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7. 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]
8. Complete androgen insensitivity syndrome. Molecular characterization in two Chinese women. Ko TM; Yang YS; Wu MY; Kao CH; Hsu PM; Chuang SM; Lee TY J Reprod Med; 1997 Jul; 42(7):424-8. PubMed ID: 9252933 [TBL] [Abstract][Full Text] [Related]
9. The clinical and molecular spectrum of androgen insensitivity syndromes. Hiort O; Sinnecker GH; Holterhus PM; Nitsche EM; Kruse K Am J Med Genet; 1996 May; 63(1):218-22. PubMed ID: 8723113 [TBL] [Abstract][Full Text] [Related]
10. Leu-676-Pro mutation of the androgen receptor causes complete androgen insensitivity syndrome in a large Hutterite kindred. Belsham DD; Pereira F; Greenberg CR; Liao S; Wrogemann K Hum Mutat; 1995; 5(1):28-33. PubMed ID: 7537149 [TBL] [Abstract][Full Text] [Related]
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12. Characterization of a novel receptor mutation A-->T at exon 4 in complete androgen insensitivity syndrome and a carrier sibling via bidirectional polymorphism sequence analysis. Sills ES; Sholes TE; Perloe M; Kaplan CR; Davis JG; Tucker MJ Int J Mol Med; 2002 Jan; 9(1):45-8. PubMed ID: 11744994 [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. Androgen receptor point mutations as the underlying molecular defect in 2 patients with androgen insensitivity syndrome. Radmayr C; Culig Z; Glatzl J; Neuschmid-Kaspar F; Bartsch G; Klocker H J Urol; 1997 Oct; 158(4):1553-6. PubMed ID: 9302173 [TBL] [Abstract][Full Text] [Related]
16. Substitution of arginine-839 by cysteine or histidine in the androgen receptor causes different receptor phenotypes in cultured cells and coordinate degrees of clinical androgen resistance. Beitel LK; Kazemi-Esfarjani P; Kaufman M; Lumbroso R; DiGeorge AM; Killinger DW; Trifiro MA; Pinsky L J Clin Invest; 1994 Aug; 94(2):546-54. PubMed ID: 8040309 [TBL] [Abstract][Full Text] [Related]
17. [Deletion of thymine at position 2298 in exon 5 of the androgenic receptor gene causing complete androgen insensitivity syndrome]. Soriano Guillén L; Muñoz Calvo MT; Martinez Pérez J; Pozo Román J; Martín Sobrino MA; González Medeiro I; Argente Oliver J An Esp Pediatr; 2002 Apr; 56(4):347-52. PubMed ID: 11927080 [TBL] [Abstract][Full Text] [Related]
18. [An acceptor-splice-site mutation responsible for complete androgen insensitivity syndrome]. Zhang W; Li X Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2001 Feb; 18(1):14-6. PubMed ID: 11172634 [TBL] [Abstract][Full Text] [Related]
19. 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]
20. Mutations in the androgen receptor gene are associated with progression of human prostate cancer to androgen independence. Tilley WD; Buchanan G; Hickey TE; Bentel JM Clin Cancer Res; 1996 Feb; 2(2):277-85. PubMed ID: 9816170 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]