Distribution of pejvakin in human spiral ganglion: An immunohistochemical study.

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Directed Differentiation of Human Embryonic Stem Cells Toward Placode-Derived Spiral Ganglion-Like Sensory Neurons.Preferentially regulated expression of connexin 43 in the developing spiral ganglion neurons and afferent terminals in post-natal rat cochlea

P2860

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P2860

Distribution of pejvakin in human spiral ganglion: An immunohistochemical study.

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http://www.wikidata.org/entity/Q46512012

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2013 nî lūn-bûn

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2013年の論文

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2013年学术文章

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2013年学术文章

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2013年学术文章

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Distribution of pejvakin in human spiral ganglion: An immunohistochemical study.

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Distribution of pejvakin in human spiral ganglion: An immunohistochemical study.

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Distribution of pejvakin in human spiral ganglion: An immunohistochemical study.

@en

Distribution of pejvakin in human spiral ganglion: An immunohistochemical study.

@nl

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Distribution of pejvakin in human spiral ganglion: An immunohistochemical study.

@en

Distribution of pejvakin in human spiral ganglion: An immunohistochemical study.

@nl

P1476

Distribution of pejvakin in human spiral ganglion: An immunohistochemical study.

@en

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Anders Kinnefors

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

Fredrik Edin

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

Helge Rask-Andersen

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

Marja Boström

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

Wei Liu

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P2860

A forward genetics screen in mice identifies recessive deafness traits and reveals that pejvakin is essential for outer hair cell function

Mutations in the gene encoding pejvakin, a newly identified protein of the afferent auditory pathway, cause DFNB59 auditory neuropathy

Spiral ganglion cell loss is unrelated to segmental cochlear sensory system degeneration in humans

Expression of myelin basic protein in the human auditory nerve - an immunohistochemical and comparative study.

A p.C343S missense mutation in PJVK causes progressive hearing loss

Truncating mutation of the DFNB59 gene causes cochlear hearing impairment and central vestibular dysfunction.

Unique expression of connexins in the human cochlea.

High frequency of autosomal-recessive DFNB59 hearing loss in an isolated Arab population in Israel.

Novel mutations in the pejvakin gene are associated with autosomal recessive non-syndromic hearing loss in Iranian families.

Involvement of DFNB59 mutations in autosomal recessive nonsyndromic hearing impairment.

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225-231

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P31

scholarly article

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10.1179/1754762812Y.0000000027

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P433

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

P478

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

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2013-02-12T00:00:00Z

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P698

23407324

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P921

immunohistochemistry

Distribution of pejvakin in human spiral ganglion: An immunohistochemical study.

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P2860

P2860

Distribution of pejvakin in human spiral ganglion: An immunohistochemical study.

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type

label

prefLabel

P1433

P1476

P2093

P2860

P304

P31

P356

P433

P478

P577

P698

P921

P356

P1433

P1476

P2093

P2860

P304

P31

P356

P433

P478

P577

P698

P921