Common variants in mismatch repair genes associated with increased risk of sperm DNA damage and male infertility
about
Refining the role of PMS2 in Lynch syndrome: germline mutational analysis improved by comprehensive assessment of variantsImpact of DNA mismatch repair system alterations on human fertility and related treatmentsThe human RHOX gene cluster: target genes and functional analysis of gene variants in infertile menA multi-faceted approach to understanding male infertility: gene mutations, molecular defects and assisted reproductive techniques (ART).Gene and pathway level analyses of germline DNA-repair gene variants and prostate cancer susceptibility using the iCOGS-genotyping array.Cytokines in the blood and semen of infertile patientsSubfertility increases risk of testicular cancer: evidence from population-based semen samples.MutS Homologues hMSH4 and hMSH5: Genetic Variations, Functions, and Implications in Human DiseasesLow-frequency germline variants across 6p22.2-6p21.33 are associated with non-obstructive azoospermia in Han Chinese men.Increased risk of cancer among azoospermic menRAB10 Interacts with the Male Germ Cell-Specific GTPase-Activating Protein during Mammalian Spermiogenesis.Novel Implications in Molecular Diagnosis of Lynch Syndrome.Human sperm DNA fragmentation and its correlation with conventional semen parameters.Meiotic Recombination: The Essence of Heredity.Childhood Cancer Risk in the Siblings and Cousins of Men with Poor Semen Quality.Cancer risk in first- and second-degree relatives of men with poor semen quality.Correlation between polymorphisms in DNA mismatch repair genes and the risk of primary hepatocellular carcinoma for the Han population in northern China.XRCC5 VNTR, XRCC6 -61C>G, and XRCC7 6721G>T Gene Polymorphisms Associated with Male Infertility Risk: Evidences from Case-Control and In Silico Studies.Review of Azoospermia.Outer dense fibers stabilize the axoneme to maintain sperm motility.Association between promoter methylation of MLH1 and MSH2 and reactive oxygen species in oligozoospermic men-A pilot study.Polymorphisms of DNA repair genes XRCC1 and LIG4 and idiopathic male infertility.Genetic intersection of male infertility and cancer.Association of C3953T transition in interleukin 1β gene with idiopathic male infertility in an Iranian population.The polymorphic hMSH5 C85T allele augments radiotherapy-induced spermatogenic impairment.
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P2860
Common variants in mismatch repair genes associated with increased risk of sperm DNA damage and male infertility
description
2012 nî lūn-bûn
@nan
2012 թուականին հրատարակուած գիտական յօդուած
@hyw
2012 թվականին հրատարակված գիտական հոդված
@hy
2012年の論文
@ja
2012年論文
@yue
2012年論文
@zh-hant
2012年論文
@zh-hk
2012年論文
@zh-mo
2012年論文
@zh-tw
2012年论文
@wuu
name
Common variants in mismatch re ...... NA damage and male infertility
@ast
Common variants in mismatch re ...... NA damage and male infertility
@en
Common variants in mismatch re ...... NA damage and male infertility
@en-gb
Common variants in mismatch re ...... NA damage and male infertility
@nl
type
label
Common variants in mismatch re ...... NA damage and male infertility
@ast
Common variants in mismatch re ...... NA damage and male infertility
@en
Common variants in mismatch re ...... NA damage and male infertility
@en-gb
Common variants in mismatch re ...... NA damage and male infertility
@nl
prefLabel
Common variants in mismatch re ...... NA damage and male infertility
@ast
Common variants in mismatch re ...... NA damage and male infertility
@en
Common variants in mismatch re ...... NA damage and male infertility
@en-gb
Common variants in mismatch re ...... NA damage and male infertility
@nl
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Common variants in mismatch re ...... NA damage and male infertility
@en
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P2860
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P356
10.1186/1741-7015-10-49
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2012-01-01T00:00:00Z
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1015412647