2014
DOI: 10.1007/s10815-014-0311-3
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Association of common SNP rs1136410 in PARP1 gene with the susceptibility to male infertility with oligospermia

Abstract: These results indicated that genotype CC of SNP rs1136410 may increase the risk of oligosoermia and genotype TT of rs1136410 may have some protective effect from oligospermia, suggesting that the polymorphism of SNP rs1136410 in PARP1 gene may modify the susceptibility to male infertility with oligospermia.

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Cited by 8 publications
(3 citation statements)
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“…Multi-factorial disorders, including genetic abnormalities and/or environment influences, potentially affect fertility parameters. It is demonstrated that abnormalities of nuclear DNA [6], mitochondrial DNA [7] and RNA [8] in human being might either directly or indirectly affect the spermatogenesis. The impact of exposure to environmental factors would be indirect but significant.…”
Section: Introductionmentioning
confidence: 99%
“…Multi-factorial disorders, including genetic abnormalities and/or environment influences, potentially affect fertility parameters. It is demonstrated that abnormalities of nuclear DNA [6], mitochondrial DNA [7] and RNA [8] in human being might either directly or indirectly affect the spermatogenesis. The impact of exposure to environmental factors would be indirect but significant.…”
Section: Introductionmentioning
confidence: 99%
“…The genetic factors involved in male infertility include Y chromosome microdeletions, chromosomal or monogenic disorders, mitochondrial DNA (MTDNA) mutations, imprinting disorders, or endocrine disorders of genetic origin [4]. Spermatogenesis impairment is the most common form of male infertility, and many genetic factors are involved in impaired spermatogenesis [4,5].…”
Section: Introductionmentioning
confidence: 99%
“…In humans, the level of MLH1 methylation in NOA patients is significantly higher than that in healthy subjects and is positively correlated with the level of reactive oxygen species (ROS; Gunes et al, ). Moreover, a recent human study indicated that single nucleotide polymorphisms (SNPs) of PARP1 are highly associated with oligospermia (Chen, Pu, Zhang, & A, ). In mice, the requirements of HSP90AA1, MAPK1 and PRMT5 for spermatogenesis have been shown, and the absence of one of these genes leads to germ cell reduction or inhibition of proliferation (Grad et al, ; Thuillier et al, ; Wang et al, ).…”
Section: Discussionmentioning
confidence: 99%