178 related articles for article (PubMed ID: 33548461)
1. In vitro functional characterization of androgen receptor gene mutations at arginine p.856 of the ligand-binding-domain associated with androgen insensitivity syndrome.
Tajouri A; Kharrat M; Trabelsi M; M'rad R; Hiort O; Werner R
J Steroid Biochem Mol Biol; 2021 Apr; 208():105834. PubMed ID: 33548461
[TBL] [Abstract][Full Text] [Related]
2. 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]
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. An examination of how different mutations at arginine 855 of the androgen receptor result in different androgen insensitivity phenotypes.
Elhaji YA; Wu JH; Gottlieb B; Beitel LK; Alvarado C; Batist G; Trifiro MA
Mol Endocrinol; 2004 Aug; 18(8):1876-86. PubMed ID: 15118070
[TBL] [Abstract][Full Text] [Related]
5. Partial androgen insensitivity and correlations with the predicted three dimensional structure of the androgen receptor ligand-binding domain.
Yong EL; Tut TG; Ghadessy FJ; Prins G; Ratnam SS
Mol Cell Endocrinol; 1998 Feb; 137(1):41-50. PubMed ID: 9607727
[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. 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]
8. AR and SRD5A2 gene mutations in a series of 51 Turkish 46,XY DSD children with a clinical diagnosis of androgen insensitivity.
Akcay T; Fernandez-Cancio M; Turan S; Güran T; Audi L; Bereket A
Andrology; 2014 Jul; 2(4):572-8. PubMed ID: 24737579
[TBL] [Abstract][Full Text] [Related]
9. Androgen receptor mutations and androgen insensitivity.
McPhaul MJ
Mol Cell Endocrinol; 2002 Dec; 198(1-2):61-7. PubMed ID: 12573815
[TBL] [Abstract][Full Text] [Related]
10. Two de novo mutations in the AR gene cause the complete androgen insensitivity syndrome in a pair of monozygotic twins.
Mongan NP; Jääskeläinen J; Green K; Schwabe JW; Shimura N; Dattani M; Hughes IA
J Clin Endocrinol Metab; 2002 Mar; 87(3):1057-61. PubMed ID: 11889162
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. The FKBP4 Gene, Encoding a Regulator of the Androgen Receptor Signaling Pathway, Is a Novel Candidate Gene for Androgen Insensitivity Syndrome.
Ilaslan E; Markosyan R; Sproll P; Stevenson BJ; Sajek M; Sajek MP; Hayrapetyan H; Sarkisian T; Livshits L; Nef S; Jaruzelska J; Kusz-Zamelczyk K
Int J Mol Sci; 2020 Nov; 21(21):. PubMed ID: 33182400
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. L712V mutation in the androgen receptor gene causes complete androgen insensitivity syndrome due to severe loss of androgen function.
Rajender S; Gupta NJ; Chakrabarty B; Singh L; Thangaraj K
Steroids; 2013 Dec; 78(12-13):1288-92. PubMed ID: 24055831
[TBL] [Abstract][Full Text] [Related]
15. Phenotypic and molecular characteristics of androgen insensitivity syndrome patients.
Yuan SM; Zhang YN; Du J; Li W; Tu CF; Meng LL; Lin G; Lu GX; Tan YQ
Asian J Androl; 2018; 20(5):473-478. PubMed ID: 29785970
[TBL] [Abstract][Full Text] [Related]
16. Four novel mutations in the androgen receptor gene from Vietnamese patients with androgen insensitivity syndrome.
Nguyen TH; Nguyen DQ; Kim LNT; Thi TNN; Nguyen TPM; Tran ND; Nguyen HH
Genes Genomics; 2023 Apr; 45(4):467-474. PubMed ID: 35445939
[TBL] [Abstract][Full Text] [Related]
17. Molecular basis of androgen insensitivity.
Brinkmann AO
Mol Cell Endocrinol; 2001 Jun; 179(1-2):105-9. PubMed ID: 11420135
[TBL] [Abstract][Full Text] [Related]
18. Androgen receptor gene mutations in androgen insensitivity syndrome cause distinct patterns of reduced activation of androgen-responsive promoter constructs.
Werner R; Schütt J; Hannema S; Röpke A; Wieacker P; Hiort O; Holterhus PM
J Steroid Biochem Mol Biol; 2006 Sep; 101(1):1-10. PubMed ID: 16930995
[TBL] [Abstract][Full Text] [Related]
19. 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]
20. Androgen insensitivity syndrome.
Mongan NP; Tadokoro-Cuccaro R; Bunch T; Hughes IA
Best Pract Res Clin Endocrinol Metab; 2015 Aug; 29(4):569-80. PubMed ID: 26303084
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]