Sequence family variant loss from the AZFc interval of the human Y chromosome, but not gene copy loss, is strongly associated with male infertility - Wikidata - awgldk - TriplyDB

Sequence family variant loss from the AZFc interval of the human Y chromosome, but not gene copy loss, is strongly associated with male infertility

Sequence family variant loss from the AZFc interval of the human Y chromosome, but not gene copy loss, is strongly associated with male infertility

http://www.wikidata.org/entity/Q35444185

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A preliminary study of copy number variation in Tibetans Tudor, MBT and chromo domains gauge the degree of lysine methylation The AZFc region of the Y chromosome: at the crossroads between genetic diversity and male infertility Epigenetics and male reproduction: the consequences of paternal lifestyle on fertility, embryo development, and children lifetime health High mutation rates have driven extensive structural polymorphism among human Y chromosomes Characterizing partial AZFc deletions of the Y chromosome with amplicon-specific sequence markers Lack of association between genetic polymorphisms in enzymes associated with folate metabolism and unexplained reduced sperm counts.Screening for Y-chromosome microdeletions in a population of infertile males in the Gaza Strip.The Y deletion gr/gr and susceptibility to testicular germ cell tumor Association of spermatogenic failure with the b2/b3 partial AZFc deletion Clinical data for 185 infertile Iranian men with Y-chromosome microdeletion Impaired spermatogenesis and gr/gr deletions related to Y chromosome haplogroups in Korean men.Developmental model for the pathogenesis of testicular carcinoma in situ: genetic and environmental aspects.Human spermatogenic failure purges deleterious mutation load from the autosomes and both sex chromosomes, including the gene DMRT1.Screening for AZFc partial deletions in Dravidian men with nonobstructive azoospermia and oligozoospermia.Structural variation of the human genome: mechanisms, assays, and role in male infertility Common AZFc structure may possess the optimal spermatogenesis efficiency relative to the rearranged structures mediated by non-allele homologous recombination.Copy number variation in the human Y chromosome in the UK population.Organizational and functional status of the Y-linked genes and loci in the infertile patients having normal spermiogram Susceptibility of gr/gr rearrangements to azoospermia or oligozoospermia is dependent on DAZ and CDY1 gene copy deletions.Discrimination of Deletion and Duplication Subtypes of the Deleted in Azoospermia Gene Family in the Context of Frequent Interloci Gene Conversion.Multiplex PCR based screening for micro/partial deletions in the AZF region of Y-chromosome in severe oligozoospermic and azoospermic infertile men in Iran Quantitative PCR technique for the identification of microrearrangements of the AZFc region.Y chromosome variants and male reproductive function.Gr/gr deletions on Y-chromosome correlate with male infertility: an original study, meta-analyses, and trial sequential analyses Genetic risk factors in male infertility.Susceptibility alleles for testicular germ cell tumour: a review.Partial deletions are associated with an increased risk of complete deletion in AZFc: a new insight into the role of partial AZFc deletions in male infertility.Analysis of sex chromosome abnormalities using X and Y chromosome DNA tiling path arrays.Partial AZFc duplications not deletions are associated with male infertility in the Yi population of Yunnan Province, China.Phenotypic variation within European carriers of the Y-chromosomal gr/gr deletion is independent of Y-chromosomal background.Human Y-chromosome variation and male dysfunction Genetic testing in couples undergoing assisted reproduction technique protocols.Partial Deletions of Y-Chromosome in Infertile Men with Non-obstructive Azoospermia and Oligoasthenoteratozoospermia in a Turkish Population.Comprehensive investigation in patients affected by sperm macrocephaly and globozoospermia.Associations of Y-chromosome subdeletion gr/gr with the prevalence of Y-chromosome haplogroups in infertile patients.Y Chromosome Microdeletions in Infertile Men with Non-obstructive Azoospermia and Severe Oligozoospermia.A significant effect of the TSPY1 copy number on spermatogenesis efficiency and the phenotypic expression of the gr/gr deletion.Genetics of the human Y chromosome and its association with male infertility.An infertile patient with Y chromosome b1/b3 deletion presenting with congenital bilateral absence of the vas deferens with normal spermatogenesis.

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P2860

Sequence family variant loss from the AZFc interval of the human Y chromosome, but not gene copy loss, is strongly associated with male infertility

http://www.wikidata.org/entity/Q35444185

description

2004 nî lūn-bûn

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2004 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած

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2004 թվականի նոյեմբերին հրատարակված գիտական հոդված

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2004年の論文

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2004年論文

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2004年論文

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2004年論文

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2004年論文

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2004年論文

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2004年论文

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name

Sequence family variant loss f ...... sociated with male infertility

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Sequence family variant loss f ...... sociated with male infertility

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type

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Sequence family variant loss f ...... sociated with male infertility

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JMG.2004.022111

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Journal of Medical Genetics

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Sequence family variant loss f ...... sociated with male infertility

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P2093

Belougne J

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Chiaroni J

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Clemente E

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Collignon P

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Ducourneau A

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Durand C

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Frances AM

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Guichaoua M

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Longepied G

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Machev N

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P2860

Previously uncharacterized histone acetyltransferases implicated in mammalian spermatogenesis.

Y-chromosomal diversity in Europe is clinal and influenced primarily by geography, rather than by language

Diverse spermatogenic defects in humans caused by Y chromosome deletions encompassing a novel RNA-binding protein gene

Four DAZ genes in two clusters found in the AZFc region of the human Y chromosome

The male-specific region of the human Y chromosome is a mosaic of discrete sequence classes

High frequency of DAZ1/DAZ2 gene deletions in patients with severe oligozoospermia

Human Y chromosome azoospermia factors (AZF) mapped to different subregions in Yq11

Y chromosomal DNA variation and the peopling of Japan

Human chromosome deletions in Yq11, AZF candidate genes and male infertility: history and update.

Localization of factors controlling spermatogenesis in the nonfluorescent portion of the human Y chromosome long arm.

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814-825

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10.1136/JMG.2004.022111

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11

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41

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Michael Mitchell

Marie-Geneviève Mattéi

Christophe Chevillard

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2004-11-01T00:00:00Z

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8200889

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15520406

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1735624

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