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Eyes shut homolog is required for maintaining the ciliary pocket and survival of photoreceptors in zebrafish
Mutations in the extracellular matrix protein eyes shut homolog (EYS) cause photoreceptor degeneration in patients with retinitis pigmentosa 25 (RP25). Functions of EYS remain poorly understood, due in part to the lack of an EYS gene in mouse. We investigated the localization of vertebrate EYS prote...
Tallennettuna:
| Julkaisussa: | Biol Open |
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| Päätekijät: | , , , , , , , |
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
The Company of Biologists Ltd
2016
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| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5155541/ https://ncbi.nlm.nih.gov/pubmed/27737822 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1242/bio.021584 |
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