BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

260 related articles for article (PubMed ID: 33182400)

  • 1. 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]  

  • 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 basis of androgen insensitivity syndromes.
    Hornig NC; Holterhus PM
    Mol Cell Endocrinol; 2021 Mar; 523():111146. PubMed ID: 33385475
    [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. 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]  

  • 6. 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]  

  • 7. Investigation of androgen receptor gene mutations in a series of 21 patients with 46,XY disorders of sex development.
    Topcu V; Ilgin-Ruhi H; Siklar Z; Karabulut HG; Berberoglu M; Hacihamdioglu B; Savas-Erdeve S; Aycan Z; Peltek-Kendirci HN; Ocal G; Tukun FA
    J Pediatr Endocrinol Metab; 2015 Nov; 28(11-12):1257-63. PubMed ID: 26197461
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Somatic mosaicism of androgen receptor gene in an androgen insensitivity syndrome patient conceived through assisted reproduction technique.
    Wang H; Zhu H; Wang N; Cheng T; Han B; Zhao S; Song H; Cheng K; Liu Y; Qiao J
    Mol Genet Genomic Med; 2019 Oct; 7(10):e00906. PubMed ID: 31429517
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. 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]  

  • 11. Mobile DNA in Endocrinology: LINE-1 Retrotransposon Causing Partial Androgen Insensitivity Syndrome.
    Batista RL; Yamaguchi K; Rodrigues ADS; Nishi MY; Goodier JL; Carvalho LR; Domenice S; Costa EMF; Kazazian HH; Mendonca BB
    J Clin Endocrinol Metab; 2019 Dec; 104(12):6385-6390. PubMed ID: 31393562
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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]  

  • 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. 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]  

  • 15. 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]  

  • 16. Androgen receptor genotyping in a large Australasian cohort with androgen insensitivity syndrome; identification of four novel mutations.
    Jeske YW; McGown IN; Cowley DM; Oley C; Thomsett MJ; Choong CS; Cotterill AM
    J Pediatr Endocrinol Metab; 2007 Aug; 20(8):893-908. PubMed ID: 17937062
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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]  

  • 18. 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]  

  • 19. Identification of an AR Mutation-Negative Class of Androgen Insensitivity by Determining Endogenous AR Activity.
    Hornig NC; Ukat M; Schweikert HU; Hiort O; Werner R; Drop SL; Cools M; Hughes IA; Audi L; Ahmed SF; Demiri J; Rodens P; Worch L; Wehner G; Kulle AE; Dunstheimer D; Müller-Roßberg E; Reinehr T; Hadidi AT; Eckstein AK; van der Horst C; Seif C; Siebert R; Ammerpohl O; Holterhus PM
    J Clin Endocrinol Metab; 2016 Nov; 101(11):4468-4477. PubMed ID: 27583472
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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]  

    [Next]    [New Search]
    of 13.