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Journal Abstract Search

227 related items for PubMed ID: 16146703

  • 1. DAX1 origin, function, and novel role.
    Niakan KK, McCabe ER.
    Mol Genet Metab; 2005; 86(1-2):70-83. PubMed ID: 16146703
    [Abstract] [Full Text] [Related]

  • 2. Molecular mechanisms of DAX1 action.
    Iyer AK, McCabe ER.
    Mol Genet Metab; 2004; 83(1-2):60-73. PubMed ID: 15464421
    [Abstract] [Full Text] [Related]

  • 3. The gene responsible for adrenal hypoplasia congenita, DAX-1, encodes a nuclear hormone receptor that defines a new class within the superfamily.
    Burris TP, Guo W, McCabe ER.
    Recent Prog Horm Res; 1996; 51():241-59; discussion 259-60. PubMed ID: 8701082
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  • 4. NR0B1A: an alternatively spliced form of NR0B1.
    Ho J, Zhang YH, Huang BL, McCabe ER.
    Mol Genet Metab; 2004 Dec; 83(4):330-6. PubMed ID: 15589120
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  • 5. Sex determination: a 'window' of DAX1 activity.
    Ludbrook LM, Harley VR.
    Trends Endocrinol Metab; 2004 Apr; 15(3):116-21. PubMed ID: 15046740
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  • 7. Nine novel mutations in NR0B1 (DAX1) causing adrenal hypoplasia congenita.
    Zhang YH, Huang BL, Anyane-Yeboa K, Carvalho JA, Clemons RD, Cole T, De Figueiredo BC, Lubinsky M, Metzger DL, Quadrelli R, Repaske DR, Reyno S, Seaver LH, Vaglio A, Van Vliet G, McCabe LL, McCabe ER, Phelan JK.
    Hum Mutat; 2001 Dec; 18(6):547. PubMed ID: 11748852
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  • 8. Thirteen novel mutations in the NR0B1 (DAX1) gene as cause of adrenal hypoplasia congenita.
    Krone N, Riepe FG, Dörr HG, Morlot M, Rudorff KH, Drop SL, Weigel J, Pura M, Kreze A, Boronat M, de Luca F, Tiulpakov A, Partsch CJ, Peter M, Sippell WG.
    Hum Mutat; 2005 May; 25(5):502-3. PubMed ID: 15841486
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  • 9. X-linked adrenal hypoplasia congenita is caused by abnormal nuclear localization of the DAX-1 protein.
    Lehmann SG, Lalli E, Sassone-Corsi P.
    Proc Natl Acad Sci U S A; 2002 Jun 11; 99(12):8225-30. PubMed ID: 12034880
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  • 10. Novel role for the orphan nuclear receptor Dax1 in embryogenesis, different from steroidogenesis.
    Niakan KK, Davis EC, Clipsham RC, Jiang M, Dehart DB, Sulik KK, McCabe ER.
    Mol Genet Metab; 2006 Jul 11; 88(3):261-71. PubMed ID: 16466956
    [Abstract] [Full Text] [Related]

  • 11. DAX1, a direct target of EWS/FLI1 oncoprotein, is a principal regulator of cell-cycle progression in Ewing's tumor cells.
    García-Aragoncillo E, Carrillo J, Lalli E, Agra N, Gómez-López G, Pestaña A, Alonso J.
    Oncogene; 2008 Oct 09; 27(46):6034-43. PubMed ID: 18591936
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  • 12. Novel mutation, c.1234delA, in the DAX1 gene in congenital adrenal hypoplasia.
    Lam CW, Cheng AW, Poon WT, Yuen YP, Huen KF.
    Clin Chim Acta; 2006 Dec 09; 374(1-2):151-2. PubMed ID: 16698006
    [No Abstract] [Full Text] [Related]

  • 13. Novel missense mutation (Leu466Arg) of the DAX1 gene in a patient with X-linked congenital adrenal hypoplasia.
    Abe S, Nakae J, Yasoshima K, Tajima T, Shinohara N, Murashita M, Satoh K, Koike A, Takahashi Y, Fujieda K.
    Am J Med Genet; 1999 May 21; 84(2):87-9. PubMed ID: 10323730
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  • 15. Dax1 is required for testis determination.
    Meeks JJ, Weiss J, Jameson JL.
    Nat Genet; 2003 May 21; 34(1):32-3. PubMed ID: 12679814
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  • 18. Somatic mutational analysis of DAX1 in testes from men with idiopathic azoospermia.
    Mantovani G, Mancini M, Gazzano G, Spada A, Colpi GM, Beck-Peccoz P, Persani L.
    Fertil Steril; 2005 Nov 21; 84(5):1542-4. PubMed ID: 16275267
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  • 20. Dax-1 knockdown in mouse embryonic stem cells induces loss of pluripotency and multilineage differentiation.
    Khalfallah O, Rouleau M, Barbry P, Bardoni B, Lalli E.
    Stem Cells; 2009 Jul 21; 27(7):1529-37. PubMed ID: 19530134
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