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Modeling of autosomal-dominant retinitis pigmentosa in Caenorhabditis elegans uncovers a nexus between global impaired functioning of certain splicing factors and cell type-specific apoptosis
Authors:Karinna Rubio-Pe?a  Laura Fontrodona  David Aristizábal-Corrales  Silvia Torres  Eric Cornes  Francisco J García-Rodríguez  Xènia Serrat  David González-Knowles  Sylvain Foissac  Montserrat Porta-De-La-Riva  Julián Cerón
Institution:1.Cancer and Human Molecular Genetics, Bellvitge Biomedical Research Institute-IDIBELL, Hospitalet de Llobregat, Barcelona 08908, Spain;2.Integromics, Integromics SL, Parque Científico de Madrid, 28760, Tres Cantos, Madrid, Spain;3.INRA, GenPhySE, F-31326 Castanet-Tolosan, France;4.C. elegans Core Facility, Bellvitge Biomedical Research Institute-IDIBELL, Hospitalet de Llobregat, Barcelona 08908, Spain
Abstract:
Keywords:C  elegans  retinitis pigmentosa  RNA-seq  spliceosome  intron retention
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