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Journal Abstract Search

397 related items for PubMed ID: 15334548

  • 21. Loss of heterozygosity at 11q23.1 and survival in breast cancer: results of a large European study. Breast Cancer Somatic Genetics Consortium.
    Laake K, Launonen V, Niederacher D, Gudlaugsdottir S, Seitz S, Rio P, Champème MH, Bièche I, Birnbaum D, White G, Sztan M, Sever N, Plummer S, Osorio A, Broeks A, Huusko P, Spurr N, Borg A, Cleton-Jansen AM, van't Veer L, Benitez J, Casey G, Peterlin B, Olah E, Børresen-Dale AL.
    Genes Chromosomes Cancer; 1999 Jul; 25(3):212-21. PubMed ID: 10379867
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  • 22. A distinct region of chromosome 19p13.3 associated with the sporadic form of adenoma malignum of the uterine cervix.
    Lee JY, Dong SM, Kim HS, Kim SY, Na EY, Shin MS, Lee SH, Park WS, Kim KM, Lee YS, Jang JJ, Yoo NJ.
    Cancer Res; 1998 Mar 15; 58(6):1140-3. PubMed ID: 9515797
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  • 23. High-density marker analysis of 11p15.5 in non-small cell lung carcinomas reveals allelic deletion of one shared and one distinct region when compared to breast carcinomas.
    Tran YK, Newsham IF.
    Cancer Res; 1996 Jul 01; 56(13):2916-21. PubMed ID: 8674040
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  • 24. Alterations of the 16q22.1 and 16q24.3 chromosomal loci in sporadic invasive breast carcinomas: correlation with proliferative activity, ploidy and hormonal status of the tumors.
    Kouvaraki M, Gorgoulis VG, Rassidakis GZ, Liodis P, Koutroumbi E, Markopoulos C, Gogas J, Kittas C.
    Anticancer Res; 2001 Jul 01; 21(2A):991-9. PubMed ID: 11396193
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  • 26. Complete germline deletion of the STK11 gene in a family with Peutz-Jeghers syndrome.
    Le Meur N, Martin C, Saugier-Veber P, Joly G, Lemoine F, Moirot H, Rossi A, Bachy B, Cabot A, Joly P, Frébourg T.
    Eur J Hum Genet; 2004 May 01; 12(5):415-8. PubMed ID: 14970844
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  • 29. Loss of heterozygosity at the BRCA1 locus in Tunisian women with sporadic breast cancer.
    Charef-Hamza S, Trimeche M, Ziadi S, Amara K, Gaddas N, Mokni M, Sriha B, Yacoubi T, Korbi S.
    Cancer Lett; 2005 Jun 28; 224(2):185-91. PubMed ID: 15914269
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  • 30. Mapping of a new target region of allelic loss to a 2-cM interval at 22q13.1 in primary breast cancer.
    Iida A, Kurose K, Isobe R, Akiyama F, Sakamoto G, Yoshimoto M, Kasumi F, Nakamura Y, Emi M.
    Genes Chromosomes Cancer; 1998 Feb 28; 21(2):108-12. PubMed ID: 9491321
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  • 31. Four regions of allelic imbalance on 17q12-qter associated with high-grade breast tumors.
    Plummer SJ, Paris MJ, Myles J, Tubbs R, Crowe J, Casey G.
    Genes Chromosomes Cancer; 1997 Dec 28; 20(4):354-62. PubMed ID: 9408751
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  • 32. Are there any more ovarian tumor suppressor genes? A new perspective using ultra high-resolution copy number and loss of heterozygosity analysis.
    Gorringe KL, Ramakrishna M, Williams LH, Sridhar A, Boyle SE, Bearfoot JL, Li J, Anglesio MS, Campbell IG.
    Genes Chromosomes Cancer; 2009 Oct 28; 48(10):931-42. PubMed ID: 19603523
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  • 38. An 800-kb region of deletion at 13q14 in human prostate and other carcinomas.
    Chen C, Frierson HF, Haggerty PF, Theodorescu D, Gregory CW, Dong JT.
    Genomics; 2001 Oct 28; 77(3):135-44. PubMed ID: 11597138
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  • 39. Loss of heterozygosity on the long arm of chromosome 6 in breast cancer: possibly four regions of deletion.
    Noviello C, Courjal F, Theillet C.
    Clin Cancer Res; 1996 Sep 28; 2(9):1601-6. PubMed ID: 9816339
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  • 40. Complex CGH alterations on chromosome arm 8p at candidate tumor suppressor gene loci in breast cancer cell lines.
    Venter DJ, Ramus SJ, Hammet FM, de Silva M, Hutchins AM, Petrovic V, Price G, Armes JE.
    Cancer Genet Cytogenet; 2005 Jul 15; 160(2):134-40. PubMed ID: 15993269
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