Myosin VIIA is a marker for the cone accessory outer segment in zebrafish.

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Recent advances in muscle research Eyes shut homolog is required for maintaining the ciliary pocket and survival of photoreceptors in zebrafish Animal modelling for inherited central vision loss.Usherin defects lead to early-onset retinal dysfunction in zebrafish

P2860

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P2860

Myosin VIIA is a marker for the cone accessory outer segment in zebrafish.

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http://www.wikidata.org/entity/Q39144674

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2014 nî lūn-bûn

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2014年の論文

@ja

2014年論文

@yue

2014年論文

@zh-hant

2014年論文

@zh-hk

2014年論文

@zh-mo

2014年論文

@zh-tw

2014年论文

@wuu

2014年论文

@zh

2014年论文

@zh-cn

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Myosin VIIA is a marker for the cone accessory outer segment in zebrafish.

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Myosin VIIA is a marker for the cone accessory outer segment in zebrafish.

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Myosin VIIA is a marker for the cone accessory outer segment in zebrafish.

@en

Myosin VIIA is a marker for the cone accessory outer segment in zebrafish.

@nl

prefLabel

Myosin VIIA is a marker for the cone accessory outer segment in zebrafish.

@en

Myosin VIIA is a marker for the cone accessory outer segment in zebrafish.

@nl

P1476

Myosin VIIA is a marker for the cone accessory outer segment in zebrafish

@en

P2093

Corinne Hodel

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

Jan Klooster

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

Maarten Kamermans

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

Martina Heidemann

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

Matthias Gesemann

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

P2860

Human Usher 1B/mouse shaker-1: the retinal phenotype discrepancy explained by the presence/absence of myosin VIIA in the photoreceptor cells

Expression in cochlea and retina of myosin VIIa, the gene product defective in Usher syndrome type 1B

Human myosin VIIA responsible for the Usher 1B syndrome: a predicted membrane-associated motor protein expressed in developing sensory epithelia

The many different cellular functions of MYO7A in the retina

Abnormal phagocytosis by retinal pigmented epithelium that lacks myosin VIIa, the Usher syndrome 1B protein

A type VII myosin encoded by the mouse deafness gene shaker-1

Mutant myosin VIIa causes defective melanosome distribution in the RPE of shaker-1 mice

Zebrafish hox clusters and vertebrate genome evolution

Localization of Usher 1 proteins to the photoreceptor calyceal processes, which are absent from mice.

A novel allele of myosin VIIa reveals a critical function for the C-terminal FERM domain for melanosome transport in retinal pigment epithelial cells.

P304

1777-1784

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

P31

scholarly article

P356

10.1002/AR.22976

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

P433

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

P478

297

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

P50

Stephan C Neuhauss

Oliver Biehlmaier

Stephanie Niklaus

P577

2014-09-01T00:00:00Z

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

P5875

264743876

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

P698

25125189

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

P921

Danio rerio

accessory outer segment

Myosin VIIA is a marker for the cone accessory outer segment in zebrafish.

about

P2860

P2860

Myosin VIIA is a marker for the cone accessory outer segment in zebrafish.

description

name

type

label

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P1433

P1476

P2093

P2860

P304

P31

P356

P433

P478

P50

P577

P5875

P698

P921

P356

P1433

P1476

P2093

P2860

P304

P31

P356

P433

P478

P50

P577

P5875

P698

P921