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Journal Abstract Search


82 related items for PubMed ID: 1993303

  • 1.
    ; . PubMed ID:
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  • 2. Preferential involvement of chromosome 11 as add(11)(p15) in ovarian cancer: is it a common cytogenetic abnormality in cancer?
    Panani AD.
    Cancer Lett; 2007 Dec 18; 258(2):262-7. PubMed ID: 17945413
    [Abstract] [Full Text] [Related]

  • 3. 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]

  • 4. Common cytogenetic findings in primary breast cancer.
    Ferti-Passantonopoulou AD, Panani AD.
    Cancer Genet Cytogenet; 1987 Aug 01; 27(2):289-98. PubMed ID: 3036341
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  • 5. Loss of heterozygosity for chromosome 11 in primary human breast tumors is associated with poor survival after metastasis.
    Winqvist R, Hampton GM, Mannermaa A, Blanco G, Alavaikko M, Kiviniemi H, Taskinen PJ, Evans GA, Wright FA, Newsham I.
    Cancer Res; 1995 Jun 15; 55(12):2660-4. PubMed ID: 7780982
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  • 6. Cytogenetic features of twenty-six primary breast cancers.
    Hainsworth PJ, Raphael KL, Stillwell RG, Bennett RC, Garson OM.
    Cancer Genet Cytogenet; 1991 Jun 15; 53(2):205-18. PubMed ID: 1648438
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  • 7. Two distinct tumor suppressor loci within chromosome 11p15 implicated in breast cancer progression and metastasis.
    Karnik P, Paris M, Williams BR, Casey G, Crowe J, Chen P.
    Hum Mol Genet; 1998 May 15; 7(5):895-903. PubMed ID: 9536095
    [Abstract] [Full Text] [Related]

  • 8. ETS1 gene in myelodysplastic syndrome with chromosome change at 11q23.
    Ohyashiki K, Ohyashiki JH, Tauchi T, Iwabuchi H, Iwabuchi A, Toyama K.
    Cancer Genet Cytogenet; 1990 Mar 15; 45(1):73-80. PubMed ID: 2302688
    [Abstract] [Full Text] [Related]

  • 9. Mutation at chromosome 11q23 in human non-familial breast cancer: a microdissection microsatellite analysis.
    Koreth J, Bethwaite PB, McGee JO.
    J Pathol; 1995 May 15; 176(1):11-8. PubMed ID: 7616353
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  • 12. Refinement of regional loss of heterozygosity for chromosome 11p15.5 in human breast tumors.
    Winqvist R, Mannermaa A, Alavaikko M, Blanco G, Taskinen PJ, Kiviniemi H, Newsham I, Cavenee W.
    Cancer Res; 1993 Oct 01; 53(19):4486-8. PubMed ID: 8402619
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  • 14. Loss of heterozygosity on chromosome 11 q in breast cancer.
    Tomlinson IP, Strickland JE, Lee AS, Bromley L, Evans MF, Morton J, McGee JO.
    J Clin Pathol; 1995 May 01; 48(5):424-8. PubMed ID: 7629288
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  • 15. Definition and refinement of chromosome 11 regions of loss of heterozygosity in breast cancer: identification of a new region at 11q23.3.
    Negrini M, Rasio D, Hampton GM, Sabbioni S, Rattan S, Carter SL, Rosenberg AL, Schwartz GF, Shiloh Y, Cavenee WK.
    Cancer Res; 1995 Jul 15; 55(14):3003-7. PubMed ID: 7606718
    [Abstract] [Full Text] [Related]

  • 16. Cloning and characterization of an interstitial deletion at chromosome 11p15 in a sporadic breast cancer.
    Miyagi M, Inazawa J, Takita K, Nakamura Y.
    Hum Mol Genet; 1992 Dec 15; 1(9):705-8. PubMed ID: 1302607
    [Abstract] [Full Text] [Related]

  • 17. 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]

  • 18. 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 30; 180(1):38-43. PubMed ID: 8943813
    [Abstract] [Full Text] [Related]

  • 19. Preferential chromosome 11q and/or 17q aberrations in short-term cultures of metastatic melanoma in resections from human brain.
    Morse HG, Gonzalez R, Moore GE, Robinson WA.
    Cancer Genet Cytogenet; 1992 Dec 30; 64(2):118-26. PubMed ID: 1486560
    [Abstract] [Full Text] [Related]

  • 20. Molecular cytogenetic analysis of breast cancer: a combined multicolor fluorescence in situ hybridization and G-banding study of uncultured tumor cells.
    Ferti AD, Stamouli MJ, Panani AD, Raptis SA, Young BD.
    Cancer Genet Cytogenet; 2004 Feb 30; 149(1):28-37. PubMed ID: 15104280
    [Abstract] [Full Text] [Related]


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