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Journal Abstract Search

309 related items for PubMed ID: 8995477

  • 1. Molecular cloning of the papillary renal cell carcinoma-associated translocation (X;1)(p11;q21) breakpoint.
    Weterman MA, Wilbrink M, Janssen I, Janssen HA, van den Berg E, Fisher SE, Craig I, Geurts van Kessel A.
    Cytogenet Cell Genet; 1996; 75(1):2-6. PubMed ID: 8995477
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  • 2. Mapping the X chromosome breakpoint in two papillary renal cell carcinoma cell lines with a t(X;1)(p11.2;q21.2) and the first report of a female case.
    Shipley JM, Birdsall S, Clark J, Crew J, Gill S, Linehan M, Gnarra J, Fisher S, Craig IW, Cooper CS.
    Cytogenet Cell Genet; 1995; 71(3):280-4. PubMed ID: 7587394
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  • 3. Fine mapping of the 1q21 breakpoint of the papillary renal cell carcinoma-associated (X;1) translocation.
    Weterman MA, Wilbrink M, Dijkhuizen T, van den Berg E, Geurts van Kessel A.
    Hum Genet; 1996 Jul; 98(1):16-21. PubMed ID: 8682500
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  • 4. Identification of a yeast artificial chromosome that spans the human papillary renal cell carcinoma-associated t(X;1) breakpoint in Xp11.2.
    Suijkerbuijk RF, Meloni AM, Sinke RJ, de Leeuw B, Wilbrink M, Janssen HA, Geraghty MT, Monaco AP, Sandberg AA, Geurts van Kessel A.
    Cancer Genet Cytogenet; 1993 Dec; 71(2):164-9. PubMed ID: 8281521
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  • 5. Localization of the synovial sarcoma t(X;18)(p11.2;q11.2) breakpoint by fluorescence in situ hybridization.
    Knight JC, Reeves BR, Kearney L, Monaco AP, Lehrach H, Cooper CS.
    Hum Mol Genet; 1992 Nov; 1(8):633-7. PubMed ID: 1338692
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  • 8. The der(17)t(X;17)(p11;q25) of human alveolar soft part sarcoma fuses the TFE3 transcription factor gene to ASPL, a novel gene at 17q25.
    Ladanyi M, Lui MY, Antonescu CR, Krause-Boehm A, Meindl A, Argani P, Healey JH, Ueda T, Yoshikawa H, Meloni-Ehrig A, Sorensen PH, Mertens F, Mandahl N, van den Berghe H, Sciot R, Dal Cin P, Bridge J.
    Oncogene; 2001 Jan 04; 20(1):48-57. PubMed ID: 11244503
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  • 9. Sublocalization of the synovial sarcoma-associated t(X;18) chromosomal breakpoint in Xp11.2 using cosmid cloning and fluorescence in situ hybridization.
    de Leeuw B, Suijkerbuijk RF, Balemans M, Sinke RJ, de Jong B, Molenaar WM, Meloni AM, Sandberg AA, Geraghty M, Hofker M.
    Oncogene; 1993 Jun 04; 8(6):1457-63. PubMed ID: 8389029
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  • 11. 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 04; 14(2):412-6. PubMed ID: 1427857
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  • 12. Fusion of the transcription factor TFE3 gene to a novel gene, PRCC, in t(X;1)(p11;q21)-positive papillary renal cell carcinomas.
    Weterman MA, Wilbrink M, Geurts van Kessel A.
    Proc Natl Acad Sci U S A; 1996 Dec 24; 93(26):15294-8. PubMed ID: 8986805
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  • 14. The t(X;18)(p11.2;q11.2) translocation found in human synovial sarcomas involves two distinct loci on the X chromosome.
    Shipley JM, Clark J, Crew AJ, Birdsall S, Rocques PJ, Gill S, Chelly J, Monaco AP, Abe S, Gusterson BA.
    Oncogene; 1994 May 24; 9(5):1447-53. PubMed ID: 8152806
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  • 16. Construction of two YAC contigs in human Xp11.23-p11.22, one encompassing the loci OATL1, GATA, TFE3, and SYP, the other linking DXS255 to DXS146.
    Fisher SE, Hatchwell E, Chand A, Ockenden N, Monaco AP, Craig IW.
    Genomics; 1995 Sep 20; 29(2):496-502. PubMed ID: 8666400
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  • 18. A 2-megabase physical contig incorporating 43 DNA markers on the human X chromosome at p11.23-p11.22 from ZNF21 to DXS255.
    Boycott KM, Halley GR, Schlessinger D, Bech-Hansen NT.
    Genomics; 1996 May 01; 33(3):488-97. PubMed ID: 8661008
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