BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

251 related articles for article (PubMed ID: 26592841)

  • 1. 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]  

  • 2. 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]  

  • 3. 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]  

  • 4. Clinical characteristics and molecular genetics of complete androgen insensitivity syndrome patients: a series study of 30 cases from a Chinese tertiary medical center.
    Zhang D; Yao F; Tian T; Deng S; Luo M; Tian Q
    Fertil Steril; 2021 May; 115(5):1270-1279. PubMed ID: 33602557
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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]  

  • 6. A double nucleotide insertion-induced frame-shift mutation of the androgen receptor gene in a familial complete androgen insensitivity syndrome.
    Rong HL; Suzuki N; Imai A
    Eur J Obstet Gynecol Reprod Biol; 2010 Jan; 148(1):53-5. PubMed ID: 19815331
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. [Identification of a novel frameshift mutation of human androgen receptor gene in a patient featuring complete androgen insensitivity syndrome].
    Xie JH; Qu JH; Xiao QZ; Zhou YQ
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2013 Feb; 30(1):99-101. PubMed ID: 23450491
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Novel mutation in the ligand-binding domain of the androgen receptor gene (l790p) associated with complete androgen insensitivity syndrome.
    Raicu F; Giuliani R; Gatta V; Palka C; Franchi PG; Lelli-Chiesa P; Tumini S; Stuppia L
    Asian J Androl; 2008 Jul; 10(4):687-91. PubMed ID: 18097502
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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]  

  • 11. Heterozygous Nonsense Mutation in the Androgen Receptor Gene Associated with Partial Androgen Insensitivity Syndrome in an Individual with 47,XXY Karyotype.
    Batista RL; Rodrigues AS; Nishi MY; Feitosa ACR; Gomes NLRA; Junior JAF; Domenice S; Costa EMF; de Mendonça BB
    Sex Dev; 2017; 11(2):78-81. PubMed ID: 28456808
    [TBL] [Abstract][Full Text] [Related]  

  • 12. A novel mutation (c.T3816 > C) in the androgen receptor gene in a 46,XY female patient with androgen insensitivity syndrome.
    Helszer Z; Dmochowska A; Borkowska E; Moczulska H; Słowikowska-Hilczer J; Pietrusiński M; Jędrzejczyk S; Kałużewski B
    Endokrynol Pol; 2013; 64(5):398-402. PubMed ID: 24186597
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [Androgen insensitivity syndrome: clinical, hormonal and molecular analysis of 33 cases].
    Melo KF; Mendonça BB; Billerbeck AE; Costa EM; Latronico AC; Arnhold IJ
    Arq Bras Endocrinol Metabol; 2005 Feb; 49(1):87-97. PubMed ID: 16544039
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 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. 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]  

  • 17. Complete androgen insensitivity syndrome caused by the R855H mutation in the androgen receptor gene.
    Skordis N; Lumbroso S; Perikleous M; Sismani C; Patsalis PC; Sultan C
    J Pediatr Endocrinol Metab; 2005 Mar; 18(3):309-13. PubMed ID: 15813610
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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]  

  • 19. 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]  

  • 20. 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]  

    [Next]    [New Search]
    of 13.