BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

213 related articles for article (PubMed ID: 24012728)

  • 21. Clinical and molecular characterization of 5α-reductase type 2 deficiency due to mutations (p.Q6X, p.R246Q) in SRD5A2 gene.
    Jia W; Zheng D; Zhang L; Li C; Zhang X; Wang F; Guan Q; Fang L; Zhao J; Xu C
    Endocr J; 2018 Jun; 65(6):645-655. PubMed ID: 29643321
    [TBL] [Abstract][Full Text] [Related]  

  • 22. The identification of 5 alpha-reductase-2 and 17 beta-hydroxysteroid dehydrogenase-3 gene defects in male pseudohermaphrodites from a Turkish kindred.
    Can S; Zhu YS; Cai LQ; Ling Q; Katz MD; Akgun S; Shackleton CH; Imperato-McGinley J
    J Clin Endocrinol Metab; 1998 Feb; 83(2):560-9. PubMed ID: 9467575
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Recognition of 5α-reductase-2 deficiency in an adult female 46XY DSD clinic.
    Berra M; Williams EL; Muroni B; Creighton SM; Honour JW; Rumsby G; Conway GS
    Eur J Endocrinol; 2011 Jun; 164(6):1019-25. PubMed ID: 21402750
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Phenotype and molecular characteristics in 45 Chinese children with 5α-reductase type 2 deficiency from South China.
    Cheng J; Lin R; Zhang W; Liu G; Sheng H; Li X; Zhou Z; Mao X; Liu L
    Clin Endocrinol (Oxf); 2015 Oct; 83(4):518-26. PubMed ID: 25899528
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Diagnosis of 5α-reductase 2 deficiency: is measurement of dihydrotestosterone essential?
    Chan AO; But BW; Lee CY; Lam YY; Ng KL; Tung JY; Kwan EY; Chan YK; Tsui TK; Lam AL; Tse WY; Cheung PT; Shek CC
    Clin Chem; 2013 May; 59(5):798-806. PubMed ID: 23513070
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Undervirilization in XY newborns may hide a 5α-reductase deficiency: report of three new SRD5A2 gene mutations.
    Maimoun L; Philibert P; Cammas B; Audran F; Pienkowski C; Kurtz F; Heinrich C; Cartigny M; Sultan C
    Int J Androl; 2010 Dec; 33(6):841-7. PubMed ID: 20132346
    [TBL] [Abstract][Full Text] [Related]  

  • 27. SRD5A1 and SRD5A2 are associated with treatment for benign prostatic hyperplasia with the combination of 5α-reductase inhibitors and α-adrenergic receptor antagonists.
    Gu X; Na R; Huang T; Wang L; Tao S; Tian L; Chen Z; Jiao Y; Kang J; Zheng S; Xu J; Sun J; Qi J
    J Urol; 2013 Aug; 190(2):615-9. PubMed ID: 23499746
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Difficulties in diagnosis and treatment of 5alpha-reductase type 2 deficiency in a newborn with 46,XY DSD.
    Walter KN; Kienzle FB; Frankenschmidt A; Hiort O; Wudy SA; van der Werf-Grohmann N; Superti-Furga A; Schwab KO
    Horm Res Paediatr; 2010; 74(1):67-71. PubMed ID: 20395661
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Steroid 5alpha-reductase 1 polymorphisms and testosterone/dihydrotestosterone ratio in male patients with hypospadias.
    Tria A; Hiort O; Sinnecker GH
    Horm Res; 2004; 61(4):180-3. PubMed ID: 14739525
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Molecular diagnosis of 5α-reductase type II deficiency in Brazilian siblings with 46,XY disorder of sex development.
    Leme de Calais FL; Soardi FC; Petroli RJ; Lusa AL; de Paiva E Silva RB; Maciel-Guerra AT; Guerra-Júnior G; de Mello MP
    Int J Mol Sci; 2011; 12(12):9471-80. PubMed ID: 22272144
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Genetic analysis of the SRD5A2 gene in Indian patients with 5alpha-reductase deficiency.
    Sahu R; Boddula R; Sharma P; Bhatia V; Greaves R; Rao S; Desai M; Wakhlu A; Phadke S; Shukla M; Dabadghao P; Mehrotra RN; Bhatia E
    J Pediatr Endocrinol Metab; 2009 Mar; 22(3):247-54. PubMed ID: 19492581
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Identification of three novel
    Cheng T; Wang H; Han B; Zhu H; Yao HJ; Zhao SX; Zhu WJ; Zhai HL; Chen FG; Song HD; Cheng KX; Liu Y; Qiao J
    Asian J Androl; 2019; 21(6):577-581. PubMed ID: 31031332
    [TBL] [Abstract][Full Text] [Related]  

  • 33. The IVS1-2A>G mutation in the SRD5A2 gene predominates in Cypriot patients with 5α reductase deficiency.
    Skordis N; Neocleous V; Kyriakou A; Efstathiou E; Sertedaki A; Philibert P; Phylactou LA; Lumbroso S; Sultan C
    J Endocrinol Invest; 2010 Dec; 33(11):810-4. PubMed ID: 20511729
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Phenotypic and molecular characteristics in eleven Chinese patients with 5α-reductase Type 2 deficiency.
    Zhu H; Liu W; Han B; Fan M; Zhao S; Wang H; Lu Y; Pan C; Chen F; Chen M; Song H; Cheng K; Qiao J
    Clin Endocrinol (Oxf); 2014 Nov; 81(5):711-20. PubMed ID: 24665940
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Mutational analysis of compound heterozygous mutation p.Q6X/p.H232R in SRD5A2 causing 46,XY disorder of sex development.
    Li L; Zhang J; Li Q; Qiao L; Li P; Cui Y; Li S; Hao S; Wu T; Liu L; Yin J; Hu P; Dou X; Li S; Yang H
    Ital J Pediatr; 2022 Mar; 48(1):47. PubMed ID: 35331321
    [TBL] [Abstract][Full Text] [Related]  

  • 36. The Molecular Basis of 5α-Reductase Type 2 Deficiency.
    Batista RL; Mendonca BB
    Sex Dev; 2022; 16(2-3):171-183. PubMed ID: 35793650
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Clinical characterization and analysis of the SRD5A2 gene in six Korean patients with 5alpha-reductase type 2 deficiency.
    Ko JM; Cheon CK; Kim GH; Kim SH; Kim KS; Yoo HW
    Horm Res Paediatr; 2010; 73(1):41-8. PubMed ID: 20190539
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Mutational analysis of SRD5A2: From gene to functional kinetics in individuals with steroid 5α-reductase 2 deficiency.
    Ramos L; Vilchis F; Chávez B; Mares L
    J Steroid Biochem Mol Biol; 2020 Jun; 200():105691. PubMed ID: 32380235
    [TBL] [Abstract][Full Text] [Related]  

  • 39. SRD5A2 gene mutations and polymorphisms in Spanish 46,XY patients with a disorder of sex differentiation.
    Fernández-Cancio M; Audí L; Andaluz P; Torán N; Piró C; Albisu M; Gussinyé M; Yeste D; Clemente M; Martínez-Mora J; Blanco A; Granada ML; Marco M; Ferragut J; López-Siguero JP; Beneyto M; Carles C; Carrascosa A
    Int J Androl; 2011 Dec; 34(6 Pt 2):e526-35. PubMed ID: 21631525
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Identification of missense mutations in the SRD5A2 gene from patients with steroid 5alpha-reductase 2 deficiency.
    Vilchis F; Méndez JP; Canto P; Lieberman E; Chávez B
    Clin Endocrinol (Oxf); 2000 Mar; 52(3):383-7. PubMed ID: 10718838
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 11.