<p>The natural 3’ss of the exon 9 in each minigene was substituted with a more functional one by site-directed mutagenesis (c.889-10_889-9delinsTT). The proportion of transcripts including exon 9 was assessed and normalized to the wild type minigene. The stripped and solid bars represent the exon 9 inclusion from the different minigenes with the natural 3’ss and the 3’ss mutated, respectively. All the differences were statistically significant (*** p<0.001).</p
To illuminate the extent and roles of exonic sequences in the splicing of human RNA transcripts, we ...
<p>The common forms of alternative splicing represented here are; exon skipping, intron retention, a...
<p>(A.) The c.474 G→A SNP induces alternative splicing <i>ex vivo</i>. Left panel: PCR fragments con...
<p>The splicing score of exon 11 5’ splice site was optimized in the 3A6T minigene by introducing th...
<p>(a) Schematic representation of the position of the mutations in <i>NF1</i> exon 9 identified in ...
<p>The upper panel shows the location and predicted splice scores of the natural and cryptic (wild t...
<p>The upper panel shows the location and sequence of the spacer introduced in the pcDNA3.1 wild typ...
<p>RT-PCR analysis of the literature-derived E<sup>+1</sup> variations. The splicing affecting seque...
<p>(A) The scheme illustrates four alternative splicing patterns regarding novel exon 9A in mice. Gr...
<p>(A) Schematic representation of FIX exon 5 sequence showing the location of the deletions, the ex...
Alternative splicing of genes is an efficient means of generating variation in protein function. Sev...
Splice site nucleotide substitutions can be analyzed by comparing the individual information content...
One of the most common splice variations are small exon length variations caused by the use of alter...
Alternative splicing of genes is an efficient means of generating variation in protein function. Sev...
<p>(A) A wild-type <i>eIF4H</i> minigene, containing exons 4–6 and the intervening introns, was muta...
To illuminate the extent and roles of exonic sequences in the splicing of human RNA transcripts, we ...
<p>The common forms of alternative splicing represented here are; exon skipping, intron retention, a...
<p>(A.) The c.474 G→A SNP induces alternative splicing <i>ex vivo</i>. Left panel: PCR fragments con...
<p>The splicing score of exon 11 5’ splice site was optimized in the 3A6T minigene by introducing th...
<p>(a) Schematic representation of the position of the mutations in <i>NF1</i> exon 9 identified in ...
<p>The upper panel shows the location and predicted splice scores of the natural and cryptic (wild t...
<p>The upper panel shows the location and sequence of the spacer introduced in the pcDNA3.1 wild typ...
<p>RT-PCR analysis of the literature-derived E<sup>+1</sup> variations. The splicing affecting seque...
<p>(A) The scheme illustrates four alternative splicing patterns regarding novel exon 9A in mice. Gr...
<p>(A) Schematic representation of FIX exon 5 sequence showing the location of the deletions, the ex...
Alternative splicing of genes is an efficient means of generating variation in protein function. Sev...
Splice site nucleotide substitutions can be analyzed by comparing the individual information content...
One of the most common splice variations are small exon length variations caused by the use of alter...
Alternative splicing of genes is an efficient means of generating variation in protein function. Sev...
<p>(A) A wild-type <i>eIF4H</i> minigene, containing exons 4–6 and the intervening introns, was muta...
To illuminate the extent and roles of exonic sequences in the splicing of human RNA transcripts, we ...
<p>The common forms of alternative splicing represented here are; exon skipping, intron retention, a...
<p>(A.) The c.474 G→A SNP induces alternative splicing <i>ex vivo</i>. Left panel: PCR fragments con...