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Journal Abstract Search

106 related items for PubMed ID: 10780782

  • 1. The human EZH2 gene: genomic organisation and revised mapping in 7q35 within the critical region for malignant myeloid disorders.
    Cardoso C, Mignon C, Hetet G, Grandchamps B, Fontes M, Colleaux L.
    Eur J Hum Genet; 2000 Mar; 8(3):174-80. PubMed ID: 10780782
    [Abstract] [Full Text] [Related]

  • 2. Cloning of a human homolog of the Drosophila enhancer of zeste gene (EZH2) that maps to chromosome 21q22.2.
    Chen H, Rossier C, Antonarakis SE.
    Genomics; 1996 Nov 15; 38(1):30-7. PubMed ID: 8954776
    [Abstract] [Full Text] [Related]

  • 3. Isolation of human and murine homologues of the Drosophila minibrain gene: human homologue maps to 21q22.2 in the Down syndrome "critical region".
    Song WJ, Sternberg LR, Kasten-Sportès C, Keuren ML, Chung SH, Slack AC, Miller DE, Glover TW, Chiang PW, Lou L, Kurnit DM.
    Genomics; 1996 Dec 15; 38(3):331-9. PubMed ID: 8975710
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  • 5. Identification and characterization of ASXL3 gene in silico.
    Katoh M, Katoh M.
    Int J Oncol; 2004 Jun 15; 24(6):1617-22. PubMed ID: 15138607
    [Abstract] [Full Text] [Related]

  • 6. The AML1 gene: a transcription factor involved in the pathogenesis of myeloid and lymphoid leukemias.
    Lo Coco F, Pisegna S, Diverio D.
    Haematologica; 1997 Jun 15; 82(3):364-70. PubMed ID: 9234595
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  • 7. cDNA cloning, tissue distribution, and chromosomal localization of myelodysplasia/myeloid leukemia factor 2 (MLF2).
    Kuefer MU, Look AT, Williams DC, Valentine V, Naeve CW, Behm FG, Mullersman JE, Yoneda-Kato N, Montgomery K, Kucherlapati R, Morris SW.
    Genomics; 1996 Jul 15; 35(2):392-6. PubMed ID: 8661158
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  • 9. The mammalian single-minded (SIM) gene: mouse cDNA structure and diencephalic expression indicate a candidate gene for Down syndrome.
    Yamaki A, Noda S, Kudoh J, Shindoh N, Maeda H, Minoshima S, Kawasaki K, Shimizu Y, Shimizu N.
    Genomics; 1996 Jul 01; 35(1):136-43. PubMed ID: 8661114
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  • 10. The murine Polycomb-group gene eed and its human orthologue: functional implications of evolutionary conservation.
    Schumacher A, Lichtarge O, Schwartz S, Magnuson T.
    Genomics; 1998 Nov 15; 54(1):79-88. PubMed ID: 9806832
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  • 11. Genomic organization, tissue expression, and cellular localization of AF3p21, a fusion partner of MLL in therapy-related leukemia.
    Hayakawa A, Matsuda Y, Daibata M, Nakamura H, Sano K.
    Genes Chromosomes Cancer; 2001 Apr 15; 30(4):364-74. PubMed ID: 11241789
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  • 12. Mapping of the human holocarboxylase synthetase gene (HCS) to the Down syndrome critical region of chromosome 21q22.
    Blouin JL, Duriaux Saïl G, Antonarakis SE.
    Ann Genet; 1996 Apr 15; 39(3):185-8. PubMed ID: 8839893
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  • 13. Transcript mapping of the human chromosome 11q12-q13.1 gene-rich region identifies several newly described conserved genes.
    Cooper PR, Nowak NJ, Higgins MJ, Church DM, Shows TB.
    Genomics; 1998 May 01; 49(3):419-29. PubMed ID: 9615227
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  • 14. The polycomb-group gene Ezh2 is required for early mouse development.
    O'Carroll D, Erhardt S, Pagani M, Barton SC, Surani MA, Jenuwein T.
    Mol Cell Biol; 2001 Jul 01; 21(13):4330-6. PubMed ID: 11390661
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  • 15. WWOX, a novel WW domain-containing protein mapping to human chromosome 16q23.3-24.1, a region frequently affected in breast cancer.
    Bednarek AK, Laflin KJ, Daniel RL, Liao Q, Hawkins KA, Aldaz CM.
    Cancer Res; 2000 Apr 15; 60(8):2140-5. PubMed ID: 10786676
    [Abstract] [Full Text] [Related]

  • 16. Isolation and characterization of a human gene containing a nuclear localization signal from the critical region for velo-cardio-facial syndrome on 22q11.
    Funke B, Puech A, Saint-Jore B, Pandita R, Skoultchi A, Morrow B.
    Genomics; 1998 Oct 15; 53(2):146-54. PubMed ID: 9790763
    [Abstract] [Full Text] [Related]

  • 17. A novel cryptic translocation t(12;17)(p13;p12-p13) in a secondary acute myeloid leukemia results in a fusion of the ETV6 gene and the antisense strand of the PER1 gene.
    Murga Penas EM, Cools J, Algenstaedt P, Hinz K, Seeger D, Schafhausen P, Schilling G, Marynen P, Hossfeld DK, Dierlamm J.
    Genes Chromosomes Cancer; 2003 May 15; 37(1):79-83. PubMed ID: 12661008
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  • 18. The NNP-1 gene (D21S2056E), which encodes a novel nuclear protein, maps in close proximity to the cystatin B gene within the EPM1 and APECED critical region on 21q22.3.
    Jansen E, Meulemans SM, Orlans IC, Van de Ven WJ.
    Genomics; 1997 Jun 01; 42(2):336-41. PubMed ID: 9192856
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  • 20. Fusion of the homeobox gene HLXB9 and the ETV6 gene in infant acute myeloid leukemias with the t(7;12)(q36;p13).
    Beverloo HB, Panagopoulos I, Isaksson M, van Wering E, van Drunen E, de Klein A, Johansson B, Slater R.
    Cancer Res; 2001 Jul 15; 61(14):5374-7. PubMed ID: 11454678
    [Abstract] [Full Text] [Related]

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