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Jun 8, 2023
Overcoming the Challenges to Clinical Development of X-Linked Retinitis Pigmentosa Therapies: Proceedings of an Expert Panel
Formulate recommendations for designing XLRP gene therapy clinical studies to provide the best chance of successful treatment development.


Jan 6, 2023
PRPF8 increases the aggressiveness of hepatocellular carcinoma by regulating FAK/AKT pathway via fibronectin 1 splicing
PRPF8 mutations have been associated with severe forms of RP and with the initiation of various types of myeloid neoplasms . . .

Jan 26, 2022
UCI researchers discover cause, develop pharmacological treatment for reducing retinitis pigmentosa vision loss
Although AdipoR1 is found in multiple organs, highest levels are found in eye and brain, suggesting its critical importance to the retina.

Jan 1, 2022
Retinitis Pigmentosa Pathway
Many genes have been identified for the inherited and highly heterogeneous disorders - some are arRP, adRP and X-linked.


Nov 25, 2016
Two novel mutations in PRPF3 causing autosomal dominant retinitis pigmentosa
Zilin Zhong , Min Yan , Wan Sun , Zehua Wu , Liyun Han , Zheng Zhou , Fang Zheng , Jianjun Chen  | Scientific Reports | 6 | 37840 | 25...


Aug 19, 2014
Recent Advances of Stem Cell Therapy for Retinitis Pigmentosa
This review provides an overview of stem cell-based treatment of RP and its main problems, providing evidence for the safety and . . .


Mar 9, 2007
Identification of photoreceptor genes affected by PRPF31 mutations associated with autosomal dominant retinitis pigmentosa
Identification of RNA transcripts associated with PRPF31-containing splicing complexes using an immunoprecipitation-coupled microarray . . .
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