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159 related items for PubMed ID: 9178887
1. 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]
2. 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 [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. 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]
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. 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]
7. 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]
8. 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]
9. 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]
10. 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]
11. Terminal deletion of chromosome 3p sequences in nonpapillary renal cell carcinomas: a breakpoint cluster between loci D3S1285 and D3S1603. Wilhelm M, Bugert P, Kenck C, Staehler G, Kovacs G. Cancer Res; 1995 Nov 15; 55(22):5383-5. PubMed ID: 7585605 [Abstract] [Full Text] [Related]
12. PCR-based RFLP screening of the commonly deleted 3p loci in renal cortical neoplasms. el-Naggar AK, Batsakis JG, Wang G, Lee MS. Diagn Mol Pathol; 1993 Dec 15; 2(4):269-76. PubMed ID: 7906993 [Abstract] [Full Text] [Related]
13. Loss of heterozygosity on the long arm of human chromosome 7 in sporadic renal cell carcinomas. Shridhar V, Sun QC, Miller OJ, Kalemkerian GP, Petros J, Smith DI. Oncogene; 1997 Nov 27; 15(22):2727-33. PubMed ID: 9400999 [Abstract] [Full Text] [Related]
14. Molecular genetic evidence for the independent origin of multifocal papillary tumors in patients with papillary renal cell carcinomas. Jones TD, Eble JN, Wang M, MacLennan GT, Delahunt B, Brunelli M, Martignoni G, Lopez-Beltran A, Bonsib SM, Ulbright TM, Zhang S, Nigro K, Cheng L. Clin Cancer Res; 2005 Oct 15; 11(20):7226-33. PubMed ID: 16243792 [Abstract] [Full Text] [Related]
15. Physical and functional mapping of a tumor suppressor locus for renal cell carcinoma within chromosome 3p12. Lott ST, Lovell M, Naylor SL, Killary AM. Cancer Res; 1998 Aug 15; 58(16):3533-7. PubMed ID: 9721855 [Abstract] [Full Text] [Related]
16. Histopathological, cytogenetic, and molecular characterization of renal cortical tumors. Presti JC, Rao PH, Chen Q, Reuter VE, Li FP, Fair WR, Jhanwar SC. Cancer Res; 1991 Mar 01; 51(5):1544-52. PubMed ID: 1671759 [Abstract] [Full Text] [Related]
17. 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]
18. 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 [Abstract] [Full Text] [Related]
20. Detection of deletions in the short arm of chromosome 3 in uncultured renal cell carcinomas by interphase cytogenetics. Siebert R, Jacobi C, Matthiesen P, Zühlke-Jenisch R, Potratz C, Zhang Y, Stöckle M, Klöppel G, Grote W, Schlegelberger B. J Urol; 1998 Aug 01; 160(2):534-9. PubMed ID: 9679924 [Abstract] [Full Text] [Related] Page: [Next] [New Search]