Exonic splicing enhancers (ESEs) are pre-mRNA cis-acting elements required for splice-site recognition. We previously developed a web-based program called ESEfinder that scores any sequence for the presence of ESE motifs recognized by the human SR proteins SF2/ASF, SRp40, SRp55 and SC35 (http://rulai.cshl.edu/tools/ESE/). Using ESEfinder, we have undertaken a large-scale analysis of ESE motif distribution in human protein-coding genes. Significantly higher frequencies of ESE motifs were observed in constitutive internal protein-coding exons, compared with both their flanking intronic regions and with pseudo exons. Statistical analysis of ESE motif frequency distributions revealed a complex relationship between splice-site strength and incre...
A very early step in splice site recognition is exon definition, a process that is as yet poorly und...
Cis-acting short sequence motifs play important roles in alternative splicing. It is now possible to...
It is widely accepted that at least 10% of all mutations causing human inherited disease disrupt spl...
Point mutations frequently cause genetic diseases by disrupting the correct pattern of pre-mRNA spli...
Using an in vitro randomization and functional selection procedure, we have identified three novel c...
Exonic Splicing enhancers (ESEs) are important cis elements required for exon inclusion. Using an in...
Numerous disease-associated point mutations exert their effects by disrupting the activity of exonic...
ABSTRACT A typical gene contains two levels of information: a sequence that encodes a particular pro...
Accurate pre-mRNA splicing requires primary splicing signals, including the splice sites, a polypyri...
Alternative splicing is a powerful means of regulating gene expression and enhancing protein diversi...
SummaryMost human genes produce multiple splicing isoforms with distinct functions. To systematicall...
AbstractExonic splicing silencers (ESSs) are cis-regulatory elements that inhibit the use of adjacen...
Abstract Background Exonic splicing enhancers (ESEs) activate nearby splice sites and promote the in...
A modified method of cycled selection was used to characterize splicing enhancers for exon inclusion...
The majority of human genes undergo alternative splicing to generate multiple isoforms with distinct...
A very early step in splice site recognition is exon definition, a process that is as yet poorly und...
Cis-acting short sequence motifs play important roles in alternative splicing. It is now possible to...
It is widely accepted that at least 10% of all mutations causing human inherited disease disrupt spl...
Point mutations frequently cause genetic diseases by disrupting the correct pattern of pre-mRNA spli...
Using an in vitro randomization and functional selection procedure, we have identified three novel c...
Exonic Splicing enhancers (ESEs) are important cis elements required for exon inclusion. Using an in...
Numerous disease-associated point mutations exert their effects by disrupting the activity of exonic...
ABSTRACT A typical gene contains two levels of information: a sequence that encodes a particular pro...
Accurate pre-mRNA splicing requires primary splicing signals, including the splice sites, a polypyri...
Alternative splicing is a powerful means of regulating gene expression and enhancing protein diversi...
SummaryMost human genes produce multiple splicing isoforms with distinct functions. To systematicall...
AbstractExonic splicing silencers (ESSs) are cis-regulatory elements that inhibit the use of adjacen...
Abstract Background Exonic splicing enhancers (ESEs) activate nearby splice sites and promote the in...
A modified method of cycled selection was used to characterize splicing enhancers for exon inclusion...
The majority of human genes undergo alternative splicing to generate multiple isoforms with distinct...
A very early step in splice site recognition is exon definition, a process that is as yet poorly und...
Cis-acting short sequence motifs play important roles in alternative splicing. It is now possible to...
It is widely accepted that at least 10% of all mutations causing human inherited disease disrupt spl...