Mutation in the splicing factor Hprp3p linked to retinitis pigmentosa impairs interactions within the U4/U6 snRNP complex.
about
Spliceosomal protein eftud2 mutation leads to p53-dependent apoptosis in zebrafish neural progenitors.Mutations in spliceosomal proteins and retina degenerationTemporal and tissue specific regulation of RP-associated splicing factor genes PRPF3, PRPF31 and PRPC8--implications in the pathogenesis of RP.Follicle-stimulating hormone receptor (FSHR) alternative skipping of exon 2 or 3 affects ovarian response to FSHUsing bacteria to determine protein kinase specificity and predict target substratesA missense mutation in PRPF6 causes impairment of pre-mRNA splicing and autosomal-dominant retinitis pigmentosaSuppressors of the cdc-25.1(gf)-associated intestinal hyperplasia reveal important maternal roles for prp-8 and a subset of splicing factors in C. elegans.Assembly of the U5 snRNP component PRPF8 is controlled by the HSP90/R2TP chaperones.Retinitis pigmentosa mutations of SNRNP200 enhance cryptic splice-site recognition.Splicing in the RNA World
P2860
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P2860
Mutation in the splicing factor Hprp3p linked to retinitis pigmentosa impairs interactions within the U4/U6 snRNP complex.
description
2007 nî lūn-bûn
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2007年の論文
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2007年学术文章
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2007年学术文章
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name
Mutation in the splicing facto ...... ithin the U4/U6 snRNP complex.
@en
type
label
Mutation in the splicing facto ...... ithin the U4/U6 snRNP complex.
@en
prefLabel
Mutation in the splicing facto ...... ithin the U4/U6 snRNP complex.
@en
P2093
P2860
P356
P1476
Mutation in the splicing facto ...... ithin the U4/U6 snRNP complex.
@en
P2093
Juana Maria Gonzalez-Santos
Rongqi Cathleen Duan
P2860
P304
P356
10.1093/HMG/DDM300
P577
2007-10-11T00:00:00Z