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Relationship Between Genetic Polymorphisms of Methylenetetrahydrofolate Reductase (C677T, A1298C, and G1793A) as Risk Factors for Idiopathic Male Infertility
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Methylation defects of imprinted genes in human testicular spermatozoa
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Alterations in sperm DNA methylation patterns at imprinted loci in two classes of infertility
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DNA methylation errors at imprinted loci after assisted conception originate in the parental sperm
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Abnormal methylation of imprinted genes in human sperm is associated with oligozoospermia
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MOLECULAR HUMAN REPRODUCTION (2008)
Aberrant DNA methylation of imprinted loci in sperm from oligospermic patients
Hisato Kobayashi et al.
HUMAN MOLECULAR GENETICS (2007)
Single nucleotide polymorphism C677T in the methylenetetrahydrofolate reductase gene might be a genetic risk factor for infertility for Chinese men with azoospermia or severe oligozoospermia
Zhou-Cun A et al.
ASIAN JOURNAL OF ANDROLOGY (2007)
Associations of MTHFR DNMT3b 4977 bp deletion in mtDNA and GSTM1 deletion, and aberrant CpG island hypermethylation of GSTM1 in non-obstructive infertility in Indian men
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Association study of four polymorphisms in three folate-related enzyme genes with non-obstructive male infertility
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The testis-specific factor CTCFL cooperates with the protein methyltransferase PRMT7 in H19 imprinting control region methylation
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MTHFR C677T polymorphism, GSTM1 deletion and male infertility: a possible suggestion of a gene-gene interaction?
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MTHFR C677T polymorphism associates with unexplained infertile male factors
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JOURNAL OF ASSISTED REPRODUCTION AND GENETICS (2005)
Mutation C677T in the methylenetetrahydrofolate reductase gene is associated with male infertility in an Indian population
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Genomic imprinting in disruptive spermatogenesis
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C677T methylenetetrahydrofolate reductase polymorphism interferes with the effects of folic acid and zinc sulfate on sperm concentration
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The methylenetethrahydrofolate reductase (MTHFR) C677T polymorphism and male infertility in Italy
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Homozygous methylenetetrahydrofolate reductase C677T mutation and male infertility.
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Isolation and initial characterization of a novel zinc finger gene, DNMT3L, on 21q22.3, related to the cytosine-5-methyltransferase 3 gene family
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