TEX11 is mutated in infertile men with azoospermia and regulates genome-wide recombination rates in mouse. - Test2 - elhamkhani - TriplyDB

TEX11 is mutated in infertile men with azoospermia and regulates genome-wide recombination rates in mouse.

TEX11 is mutated in infertile men with azoospermia and regulates genome-wide recombination rates in mouse.

http://www.wikidata.org/entity/Q36057591

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Y-chromosomal genes affecting male fertility: A review Experimental methods to preserve male fertility and treat male factor infertility The human RHOX gene cluster: target genes and functional analysis of gene variants in infertile men Altered Crossover Distribution and Frequency in Spermatocytes of Infertile Men with Azoospermia Hybrid Sterility Locus on Chromosome X Controls Meiotic Recombination Rate in Mouse.Meiotic Recombination: The Essence of Heredity.Single gene defects leading to sperm quantitative anomalies.RNA immunoprecipitation identifies novel targets of DAZL in human foetal ovary.Genetics of Male Infertility.Approaches for targeting cancer stem cells drug resistance.Validation and application of a novel integrated genetic screening method to a cohort of 1,112 men with idiopathic azoospermia or severe oligozoospermia.SPINK2 deficiency causes infertility by inducing sperm defects in heterozygotes and azoospermia in homozygotes.Relationship of genetic causes and inhibin B in non obstructive azoospermia spermatogenic failure.Meiotic Centromere Coupling and Pairing Function by Two Separate Mechanisms in Saccharomyces cerevisiae.A no-stop mutation in MAGEB4 is a possible cause of rare X-linked azoospermia and oligozoospermia in a consanguineous Turkish family.Distinct prophase arrest mechanisms in human male meiosis.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.Evolutionarily-conserved MZIP2 is essential for crossover formation in mammalian meiosis

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P2860

TEX11 is mutated in infertile men with azoospermia and regulates genome-wide recombination rates in mouse.

http://www.wikidata.org/entity/Q36057591

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2015 nî lūn-bûn

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TEX11 is mutated in infertile ...... recombination rates in mouse.

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TEX11 is mutated in infertile ...... recombination rates in mouse.

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TEX11 is mutated in infertile ...... recombination rates in mouse.

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TEX11 is mutated in infertile ...... recombination rates in mouse.

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TEX11 is mutated in infertile ...... recombination rates in mouse.

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TEX11 is mutated in infertile ...... recombination rates in mouse.

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TEX11 is mutated in infertile ...... e recombination rates in mouse

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David C Page

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Fang Yang

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Helen Skaletsky

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Laura G Brown

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N Adrian Leu

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P Jeremy Wang

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P2860

An abundance of X-linked genes expressed in spermatogonia

Human testis-specific PGK gene lacks introns and possesses characteristics of a processed gene

Azoospermia in patients heterozygous for a mutation in SYCP3

Recombination between palindromes P5 and P1 on the human Y chromosome causes massive deletions and spermatogenic failure

Deletion of the pluripotency-associated Tex19.1 gene causes activation of endogenous retroviruses and defective spermatogenesis in mice

The meiosis-specific zip4 protein regulates crossover distribution by promoting synaptonemal complex formation together with zip2.

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

An azoospermic man with a de novo point mutation in the Y-chromosomal gene USP9Y

The tetratricopeptide repeat: a structural motif mediating protein-protein interactions

Spermatogenesis in a man with complete deletion of USP9Y

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