CERKL, a Retinal Disease Gene, Encodes an mRNA-Binding Protein That Localizes in Compact and Untranslated mRNPs Associated with Microtubules

The function of CERKL (CERamide Kinase Like), a causative gene of retinitis pigmentosa and cone-rod dystrophy, still awaits characterization. To approach its cellular role we have investigated the subcellular localization and interaction partners of the full length CERKL isoform, CERKLa of 532 amino...

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Detalles Bibliográficos
Autores principales: Fathinajafabadi, Alihamze, Pérez-Jiménez, Eva, Riera, Marina, Knecht, Erwin, Gonzàlez-Duarte, Roser
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2014
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3912138/
https://www.ncbi.nlm.nih.gov/pubmed/24498393
http://dx.doi.org/10.1371/journal.pone.0087898

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3912138/
https://www.ncbi.nlm.nih.gov/pubmed/24498393
http://dx.doi.org/10.1371/journal.pone.0087898

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