Cdc42 and sec10 Are Required for Normal Retinal Development in Zebrafish.

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Gene expression changes in the retina following subretinal injection of human neural progenitor cells into a rodent model for retinal degeneration.The exocyst is required for photoreceptor ciliogenesis and retinal development.

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Cdc42 and sec10 Are Required for Normal Retinal Development in Zebrafish.

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2015 nî lūn-bûn

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2015年の論文

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2015年論文

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2015年論文

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2015年論文

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2015年論文

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2015年論文

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Cdc42 and sec10 Are Required for Normal Retinal Development in Zebrafish.

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Cdc42 and sec10 Are Required for Normal Retinal Development in Zebrafish.

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Cdc42 and sec10 Are Required for Normal Retinal Development in Zebrafish.

@ast

Cdc42 and sec10 Are Required for Normal Retinal Development in Zebrafish.

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Cdc42 and sec10 Are Required for Normal Retinal Development in Zebrafish.

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Cdc42 and sec10 Are Required for Normal Retinal Development in Zebrafish.

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P1476

Cdc42 and sec10 Are Required for Normal Retinal Development in Zebrafish.

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Jeong-In Baek

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

Joshua H Lipschutz

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

Joshua L Dunaief

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

Seok-Hyung Kim

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

Soo Young Choi

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

Xiaofeng Zuo

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P2860

The Ciliopathies: An Emerging Class of Human Genetic Disorders

Bardet-Biedl syndrome genes are important in retrograde intracellular trafficking and Kupffer's vesicle cilia function

Mutations in the gene encoding the basal body protein RPGRIP1L, a nephrocystin-4 interactor, cause Joubert syndrome

A core complex of BBS proteins cooperates with the GTPase Rab8 to promote ciliary membrane biogenesis

Interaction of nephrocystin-4 and RPGRIP1 is disrupted by nephronophthisis or Leber congenital amaurosis-associated mutations.

Usher syndrome: animal models, retinal function of Usher proteins, and prospects for gene therapy

The exocyst protein Sec10 interacts with Polycystin-2 and knockdown causes PKD-phenotypes

Stages of embryonic development of the zebrafish

The exocyst localizes to the primary cilium in MDCK cells.

The homodimeric kinesin, Kif17, is essential for vertebrate photoreceptor sensory outer segment development

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3361-3370

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scholarly article

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10.1167/IOVS.14-15692

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English

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2015-05-01T00:00:00Z

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26024121

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4453986

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Cdc42 and sec10 Are Required for Normal Retinal Development in Zebrafish.

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P2860

P2860

Cdc42 and sec10 Are Required for Normal Retinal Development in Zebrafish.

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P1433

P1476

P2093

P2860

P304

P31

P356

P407

P433

P478

P577

P698

P932

P356

P1433

P1476

P2093

P2860

P304

P31

P356

P407

P433

P478

P577

P698

P932