Sperm dysfunction and ciliopathy.

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Protein biomarkers for male artificial insemination subfertility in bovine spermatozoa.Identification of oxidatively modified proteins due to cryopreservation of carp semen

P2860

Q47132616-CE7D487E-2DA9-42E4-B6BC-5B8D32E4D0B2 Q57963028-52E7F6B7-7779-40DA-B9DC-2A374628C73F

P2860

Sperm dysfunction and ciliopathy.

Item

http://www.wikidata.org/entity/Q47171971

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2015 nî lūn-bûn

@nan

2015年の論文

@ja

2015年学术文章

@wuu

2015年学术文章

@zh

2015年学术文章

@zh-cn

2015年学术文章

@zh-hans

2015年学术文章

@zh-my

2015年学术文章

@zh-sg

2015年學術文章

@yue

2015年學術文章

@zh-hant

name

Sperm dysfunction and ciliopathy.

@en

Sperm dysfunction and ciliopathy.

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type

Item

label

Sperm dysfunction and ciliopathy.

@en

Sperm dysfunction and ciliopathy.

@nl

prefLabel

Sperm dysfunction and ciliopathy.

@en

Sperm dysfunction and ciliopathy.

@nl

P1476

Sperm dysfunction and ciliopathy

@en

P2093

Kazuo Inaba

http://www.w3.org/2001/XMLSchema#string

P2860

Randomization of left-right asymmetry due to loss of nodal cilia generating leftward flow of extraembryonic fluid in mice lacking KIF3B motor protein

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

Disruption of an inner arm dynein heavy chain gene results in asthenozoospermia and reduced ciliary beat frequency

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

Identification of dynein heavy chain 7 as an inner arm component of human cilia that is synthesized but not assembled in a case of primary ciliary dyskinesia

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

Human and mouse mutations in WDR35 cause short-rib polydactyly syndromes due to abnormal ciliogenesis

A common variant in combination with a nonsense mutation in a member of the thioredoxin family causes primary ciliary dyskinesia

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

Primary ciliary dyskinesia associated with normal axoneme ultrastructure is caused by DNAH11 mutations

P2888

s12522-015-0225-5

P304

77-94

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P31

scholarly article

review article

P356

10.1007/S12522-015-0225-5

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P433

http://www.w3.org/2001/XMLSchema#string

P478

http://www.w3.org/2001/XMLSchema#string

P50

Katsutoshi Mizuno

P577

2015-10-14T00:00:00Z

http://www.w3.org/2001/XMLSchema#dateTime

P698

29259424

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P932

5715842

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Sperm dysfunction and ciliopathy.

about

P2860

P2860

Sperm dysfunction and ciliopathy.

description

name

type

label

prefLabel

P1433

P1476

P2093

P2860

P2888

P304

P31

P356

P433

P478

P50

P577

P698

P932

P356

P1433

P1476

P2093

P2860

P2888

P304

P31

P356

P433

P478

P50

P577

P698

P932