601 related articles for article (PubMed ID: 19178528)
1. 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
[TBL] [Abstract][Full Text] [Related]
2. 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
[TBL] [Abstract][Full Text] [Related]
3. Correlation between genotype, phenotype and sex of rearing in 111 patients with partial androgen insensitivity syndrome.
Deeb A; Mason C; Lee YS; Hughes IA
Clin Endocrinol (Oxf); 2005 Jul; 63(1):56-62. PubMed ID: 15963062
[TBL] [Abstract][Full Text] [Related]
4. 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
[TBL] [Abstract][Full Text] [Related]
5. Detailed functional studies on androgen receptor mild mutations demonstrate their association with male infertility.
Zuccarello D; Ferlin A; Vinanzi C; Prana E; Garolla A; Callewaert L; Claessens F; Brinkmann AO; Foresta C
Clin Endocrinol (Oxf); 2008 Apr; 68(4):580-8. PubMed ID: 17970778
[TBL] [Abstract][Full Text] [Related]
6. 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
[TBL] [Abstract][Full Text] [Related]
7. 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; 46(10):560-5. PubMed ID: 11587068
[TBL] [Abstract][Full Text] [Related]
8. 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; 2(2):73-83. PubMed ID: 18577874
[TBL] [Abstract][Full Text] [Related]
9. 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; 113(8):457-63. PubMed ID: 16151980
[TBL] [Abstract][Full Text] [Related]
10. Impaired helix 12 dynamics due to proline 892 substitutions in the androgen receptor are associated with complete androgen insensitivity.
Elhaji YA; Stoica I; Dennis S; Purisima EO; Lumbroso R; Beitel LK; Trifiro MA
Hum Mol Genet; 2006 Mar; 15(6):921-31. PubMed ID: 16449235
[TBL] [Abstract][Full Text] [Related]
11. 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
[TBL] [Abstract][Full Text] [Related]
12. 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; 125(10-11):683-95. PubMed ID: 15541764
[TBL] [Abstract][Full Text] [Related]
13. 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; 32(2):193-8. PubMed ID: 20671138
[TBL] [Abstract][Full Text] [Related]
14. 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; 27(4):510-6. PubMed ID: 16582414
[TBL] [Abstract][Full Text] [Related]
15. Analysis of exon 1 mutations in the androgen receptor gene.
Gottlieb B; Vasiliou DM; Lumbroso R; Beitel LK; Pinsky L; Trifiro MA
Hum Mutat; 1999; 14(6):527-39. PubMed ID: 10571951
[TBL] [Abstract][Full Text] [Related]
16. Bridging structural biology and genetics by computational methods: an investigation into how the R774C mutation in the AR gene can result in complete androgen insensitivity syndrome.
Wu JH; Gottlieb B; Batist G; Sulea T; Purisima EO; Beitel LK; Trifiro M
Hum Mutat; 2003 Dec; 22(6):465-75. PubMed ID: 14635106
[TBL] [Abstract][Full Text] [Related]
17. 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; 28(5):772-6. PubMed ID: 17522416
[TBL] [Abstract][Full Text] [Related]
18. Human androgen insensitivity syndrome.
Brown TR
J Androl; 1995; 16(4):299-303. PubMed ID: 8537246
[TBL] [Abstract][Full Text] [Related]
19. [Androgen insensitivity syndrome. Clinical features and molecular genetics].
Sólyom J; Scheiber D; Fekete G
Orv Hetil; 2001 Aug; 142(31):1659-65. PubMed ID: 11556259
[TBL] [Abstract][Full Text] [Related]
20. [Mutation analysis of the androgen receptor gene in a complete androgen insensitivity syndrome family].
Wu W; Luo F; Geng Q; Hao Y; Chen W; Cai J; Xie J
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2009 Dec; 26(6):606-9. PubMed ID: 19953479
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
