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Journal Abstract Search

127 related items for PubMed ID: 7816807

  • 21. Hybrid selection of transcribed sequences from microdissected DNA: isolation of genes within amplified region at 20q11-q13.2 in breast cancer.
    Guan XY, Xu J, Anzick SL, Zhang H, Trent JM, Meltzer PS.
    Cancer Res; 1996 Aug 01; 56(15):3446-50. PubMed ID: 8758910
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  • 22. DNA microarrays for comparative genomic hybridization based on DOP-PCR amplification of BAC and PAC clones.
    Fiegler H, Carr P, Douglas EJ, Burford DC, Hunt S, Scott CE, Smith J, Vetrie D, Gorman P, Tomlinson IP, Carter NP.
    Genes Chromosomes Cancer; 2003 Apr 01; 36(4):361-74. PubMed ID: 12619160
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  • 27. 20q gain associates with immortalization: 20q13.2 amplification correlates with genome instability in human papillomavirus 16 E7 transformed human uroepithelial cells.
    Savelieva E, Belair CD, Newton MA, DeVries S, Gray JW, Waldman F, Reznikoff CA.
    Oncogene; 1997 Feb 06; 14(5):551-60. PubMed ID: 9053853
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  • 28. Specific loss of chromosomes 1, 2, 6, 10, 13, 17, and 21 in chromophobe renal cell carcinomas revealed by comparative genomic hybridization.
    Speicher MR, Schoell B, du Manoir S, Schröck E, Ried T, Cremer T, Störkel S, Kovacs A, Kovacs G.
    Am J Pathol; 1994 Aug 06; 145(2):356-64. PubMed ID: 7519827
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  • 29. Microcell-mediated chromosome transfer provides evidence that polysomy promotes structural instability in tumor cell chromosomes through asynchronous replication and breakage within late-replicating regions.
    Kost-Alimova M, Fedorova L, Yang Y, Klein G, Imreh S.
    Genes Chromosomes Cancer; 2004 Aug 06; 40(4):316-24. PubMed ID: 15188454
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  • 30. A microdissection technique for archival DNA analysis of specific cell populations in lesions < 1 mm in size.
    Zhuang Z, Bertheau P, Emmert-Buck MR, Liotta LA, Gnarra J, Linehan WM, Lubensky IA.
    Am J Pathol; 1995 Mar 06; 146(3):620-5. PubMed ID: 7887444
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  • 31. Isolation of YAC insert sequences by representational difference analysis.
    Schutte M, da Costa LT, Moskaluk CA, Rozenblum E, Guan X, de Jong PJ, Bittner M, Meltzer PS, Trent JM, Kern SE.
    Nucleic Acids Res; 1995 Oct 25; 23(20):4127-33. PubMed ID: 7479076
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  • 32. Inactivation of the retinoblastoma gene in human bladder and renal cell carcinomas.
    Ishikawa J, Xu HJ, Hu SX, Yandell DW, Maeda S, Kamidono S, Benedict WF, Takahashi R.
    Cancer Res; 1991 Oct 15; 51(20):5736-43. PubMed ID: 1913692
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  • 35. Common regions of deletion on chromosomes 5q, 6q, and 10q in renal cell carcinoma.
    Morita R, Saito S, Ishikawa J, Ogawa O, Yoshida O, Yamakawa K, Nakamura Y.
    Cancer Res; 1991 Nov 01; 51(21):5817-20. PubMed ID: 1682036
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  • 36. The candidate oncogene ZNF217 is frequently amplified in colon cancer.
    Rooney PH, Boonsong A, McFadyen MC, McLeod HL, Cassidy J, Curran S, Murray GI.
    J Pathol; 2004 Nov 01; 204(3):282-8. PubMed ID: 15476264
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  • 37. Definition of a 1-Mb homozygous deletion at 9q32-q33 in a human bladder-cancer cell line.
    Fujiwara H, Emi M, Nagai H, Ohgaki K, Imoto I, Akimoto M, Ogawa O, Habuchi T.
    J Hum Genet; 2001 Nov 01; 46(7):372-7. PubMed ID: 11450846
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  • 38. Detection of CDKN2 deletions in tumor cell lines and primary glioma by interphase fluorescence in situ hybridization.
    Dreyling MH, Bohlander SK, Adeyanju MO, Olopade OI.
    Cancer Res; 1995 Mar 01; 55(5):984-8. PubMed ID: 7867008
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  • 39. p53 mutation and loss of heterozygosity on chromosomes 17 and 10 during human astrocytoma progression.
    Fults D, Brockmeyer D, Tullous MW, Pedone CA, Cawthon RM.
    Cancer Res; 1992 Feb 01; 52(3):674-9. PubMed ID: 1346255
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  • 40. Methylation of the 5' CpG island of the p16/CDKN2 tumor suppressor gene in normal and transformed human tissues correlates with gene silencing.
    Gonzalez-Zulueta M, Bender CM, Yang AS, Nguyen T, Beart RW, Van Tornout JM, Jones PA.
    Cancer Res; 1995 Oct 15; 55(20):4531-5. PubMed ID: 7553622
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