167 related articles for article (PubMed ID: 16737911)
1. Molecular cytogenetic characterization of a metastatic lung sarcomatoid carcinoma: 9p23 neocentromere and 9p23-p24 amplification including JAK2 and JMJD2C.
Italiano A; Attias R; Aurias A; Pérot G; Burel-Vandenbos F; Otto J; Venissac N; Pedeutour F
Cancer Genet Cytogenet; 2006 Jun; 167(2):122-30. PubMed ID: 16737911
[TBL] [Abstract][Full Text] [Related]
2. Polycythemia vera transforming to acute myeloid leukemia and complex abnormalities including 9p homogeneously staining region with amplification of MLLT3, JMJD2C, JAK2, and SMARCA2.
Hélias C; Struski S; Gervais C; Leymarie V; Mauvieux L; Herbrecht R; Lessard M
Cancer Genet Cytogenet; 2008 Jan; 180(1):51-5. PubMed ID: 18068534
[TBL] [Abstract][Full Text] [Related]
3. Genomic imbalances including amplification of the tyrosine kinase gene JAK2 in CD30+ Hodgkin cells.
Joos S; Küpper M; Ohl S; von Bonin F; Mechtersheimer G; Bentz M; Marynen P; Möller P; Pfreundschuh M; Trümper L; Lichter P
Cancer Res; 2000 Feb; 60(3):549-52. PubMed ID: 10676635
[TBL] [Abstract][Full Text] [Related]
4. Characterization of an analphoid supernumerary marker chromosome derived from 15q25-->qter using high-resolution CGH and multiplex FISH analyses.
Huang XL; de Michelena MI; Mark H; Harston R; Benke PJ; Price SJ; Milunsky A
Clin Genet; 2005 Dec; 68(6):513-9. PubMed ID: 16283881
[TBL] [Abstract][Full Text] [Related]
5. Identification of a novel gene, GASC1, within an amplicon at 9p23-24 frequently detected in esophageal cancer cell lines.
Yang ZQ; Imoto I; Fukuda Y; Pimkhaokham A; Shimada Y; Imamura M; Sugano S; Nakamura Y; Inazawa J
Cancer Res; 2000 Sep; 60(17):4735-9. PubMed ID: 10987278
[TBL] [Abstract][Full Text] [Related]
6. Prenatal molecular cytogenetic diagnosis of partial tetrasomy 10p due to neocentromere formation in an inversion duplication analphoid marker chromosome.
Levy B; Papenhausen P; Tepperberg J; Dunn T; Fallet S; Magid M; Kardon N; Hirschhorn K; Warburton P
Cytogenet Cell Genet; 2000; 91(1-4):165-70. PubMed ID: 11173851
[TBL] [Abstract][Full Text] [Related]
7. Variability of origin for the neocentromeric sequences in analphoid supernumerary marker chromosomes of well-differentiated liposarcomas.
Italiano A; Maire G; Sirvent N; Nuin PA; Keslair F; Foa C; Louis C; Aurias A; Pedeutour F
Cancer Lett; 2009 Jan; 273(2):323-30. PubMed ID: 18823700
[TBL] [Abstract][Full Text] [Related]
8. Chromosome 13q neocentromeres: molecular cytogenetic characterization of three additional cases and clinical spectrum.
Li S; Malafiej P; Levy B; Mahmood R; Field M; Hughes T; Lockhart LH; Wu Z; Huang M; Hirschhorn K; Velagaleti GV; Daniel A; Warburton PE
Am J Med Genet; 2002 Jul; 110(3):258-67. PubMed ID: 12116235
[TBL] [Abstract][Full Text] [Related]
9. Chromosome 9p24 abnormalities: prevalence, description of novel JAK2 translocations, JAK2V617F mutation analysis and clinicopathologic correlates.
Patnaik MM; Knudson RA; Gangat N; Hanson CA; Pardanani A; Tefferi A; Ketterling RP
Eur J Haematol; 2010 Jun; 84(6):518-24. PubMed ID: 20331734
[TBL] [Abstract][Full Text] [Related]
10. Genomic alterations in lung adenocarcinomas detected by multicolor fluorescence in situ hybridization and comparative genomic hybridization.
Shen H; Zhu Y; Wu YJ; Qiu HR; Shu YQ
Cancer Genet Cytogenet; 2008 Mar; 181(2):100-7. PubMed ID: 18295661
[TBL] [Abstract][Full Text] [Related]
11. Global search for chromosomal abnormalities in infiltrating ductal carcinoma of the breast using array-comparative genomic hybridization.
Somiari SB; Shriver CD; He J; Parikh K; Jordan R; Hooke J; Hu H; Deyarmin B; Lubert S; Malicki L; Heckman C; Somiari RI
Cancer Genet Cytogenet; 2004 Dec; 155(2):108-18. PubMed ID: 15571796
[TBL] [Abstract][Full Text] [Related]
12. Combined spectral karyotyping, multicolor banding, and microarray comparative genomic hybridization analysis provides a detailed characterization of complex structural chromosomal rearrangements associated with gene amplification in the osteosarcoma cell line MG-63.
Lim G; Karaskova J; Vukovic B; Bayani J; Beheshti B; Bernardini M; Squire JA; Zielenska M
Cancer Genet Cytogenet; 2004 Sep; 153(2):158-64. PubMed ID: 15350306
[TBL] [Abstract][Full Text] [Related]
13. Genomic microarray analysis reveals distinct locations for the CENP-A binding domains in three human chromosome 13q32 neocentromeres.
Alonso A; Mahmood R; Li S; Cheung F; Yoda K; Warburton PE
Hum Mol Genet; 2003 Oct; 12(20):2711-21. PubMed ID: 12928482
[TBL] [Abstract][Full Text] [Related]
14. A combination of molecular cytogenetic analyses reveals complex genetic alterations in conventional renal cell carcinoma.
Strefford JC; Stasevich I; Lane TM; Lu YJ; Oliver T; Young BD
Cancer Genet Cytogenet; 2005 May; 159(1):1-9. PubMed ID: 15860350
[TBL] [Abstract][Full Text] [Related]
15. Trisomy 20p resulting from inverted duplication and neocentromere formation.
Voullaire L; Saffery R; Davies J; Earle E; Kalitsis P; Slater H; Irvine DV; Choo KH
Am J Med Genet; 1999 Aug; 85(4):403-8. PubMed ID: 10398268
[TBL] [Abstract][Full Text] [Related]
16. Molecular cytogenetic characterization of head and neck squamous cell carcinoma and refinement of 3q amplification.
Singh B; Gogineni SK; Sacks PG; Shaha AR; Shah JP; Stoffel A; Rao PH
Cancer Res; 2001 Jun; 61(11):4506-13. PubMed ID: 11389082
[TBL] [Abstract][Full Text] [Related]
17. Comparative genomic hybridization of squamous cell carcinoma of the esophagus: the possible involvement of the DPI gene in the 13q34 amplicon.
Shinomiya T; Mori T; Ariyama Y; Sakabe T; Fukuda Y; Murakami Y; Nakamura Y; Inazawa J
Genes Chromosomes Cancer; 1999 Apr; 24(4):337-44. PubMed ID: 10092132
[TBL] [Abstract][Full Text] [Related]
18. Constitutional genomic instability with inversions, duplications, and amplifications in 9p23-24 in BRCA2 mutation carriers.
Savelyeva L; Claas A; Matzner I; Schlag P; Hofmann W; Scherneck S; Weber B; Schwab M
Cancer Res; 2001 Jul; 61(13):5179-85. PubMed ID: 11431357
[TBL] [Abstract][Full Text] [Related]
19. Detection of c-myc oncogene amplification and chromosomal anomalies in metastatic prostatic carcinoma by fluorescence in situ hybridization.
Jenkins RB; Qian J; Lieber MM; Bostwick DG
Cancer Res; 1997 Feb; 57(3):524-31. PubMed ID: 9012485
[TBL] [Abstract][Full Text] [Related]
20. Establishment and molecular cytogenetic characterization of non-small cell lung cancer cell line KU-T1 by multicolor fluorescence in situ hybridization, comparative genomic hybridization, and chromosome microdissection.
Kume M; Taguchi T; Okada H; Anayama T; Tominaga A; Shuin T; Sasaguri S
Cancer Genet Cytogenet; 2007 Dec; 179(2):93-101. PubMed ID: 18036395
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]