K, Wolf G, Thasler Z, Petersen S, and Petersen I.
Chromosomal imbalances of primary and metastatic lung adenocarcinomas.
J Pathol, 196(1) 2002, 8-16.
(PMID 11748636)
|
|
| CGH: 94
|
Stokke T, DeAngelis P, Smedshammer L, Galteland E, Steen HB, Smeland EB, Delabie J, et al.
Loss of chromosome 11q21-23.1 and 17p and gain of chromosome 6p are independent prognostic indicators in B-cell non-Hodgkins lymphoma.
Br J Cancer, 85(12) 2001, 1900-13.
(PMID 11747333)
|
|
| CGH: 60
|
Umayahara K, Numa F, Suehiro Y, Sakata A, Nawata S, Ogata H, Suminami Y, Sakamoto M, et al.
Comparative genomic hybridization detects genetic alterations during early stages of cervical cancer progression.
Genes Chromosomes Cancer, 33(1) 2002, 98-102.
(PMID 11746992)
|
|
| CGH: 92
|
Bockmuhl U, Schluns K, Schmidt S, Matthias S, and Petersen I.
Chromosomal alterations during metastasis formation of head and neck squamous cell carcinoma.
Genes Chromosomes Cancer, 33(1) 2002, 29-35.
(PMID 11746985)
|
|
| CGH: 62
|
Zhao J, Moch H, Scheidweiler AF, Baer A, Schaffer AA, Speel EJ, Roth J, Heitz PU, et al.
Genomic imbalances in the progression of endocrine pancreatic tumors.
Genes Chromosomes Cancer, 32(4) 2001, 364-72.
(PMID 11746977)
|
|
| CGH: 9
banding: 3 |
Kanerva J, Niini T, Vettenranta K, Riikonen P, Makipernaa A, Karhu R, Knuutila S, et al.
Loss at 12p detected by comparative genomic hybridization (CGH): association with TEL-AML1 fusion and favorable prognostic features in childhood acute lymphoblastic leukemia (ALL). A . . .
Med Pediatr Oncol, 37(5) 2001, 419-25.
(PMID 11745869)
|
|
| CGH: 46
|
Aragane H, Sakakura C, Nakanishi M, Yasuoka R, Fujita Y, Taniguchi H, Hagiwara A, et al.
Chromosomal aberrations in colorectal cancers and liver metastases analyzed by comparative genomic hybridization.
Int J Cancer, 94(5) 2001, 623-29.
(PMID 11745455)
|
|
| CGH: 27
|
Tarkkanen M, Wiklund TA, Virolainen MJ, Larramendy ML, Mandahl N, Mertens F, et al.
Comparative genomic hybridization of postirradiation sarcomas.
Cancer, 92(7) 2001, 1992-98.
(PMID 11745275)
|
|
| CGH: 15
|
Kitay-Cohen Y, Amiel A, Ashur Y, Fejgin MD, Herishanu Y, Afanasyev F, Bomstein Y, et al.
Analysis of chromosomal aberrations in large hepatocellular carcinomas by comparative genomic hybridization.
Cancer Genet Cytogenet, 131(1) 2001, 60-64.
(PMID 11734320)
|
|
| CGH: 20
|
Yang YC, Shyong WY, Chang MS, Chen YJ, Lin CH, Huang ZD, Wang Hsu MT, et al.
Frequent gain of copy number on the long arm of chromosome 3 in human cervical adenocarcinoma.
Cancer Genet Cytogenet, 131(1) 2001, 48-53.
(PMID 11734318)
|
|
| CGH: 1
banding: 1 |
Micci F, Teixeira MR, and Heim S.
Complete cytogenetic characterization of the human breast cancer cell line MA11 combining G-banding, comparative genomic hybridization, multicolor fluorescence in situ hybridization, RxFISH, . . .
Cancer Genet Cytogenet, 131(1) 2001, 25-30.
(PMID 11734314)
|
|
| CGH: 2
banding: 2 |
Phillips JL, Hayward SW, Wang Y, Vasselli J, Pavlovich C, Padilla-Nash H, Pezullo JR, et al.
The consequences of chromosomal aneuploidy on gene expression profiles in a cell line model for prostate carcinogenesis.
Cancer Res, 61(22) 2001, 8143-49.
(PMID 11719443)
|
|
| CGH: 28
banding: 21 |
Martinez-Climent JA, Vizcarra E, Sanchez D, Blesa D, Marugan I, Benet I, Sole F, et al.
Loss of a novel tumor suppressor gene locus at chromosome 8p is associated with leukemic mantle cell lymphoma.
Blood, 98(12) 2001, 3479-82.
(PMID 11719392)
|
|
| CGH: 1
banding: 1 |
Strefford JC, Foot NJ, Chaplin T, Neat MJ, Oliver RT, Young BD, et al.
The characterisation of the lymphoma cell line U937, using comparative genomic hybridisation and multi-plex FISH.
Cytogenet Cell Genet, 94(1-2) 2001, 9-14.
(PMID 11701946)
|
|
| CGH: 34
|
Rantanen S, Monni O, Joensuu H, Franssila K, and Knuutila S.
Causes and consequences of BCL2 overexpression in diffuse large B-cell lymphoma.
Leuk Lymphoma, 42(5) 2001, 1089-98.
(PMID 11697626)
|
|
| CGH: 22
banding: 22 |
Lindvall C, Nordenskjold M, Porwit A, Bjorkholm M, and Blennow E.
Molecular cytogenetic characterization of acute myeloid leukemia and myelodysplastic syndromes with multiple chromosome rearrangements.
Haematologica, 86(11) 2001, 1158-64.
(PMID 11694401)
|
|
| CGH: 31
|
Buerger H, Schmidt H, Beckmann A, Zanker KS, Boecker W, and Brandt B.
Genetic characterisation of invasive breast cancer: a comparison of CGH and PCR based multiplex microsatellite analysis.
J Clin Pathol, 54(11) 2001, 836-40.
(PMID 11684716)
|
|
| CGH: 18
|
Ullmann R, Petzmann S, Sharma A, Cagle PT, and Popper HH.
Chromosomal aberrations in a series of large-cell neuroendocrine carcinomas: unexpected divergence from small-cell carcinoma of the lung.
Hum Pathol, 32(10) 2001, 1059-63.
(PMID 11679939)
|
|
| CGH: 20
|
Takeo S, Arai H, Kusano N, Harada T, Furuya T, Kawauchi S, Oga A, Hirano T, et al.
Examination of oncogene amplification by genomic DNA microarray in hepatocellular carcinomas: comparison with comparative genomic hybridization analysis.
Cancer Genet Cytogenet, 130(2) 2001, 127-32.
(PMID 11675133)
|
|
| CGH: 43
|
Brisset S, Schleiermacher G, Peter M, Mairal A, Oberlin O, Delattre O, et al.
CGH analysis of secondary genetic changes in Ewing tumors: correlation with metastatic disease in a series of 43 cases.
Cancer Genet Cytogenet, 130(1) 2001, 57-61.
(PMID 11672775)
|
|
| CGH: 35
|
Koo SH, Ihm CH, Kwon KC, Park JW, Kim JM, and Kong G.
Genetic alterations in hepatocellular carcinoma and intrahepatic cholangiocarcinoma.
Cancer Genet Cytogenet, 130(1) 2001, 22-28.
(PMID 11672769)
|
|
| CGH: 18
banding: 4 |
Zielenska M, Bayani J, Pandita A, Toledo S, Marrano P, Andrade J, Petrilli A, et al.
Comparative genomic hybridization analysis identifies gains of 1p35 approximately p36 and chromosome 19 in osteosarcoma.
Cancer Genet Cytogenet, 130(1) 2001, 14-21.
(PMID 11672768)
|
|
| CGH: 23
banding: 6 |
Odero MD, Soto JL, Matutes E, Martin-Subero JI, Zudaire I, Rao PH, Cigudosa JC, et al.
Comparative genomic hybridization and amplotyping by arbitrarily primed PCR in stage A B-CLL.
Cancer Genet Cytogenet, 130(1) 2001, 8-13.
(PMID 11672767)
|
|
| CGH: 80
|
Kunwar S, Mohapatra G, Bollen A, Lamborn KR, Prados M, and Feuerstein BG.
Genetic subgroups of anaplastic astrocytomas correlate with patient age and survival.
Cancer Res, 61(20) 2001, 7683-88.
(PMID 11606412)
|
|
| CGH: 38
|
Su XY, Cao Q, and He KL.
[Chromosomal abnormalities in 38 CML cases of various phases].
Zhonghua Yi Xue Za Zhi, 79(1) 1999, 34-37.
(PMID 11601004)
|
|
| CGH: 40
|
Popov P, Virolainen M, Tukiainen E, Asko-Scljavaara S, Huuhtanen R, Knuutila S, et al.
Primary soft tissue sarcoma and its local recurrence: genetic changes studied by comparative genomic hybridization.
Mod Pathol, 14(10) 2001, 978-84.
(PMID 11598167)
|
|
| CGH: 36
|
Zweemer RP, Ryan A, Snijders AM, Hermsen MA, Meijer GA, Beller U, Menko FH, Jacobs IJ, et al.
Comparative genomic hybridization of microdissected familial ovarian carcinoma: two deleted regions on chromosome 15q not previously identified in sporadic ovarian . . .
Lab Invest, 81(10) 2001, 1363-70.
(PMID 11598149)
|
|
| CGH: 18
|
Li Z, Wang L, Zhang X, Zhang L, Zhang B, Yu Y, Zeng Z, Zhou M, Huang W, Chen Z, et al.
[Chromosomal aberration analyzed by comparative genomic hybridization in nasopharyngeal carcinoma].
Zhonghua Yi Xue Yi Chuan Xue Za Zhi, 18(5) 2001, 338-42.
(PMID 11592038)
|
|
| CGH: 37
|
Renedo M, Martinez-Delgado B, Arranz E, Garcia M, Urioste M, Martinez-Ramirez A, et al.
Chromosomal changes pattern and gene amplification in T cell non-Hodgkins lymphomas.
Leukemia, 15(10) 2001, 1627-32.
(PMID 11587222)
|
|
| CGH: 2
banding: 2 |
Zimonjic DB, Keck-Waggoner C, and Popescu NC.
Novel genomic imbalances and chromosome translocations involving c-myc gene in Burkitts lymphoma.
Leukemia, 15(10) 2001, 1582-88.
(PMID 11587216)
|
|
| CGH: 29
|
Hirai Y, Tanaka N, Furuta R, Kawaguchi T, Sakamoto M, Shirahama S, et al.
Somatic mutations of the PTEN/NMAC1 gene associated with frequent chromosomal loss detected using comparative genomic hybridization in endometrial cancer.
Gynecol Oncol, 83(1) 2001, 81-88.
(PMID 11585417)
|
|
| CGH: 12
banding: 6 |
Alvarez S, MacGrogan D, Calasanz MJ, Nimer SD, and Jhanwar SC.
Frequent gain of chromosome 19 in megakaryoblastic leukemias detected by comparative genomic hybridization.
Genes Chromosomes Cancer, 32(3) 2001, 285-93.
(PMID 11579469)
|
|
| CGH: 16
|
Scheil S, Bruderlein S, Liehr T, Starke H, Herms J, Schulte M, et al.
Genome-wide analysis of sixteen chordomas by comparative genomic hybridization and cytogenetics of the first human chordoma cell line, U-CH1.
Genes Chromosomes Cancer, 32(3) 2001, 203-11.
(PMID 11579460)
|
|
| CGH: 10
|
Larramendy ML, Knuutila S, Jantunen R, Ruutu T, and Juvonen E.
No DNA sequence copy number changes in essential thrombocythemia.
Cancer Genet Cytogenet, 129(2) 2001, 181-82.
(PMID 11572227)
|
|
| CGH: 15
|
Ashton KJ, Weinstein SR, Maguire DJ, and Griffiths LR.
Molecular cytogenetic analysis of basal cell carcinoma DNA using comparative genomic hybridization.
J Invest Dermatol, 117(3) 2001, 683-86.
|
