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Genetic factors contributing to human primary ciliary dyskinesia and male infertility

Genetic factors contributing to human primary ciliary dyskinesia and male infertility

http://www.wikidata.org/entity/Q26748534

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Recurrent deletions of the X chromosome linked CNV64, CNV67, and CNV69 shows geographic differences across China and no association with idiopathic infertility in men.Ran-binding protein M is associated with human spermatogenesis and oogenesis.

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Genetic factors contributing to human primary ciliary dyskinesia and male infertility

http://www.wikidata.org/entity/Q26748534

description

2016 nî lūn-bûn

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2016 թուականի Յունիսին հրատարակուած գիտական յօդուած

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2016 թվականի հունիսին հրատարակված գիտական հոդված

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2016年の論文

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2016年論文

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2016年論文

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2016年論文

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2016年論文

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2016年論文

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2016年论文

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name

Genetic factors contributing to human primary ciliary dyskinesia and male infertility

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Genetic factors contributing to human primary ciliary dyskinesia and male infertility

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Genetic factors contributing to human primary ciliary dyskinesia and male infertility

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type

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Genetic factors contributing to human primary ciliary dyskinesia and male infertility

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Genetic factors contributing to human primary ciliary dyskinesia and male infertility

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Genetic factors contributing to human primary ciliary dyskinesia and male infertility

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prefLabel

Genetic factors contributing to human primary ciliary dyskinesia and male infertility

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Genetic factors contributing to human primary ciliary dyskinesia and male infertility

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Genetic factors contributing to human primary ciliary dyskinesia and male infertility

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1008-682X.181227

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Asian Journal of Andrology

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Genetic factors contributing to human primary ciliary dyskinesia and male infertility

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Lu Ding

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Ping Li

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Zhi-Yong Ji

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P2860

Loss-of-function mutations in a human gene related to Chlamydomonas reinhardtii dynein IC78 result in primary ciliary dyskinesia.

The Chlamydomonas genome reveals the evolution of key animal and plant functions.

Identification of a novel testis-specific leucine-rich protein in humans and mice

Homozygosity mapping of a gene locus for primary ciliary dyskinesia on chromosome 5p and identification of the heavy dynein chain DNAH5 as a candidate gene

The human dynein intermediate chain 2 gene (DNAI2): cloning, mapping, expression pattern, and evaluation as a candidate for primary ciliary dyskinesia

Axonemal dynein intermediate-chain gene (DNAI1) mutations result in situs inversus and primary ciliary dyskinesia (Kartagener syndrome)

Mutations in DNAH5 cause primary ciliary dyskinesia and randomization of left-right asymmetry

Mislocalization of DNAH5 and DNAH9 in respiratory cells from patients with primary ciliary dyskinesia

Mutations of DNAI1 in primary ciliary dyskinesia: evidence of founder effect in a common mutation

Whole-exome capture and sequencing identifies HEATR2 mutation as a cause of primary ciliary dyskinesia

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scholarly article

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Kartagener syndrome

male infertility

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5566842

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