These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

214 related articles for article (PubMed ID: 31499074)

  • 1. 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]  

  • 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. 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]  

  • 4. 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]  

  • 5. 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]  

  • 6. 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]  

  • 7. 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]  

  • 8. 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]  

  • 9. 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]  

  • 10. 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]  

  • 11. AR mutations in 28 patients with androgen insensitivity syndrome (Prader grade 0-3).
    Wang Y; Gong C; Wang X; Qin M
    Sci China Life Sci; 2017 Jul; 60(7):700-706. PubMed ID: 28624954
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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]  

  • 13. 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]  

  • 14. Androgen Insensitivity Syndrome: Clinical Phenotype and Molecular Analysis in a Single Tertiary Center Cohort.
    Touzon MS; Garrido NP; Marino R; Ramirez P; Costanzo M; Guercio G; Berensztein E; Rivarola MA; Belgorosky A
    J Clin Res Pediatr Endocrinol; 2019 Feb; 11(1):24-33. PubMed ID: 30251955
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [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]  

  • 16. 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]  

  • 17. 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]  

  • 18. Severe forms of complete androgen insensitivity syndrome caused by a p.Q65X novel mutation in androgen receptor: Clinical manifestations, imaging findings and molecular genetics.
    Liu S; Wang Z; Jiang J; OuYang H; Wei S; Liang J; Chen N; Zeng W; Chen L; Xie X
    Steroids; 2019 Apr; 144():47-51. PubMed ID: 30742848
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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]  

  • 20. 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]  

    [Next]    [New Search]
    of 11.