Single nucleotide polymorphism-based validation of exonic splicing enhancers
about
Positive selection acting on splicing motifs reflects compensatory evolutionSplicing factor SFRS1 recognizes a functionally diverse landscape of RNA transcriptsGeneral and specific functions of exonic splicing silencers in splicing controlAntisense-mediated exon skipping: a versatile tool with therapeutic and research applicationsDistribution of SR protein exonic splicing enhancer motifs in human protein-coding genes.Protein modularity of alternatively spliced exons is associated with tissue-specific regulation of alternative splicing.Evidence for selection on synonymous mutations affecting stability of mRNA secondary structure in mammalsRegions of extreme synonymous codon selection in mammalian genesDecoding mechanisms by which silent codon changes influence protein biogenesis and functionOrigin and evolution of spliceosomal intronsAlternative splicing and genetic diversity: silencers are more frequently modified by SNVs associated with alternative exon/intron bordersInference of splicing regulatory activities by sequence neighborhood analysisCRPV genomes with synonymous codon optimizations in the CRPV E7 gene show phenotypic differences in growth and altered immunity upon E7 vaccinationCYP2B6 non-coding variation associated with smoking cessation is also associated with differences in allelic expression, splicing, and nicotine metabolism independent of common amino-acid changesImpairment of translation in neurons as a putative causative factor for autismComputational prediction of splicing regulatory elements shared by Tetrapoda organismsThe pivotal roles of TIA proteins in 5' splice-site selection of alu exons and across evolutionAlternative splicing of Alu exons--two arms are better than oneStatistical signals in bioinformatics.Rethinking gene regulatory networks in light of alternative splicing, intrinsically disordered protein domains, and post-translational modificationsSNPinfo: integrating GWAS and candidate gene information into functional SNP selection for genetic association studiesBoth Maintenance and Avoidance of RNA-Binding Protein Interactions Constrain Coding Sequence Evolution.First- and second-shell metal binding residues in human proteins are disproportionately associated with disease-related SNPs.Natural selection on human microRNA binding sites inferred from SNP data.The action of selection on codon bias in the human genome is related to frequency, complexity, and chronology of amino acidsThe effects of multiple features of alternatively spliced exons on the K(A)/K(S) ratio test.Differentiated evolutionary rates in alternative exons and the implications for splicing regulation.Compensatory relationship between splice sites and exonic splicing signals depending on the length of vertebrate introns.Genomic selective constraints in murid noncoding DNASplicing and the evolution of proteins in mammalsThe emergence of alternative 3' and 5' splice site exons from constitutive exonsStrategies for identifying RNA splicing regulatory motifs and predicting alternative splicing eventsGenome-wide survey of allele-specific splicing in humans.Identify alternative splicing events based on position-specific evolutionary conservation.Splice-mediated Variants of Proteins (SpliVaP) - data and characterization of changes in signatures among protein isoforms due to alternative splicingDiverse splicing patterns of exonized Alu elements in human tissuesThe impact of the nucleosome code on protein-coding sequence evolution in yeastReexamining microRNA site accessibility in Drosophila: a population genomics studyEvolution of alternative splicing regulation: changes in predicted exonic splicing regulators are not associated with changes in alternative splicing levels in primates.Exonic splicing signals impose constraints upon the evolution of enzymatic activity.
P2860
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P2860
Single nucleotide polymorphism-based validation of exonic splicing enhancers
description
2004 nî lūn-bûn
@nan
2004 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած
@hyw
2004 թվականի սեպտեմբերին հրատարակված գիտական հոդված
@hy
2004年の論文
@ja
2004年論文
@yue
2004年論文
@zh-hant
2004年論文
@zh-hk
2004年論文
@zh-mo
2004年論文
@zh-tw
2004年论文
@wuu
name
Single nucleotide polymorphism-based validation of exonic splicing enhancers
@ast
Single nucleotide polymorphism-based validation of exonic splicing enhancers
@en
Single nucleotide polymorphism-based validation of exonic splicing enhancers
@en-gb
Single nucleotide polymorphism-based validation of exonic splicing enhancers
@nl
type
label
Single nucleotide polymorphism-based validation of exonic splicing enhancers
@ast
Single nucleotide polymorphism-based validation of exonic splicing enhancers
@en
Single nucleotide polymorphism-based validation of exonic splicing enhancers
@en-gb
Single nucleotide polymorphism-based validation of exonic splicing enhancers
@nl
altLabel
Single Nucleotide Polymorphism–Based Validation of Exonic Splicing Enhancers
@en
prefLabel
Single nucleotide polymorphism-based validation of exonic splicing enhancers
@ast
Single nucleotide polymorphism-based validation of exonic splicing enhancers
@en
Single nucleotide polymorphism-based validation of exonic splicing enhancers
@en-gb
Single nucleotide polymorphism-based validation of exonic splicing enhancers
@nl
P2860
P1433
P1476
Single nucleotide polymorphism-based validation of exonic splicing enhancers
@en
P2093
Christopher B Burge
Dirk Holste
P2860
P356
10.1371/JOURNAL.PBIO.0020268
P407
P577
2004-09-01T00:00:00Z