Molecular genetics of steroid 5 alpha-reductase 2 deficiency - Wikidata - wikimedia - TriplyDB

Molecular genetics of steroid 5 alpha-reductase 2 deficiency

Molecular genetics of steroid 5 alpha-reductase 2 deficiency

http://www.wikidata.org/entity/Q24619385

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Tissue distribution and ontogeny of steroid 5 alpha-reductase isozyme expression Male pseudohermaphroditism resulting from a novel mutation in the human steroid 5 alpha-reductase type 2 gene (SRD5A2)Current medical therapies for men with lower urinary tract symptoms and benign prostatic hyperplasia: achievements and limitations Expanding the therapeutic use of androgens via selective androgen receptor modulators (SARMs)Identification of missense mutations in the SRD5A2 gene from patients with steroid 5alpha-reductase 2 deficiency The genomic substrate for adaptive radiation in African cichlid fish Molecular diagnosis of 5α-reductase type II deficiency in Brazilian siblings with 46,XY disorder of sex development The effect of 5α-reductase-2 deficiency on human fertility Phosphorylation of a UDP-glucuronosyltransferase regulates substrate specificity 46,XY disorder of sexual development resulting from a novel monoallelic mutation (p.Ser31Phe) in the steroid 5α-reductase type-2 (SRD5A2) gene.Pharmacogenetics of human androgens and prostatic diseases.Disorders of sex development: a genetic study of patients in a multidisciplinary clinic.Homozygous Ala65Pro Mutation with V89L Polymorphism in SRD5A2 Deficiency.The genetics of male undermasculinization.Hormones and prostate cancer: current perspectives and future directions.Male androgenetic alopecia.Targeted next-generation sequencing identification of mutations in patients with disorders of sex development.SRD5A2 and HSD3B2 polymorphisms are associated with prostate cancer risk and aggressiveness.Fine mapping analysis confirms and strengthens linkage of four chromosomal regions in familial hypospadias Cell-type-specific expression of rat steroid 5 alpha-reductase isozymes.Novel mutation of SRD5A2 gene in a patient with 5α-reductase 2 deficiency from India.The role of testosterone in the pathogenesis of prostate cancer.Finasteride.Mutation analysis of five candidate genes in Chinese patients with hypospadias.Expression of androgen receptor and 5alpha-reductases in the human normal endometrium and its disorders.SRD5A2 gene expression inhibits cell migration and invasion in prostate cancer cell line via F-actin reorganization.5Alpha-reductase type 2 and androgen receptor expression in gonadotropin releasing hormone GT1-1 cells.Phenotype and molecular characteristics in 45 Chinese children with 5α-reductase type 2 deficiency from South China.Association between SRD5A2 rs523349 and rs9282858 Polymorphisms and Risk of Benign Prostatic Hyperplasia: A Meta-Analysis.Regulation of sexual dimorphism in mammals.Genetic sequencing of a patient with Kallmann syndrome plus 5α-reductase type 2 deficiency The IVS1-2A>G mutation in the SRD5A2 gene predominates in Cypriot patients with 5α reductase deficiency.Allelic frequencies of six polymorphic markers for risk of prostate cancer.Type-1 steroid 5 alpha-reductase is functionally active in the hair follicle as evidenced by new selective inhibitors of either type-1 or type-2 human steroid 5 alpha-reductase.Stable maintenance of 5alpha-reductase activity in long-term subcultures of fibroblasts derived from the foreskin.Association of polymorphisms within androgen receptor, 5alpha-reductase, and PSA genes with prostate volume, clinical parameters, and endocrine status in elderly men.Polymorphisms in the androgen receptor and type II 5 alpha-reductase genes and prostate cancer prognosis.Molecular analysis of the androgen receptor in ten prostate cancer specimens obtained before and after androgen ablation.Compound heterozygous mutations in the SRD5A2 gene exon 4 in a male pseudohermaphrodite patient of Chinese origin.Identification and characterization of somatic steroid 5alpha-reductase (SRD5A2) mutations in human prostate cancer tissue.

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P2860

Molecular genetics of steroid 5 alpha-reductase 2 deficiency

http://www.wikidata.org/entity/Q24619385

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1992 nî lūn-bûn

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1992 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած

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1992 թվականի սեպտեմբերին հրատարակված գիտական հոդված

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1992年の論文

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1992年学术文章

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1992年学术文章

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1992年学术文章

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1992年学术文章

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1992年学术文章

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1992年學術文章

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name

Molecular genetics of steroid 5 alpha-reductase 2 deficiency

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Molecular genetics of steroid 5 alpha-reductase 2 deficiency

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Molecular genetics of steroid 5 alpha-reductase 2 deficiency

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Molecular genetics of steroid 5 alpha-reductase 2 deficiency

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Molecular genetics of steroid 5 alpha-reductase 2 deficiency

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Molecular genetics of steroid 5 alpha-reductase 2 deficiency

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Molecular genetics of steroid 5 alpha-reductase 2 deficiency

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Molecular genetics of steroid 5 alpha-reductase 2 deficiency

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Molecular genetics of steroid 5 alpha-reductase 2 deficiency

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Journal of Clinical Investigation

P1476

Molecular genetics of steroid 5 alpha-reductase 2 deficiency

@en

P2093

A E Thigpen

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A Milatovich

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B B Mendonca

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D L Davis

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D W Russell

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J D Wilson

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J E Griffin

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J Imperato-McGinley

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U Francke

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P2860

Characterization and chromosomal mapping of a human steroid 5 alpha-reductase gene and pseudogene and mapping of the mouse homologue

Deletion of steroid 5 alpha-reductase 2 gene in male pseudohermaphroditism

Structural and biochemical properties of cloned and expressed human and rat steroid 5 alpha-reductases

Genetic and pharmacological evidence for more than one human steroid 5 alpha-reductase

Genomic sequencing

Primer-directed enzymatic amplification of DNA with a thermostable DNA polymerase

Rapid and efficient site-specific mutagenesis without phenotypic selection

The measurement of triphosphopyridine nucleotide and reduced triphosphopyridine nucleotide and the role of hemoglobin in producing erroneous triphosphopyridine nucleotide values

Gene for lymphoid enhancer-binding factor 1 (LEF1) mapped to human chromosome 4 (q23-q25) and mouse chromosome 3 near Egf

Detection of polymorphisms of human DNA by gel electrophoresis as single-strand conformation polymorphisms

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799-809

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10.1172/JCI115954

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3

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90

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21633958

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1522235

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329933

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