353 related articles for article (PubMed ID: 22334387)
1. The androgen receptor gene mutations database: 2012 update.
Gottlieb B; Beitel LK; Nadarajah A; Paliouras M; Trifiro M
Hum Mutat; 2012 May; 33(5):887-94. PubMed ID: 22334387
[TBL] [Abstract][Full Text] [Related]
2. The androgen receptor gene mutations database (ARDB): 2004 update.
Gottlieb B; Beitel LK; Wu JH; Trifiro M
Hum Mutat; 2004 Jun; 23(6):527-33. PubMed ID: 15146455
[TBL] [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
[TBL] [Abstract][Full Text] [Related]
4. Update of the androgen receptor gene mutations database.
Gottlieb B; Beitel LK; Lumbroso R; Pinsky L; Trifiro M
Hum Mutat; 1999; 14(2):103-14. PubMed ID: 10425033
[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. 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]
7. 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]
8. Healthy birth after testicular extraction of sperm and ICSI from an azoospermic man with mild androgen insensitivity syndrome caused by an androgen receptor partial loss-of-function mutation.
Massin N; Bry H; Vija L; Maione L; Constancis E; Haddad B; Morel Y; Claessens F; Young J
Clin Endocrinol (Oxf); 2012 Oct; 77(4):593-8. PubMed ID: 22469007
[TBL] [Abstract][Full Text] [Related]
9. 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]
10. 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]
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; 10(4):687-91. PubMed ID: 18097502
[TBL] [Abstract][Full Text] [Related]
12. Collocation of androgen receptor gene mutations in prostate cancer.
Buchanan G; Greenberg NM; Scher HI; Harris JM; Marshall VR; Tilley WD
Clin Cancer Res; 2001 May; 7(5):1273-81. PubMed ID: 11350894
[TBL] [Abstract][Full Text] [Related]
13. 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]
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; 46(10):560-5. PubMed ID: 11587068
[TBL] [Abstract][Full Text] [Related]
15. Androgen receptor mutations identified in prostate cancer and androgen insensitivity syndrome display aberrant ART-27 coactivator function.
Li W; Cavasotto CN; Cardozo T; Ha S; Dang T; Taneja SS; Logan SK; Garabedian MJ
Mol Endocrinol; 2005 Sep; 19(9):2273-82. PubMed ID: 15919721
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. Human androgen insensitivity syndrome.
Brown TR
J Androl; 1995; 16(4):299-303. PubMed ID: 8537246
[TBL] [Abstract][Full Text] [Related]
18. 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; 66(6):822-6. PubMed ID: 17408421
[TBL] [Abstract][Full Text] [Related]
19. 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]
20. 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]
[Next] [New Search]
