203 related articles for article (PubMed ID: 31936796)
1. Androgen Receptor Gene Variants in New Cases of Equine Androgen Insensitivity Syndrome.
Villagomez DAF; Welsford EG; King WA; Revay T
Genes (Basel); 2020 Jan; 11(1):. PubMed ID: 31936796
[TBL] [Abstract][Full Text] [Related]
2. Androgen Insensitivity Syndrome in a Family of Warmblood Horses Caused by a 25-bp Deletion of the DNA-Binding Domain of the Androgen Receptor Gene.
Welsford GE; Munk R; Villagómez DA; Hyttel P; King WA; Revay T
Sex Dev; 2017; 11(1):40-45. PubMed ID: 28192783
[TBL] [Abstract][Full Text] [Related]
3. Androgen insensitivity syndrome: somatic mosaicism of the androgen receptor in seven families and consequences for sex assignment and genetic counseling.
Köhler B; Lumbroso S; Leger J; Audran F; Grau ES; Kurtz F; Pinto G; Salerno M; Semitcheva T; Czernichow P; Sultan C
J Clin Endocrinol Metab; 2005 Jan; 90(1):106-11. PubMed ID: 15522944
[TBL] [Abstract][Full Text] [Related]
4. Phenotypic features, androgen receptor binding, and mutational analysis in 278 clinical cases reported as androgen insensitivity syndrome.
Ahmed SF; Cheng A; Dovey L; Hawkins JR; Martin H; Rowland J; Shimura N; Tait AD; Hughes IA
J Clin Endocrinol Metab; 2000 Feb; 85(2):658-65. PubMed ID: 10690872
[TBL] [Abstract][Full Text] [Related]
5. 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]
6. Molecular features and clinical phenotypes in androgen insensitivity syndrome in the absence and presence of androgen receptor gene mutations.
Holterhus PM; Werner R; Hoppe U; Bassler J; Korsch E; Ranke MB; Dörr HG; Hiort O
J Mol Med (Berl); 2005 Dec; 83(12):1005-13. PubMed ID: 16283146
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. Phenotypic variation in a family with partial androgen insensitivity syndrome explained by differences in 5alpha dihydrotestosterone availability.
Boehmer AL; Brinkmann AO; Nijman RM; Verleun-Mooijman MC; de Ruiter P; Niermeijer MF; Drop SL
J Clin Endocrinol Metab; 2001 Mar; 86(3):1240-6. PubMed ID: 11238515
[TBL] [Abstract][Full Text] [Related]
9. 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]
10. Genotype versus phenotype in families with androgen insensitivity syndrome.
Boehmer AL; Brinkmann O; Brüggenwirth H; van Assendelft C; Otten BJ; Verleun-Mooijman MC; Niermeijer MF; Brunner HG; Rouwé CW; Waelkens JJ; Oostdijk W; Kleijer WJ; van der Kwast TH; de Vroede MA; Drop SL
J Clin Endocrinol Metab; 2001 Sep; 86(9):4151-60. PubMed ID: 11549642
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. Partial androgen insensitivity syndrome due to somatic mosaicism of the androgen receptor.
Batista RL; Rodrigues AS; Machado AZ; Nishi MY; Cunha FS; Silva RB; Costa EMF; Mendonca BB; Domenice S
J Pediatr Endocrinol Metab; 2018 Jan; 31(2):223-228. PubMed ID: 29267169
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. Missense Mutation in the Ligand-Binding Domain of the Horse Androgen Receptor Gene in a Thoroughbred Family with Inherited 64,XY (SRY+) Disorder of Sex Development.
Bolzon C; Joonè CJ; Schulman ML; Harper CK; Villagómez DA; King WA; Révay T
Sex Dev; 2016; 10(1):37-44. PubMed ID: 27073903
[TBL] [Abstract][Full Text] [Related]
15. A hemizygous mutation in the androgen receptor gene causes different phenotypes of androgen insensitivity syndrome in two siblings by disrupting the nuclear translocation.
Liu C; Lyu Y; Li P
Mol Genet Genomics; 2020 Sep; 295(5):1103-1111. PubMed ID: 32435981
[TBL] [Abstract][Full Text] [Related]
16. Sequence variations in equine candidate genes For XX and XY inherited disorders of sexual development.
Pujar S; Meyers-Wallen VN
Reprod Domest Anim; 2012 Oct; 47(5):827-34. PubMed ID: 22239239
[TBL] [Abstract][Full Text] [Related]
17. Clinical characteristics, AR gene variants, and functional domains in 64 patients with androgen insensitivity syndrome.
Liu Q; Yin X; Li P
J Endocrinol Invest; 2023 Jan; 46(1):151-158. PubMed ID: 35974208
[TBL] [Abstract][Full Text] [Related]
18. A novel mutation (c.2735_2736delTC) in the androgen receptor gene in 46,XY females with complete androgen insensitivity syndrome in an Egyptian family.
Mazen I; Soliman H; El-Gammal M; Torky A; Mekkawy M; Abdel-Hamid MS; Essawi M
Horm Res Paediatr; 2014; 82(6):411-4. PubMed ID: 25034089
[TBL] [Abstract][Full Text] [Related]
19. Frame-shift mutation in hormone binding domain of human androgen receptor gene causes complete androgen insensitivity.
Chung HW; Kim SC; Kim HL
Mol Cells; 1998 Dec; 8(6):741-5. PubMed ID: 9895128
[TBL] [Abstract][Full Text] [Related]
20. 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]
[Next] [New Search]