260 related articles for article (PubMed ID: 27994190)
21. 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]
22. Investigation of androgen receptor gene mutations in a series of 21 patients with 46,XY disorders of sex development.
Topcu V; Ilgin-Ruhi H; Siklar Z; Karabulut HG; Berberoglu M; Hacihamdioglu B; Savas-Erdeve S; Aycan Z; Peltek-Kendirci HN; Ocal G; Tukun FA
J Pediatr Endocrinol Metab; 2015 Nov; 28(11-12):1257-63. PubMed ID: 26197461
[TBL] [Abstract][Full Text] [Related]
23. Molecular biology of androgen insensitivity.
Jääskeläinen J
Mol Cell Endocrinol; 2012 Apr; 352(1-2):4-12. PubMed ID: 21871529
[TBL] [Abstract][Full Text] [Related]
24. Androgen insensitivity syndrome in a cohort of Sri Lankan children with 46, XY disorders of sex development (46, XY DSD).
de Silva KS; Sirisena ND; Wijenayaka HK; Cooray JG; Jayasekara RW; Dissanayake VH
Ceylon Med J; 2015 Dec; 60(4):139-42. PubMed ID: 26778393
[TBL] [Abstract][Full Text] [Related]
25. A recurrent synonymous mutation in the human androgen receptor gene causing complete androgen insensitivity syndrome.
Batista RL; Rodrigues ADS; Nishi MY; Gomes NL; Faria JAD; Moraes DR; Carvalho LR; Costa EMF; Domenice S; Mendonca BB
J Steroid Biochem Mol Biol; 2017 Nov; 174():14-16. PubMed ID: 28743543
[TBL] [Abstract][Full Text] [Related]
26. Identification of two additional novel mutations in the AR gene associated with severe forms of androgen insensitivity syndrome.
Kharrat M; Tajouri A; Nacef IB; Hizem C; Trabelsi M; Maazoul F; M'rad R; Chaabouni HB
Steroids; 2019 Dec; 152():108489. PubMed ID: 31499074
[TBL] [Abstract][Full Text] [Related]
27. Six novel Mutation analysis of the androgen receptor gene in 17 Chinese patients with androgen insensitivity syndrome.
Jiang X; Teng Y; Chen X; Liang N; Li Z; Liang D; Wu L
Clin Chim Acta; 2020 Jul; 506():180-186. PubMed ID: 32229106
[TBL] [Abstract][Full Text] [Related]
28. Sequence of the intron/exon junctions of the coding region of the human androgen receptor gene and identification of a point mutation in a family with complete androgen insensitivity.
Lubahn DB; Brown TR; Simental JA; Higgs HN; Migeon CJ; Wilson EM; French FS
Proc Natl Acad Sci U S A; 1989 Dec; 86(23):9534-8. PubMed ID: 2594783
[TBL] [Abstract][Full Text] [Related]
29. A novel mutation of the androgen receptor gene in familial complete androgen insensitivity syndrome.
Li Y; Qu S; Li P
Eur Rev Med Pharmacol Sci; 2015 Nov; 19(21):4146-52. PubMed ID: 26592841
[TBL] [Abstract][Full Text] [Related]
30. Novel and recurrent mutations in patients with androgen insensitivity syndromes.
Ledig S; Jakubiczka S; Neulen J; Aulepp U; Burck-Lehmann U; Mohnike K; Thiele H; Zierler H; Brewer C; Wieacker P
Horm Res; 2005; 63(6):263-9. PubMed ID: 15925895
[TBL] [Abstract][Full Text] [Related]
31. Single base mutations in the human androgen receptor gene causing complete androgen insensitivity: rapid detection by a modified denaturing gradient gel electrophoresis technique.
De Bellis A; Quigley CA; Cariello NF; el-Awady MK; Sar M; Lane MV; Wilson EM; French FS
Mol Endocrinol; 1992 Nov; 6(11):1909-20. PubMed ID: 1480178
[TBL] [Abstract][Full Text] [Related]
32. Complete androgen insensitivity syndrome caused by a novel mutation in the ligand-binding domain of the androgen receptor: functional characterization.
Rosa S; Biason-Lauber A; Mongan NP; Navratil F; Schoenle EJ
J Clin Endocrinol Metab; 2002 Sep; 87(9):4378-82. PubMed ID: 12213902
[TBL] [Abstract][Full Text] [Related]
33. A novel mutation in the CAG triplet region of exon 1 of androgen receptor gene causes complete androgen insensitivity syndrome in a large kindred.
Zhu YS; Cai LQ; Cordero JJ; Canovatchel WJ; Katz MD; Imperato-McGinley J
J Clin Endocrinol Metab; 1999 May; 84(5):1590-4. PubMed ID: 10323385
[TBL] [Abstract][Full Text] [Related]
34. Prenatal diagnosis of androgen insensitivity syndrome.
Bianca S; Cataliotti A; Bartoloni G; Torrente I; Barrano B; Boemi G; Lo Presti M; Indaco L; Barone C; Ettore G
Fetal Diagn Ther; 2009; 26(3):167-9. PubMed ID: 19844078
[TBL] [Abstract][Full Text] [Related]
35. Mutations of androgen receptor gene in androgen insensitivity syndromes.
Sultan C; Lumbroso S; Poujol N; Belon C; Boudon C; Lobaccaro JM
J Steroid Biochem Mol Biol; 1993 Nov; 46(5):519-30. PubMed ID: 8240973
[TBL] [Abstract][Full Text] [Related]
36. 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]
37. Mutational analysis of the androgen receptor (NR3C4) gene in patients with 46,XY DSD.
Ramos L; Chávez B; Mares L; Valdés E; Vilchis F
Gene; 2018 Jan; 641():86-93. PubMed ID: 29051026
[TBL] [Abstract][Full Text] [Related]
38. Clinical and molecular characteristics in 15 patients with androgen receptor gene mutations from South China.
Su L; Cheng J; Yin X; Liu G; Lu Z; Sheng H; Cai Y; Shi Q; Liu L
Andrologia; 2017 Dec; 49(10):. PubMed ID: 28261839
[TBL] [Abstract][Full Text] [Related]
39. Novel compound variants of the AR and MAP3K1 genes are related to the clinical heterogeneity of androgen insensitivity syndrome.
Cheng Y; Sun Y; Ji Y; Jiang D; Teng G; Zhou X; Zhou X; Li G; Xu C
Biosci Rep; 2020 May; 40(5):. PubMed ID: 32338288
[TBL] [Abstract][Full Text] [Related]
40. 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]
[Previous] [Next] [New Search]