BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

134 related articles for article (PubMed ID: 16500352)

  • 41. Novel nucleotide insertions in two unrelated Indian patients with 5α reductase 2 deficiency leading to premature termination of SRD5A2 enzyme.
    Shabir I; Khurana ML; Marumudi E; Khadgawat R; Ammini AC
    Steroids; 2013 Dec; 78(12-13):1159-63. PubMed ID: 24012728
    [TBL] [Abstract][Full Text] [Related]  

  • 42. Deletion of steroid 5 alpha-reductase 2 gene in male pseudohermaphroditism.
    Andersson S; Berman DM; Jenkins EP; Russell DW
    Nature; 1991 Nov; 354(6349):159-61. PubMed ID: 1944596
    [TBL] [Abstract][Full Text] [Related]  

  • 43. Novel Deleterious Mutation in Steroid-5α-Reductase-2 in 46, XY Disorders of Sex Development: Case Report Study.
    Rafigh M; Salmaninejad A; Sorouri Khorashad B; Arabi A; Milanizadeh S; Hiradfar M; Abbaszadegan MR
    Fetal Pediatr Pathol; 2022 Feb; 41(1):141-148. PubMed ID: 32449406
    [No Abstract]   [Full Text] [Related]  

  • 44. Molecular genetics of steroid 5 alpha-reductase 2 deficiency.
    Thigpen AE; Davis DL; Milatovich A; Mendonca BB; Imperato-McGinley J; Griffin JE; Francke U; Wilson JD; Russell DW
    J Clin Invest; 1992 Sep; 90(3):799-809. PubMed ID: 1522235
    [TBL] [Abstract][Full Text] [Related]  

  • 45. Molecular investigation of mutations in androgen receptor and 5-alpha-reductase-2 genes in 46,XY Disorders of Sex Development with normal testicular development.
    Ahmadifard M; Kajbafzadeh A; Panjeh-Shahi S; Vand-Rajabpour F; Ahmadi-Beni R; Arshadi H; Setoodeh A; Rostami P; Tavakkoly-Bazzaz J; Tabrizi M
    Andrologia; 2019 Jun; 51(5):e13250. PubMed ID: 30815925
    [TBL] [Abstract][Full Text] [Related]  

  • 46. 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]  

  • 47. 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]  

  • 48. 46,XY disorder of sex development (DSD) due to 17β-hydroxysteroid dehydrogenase type 3 deficiency.
    Mendonca BB; Gomes NL; Costa EM; Inacio M; Martin RM; Nishi MY; Carvalho FM; Tibor FD; Domenice S
    J Steroid Biochem Mol Biol; 2017 Jan; 165(Pt A):79-85. PubMed ID: 27163392
    [TBL] [Abstract][Full Text] [Related]  

  • 49. Molecular analysis of the SRD5A2 in 46,XY subjects with incomplete virilization: the P212R substitution of the steroid 5alpha-reductase 2 may constitute an ancestral founder mutation in Mexican patients.
    Vilchis F; Ramos L; Méndez JP; Benavides S; Canto P; Chávez B
    J Androl; 2010; 31(4):358-64. PubMed ID: 20019388
    [TBL] [Abstract][Full Text] [Related]  

  • 50. Mutations in
    Akcan N; Uyguner O; Baş F; Altunoğlu U; Toksoy G; Karaman B; Avcı Ş; Yavaş Abalı Z; Poyrazoğlu Ş; Aghayev A; Karaman V; Bundak R; Başaran S; Darendeliler F
    J Clin Res Pediatr Endocrinol; 2022 Jun; 14(2):153-171. PubMed ID: 35135181
    [TBL] [Abstract][Full Text] [Related]  

  • 51. 5α-Reductase-2 Deficiency: Clinical Findings, Endocrine Pitfalls, and Genetic Features in a Large Italian Cohort.
    Bertelloni S; Baldinotti F; Russo G; Ghirri P; Dati E; Michelucci A; Moscuzza F; Meroni S; Colombo I; Sessa MR; Baroncelli GI
    Sex Dev; 2016; 10(1):28-36. PubMed ID: 27070133
    [TBL] [Abstract][Full Text] [Related]  

  • 52. Diagnosis of 5alpha-reductase 2 deficiency: a local experience.
    Chan AO; But BW; Lau GT; Lam AL; Ng KL; Lam YY; Lee CY; Shek CC
    Hong Kong Med J; 2009 Apr; 15(2):130-5. PubMed ID: 19342739
    [TBL] [Abstract][Full Text] [Related]  

  • 53. Steroid 5 alpha-reductase 2 deficiency: virilization in early infancy may be due to partial function of mutant enzyme.
    Forti G; Falchetti A; Santoro S; Davis DL; Wilson JD; Russell DW
    Clin Endocrinol (Oxf); 1996 Apr; 44(4):477-82. PubMed ID: 8706317
    [TBL] [Abstract][Full Text] [Related]  

  • 54. Molecular analysis of 5alpha-reductase type 2 gene in eight unrelated egyptian children with suspected 5alpha-reductase deficiency: prevalence of the G34R mutation.
    Mazen I; Gad YZ; Hafez M; Sultan C; Lumbroso S
    Clin Endocrinol (Oxf); 2003 May; 58(5):627-31. PubMed ID: 12699446
    [TBL] [Abstract][Full Text] [Related]  

  • 55. Molecular study of the 5 alpha-reductase type 2 gene in three European families with 5 alpha-reductase deficiency.
    Boudon C; Lumbroso S; Lobaccaro JM; Szarras-Czapnik M; Romer TE; Garandeau P; Montoya P; Sultan C
    J Clin Endocrinol Metab; 1995 Jul; 80(7):2149-53. PubMed ID: 7608269
    [TBL] [Abstract][Full Text] [Related]  

  • 56. Five novel mutations of SRD5A2 found in eight Chinese patients with 46,XY disorders of sex development.
    Nie M; Zhou Q; Mao J; Lu S; Wu X
    Mol Hum Reprod; 2011 Jan; 17(1):57-62. PubMed ID: 20736251
    [TBL] [Abstract][Full Text] [Related]  

  • 57. [5alpha-reductase type 2 deficiency: experiences from Campinas (SP) and Salvador (BA)].
    Hackel C; Oliveira LE; Toralles MB; Nunes-Silva D; Tonini MM; Ferraz LF; Steinmetz L; Damiani D; Oliveira LC; Maciel-Guerra AT; Stuchi-Perez EG; Guerra-Júnior G
    Arq Bras Endocrinol Metabol; 2005 Feb; 49(1):103-11. PubMed ID: 16544041
    [TBL] [Abstract][Full Text] [Related]  

  • 58. Molecular genetics of disorders of sex development in a highly consanguineous population.
    Alswailem M; Alsagheir A; Abbas BB; Alzahrani O; Alzahrani AS
    J Steroid Biochem Mol Biol; 2021 Apr; 208():105736. PubMed ID: 32784047
    [TBL] [Abstract][Full Text] [Related]  

  • 59. Codon 89 polymorphism of the human 5alpha-steroid reductase type 2 gene.
    Vilchis F; Hernández D; Canto P; Méndez JP; Chávez B
    Clin Genet; 1997 Jun; 51(6):399-402. PubMed ID: 9237503
    [TBL] [Abstract][Full Text] [Related]  

  • 60. Genetic Analysis of 25 Patients with 5
    Han B; Cheng T; Zhu H; Yu J; Zhu WJ; Song HD; Yao H; Qiao J
    Biomed Res Int; 2020; 2020():1789514. PubMed ID: 32596280
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 7.