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Journal Abstract Search

176 related items for PubMed ID: 14635106

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  • 3. 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
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  • 4. 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; 10(4):687-91. PubMed ID: 18097502
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  • 7. 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 Jul; 125(10-11):683-95. PubMed ID: 15541764
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  • 9. In-vitro characterization of androgen receptor mutations associated with complete androgen insensitivity syndrome reveals distinct functional deficits.
    Werner R, Zhan J, Gesing J, Struve D, Hiort O.
    Sex Dev; 2008 Jul; 2(2):73-83. PubMed ID: 18577874
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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; 23(3):287. PubMed ID: 14974091
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  • 13. Ala 586 Asp mutation in androgen receptor disrupts transactivation function without affecting androgen binding.
    Rajender S, Gupta NJ, Chakrabarty B, Singh L, Thangaraj K.
    Fertil Steril; 2009 Mar; 91(3):933.e23-8. PubMed ID: 19062009
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  • 14. 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 Mar; 46(10):560-5. PubMed ID: 11587068
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  • 15. A novel androgen receptor mutation resulting in complete androgen insensitivity syndrome and bilateral Leydig cell hyperplasia.
    Singh R, Shastry PK, Rasalkar AA, Singh L, Thangaraj K.
    J Androl; 2006 Mar; 27(4):510-6. PubMed ID: 16582414
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  • 16. L712V mutation in the androgen receptor gene causes complete androgen insensitivity syndrome due to severe loss of androgen function.
    Rajender S, Gupta NJ, Chakrabarty B, Singh L, Thangaraj K.
    Steroids; 2013 Dec 11; 78(12-13):1288-92. PubMed ID: 24055831
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  • 17. Functional characterisation of a natural androgen receptor missense mutation (N771H) causing human androgen insensitivity syndrome.
    Cai J, Cai LQ, Hong Y, Zhu YS.
    Andrologia; 2012 May 11; 44 Suppl 1():523-9. PubMed ID: 21950590
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  • 18. A mutation c.C2812T in the androgen receptor gene resulting in Pro817Leu substitution may affect dimerization of the androgen receptor and result in androgen insensitivity syndrome.
    Turek-Plewa J, Eckersdorf-Mastalerz A, Kaluzewski B, Helszer Z, Trzeciak WH.
    Fertil Steril; 2006 Jun 11; 85(6):1822.e1-4. PubMed ID: 16759930
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  • 19. Complete androgen insensitivity without Wolffian duct development: the AR-A form of the androgen receptor is not sufficient for male genital development.
    Barbaro M, Oscarson M, Almskog I, Hamberg H, Wedell A.
    Clin Endocrinol (Oxf); 2007 Jun 11; 66(6):822-6. PubMed ID: 17408421
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  • 20. Dynamic communication between androgen and coactivator: mutually induced conformational perturbations in androgen receptor ligand-binding domain.
    Xu X, Yang W, Wang X, Li Y, Wang Y, Ai C.
    Proteins; 2011 Apr 11; 79(4):1154-71. PubMed ID: 21322031
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