Gene polymorphisms/mutations relevant to abnormal spermatogenesis.
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Common variants in mismatch repair genes associated with increased risk of sperm DNA damage and male infertilityClinical genetic testing for male factor infertility: current applications and future directionsA genome-wide association study reveals that variants within the HLA region are associated with risk for nonobstructive azoospermiaClinical evaluation of the infertile male with respect to genetic etiologies.Copy number variants in patients with severe oligozoospermia and Sertoli-cell-only syndrome.Regulation of male fertility by X-linked genes.Methylenetetrahydrofolate Reductase C677T and A1298C Polymorphism in Iranian Women With Idiopathic Recurrent Pregnancy LossesArray comparative genomic hybridization in male infertility.AZFc deletions and spermatogenic failure: a population-based survey of 20,000 Y chromosomes.Comprehensive sequence analysis of the NR5A1 gene encoding steroidogenic factor 1 in a large group of infertile males.High resolution X chromosome-specific array-CGH detects new CNVs in infertile malesDeregulated sex chromosome gene expression with male germ cell-specific loss of Dicer1Association study of HLA-B alleles with idiopathic male infertility in Han population of China.TEX11 is mutated in infertile men with azoospermia and regulates genome-wide recombination rates in mouse.New single nucleotide polymorphism G5508A in the SEPT12 gene may be associated with idiopathic male infertility in Iranian men.Copy number variation and microdeletions of the Y chromosome linked genes and loci across different categories of Indian infertile malesA comprehensive review of genetics and genetic testing in azoospermia.Greater prevalence of Y chromosome Q1a3a haplogroup in Y-microdeleted Chilean men: a case-control study.Genetic causes of spermatogenic failure.Prevalent false positives of azoospermia factor a (AZFa) microdeletions caused by single-nucleotide polymorphism rs72609647 in the sY84 screening of male infertility.The search for SNPs, CNVs, and epigenetic variants associated with the complex disease of male infertility.Emerging evidence for the role of genomic instability in male factor infertility.TSPY and Male Fertility.Environmental PAH exposure and male idiopathic infertility: a review on early life exposures and adult diagnosis.Localization of ubiquitin specific protease 26 at blood-testis barrier and near Sertoli cell-germ cell interface in mouse testes.Association study of human leucocyte antigen-A gene with idiopathic male infertility in Han population of China.The c.-190 C>A transversion in promoter region of protamine1 gene as a genetic risk factor for idiopathic oligozoospermia.Association of a TDRD1 variant with spermatogenic failure susceptibility in the Han Chinese.MTHFR 3'-untranslated region polymorphisms contribute to recurrent pregnancy loss risk and alterations in peripheral natural killer cell proportions.TSPY1 copy number variation influences spermatogenesis and shows differences among Y lineages.Polymorphisms in microRNA targets: a source of new molecular markers for male reproductionNo CAG repeat expansion of polymerase gamma is associated with male infertility in Tamil Nadu, South India.Relationship of SNP of H2BFWT gene to male infertility in a Chinese population with idiopathic spermatogenesis impairment.Association of the c.-9C>T and c.368A>G transitions in H2BFWT gene with male infertility in an Iranian population.Effect of B9 and B12 vitamin intake on semen parameters and fertility of men with MTHFR polymorphisms.Genetic variants of eNOS gene may modify the susceptibility to idiopathic male infertility.A novel TEX11 mutation induces azoospermia: a case report of infertile brothers and literature review.Disorders of spermatogenesis: Perspectives for novel genetic diagnostics after 20 years of unchanged routine.Abnormal synapses, recombination, and impaired double-strand break repair in a man with nonobstructive azoospermia.Evidence from enzymatic and meta-analyses does not support a direct association between USP26 gene variants and male infertility.
P2860
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P2860
Gene polymorphisms/mutations relevant to abnormal spermatogenesis.
description
article científic
@ca
article scientifique
@fr
articolo scientifico
@it
artigo científico
@pt
bilimsel makale
@tr
scientific article published on April 2008
@en
vedecký článok
@sk
vetenskaplig artikel
@sv
videnskabelig artikel
@da
vědecký článek
@cs
name
Gene polymorphisms/mutations relevant to abnormal spermatogenesis.
@en
Gene polymorphisms/mutations relevant to abnormal spermatogenesis.
@nl
type
label
Gene polymorphisms/mutations relevant to abnormal spermatogenesis.
@en
Gene polymorphisms/mutations relevant to abnormal spermatogenesis.
@nl
prefLabel
Gene polymorphisms/mutations relevant to abnormal spermatogenesis.
@en
Gene polymorphisms/mutations relevant to abnormal spermatogenesis.
@nl
P1476
Gene polymorphisms/mutations relevant to abnormal spermatogenesis.
@en
P2093
Csilla Krausz
Francesca Nuti
P304
P356
10.1016/S1472-6483(10)60457-9
P577
2008-04-01T00:00:00Z