These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

531 related items for PubMed ID: 7806217

  • 1. Multicolor FISH mapping of YAC clones in 3p14 and identification of a YAC spanning both FRA3B and the t(3;8) associated with hereditary renal cell carcinoma.
    Wilke CM, Guo SW, Hall BK, Boldog F, Gemmill RM, Chandrasekharappa SC, Barcroft CL, Drabkin HA, Glover TW.
    Genomics; 1994 Jul 15; 22(2):319-26. PubMed ID: 7806217
    [Abstract] [Full Text] [Related]

  • 2. A 350-kb cosmid contig in 3p14.2 that crosses the t(3;8) hereditary renal cell carcinoma translocation breakpoint and 17 aphidicolin-induced FRA3B breakpoints.
    Paradee W, Wilke CM, Wang L, Shridhar R, Mullins CM, Hoge A, Glover TW, Smith DI.
    Genomics; 1996 Jul 01; 35(1):87-93. PubMed ID: 8661108
    [Abstract] [Full Text] [Related]

  • 3. Positions of chromosome 3p14.2 fragile sites (FRA3B) within the FHIT gene.
    Zimonjic DB, Druck T, Ohta M, Kastury K, Croce CM, Popescu NC, Huebner K.
    Cancer Res; 1997 Mar 15; 57(6):1166-70. PubMed ID: 9067288
    [Abstract] [Full Text] [Related]

  • 4. Integrated YAC contig containing the 3p14.2 hereditary renal carcinoma 3;8 translocation breakpoint and the fragile site FRA3B.
    Boldog FL, Waggoner B, Glover TW, Chumakov I, Le Paslier D, Cohen D, Gemmill RM, Drabkin HA.
    Genes Chromosomes Cancer; 1994 Dec 15; 11(4):216-21. PubMed ID: 7533524
    [Abstract] [Full Text] [Related]

  • 5. Identification of unstable sequences within the common fragile site at 3p14.2: implications for the mechanism of deletions within fragile histidine triad gene/common fragile site at 3p14.2 in tumors.
    Corbin S, Neilly ME, Espinosa R, Davis EM, McKeithan TW, Le Beau MM.
    Cancer Res; 2002 Jun 15; 62(12):3477-84. PubMed ID: 12067991
    [Abstract] [Full Text] [Related]

  • 6. FHIT gene and the FRA3B region are not involved in the genetics of renal cell carcinomas.
    Bugert P, Wilhelm M, Kovacs G.
    Genes Chromosomes Cancer; 1997 Sep 15; 20(1):9-15. PubMed ID: 9290948
    [Abstract] [Full Text] [Related]

  • 7. Mapping of 29 YAC clones and identification of 3 YACs spanning the translocation t(3;8)(p14.2;q24.1) breakpoint at 8q24.1 in hereditary renal cell carcinoma.
    Shi G, Cannizzaro LA.
    Cytogenet Cell Genet; 1996 Sep 15; 75(2-3):180-5. PubMed ID: 9040788
    [Abstract] [Full Text] [Related]

  • 8. Determination of the specificity of aphidicolin-induced breakage of the human 3p14.2 fragile site.
    Wang ND, Testa JR, Smith DI.
    Genomics; 1993 Aug 15; 17(2):341-7. PubMed ID: 8406484
    [Abstract] [Full Text] [Related]

  • 9. Precise localization of aphidicolin-induced breakpoints on the short arm of human chromosome 3.
    Paradee W, Mullins C, He Z, Glover T, Wilke C, Opalka B, Schutte J, Smith DI.
    Genomics; 1995 May 20; 27(2):358-61. PubMed ID: 7558007
    [Abstract] [Full Text] [Related]

  • 10. Frequent breakpoints in the region surrounding FRA3B in sporadic renal cell carcinomas.
    Shridhar V, Wang L, Rosati R, Paradee W, Shridhar R, Mullins C, Sakr W, Grignon D, Miller OJ, Sun QC, Petros J, Smith DI.
    Oncogene; 1997 Mar 20; 14(11):1269-77. PubMed ID: 9178887
    [Abstract] [Full Text] [Related]

  • 11. Aphidicolin-induced FRA3B breakpoints cluster in two distinct regions.
    Wang L, Paradee W, Mullins C, Shridhar R, Rosati R, Wilke CM, Glover TW, Smith DI.
    Genomics; 1997 May 01; 41(3):485-8. PubMed ID: 9169152
    [Abstract] [Full Text] [Related]

  • 12. Detailed mapping around the breakpoint of (3;8) translocation in familial renal cell carcinoma and FRA3B.
    Yamakawa K, Takahashi E, Murata M, Okui K, Yokoyama S, Nakamura Y.
    Genomics; 1992 Oct 01; 14(2):412-6. PubMed ID: 1427857
    [Abstract] [Full Text] [Related]

  • 13. Translocation t(3;8)(p14.2;q24.1) in renal cell carcinoma affects expression of the common fragile site at 3p14(FRA3B) in lymphocytes.
    Glover TW, Coyle-Morris JF, Li FP, Brown RS, Berger CS, Gemmill RM, Hecht F.
    Cancer Genet Cytogenet; 1988 Mar 01; 31(1):69-73. PubMed ID: 3125959
    [Abstract] [Full Text] [Related]

  • 14. Detailed genetic and physical map of the 3p chromosome region surrounding the familial renal cell carcinoma chromosome translocation, t(3;8)(p14.2;q24.1).
    LaForgia S, Lasota J, Latif F, Boghosian-Sell L, Kastury K, Ohta M, Druck T, Atchison L, Cannizzaro LA, Barnea G.
    Cancer Res; 1993 Jul 01; 53(13):3118-24. PubMed ID: 8319219
    [Abstract] [Full Text] [Related]

  • 15. Positional cloning of the hereditary renal carcinoma 3;8 chromosome translocation breakpoint.
    Boldog FL, Gemmill RM, Wilke CM, Glover TW, Nilsson AS, Chandrasekharappa SC, Brown RS, Li FP, Drabkin HA.
    Proc Natl Acad Sci U S A; 1993 Sep 15; 90(18):8509-13. PubMed ID: 7690964
    [Abstract] [Full Text] [Related]

  • 16. [Identification of the breakpoint-flanking markers on chromosomes 1 and 17 of a constitutional translocation T(1;17)(P36;Q12-21) in a patient with neuroblastoma].
    Laureys GG.
    Verh K Acad Geneeskd Belg; 1995 Sep 15; 57(5):389-422. PubMed ID: 8571670
    [Abstract] [Full Text] [Related]

  • 17. Structure of the human receptor tyrosine phosphatase gamma gene (PTPRG) and relation to the familial RCC t(3;8) chromosome translocation.
    Kastury K, Ohta M, Lasota J, Moir D, Dorman T, LaForgia S, Druck T, Huebner K.
    Genomics; 1996 Mar 01; 32(2):225-35. PubMed ID: 8833149
    [Abstract] [Full Text] [Related]

  • 18. Defining the position of the breakpoint of the constitutional t(3;6) occurring in a family with renal cell carcinoma.
    van den Berg A, van der Veen AY, Hulsbeek MM, Kovacs G, Gemmill RM, Drabkin HA, Buys CH.
    Genes Chromosomes Cancer; 1995 Mar 01; 12(3):224-8. PubMed ID: 7536463
    [Abstract] [Full Text] [Related]

  • 19. Direct cloning of DNA sequences from the common fragile site region at chromosome band 3p14.2.
    Rassool FV, Le Beau MM, Shen ML, Neilly ME, Espinosa R, Ong ST, Boldog F, Drabkin H, McCarroll R, McKeithan TW.
    Genomics; 1996 Jul 01; 35(1):109-17. PubMed ID: 8661111
    [Abstract] [Full Text] [Related]

  • 20. Frequent homozygous deletions in the FRA3B region in tumor cell lines still leave the FHIT exons intact.
    Wang L, Darling J, Zhang JS, Qian CP, Hartmann L, Conover C, Jenkins R, Smith DI.
    Oncogene; 1998 Feb 05; 16(5):635-42. PubMed ID: 9482109
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 27.