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Journal Abstract Search

200 related items for PubMed ID: 9702070

  • 1. [Pathogenesis of androgen insensitivity syndrome].
    Okabe T, Nawata H.
    Nihon Rinsho; 1998 Jul; 56(7):1881-6. PubMed ID: 9702070
    [Abstract] [Full Text] [Related]

  • 2. [Androgen insensitivity syndrome and co-activator disease].
    Tanaka K, Nomura M, Nawata H.
    Nihon Rinsho; 2004 Feb; 62(2):344-50. PubMed ID: 14968543
    [Abstract] [Full Text] [Related]

  • 3. Comparison of the molecular consequences of different mutations at residue 754 and 690 of the androgen receptor (AR) and androgen insensitivity syndrome (AIS) phenotype.
    Tadokoro R, Bunch T, Schwabe JW, Hughes IA, Murphy JC.
    Clin Endocrinol (Oxf); 2009 Aug; 71(2):253-60. PubMed ID: 19178528
    [Abstract] [Full Text] [Related]

  • 4. Human androgen insensitivity due to point mutations encoding amino acid substitutions in the androgen receptor steroid-binding domain.
    Murono K, Mendonca BB, Arnhold IJ, Rigon AC, Migeon CJ, Brown TR.
    Hum Mutat; 1995 Aug; 6(2):152-62. PubMed ID: 7581399
    [Abstract] [Full Text] [Related]

  • 5. Five novel androgen receptor gene mutations associated with complete androgen insensitivity syndrome.
    Jääskeläinen J, Mongan NP, Harland S, Hughes IA.
    Hum Mutat; 2006 Mar; 27(3):291. PubMed ID: 16470553
    [Abstract] [Full Text] [Related]

  • 6. Partial androgen insensitivity with phenotypic variation caused by androgen receptor mutations that disrupt activation function 2 and the NH(2)- and carboxyl-terminal interaction.
    Quigley CA, Tan JA, He B, Zhou ZX, Mebarki F, Morel Y, Forest MG, Chatelain P, Ritzén EM, French FS, Wilson EM.
    Mech Ageing Dev; 2004 Mar; 125(10-11):683-95. PubMed ID: 15541764
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  • 9. [Androgen receptor and insensitivity to androgens].
    Mowszowicz I, Kuttenn F.
    Rev Prat; 1994 May 15; 44(10):1304-9. PubMed ID: 7939189
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  • 10. Mutations in the amino-terminal domain of the human androgen receptor may be associated with partial androgen insensitivity and impaired transactivation in vitro.
    Holterhus PM, Werner R, Struve D, Hauffa BP, Schroeder C, Hiort O.
    Exp Clin Endocrinol Diabetes; 2005 Sep 15; 113(8):457-63. PubMed ID: 16151980
    [Abstract] [Full Text] [Related]

  • 11. Novel mutation in the ligand-binding domain of the androgen receptor gene (l790p) associated with complete androgen insensitivity syndrome.
    Raicu F, Giuliani R, Gatta V, Palka C, Franchi PG, Lelli-Chiesa P, Tumini S, Stuppia L.
    Asian J Androl; 2008 Jul 15; 10(4):687-91. PubMed ID: 18097502
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  • 12. Novel androgen receptor gene mutations in Australian patients with complete androgen insensitivity syndrome.
    MacLean HE, Ball EM, Rekaris G, Warne GL, Zajac JD.
    Hum Mutat; 2004 Mar 15; 23(3):287. PubMed ID: 14974091
    [Abstract] [Full Text] [Related]

  • 13. Molecular biology of androgen insensitivity.
    Jääskeläinen J.
    Mol Cell Endocrinol; 2012 Apr 16; 352(1-2):4-12. PubMed ID: 21871529
    [Abstract] [Full Text] [Related]

  • 14. G708E mutation in the androgen receptor results in complete loss of androgen function.
    Rajender S, Pooja S, Gupta NJ, Chakrabarty B, Singh L, Thangaraj K.
    J Androl; 2011 Apr 16; 32(2):193-8. PubMed ID: 20671138
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  • 16. L859F mutation in androgen receptor gene results in complete loss of androgen binding to the receptor.
    Rajender S, Singh L, Thangaraj K.
    J Androl; 2007 Apr 16; 28(5):772-6. PubMed ID: 17522416
    [Abstract] [Full Text] [Related]

  • 17. Two de novo mutations in the AR gene cause the complete androgen insensitivity syndrome in a pair of monozygotic twins.
    Mongan NP, Jääskeläinen J, Green K, Schwabe JW, Shimura N, Dattani M, Hughes IA.
    J Clin Endocrinol Metab; 2002 Mar 16; 87(3):1057-61. PubMed ID: 11889162
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  • 20. Androgen insensitivity syndrome (or Morris syndrome) and other associated pathologies.
    Dell'Edera D, Malvasi A, Vitullo E, Epifania AA, Tinelli A, Laterza F, Novelli A, Pacella E, Mazzone E, Novelli G.
    Eur Rev Med Pharmacol Sci; 2010 Nov 16; 14(11):947-57. PubMed ID: 21284344
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