IndraLab

Statements


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"The interaction of PRP31 or PRP3 and the U5 snRNP component PRP8 is reported to be regulated by the ubiquitination and deubiquitination status of PRP31 and PRP3, which is required for efficient RNA sp[MISSING/INVALID CREDENTIALS: limited to 200 char for Elsevier]"

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"The SNRNP200, PRPF8, PRPF3, and PRPF31 gene products are all triple-snRNP components, 15,31 and PAP1 binds PRPF3 to negatively regulate splicing, 32,49 suggesting a common mechanism for pathogenesis."

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"It is interesting to note that the interaction of PRPF8 with ubiquitinated PRPF3 is regulated by the deubiquitinating enzyme USP4, and that loss of USP4 prevents the correct splicing of mRNAs including those for α-tubulin xref ."

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sparser
"As the second and third PE targets, we chose PRPF3 and PRPF8 associated with autosomal dominant (ad) forms of retinitis pigmentosa (RP) [ xref , xref ]."

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