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103 related items for PubMed ID: 7585599

  • 1. Loss of heterozygosity at the familial RCC t(3;8) locus in most clear cell renal carcinomas.
    Druck T, Kastury K, Hadaczek P, Podolski J, Toloczko A, Sikorski A, Ohta M, LaForgia S, Lasota J, McCue P.
    Cancer Res; 1995 Nov 15; 55(22):5348-53. PubMed ID: 7585599
    [Abstract] [Full Text] [Related]

  • 2. 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]

  • 3. Common regions of deletion in chromosome regions 3p12 and 3p14.2 in primary clear cell renal carcinomas.
    Lubinski J, Hadaczek P, Podolski J, Toloczko A, Sikorski A, McCue P, Druck T, Huebner K.
    Cancer Res; 1994 Jul 15; 54(14):3710-3. PubMed ID: 8033088
    [Abstract] [Full Text] [Related]

  • 4. 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]

  • 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. Loss of heterozygosity at 3p14.2 in clear cell renal cell carcinoma is an early event and is highly localized to the FHIT gene locus.
    Velickovic M, Delahunt B, Grebe SK.
    Cancer Res; 1999 Mar 15; 59(6):1323-6. PubMed ID: 10096566
    [Abstract] [Full Text] [Related]

  • 7. Cytogenetic and molecular findings in 75 clear cell renal cell carcinomas.
    Kardas I, Mrózek K, Babinska M, Krajka K, Hadaczek P, Lubinski J, Roszkiewicz A, Kuziemska E, Limon J.
    Oncol Rep; 2005 May 15; 13(5):949-56. PubMed ID: 15809763
    [Abstract] [Full Text] [Related]

  • 8. Major role for a 3p21 region and lack of involvement of the t(3;8) breakpoint region in the development of renal cell carcinoma suggested by loss of heterozygosity analysis.
    van den Berg A, Hulsbeek MF, de Jong D, Kok K, Veldhuis PM, Roche J, Buys CH.
    Genes Chromosomes Cancer; 1996 Jan 15; 15(1):64-72. PubMed ID: 8824727
    [Abstract] [Full Text] [Related]

  • 9. 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]

  • 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. Characteristic loss of heterozygosity in chromosome 3P and low frequency of replication errors in sporadic renal cell carcinoma.
    Chino K, Esumi M, Ishida H, Okada K.
    J Urol; 1999 Aug 01; 162(2):614-8. PubMed ID: 10411097
    [Abstract] [Full Text] [Related]

  • 12. Genomic alterations and instabilities in renal cell carcinomas and their relationship to tumor pathology.
    Thrash-Bingham CA, Salazar H, Freed JJ, Greenberg RE, Tartof KD.
    Cancer Res; 1995 Dec 15; 55(24):6189-95. PubMed ID: 8521412
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  • 15. 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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  • 16. 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 20; 2(4):269-76. PubMed ID: 7906993
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  • 18. [The loss of heterozygosity on the short arm of chromosome 3 in renal carcinoma].
    Maestro de las Casas ML, del Barco Barriuso V, Moreno Sierra J, Izquierdo López L, Sanz Casla MT, Zanna I, Redondo González E, Chicharro Almarza J, Fernández Pérez C, Resel Estévez L.
    Arch Esp Urol; 1999 Dec 20; 52(1):3-9. PubMed ID: 10101881
    [Abstract] [Full Text] [Related]

  • 19. Potential gastrointestinal tumor suppressor locus at the 3p14.2 FRA3B site identified by homozygous deletions in tumor cell lines.
    Kastury K, Baffa R, Druck T, Ohta M, Cotticelli MG, Inoue H, Negrini M, Rugge M, Huang D, Croce CM, Palazzo J, Huebner K.
    Cancer Res; 1996 Mar 01; 56(5):978-83. PubMed ID: 8640789
    [Abstract] [Full Text] [Related]

  • 20. 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 01; 20(1):9-15. PubMed ID: 9290948
    [Abstract] [Full Text] [Related]


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