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Journal Abstract Search

444 related items for PubMed ID: 7581399

  • 1. 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; 6(2):152-62. PubMed ID: 7581399
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  • 2. A new missense substitution at a mutational hot spot of the androgen receptor in siblings with complete androgen insensitivity syndrome.
    Dörk T, Schnieders F, Jakubiczka S, Wieacker P, Schroeder-Kurth T, Schmidtke J.
    Hum Mutat; 1998; 11(4):337-9. PubMed ID: 9554754
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  • 3. 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; 23(3):287. PubMed ID: 14974091
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  • 4. A naturally occurring mutation in the human androgen receptor of a subject with complete androgen insensitivity confers binding and transactivation by estradiol.
    Bonagura TW, Deng M, Brown TR.
    Mol Cell Endocrinol; 2007 Jan 15; 263(1-2):79-89. PubMed ID: 17011702
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  • 6. Eight novel mutations of the androgen receptor gene in patients with androgen insensitivity syndrome.
    Chávez B, Méndez JP, Ulloa-Aguirre A, Larrea F, Vilchis F.
    J Hum Genet; 2001 Jan 15; 46(10):560-5. PubMed ID: 11587068
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  • 7. Five novel androgen receptor gene mutations associated with complete androgen insensitivity syndrome.
    Jääskeläinen J, Mongan NP, Harland S, Hughes IA.
    Hum Mutat; 2006 Mar 15; 27(3):291. PubMed ID: 16470553
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  • 9. 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 15; 71(2):253-60. PubMed ID: 19178528
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  • 11. A novel point mutation (R840S) in the androgen receptor in a Brazilian family with partial androgen insensitivity syndrome.
    Melo KF, Latronico AC, Costa EM, Billerbeck AE, Mendonca BB, Arnhold IJ.
    Hum Mutat; 1999 Oct 15; 14(4):353. PubMed ID: 10502786
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  • 13. 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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  • 16. [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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  • 17. Substitution of valine-865 by methionine or leucine in the human androgen receptor causes complete or partial androgen insensitivity, respectively with distinct androgen receptor phenotypes.
    Kazemi-Esfarjani P, Beitel LK, Trifiro M, Kaufman M, Rennie P, Sheppard P, Matusik R, Pinsky L.
    Mol Endocrinol; 1993 Jan 15; 7(1):37-46. PubMed ID: 8446106
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  • 19. Identification of a critical novel mutation in the exon 1 of androgen receptor gene in 2 brothers with complete androgen insensitivity syndrome.
    Radpour R, Falah M, Aslani A, Zhong XY, Saleki A.
    J Androl; 2009 Jan 15; 30(3):230-2. PubMed ID: 19023143
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  • 20. 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 Jan 15; 125(10-11):683-95. PubMed ID: 15541764
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