Temporal and Tissue Specific Regulation of RP-Associated Splicing Factor Genes PRPF3, PRPF31 and PRPC8—Implications in the Pathogenesis of RP

BACKGROUND: Genetic mutations in several ubiquitously expressed RNA splicing genes such as PRPF3, PRP31 and PRPC8, have been found to cause retina-specific diseases in humans. To understand this intriguing phenomenon, most studies have been focused on testing two major hypotheses. One hypothesis ass...

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Wedi'i Gadw mewn:
Manylion Llyfryddiaeth
Prif Awduron: Cao, Huibi, Wu, Jing, Lam, Simon, Duan, Rongqi, Newnham, Catherine, Molday, Robert S., Graziotto, John J., Pierce, Eric A., Hu, Jim
Fformat: Artigo
Iaith:Inglês
Cyhoeddwyd: Public Library of Science 2011
Pynciau:
Research Article
Mynediad Ar-lein:https://ncbi.nlm.nih.gov/pmc/articles/PMC3023711/
https://ncbi.nlm.nih.gov/pubmed/21283520
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0015860
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