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Transcriptional Profile Analysis of RPGRORF15 Frameshift Mutation Identifies Novel Genes Associated with Retinal Degeneration

PURPOSE. To identify genes and molecular mechanisms associated with photoreceptor degeneration in a canine model of XLRP caused by an RPGR exon ORF15 microdeletion. METHODS. Expression profiles of mutant and normal retinas were compared by using canine retinal custom cDNA microarrays. qRT-PCR, Weste...

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Detalhes bibliográficos
Main Authors: Genini, Sem, Zangerl, Barbara, Slavik, Julianna, Acland, Gregory M., Beltran, William A., Aguirre, Gustavo D.
Formato: Artigo
Idioma:Inglês
Publicado em: Association for Research in Vision and Ophthalmology, Inc. 2010
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Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3061521/
https://ncbi.nlm.nih.gov/pubmed/20574030
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1167/iovs.10-5443
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