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Journal Abstract Search

222 related items for PubMed ID: 7616353

  • 1. Mutation at chromosome 11q23 in human non-familial breast cancer: a microdissection microsatellite analysis.
    Koreth J, Bethwaite PB, McGee JO.
    J Pathol; 1995 May; 176(1):11-8. PubMed ID: 7616353
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  • 2. Loss of heterozygosity in ductal carcinoma in situ of the breast.
    Stratton MR, Collins N, Lakhani SR, Sloane JP.
    J Pathol; 1995 Feb; 175(2):195-201. PubMed ID: 7738715
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  • 4. 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; 74(2):100-7. PubMed ID: 10914818
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  • 5. Loss of heterozygosity from the short arm of chromosome 8 is associated with invasive behavior in breast cancer.
    Yaremko ML, Kutza C, Lyzak J, Mick R, Recant WM, Westbrook CA.
    Genes Chromosomes Cancer; 1996 Jul; 16(3):189-95. PubMed ID: 8814452
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  • 9. 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
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  • 10. Analysis of the FHIT gene and FRA3B region in sporadic breast cancer, preneoplastic lesions, and familial breast cancer probands.
    Ahmadian M, Wistuba II, Fong KM, Behrens C, Kodagoda DR, Saboorian MH, Shay J, Tomlinson GE, Blum J, Minna JD, Gazdar AF.
    Cancer Res; 1997 Sep 01; 57(17):3664-8. PubMed ID: 9288768
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  • 11. Genetic abnormalities in mammary ductal intraepithelial neoplasia-flat type ("clinging ductal carcinoma in situ"): a simulator of normal mammary epithelium.
    Moinfar F, Man YG, Bratthauer GL, Ratschek M, Tavassoli FA.
    Cancer; 2000 May 01; 88(9):2072-81. PubMed ID: 10813719
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  • 12. Pattern of chromosome 16q loss differs between an atypical proliferative lesion and an intraductal or invasive ductal carcinoma occurring subsequently in the same area of the breast.
    Tsuda H, Takarabe T, Akashi-Tanaka S, Fukutomi T, Hirohashi S.
    Mod Pathol; 2001 May 01; 14(5):382-8. PubMed ID: 11353046
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  • 14. Loss of heterozygosity occurs at the D11S29 locus on chromosome 11q23 in invasive cervical carcinoma.
    Bethwaite PB, Koreth J, Herrington CS, McGee JO.
    Br J Cancer; 1995 Apr 01; 71(4):814-8. PubMed ID: 7710949
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  • 16. Allelotyping of ductal carcinoma in situ of the breast: deletion of loci on 8p, 13q, 16q, 17p and 17q.
    Radford DM, Fair KL, Phillips NJ, Ritter JH, Steinbrueck T, Holt MS, Donis-Keller H.
    Cancer Res; 1995 Aug 01; 55(15):3399-405. PubMed ID: 7614479
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  • 17. Microsatellite instability in ductal carcinoma in situ of the breast.
    Walsh T, Chappell SA, Shaw JA, Walker RA.
    J Pathol; 1998 May 01; 185(1):18-24. PubMed ID: 9713355
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  • 18. Deletion map of chromosome 16q in ductal carcinoma in situ of the breast: refining a putative tumor suppressor gene region.
    Chen T, Sahin A, Aldaz CM.
    Cancer Res; 1996 Dec 15; 56(24):5605-9. PubMed ID: 8971163
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  • 19. Genome-wide search for loss of heterozygosity using laser capture microdissected tissue of breast carcinoma: an implication for mutator phenotype and breast cancer pathogenesis.
    Shen CY, Yu JC, Lo YL, Kuo CH, Yue CT, Jou YS, Huang CS, Lung JC, Wu CW.
    Cancer Res; 2000 Jul 15; 60(14):3884-92. PubMed ID: 10919664
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  • 20. Identification of multiple breast cancers of multicentric origin by histological observations and distribution of allele loss on chromosome 16q.
    Tsuda H, Hirohashi S.
    Cancer Res; 1995 Aug 01; 55(15):3395-8. PubMed ID: 7614478
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