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Journal Abstract Search

184 related items for PubMed ID: 7558007

  • 1. 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]

  • 2. Determination of the specificity of aphidicolin-induced breakage of the human 3p14.2 fragile site.
    Wang ND, Testa JR, Smith DI.
    Genomics; 1993 Aug 20; 17(2):341-7. PubMed ID: 8406484
    [Abstract] [Full Text] [Related]

  • 3. 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]

  • 4. 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]

  • 5. 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]

  • 6. 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]

  • 7. 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]

  • 8. 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]

  • 9. Frequent breakpoints in the 3p14.2 fragile site, FRA3B, in pancreatic tumors.
    Shridhar R, Shridhar V, Wang X, Paradee W, Dugan M, Sarkar F, Wilke C, Glover TW, Vaitkevicius VK, Smith DI.
    Cancer Res; 1996 Oct 01; 56(19):4347-50. PubMed ID: 8813121
    [Abstract] [Full Text] [Related]

  • 10. Chromosome breakage and recombination at fragile sites.
    Glover TW, Stein CK.
    Am J Hum Genet; 1988 Sep 01; 43(3):265-73. PubMed ID: 3137811
    [Abstract] [Full Text] [Related]

  • 11. 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]

  • 12. Chromosomal fragile site FRA16D and DNA instability in cancer.
    Mangelsdorf M, Ried K, Woollatt E, Dayan S, Eyre H, Finnis M, Hobson L, Nancarrow J, Venter D, Baker E, Richards RI.
    Cancer Res; 2000 Mar 15; 60(6):1683-9. PubMed ID: 10749140
    [Abstract] [Full Text] [Related]

  • 13. Common fragile sites and cancer (review).
    Smith DI, Huang H, Wang L.
    Int J Oncol; 1998 Jan 15; 12(1):187-96. PubMed ID: 9454904
    [Abstract] [Full Text] [Related]

  • 14. Direct correlation between FRA3B expression and cigarette smoking.
    Stein CK, Glover TW, Palmer JL, Glisson BS.
    Genes Chromosomes Cancer; 2002 Jul 15; 34(3):333-40. PubMed ID: 12007194
    [Abstract] [Full Text] [Related]

  • 15. Preferential integration of marker DNA into the chromosomal fragile site at 3p14: an approach to cloning fragile sites.
    Rassool FV, McKeithan TW, Neilly ME, van Melle E, Espinosa R, Le Beau MM.
    Proc Natl Acad Sci U S A; 1991 Aug 01; 88(15):6657-61. PubMed ID: 1862089
    [Abstract] [Full Text] [Related]

  • 16. Induction of the common fragile site FRA3B does not affect FHIT expression.
    Michael D, Rajewsky MF.
    Oncogene; 2001 Mar 29; 20(14):1798-801. PubMed ID: 11313927
    [Abstract] [Full Text] [Related]

  • 17. Increased genetic instability of the common fragile site at 3p14 after integration of exogenous DNA.
    Rassool FV, Le Beau MM, Neilly ME, van Melle E, Espinosa R, McKeithan TW.
    Am J Hum Genet; 1992 Jun 29; 50(6):1243-51. PubMed ID: 1317992
    [Abstract] [Full Text] [Related]

  • 18. Definitive functional evidence for a tumor suppressor gene on human chromosome 7q31.1 neighboring the Fra7G site.
    Zenklusen JC, Hodges LC, LaCava M, Green ED, Conti CJ.
    Oncogene; 2000 Mar 23; 19(13):1729-33. PubMed ID: 10763831
    [Abstract] [Full Text] [Related]

  • 19. 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]

  • 20. Cloning and characterization of the common fragile site FRA6F harboring a replicative senescence gene and frequently deleted in human tumors.
    Morelli C, Karayianni E, Magnanini C, Mungall AJ, Thorland E, Negrini M, Smith DI, Barbanti-Brodano G.
    Oncogene; 2002 Oct 17; 21(47):7266-76. PubMed ID: 12370818
    [Abstract] [Full Text] [Related]

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