<p>(<b>A–B</b>) <b>A.</b> Ψ values for ten misspliced ASEs are represented as histograms for 4 adult controls (white bars) and 5 DM1 patients (black bars). Error bars represent standard deviations for each ASE. Hits were defined as changes displaying <i>q</i> values <0.05 and |ΔΨ| >5%. <b>B.</b> Sample UCSC Genome Browser (<a href="http://genome.ucsc.edu" target="_blank">http://genome.ucsc.edu</a>) adaptation showing the chromosome 19 region harboring human insulin receptor, INSR. Top image shows reported full-length RefSeq transcripts, the targeted ASE is boxed and shown in detail in the bottom image. The positions and names of the primers used for mRNA amplification by RT-PCR are shown above the transcripts. Links to transcript maps and p...
<p>Splicing sensitive microarrays of candidate factors (A) <i>bdf1Δ</i> and <i>bdf2Δ</i>, (B) <i>vps...
In recent years, genes encoding components of the RNA splicing machinery and regulatory factors have...
Myotonic dystrophy (DM) is caused by either an untranslated CTG expansion in the 3′ untranslated reg...
<p><b>(A)</b><i>INSR</i> splicing products obtained by RT-PCR amplification of RNA isolated from <i>...
<p><b>(A)</b><i>INSR</i> splicing products obtained by RT-PCR amplification of RNA isolated from <i>...
<p>(A) A total of 33 ASEs were considered for this analysis based on the following criteria. First, ...
<p>(<b>A</b>) Relative abundance of <i>St5</i>, <i>Asb1</i> and <i>Plg2g10</i> is significantly incr...
DMD is the largest gene in the human genome, spanning over 2.2Mb of the X chromosome, and more than ...
(A)INSR splicing products obtained by RT-PCR amplification of RNA isolated from skeletal muscle biop...
<p>Total RNA from muscle tissues of transgenic C57BL6 mice expressing 600 and 1200 CUG-repeats were ...
AbstractMyotonic dystrophy (DM1) is a dominant autosomal multisystemic disorder caused by the expans...
<p><b>Copyright information:</b></p><p>Taken from "Computational analysis of splicing errors and mut...
Predisposition to type 1 diabetes and juvenile obesity is influenced by the susceptibility locus IDD...
High-throughput next-generation sequencing technologies have led to a rapid increase in the number o...
<p><b>Copyright information:</b></p><p>Taken from "Computational analysis of splicing errors and mut...
<p>Splicing sensitive microarrays of candidate factors (A) <i>bdf1Δ</i> and <i>bdf2Δ</i>, (B) <i>vps...
In recent years, genes encoding components of the RNA splicing machinery and regulatory factors have...
Myotonic dystrophy (DM) is caused by either an untranslated CTG expansion in the 3′ untranslated reg...
<p><b>(A)</b><i>INSR</i> splicing products obtained by RT-PCR amplification of RNA isolated from <i>...
<p><b>(A)</b><i>INSR</i> splicing products obtained by RT-PCR amplification of RNA isolated from <i>...
<p>(A) A total of 33 ASEs were considered for this analysis based on the following criteria. First, ...
<p>(<b>A</b>) Relative abundance of <i>St5</i>, <i>Asb1</i> and <i>Plg2g10</i> is significantly incr...
DMD is the largest gene in the human genome, spanning over 2.2Mb of the X chromosome, and more than ...
(A)INSR splicing products obtained by RT-PCR amplification of RNA isolated from skeletal muscle biop...
<p>Total RNA from muscle tissues of transgenic C57BL6 mice expressing 600 and 1200 CUG-repeats were ...
AbstractMyotonic dystrophy (DM1) is a dominant autosomal multisystemic disorder caused by the expans...
<p><b>Copyright information:</b></p><p>Taken from "Computational analysis of splicing errors and mut...
Predisposition to type 1 diabetes and juvenile obesity is influenced by the susceptibility locus IDD...
High-throughput next-generation sequencing technologies have led to a rapid increase in the number o...
<p><b>Copyright information:</b></p><p>Taken from "Computational analysis of splicing errors and mut...
<p>Splicing sensitive microarrays of candidate factors (A) <i>bdf1Δ</i> and <i>bdf2Δ</i>, (B) <i>vps...
In recent years, genes encoding components of the RNA splicing machinery and regulatory factors have...
Myotonic dystrophy (DM) is caused by either an untranslated CTG expansion in the 3′ untranslated reg...