Possible role of USP26 in patients with severely impaired spermatogenesis
about
Male infertility and the involvement of the X chromosomeUbiquitin Specific Protease 26 (USP26) expression analysis in human testicular and extragonadal tissues indicates diverse action of USP26 in cell differentiation and tumorigenesis.A multi-faceted approach to understanding male infertility: gene mutations, molecular defects and assisted reproductive techniques (ART).Association of 370-371insACA, 494T>C, and 1423C>T haplotype in ubiquitin-specific protease 26 gene and male infertility: a meta-analysis.Mice lacking the USP2 deubiquitinating enzyme have severe male subfertility associated with defects in fertilization and sperm motility.Deubiquitinases in cancer.Incidental medical information in whole-exome sequencing.TEX11 is mutated in infertile men with azoospermia and regulates genome-wide recombination rates in mouse.A comprehensive review of genetics and genetic testing in azoospermia.Genetic risk factors in male infertility.Ubiquitin-specific protease (USP26) gene alterations associated with male infertility and recurrent pregnancy loss (RPL) in Iranian infertile patients.The expression of Usp26 gene in mouse testis and brain.Ubiquitination regulates the morphogenesis and function of sperm organellesComparative genomics approach to identify candidate genetic loci for male fertility.The search for SNPs, CNVs, and epigenetic variants associated with the complex disease of male infertility.Human male infertility: a complex multifactorial phenotype.The role of deubiquitinating enzymes in spermatogenesis.Single gene defects leading to sperm quantitative anomalies.Localization of ubiquitin specific protease 26 at blood-testis barrier and near Sertoli cell-germ cell interface in mouse testes.Genome-wide Loci linked to non-obstructive azoospermia susceptibility may be independent of reduced sperm production in males with normozoospermia.RHOXF2 gene, a new candidate gene for spermatogenesis failure.Single nucleotide polymorphisms of USP26 in azoospermic men.Mutation analysis of the X-chromosome linked, testis-specific TAF7L gene in spermatogenic failure.A no-stop mutation in MAGEB4 is a possible cause of rare X-linked azoospermia and oligozoospermia in a consanguineous Turkish family.Disorders of spermatogenesis: Perspectives for novel genetic diagnostics after 20 years of unchanged routine.Analysis of Parent-of-Origin Effects on the X Chromosome in Asian and European Orofacial Cleft Triads Identifies Associations with DMD, FGF13, EGFL6, and Additional Loci at Xp22.2.Evidence from enzymatic and meta-analyses does not support a direct association between USP26 gene variants and male infertility.A Novel Missense Mutation in USP26 Gene Is Associated With Nonobstructive Azoospermia.Alterations of the USP26 gene in Caucasian men
P2860
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P2860
Possible role of USP26 in patients with severely impaired spermatogenesis
description
2005 nî lūn-bûn
@nan
2005 թուականի Մարտին հրատարակուած գիտական յօդուած
@hyw
2005 թվականի մարտին հրատարակված գիտական հոդված
@hy
2005年の論文
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2005年論文
@yue
2005年論文
@zh-hant
2005年論文
@zh-hk
2005年論文
@zh-mo
2005年論文
@zh-tw
2005年论文
@wuu
name
Possible role of USP26 in patients with severely impaired spermatogenesis
@ast
Possible role of USP26 in patients with severely impaired spermatogenesis
@en
Possible role of USP26 in patients with severely impaired spermatogenesis
@nl
type
label
Possible role of USP26 in patients with severely impaired spermatogenesis
@ast
Possible role of USP26 in patients with severely impaired spermatogenesis
@en
Possible role of USP26 in patients with severely impaired spermatogenesis
@nl
prefLabel
Possible role of USP26 in patients with severely impaired spermatogenesis
@ast
Possible role of USP26 in patients with severely impaired spermatogenesis
@en
Possible role of USP26 in patients with severely impaired spermatogenesis
@nl
P2860
P50
P356
P1476
Possible role of USP26 in patients with severely impaired spermatogenesis
@en
P2093
Inge Liebaers
P2860
P2888
P304
P356
10.1038/SJ.EJHG.5201335
P407
P577
2005-03-01T00:00:00Z