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106 related items for PubMed ID: 8943813

  • 1. The frequency and mechanism of loss of heterozygosity on chromosome 11q in breast cancer.
    Tomlinson IP, Nicolai H, Solomon E, Bodmer WF.
    J Pathol; 1996 Sep; 180(1):38-43. PubMed ID: 8943813
    [Abstract] [Full Text] [Related]

  • 2. Loss of heterozygosity at 11q22-q23 in breast cancer.
    Carter SL, Negrini M, Baffa R, Gillum DR, Rosenberg AL, Schwartz GF, Croce CM.
    Cancer Res; 1994 Dec 01; 54(23):6270-4. PubMed ID: 7954477
    [Abstract] [Full Text] [Related]

  • 3. Allelic deletions at chromosome 11q22-q23.1 and 11q25-qterm are frequent in sporadic breast but not colorectal cancers.
    Koreth J, Bakkenist CJ, McGee JO.
    Oncogene; 1997 Jan 30; 14(4):431-7. PubMed ID: 9053840
    [Abstract] [Full Text] [Related]

  • 4. Mutation at chromosome 11q23 in human non-familial breast cancer: a microdissection microsatellite analysis.
    Koreth J, Bethwaite PB, McGee JO.
    J Pathol; 1995 May 30; 176(1):11-8. PubMed ID: 7616353
    [Abstract] [Full Text] [Related]

  • 5. Allele loss on chromosome 11q and microsatellite instability in malignant melanoma.
    Tomlinson IP, Beck NE, Bodmer WF.
    Eur J Cancer; 1996 Sep 30; 32A(10):1797-802. PubMed ID: 8983292
    [Abstract] [Full Text] [Related]

  • 6. Chromosome 11q in sporadic colorectal carcinoma: patterns of allele loss and their significance for tumorigenesis.
    Tomlinson IP, Bodmer WF.
    J Clin Pathol; 1996 May 30; 49(5):386-90. PubMed ID: 8707952
    [Abstract] [Full Text] [Related]

  • 7. Microsatellite alterations on human chromosome 11 in in situ and invasive breast cancer: a microdissection microsatellite analysis and correlation with p53, ER (estrogen receptor), and PR (progesterone receptor) protein immunoreactivity.
    Shen KL, Yang LS, Hsieh HF, Chen CJ, Yu JC, Tsai NM, Harn HJ.
    J Surg Oncol; 2000 Jun 30; 74(2):100-7. PubMed ID: 10914818
    [Abstract] [Full Text] [Related]

  • 8. Loss of heterozygosity in sporadic human breast carcinoma: a common region between 11q22 and 11q23.3.
    Hampton GM, Mannermaa A, Winqvist R, Alavaikko M, Blanco G, Taskinen PJ, Kiviniemi H, Newsham I, Cavenee WK, Evans GA.
    Cancer Res; 1994 Sep 01; 54(17):4586-9. PubMed ID: 8062246
    [Abstract] [Full Text] [Related]

  • 9. Loss of heterozygosity on the long arm of chromosome 11 in nasopharyngeal carcinoma.
    Hui AB, Lo KW, Leung SF, Choi PH, Fong Y, Lee JC, Huang DP.
    Cancer Res; 1996 Jul 15; 56(14):3225-9. PubMed ID: 8764112
    [Abstract] [Full Text] [Related]

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  • 11. Cluster of allele losses within a 2.5 cM region of chromosome 10 in high-grade invasive bladder cancer.
    Kagan J, Liu J, Stein JD, Wagner SS, Babkowski R, Grossman BH, Katz RL.
    Oncogene; 1998 Feb 19; 16(7):909-13. PubMed ID: 9484782
    [Abstract] [Full Text] [Related]

  • 12. Detailed deletion mapping at chromosome 11q23 in colorectal carcinoma.
    Lee AS, Seo YC, Chang A, Tohari S, Eu KW, Seow-Choen F, McGee JO.
    Br J Cancer; 2000 Sep 19; 83(6):750-5. PubMed ID: 10952779
    [Abstract] [Full Text] [Related]

  • 13. High resolution chromosome 3p allelotyping of human lung cancer and preneoplastic/preinvasive bronchial epithelium reveals multiple, discontinuous sites of 3p allele loss and three regions of frequent breakpoints.
    Wistuba II, Behrens C, Virmani AK, Mele G, Milchgrub S, Girard L, Fondon JW, Garner HR, McKay B, Latif F, Lerman MI, Lam S, Gazdar AF, Minna JD.
    Cancer Res; 2000 Apr 01; 60(7):1949-60. PubMed ID: 10766185
    [Abstract] [Full Text] [Related]

  • 14. High frequency of LOH at chromosome 18q in human breast cancer: association with high S-phase fraction and low progesterone receptor content.
    Huiping C, Eiriksdottir G, Sigurdsson A, Sigurgeirsdottir JR, Barkardottir RB, Egilsson V, Ingvarsson S.
    Anticancer Res; 1998 Apr 01; 18(2A):1031-6. PubMed ID: 9615760
    [Abstract] [Full Text] [Related]

  • 15. Microsatellite analysis of breast carcinoma and corresponding local recurrences.
    Regitnig P, Moser R, Thalhammer M, Luschin-Ebengreuth G, Ploner F, Papadi H, Tsybrovskyy O, Lax SF.
    J Pathol; 2002 Oct 01; 198(2):190-7. PubMed ID: 12237878
    [Abstract] [Full Text] [Related]

  • 16. Mapping of a new target region of allelic loss to a 6-cM interval at 21q21 in primary breast cancers.
    Ohgaki K, Iida A, Kasumi F, Sakamoto G, Akimoto M, Nakamura Y, Emi M.
    Genes Chromosomes Cancer; 1998 Nov 01; 23(3):244-7. PubMed ID: 9790505
    [Abstract] [Full Text] [Related]

  • 17. Consortium study on 1280 breast carcinomas: allelic loss on chromosome 17 targets subregions associated with family history and clinical parameters.
    Phelan CM, Borg A, Cuny M, Crichton DN, Baldersson T, Andersen TI, Caligo MA, Lidereau R, Lindblom A, Seitz S, Kelsell D, Hamann U, Rio P, Thorlacius S, Papp J, Olah E, Ponder B, Bignon YJ, Scherneck S, Barkardottir R, Borresen-Dale AL, Eyfjörd J, Theillet C, Thompson AM, Larsson C.
    Cancer Res; 1998 Mar 01; 58(5):1004-12. PubMed ID: 9500463
    [Abstract] [Full Text] [Related]

  • 18. Loss of heterozygosity at 17p13.3-ter, distal to TP53, correlates with negative hormonal phenotype in sporadic breast cancer.
    Roncuzzi L, Brognara I, Baiocchi D, Amadori D, Gasperi-Campani A.
    Oncol Rep; 2005 Aug 01; 14(2):471-4. PubMed ID: 16012732
    [Abstract] [Full Text] [Related]

  • 19. Loss of heterozygosity at chromosome 7q in human breast cancer: association with clinical variables.
    Kristjansson AK, Eiriksdottir G, Ragnarsson G, Sigurdsson A, Gudmundsson J, Barkardottir RB, Jonasson JG, Egilsson V, Ingvarsson S.
    Anticancer Res; 1997 Aug 01; 17(1A):93-8. PubMed ID: 9066635
    [Abstract] [Full Text] [Related]

  • 20. High-resolution 19p13.2-13.3 allelotyping of breast carcinomas demonstrates frequent loss of heterozygosity.
    Yang TL, Su YR, Huang CS, Yu JC, Lo YL, Wu PE, Shen CY.
    Genes Chromosomes Cancer; 2004 Nov 01; 41(3):250-6. PubMed ID: 15334548
    [Abstract] [Full Text] [Related]

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