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Journal Abstract Search

489 related items for PubMed ID: 8661108

  • 1. 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
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  • 2. 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
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  • 3. 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
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  • 4. 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
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  • 6. 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
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  • 7. 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
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  • 10. 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 20; 20(1):9-15. PubMed ID: 9290948
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  • 11. 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
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  • 12. 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
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  • 13. 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
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  • 14. 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
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  • 15. 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
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  • 18. 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 Oct 01; 75(2-3):180-5. PubMed ID: 9040788
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  • 20. 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
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