CERKL, a retinal dystrophy gene, regulates mitochondrial function and dynamics in the mammalian retina

Author:

Mirra Serena,García-Arroyo Rocío,B. Domènech Elena,Gavaldà-Navarro Aleix,Herrera-Úbeda Carlos,Oliva Clara,Garcia-Fernàndez Jordi,Artuch Rafael,Villarroya Francesc,Marfany Gemma

Funder

Ministerio de Economía y Competitividad

Espana Ministerio de Ciencia e Innovacion

CIBER

Publisher

Elsevier BV

Subject

Neurology

Reference62 articles.

1. Characterization of the cone-rod dystrophy retinal phenotype caused by novel homozygous DRAM2 mutations;Abad-Morales;Exp. Eye Res.,2019

2. CERKL mutations cause an autosomal recessive cone-rod dystrophy with inner retinopathy;Aleman;Investig. Ophthalmol. Vis. Sci.,2009

3. A missense mutation in the nuclear localization signal sequence of CERKL (p.R106S) causes autosomal recessive retinal degeneration;Ali;Mol. Vis.,2008

4. The pathways of mitophagy for quality control and clearance of mitochondria;Ashrafi;Cell Death Differ.,2012

5. Sestrins activate Nrf2 by promoting p62-dependent autophagic degradation of keap1 and prevent oxidative liver damage;Bae;Cell Metab.,2013

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