151 related articles for article (PubMed ID: 36708848)
1. Novel pathogenic variants in the androgen receptor gene associated with androgen insensitivity syndrome identified through exome sequencing and in silico analysis.
Li C; Wang X; Wang X; Li X; Chen W; Zhao M; Liu X; Li P; Xue M
Gene; 2023 Apr; 860():147225. PubMed ID: 36708848
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. Clinical, Biochemical, and Molecular Characterization of Indian Children with Clinically Suspected Androgen Insensitivity Syndrome.
Kumar A; Sharma R; Faruq M; Kumar M; Sharma S; Werner R; Hiort O; Vandana J
Sex Dev; 2022; 16(1):34-45. PubMed ID: 34689141
[TBL] [Abstract][Full Text] [Related]
4. Characterization of a novel androgen receptor gene variant identified in an Iranian family with complete androgen insensitivity syndrome (CAIS): a molecular dynamics simulation study.
Aghaei S; Parvizpour S; Farrokhi E; Molavi N; Hoseinzadeh M; Tabatabaiefar MA
J Biomol Struct Dyn; 2023 Nov; 41(19):9850-9864. PubMed ID: 36411944
[TBL] [Abstract][Full Text] [Related]
5. Novel androgen receptor gene variant containing a frameshift mutation in a patient with complete androgen insensitivity syndrome.
Chen G; Zhao D; Zhu L; Zhao Y; Zhang J; Wang X; Tian H; Tang D; Shu Q; Qiao S
Andrologia; 2022 Mar; 54(2):e14292. PubMed ID: 34700362
[TBL] [Abstract][Full Text] [Related]
6. 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]
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. 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]
9. Complete androgen insensitivity syndrome caused by c.1769-1G > C mutation and activation of a cryptic splice acceptor site in the androgen receptor gene.
Wang S; Xia P; Cacalano NA; Xu H; Li D
Steroids; 2018 Sep; 137():64-69. PubMed ID: 29859233
[TBL] [Abstract][Full Text] [Related]
10. 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]
11. 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]
12. A large deletion/insertion-induced frameshift mutation of the androgen receptor gene in a family with a familial complete androgen insensitivity syndrome.
Cong P; Ye Y; Wang Y; Lu L; Yong J; Yu P; Joseph KK; Jin F; Qi M
Gene; 2012 Jun; 500(2):220-3. PubMed ID: 22487869
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. 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]
15. Complete Androgen Insensitivity Syndrome: From the Relevance of an Accurate Genetic Diagnosis to the Challenge of Clinical Management. A Case Report.
Barbagallo F; Cannarella R; Bertelli M; Crafa A; La Vignera S; Condorelli RA; Calogero AE
Medicina (Kaunas); 2021 Oct; 57(11):. PubMed ID: 34833359
[No Abstract] [Full Text] [Related]
16. 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]
17. 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]
18. 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]
19. Complete androgen insensitivity syndrome caused by a novel mutation in the androgen receptor gene and its mechanism.
Zhou D; Xu H; Shen X; Gu R; Chen Y; Chen G; Li P; Shi H; Sun X; Xin A
Clin Chim Acta; 2022 Jun; 531():94-99. PubMed ID: 35351434
[TBL] [Abstract][Full Text] [Related]
20. Clinical, Hormonal, Genetic, and Molecular Characteristics in Androgen Insensitivity Syndrome in an Asian Indian Cohort from a Single Centre in Western India.
Arya S; Barnabas R; Lila AR; Sarathi V; Memon SS; Bhandare VV; Thakkar K; Patil V; Shah NS; Kunwar A; Bandgar T
Sex Dev; 2021; 15(4):253-261. PubMed ID: 34333495
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
