60 related articles for article (PubMed ID: 9554755)
1. An androgen receptor gene mutation (A645D) in a boy with a normal phenotype.
Nordenskjöld A; Söderhäll S
Hum Mutat; 1998; 11(4):339. PubMed ID: 9554755
[TBL] [Abstract][Full Text] [Related]
2. 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]
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. Altered mRNA expression due to insertion or substitution of thymine at position +3 of two splice-donor sites in the androgen receptor gene.
Trifiro MA; Lumbroso R; Beitel LK; Vasiliou DM; Bouchard J; Deal C; Van Vliet G; Pinsky L
Eur J Hum Genet; 1997; 5(1):50-8. PubMed ID: 9156321
[TBL] [Abstract][Full Text] [Related]
5. 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
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. 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]
8. 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]
9. GTG mutation in the start codon of the androgen receptor gene in a family of horses with 64,XY disorder of sex development.
Révay T; Villagómez DA; Brewer D; Chenier T; King WA
Sex Dev; 2012; 6(1-3):108-16. PubMed ID: 22095250
[TBL] [Abstract][Full Text] [Related]
10. Genetic analysis of a family with 46,XY "female" associated with infertility.
Wang X; Wang XR; Liu MG; Wang Q; Liu JY
Yi Chuan Xue Bao; 2006 Jan; 33(1):19-25. PubMed ID: 16450583
[TBL] [Abstract][Full Text] [Related]
11. The same mutation affecting the splicing of WT1 gene is present on Frasier syndrome patients with or without Wilms' tumor.
Barbosa AS; Hadjiathanasiou CG; Theodoridis C; Papathanasiou A; Tar A; Merksz M; Györvári B; Sultan C; Dumas R; Jaubert F; Niaudet P; Moreira-Filho CA; Cotinot C; Fellous M
Hum Mutat; 1999; 13(2):146-53. PubMed ID: 10094551
[TBL] [Abstract][Full Text] [Related]
12. Molecular analysis of androgen resistance syndromes in Egyptian patients.
Essawi M; Gad YZ; el-Rouby O; Temtamy SA; Sabour YA; el-Awady MK
Dis Markers; 1997 Apr; 13(2):99-105. PubMed ID: 9160185
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. A point mutation within exon 5 of the WT1 gene of a sporadic unilateral Wilms' tumor alters gene function.
Guan LS; Liu JJ; Xu YH; Wang ZY
Cancer Res; 1998 Sep; 58(18):4180-4. PubMed ID: 9751632
[TBL] [Abstract][Full Text] [Related]
15. 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]
16. 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; 30(3):230-2. PubMed ID: 19023143
[TBL] [Abstract][Full Text] [Related]
17. Alport syndrome. Molecular genetic aspects.
Hertz JM
Dan Med Bull; 2009 Aug; 56(3):105-52. PubMed ID: 19728970
[TBL] [Abstract][Full Text] [Related]
18. 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]
19. 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]
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; 125(10-11):683-95. PubMed ID: 15541764
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]