Comparative Analysis Identifies Exonic Splicing Regulatory Sequences—The Complex Definition of Enhancers and Silencers

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Comparative analysis detects dependencies among the 5′ splice-site positions

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Single Nucleotide Polymorphism–Based Validation of Exonic Splicing Enhancers

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Minimal Conditions for Exonization of Intronic Sequences

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A Combinatorial Code for Splicing Silencing: UAGG and GGGG Motifs

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Multiple roles of arginine/serine-rich splicing factors in RNA processing

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OligoArray: genome-scale oligonucleotide design for microarrays

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Distribution of SR protein exonic splicing enhancer motifs in human protein-coding genes

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Weak selection revealed by the whole-genome comparison of the X chromosome and autosomes of human and chimpanzee

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Evidence of functional selection pressure for alternative splicing events that accelerate evolution of protein subsequences

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Determinants of the inherent strength of human 5′ splice sites

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Exon Inclusion Is Dependent on Predictable Exonic Splicing Enhancers

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Human–mouse comparative analysis reveals that branch-site plasticity contributes to splicing regulation

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Characteristics and regulatory elements defining constitutive splicing and different modes of alternative splicing in human and mouse

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hnRNP H binding at the 5' splice site correlates with the pathological effect of two intronic mutations in the NF-1 and TSH genes

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Comparison of intron-containing and intron-lacking human genes elucidates putative exonic splicing enhancers

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Splicing mutations in human genetic disorders: Examples, detection, and confirmation

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Chromatin organization marks exon-intron structure

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An RNA code for the FOX2 splicing regulator revealed by mapping RNA-protein interactions in stem cells

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