Cargando…
Aipl1 is required for cone photoreceptor function and survival through the stability of Pde6c and Gc3 in zebrafish
Genetic mutations in aryl hydrocarbon receptor interacting protein-like 1 (AIPL1) cause photoreceptor degeneration associated with Leber congenital amaurosis 4 (LCA4) in human patients. Here we report retinal phenotypes of a zebrafish aipl1 mutant, gold rush (gosh). In zebrafish, there are two aipl1...
Autores principales: | Iribarne, Maria, Nishiwaki, Yuko, Nakamura, Shohei, Araragi, Masato, Oguri, Eri, Masai, Ichiro |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2017
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5381001/ https://www.ncbi.nlm.nih.gov/pubmed/28378769 http://dx.doi.org/10.1038/srep45962 |
Ejemplares similares
-
β-SNAP activity in the outer segment growth period is critical for preventing BNip1-dependent apoptosis in zebrafish photoreceptors
por: Nishiwaki, Yuko, et al.
Publicado: (2020) -
TNFα Induces Müller Glia to Transition From Non-proliferative Gliosis to a Regenerative Response in Mutant Zebrafish Presenting Chronic Photoreceptor Degeneration
por: Iribarne, Maria, et al.
Publicado: (2019) -
The Leber Congenital Amaurosis Protein AIPL1 and EB Proteins Co-Localize at the Photoreceptor Cilium
por: Hidalgo-de-Quintana, Juan, et al.
Publicado: (2015) -
Action Spectra of Zebrafish Cone Photoreceptors
por: Endeman, Duco, et al.
Publicado: (2013) -
Endocytic trafficking factor VPS45 is essential for spatial regulation of lens fiber differentiation in zebrafish
por: Mochizuki, Toshiaki, et al.
Publicado: (2018)