Exon definition may facilitate splice site selection in RNAs with multiple exons.
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Regulation of alternative splicing by SRrp86 and its interacting proteinsAssociation of polyadenylation cleavage factor I with U1 snRNP.A splice site mutation in the gene of the human type I hair keratin hHa1 results in the expression of a tailless keratin isoformMolecular basis of Fabry disease: mutations and polymorphisms in the human alpha-galactosidase A geneHuman peroxisome assembly factor-2 (PAF-2): a gene responsible for group C peroxisome biogenesis disorder in humansPrp5 bridges U1 and U2 snRNPs and enables stable U2 snRNP association with intron RNAGenomic sequence, splicing, and gene annotationTargeted 'knockdown' of spliceosome function in mammalian cellsSequence information for the splicing of human pre-mRNA identified by support vector machine classificationNovel splice donor site mutation in the cardiac myosin-binding protein-C gene in familial hypertrophic cardiomyopathy. Characterization Of cardiac transcript and proteinA bidirectional SF2/ASF- and SRp40-dependent splicing enhancer regulates human immunodeficiency virus type 1 rev, env, vpu, and nef gene expressionMultiple forms of mRNA encoding human pregnancy-associated endometrial alpha 2-globulin, a beta-lactoglobulin homologueStructure and expression of the excision repair gene ERCC6, involved in the human disorder Cockayne's syndrome group BAn intronic enhancer regulates splicing of the twintron of Drosophila melanogaster prospero pre-mRNA by two different spliceosomesCan, a putative oncogene associated with myeloid leukemogenesis, may be activated by fusion of its 3' half to different genes: characterization of the set geneSplicing regulation: from a parts list of regulatory elements to an integrated splicing codeRole of polyadenylation in nucleocytoplasmic transport of mRNAA subset of SR proteins activates splicing of the cardiac troponin T alternative exon by direct interactions with an exonic enhancerIdentification of RNA splicing errors resulting in human ornithine transcarbamylase deficiencyAntisense-mediated exon skipping: a versatile tool with therapeutic and research applicationsConsensus sequence ZenGene trap mutagenesis of hnRNP A2/B1: a cryptic 3' splice site in the neomycin resistance gene allows continued expression of the disrupted cellular genemRNA trans-splicing in gene therapy for genetic diseasesPrp40 and early events in splice site definitionRecursive splicing in long vertebrate genes.Cross-kingdom patterns of alternative splicing and splice recognitionMolecular basis of the Kell-null phenotype: a mutation at the splice site of human KEL gene abolishes the expression of Kell blood group antigensSerine-arginine-rich protein p30 directs alternative splicing of glucocorticoid receptor pre-mRNA to glucocorticoid receptor beta in neutrophilsScreening for mutations by expressing patient cDNA segments in E. coli: homocystinuria due to cystathionine beta-synthase deficiencyContext-dependent control of alternative splicing by RNA-binding proteinsAn activated 5' cryptic splice site in the human ALG3 gene generates a premature termination codon insensitive to nonsense-mediated mRNA decay in a new case of congenital disorder of glycosylation type Id (CDG-Id)RNA editing: exploring one mode with apolipoprotein B mRNAA point mutation in an invariant splice donor site leads to exon skipping in two unrelated Dutch patients with dihydropyrimidine dehydrogenase deficiencyA purine-rich intronic element enhances alternative splicing of thyroid hormone receptor mRNADirect selection for mutations affecting specific splice sites in a hamster dihydrofolate reductase minigeneInterplay between exonic splicing enhancers, mRNA processing, and mRNA surveillance in the dystrophic Mdx mouseThe CUGBP2 splicing factor regulates an ensemble of branchpoints from perimeter binding sites with implications for autoregulationMouse pseudouridine synthase 1: gene structure and alternative splicing of pre-mRNAIdentification of mutations in the alpha-L-iduronidase gene (IDUA) that cause Hurler and Scheie syndromesMultiple interdependent sequence elements control splicing of a fibroblast growth factor receptor 2 alternative exon
P2860
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P2860
Exon definition may facilitate splice site selection in RNAs with multiple exons.
description
1990 nî lūn-bûn
@nan
1990年の論文
@ja
1990年論文
@yue
1990年論文
@zh-hant
1990年論文
@zh-hk
1990年論文
@zh-mo
1990年論文
@zh-tw
1990年论文
@wuu
1990年论文
@zh
1990年论文
@zh-cn
name
Exon definition may facilitate splice site selection in RNAs with multiple exons.
@ast
Exon definition may facilitate splice site selection in RNAs with multiple exons.
@en
type
label
Exon definition may facilitate splice site selection in RNAs with multiple exons.
@ast
Exon definition may facilitate splice site selection in RNAs with multiple exons.
@en
prefLabel
Exon definition may facilitate splice site selection in RNAs with multiple exons.
@ast
Exon definition may facilitate splice site selection in RNAs with multiple exons.
@en
P2093
P2860
P356
P1476
Exon definition may facilitate splice site selection in RNAs with multiple exons.
@en
P2093
P2860
P356
10.1128/MCB.10.1.84
P407
P577
1990-01-01T00:00:00Z