117 related articles for article (PubMed ID: 8537246)
1. Human androgen insensitivity syndrome.
Brown TR
J Androl; 1995; 16(4):299-303. PubMed ID: 8537246
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. 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]
4. 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]
5. 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]
6. 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]
7. 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
[TBL] [Abstract][Full Text] [Related]
8. 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]
9. Male infertility and androgen receptor gene mutations: clinical features and identification of seven novel mutations.
Ferlin A; Vinanzi C; Garolla A; Selice R; Zuccarello D; Cazzadore C; Foresta C
Clin Endocrinol (Oxf); 2006 Nov; 65(5):606-10. PubMed ID: 17054461
[TBL] [Abstract][Full Text] [Related]
10. 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]
11. 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]
12. 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]
13. Partial androgen insensitivity syndrome with R840H mutation in androgen receptor: report of one case.
Yen JL; Chang KH; Sheu JC; Lee YJ; Tsai LP
Acta Paediatr Taiwan; 2005; 46(2):101-5. PubMed ID: 16302589
[TBL] [Abstract][Full Text] [Related]
14. Androgen resistance.
Hughes IA; Deeb A
Best Pract Res Clin Endocrinol Metab; 2006 Dec; 20(4):577-98. PubMed ID: 17161333
[TBL] [Abstract][Full Text] [Related]
15. [The androgen receptor: molecular pathology].
Sultan Ch; Gobinet J; Terouanne B; Paris F; Belon Ch; Jalaguier S; Georget V; Poujol N; Auzou G; Lumbroso S
J Soc Biol; 2002; 196(3):223-40. PubMed ID: 12465595
[TBL] [Abstract][Full Text] [Related]
16. A novel E153X point mutation in the androgen receptor gene in a patient with complete androgen insensitivity syndrome.
Copelli SB; Lumbroso S; Audran F; Pellizzari EH; Heinrich JJ; Cigorraga SB; Sultan C; Chemes HE
Asian J Androl; 1999 Jun; 1(1-2):73-7. PubMed ID: 11225909
[TBL] [Abstract][Full Text] [Related]
17. Clinical, hormonal and genetic characteristics of androgen insensitivity syndrome in 39 Chinese patients.
Liu Q; Yin X; Li P
Reprod Biol Endocrinol; 2020 Apr; 18(1):34. PubMed ID: 32345305
[TBL] [Abstract][Full Text] [Related]
18. 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; 44 Suppl 1():523-9. PubMed ID: 21950590
[TBL] [Abstract][Full Text] [Related]
19. 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]
20. Functional analysis of novel androgen receptor mutations in a unique cohort of Indonesian patients with a disorder of sex development.
Elfferich P; Juniarto AZ; Dubbink HJ; van Royen ME; Molier M; Hoogerbrugge J; Houtsmuller AB; Trapman J; Santosa A; de Jong FH; Drop SL; Faradz SM; Bruggenwirth H; Brinkmann AO
Sex Dev; 2009; 3(5):237-44. PubMed ID: 19851057
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]