<p>(A) A total of 33 ASEs were considered for this analysis based on the following criteria. First, ASEs that showed a ≥10% ΔPSI from WT to DM1 conditions were selected. From this, ASEs that showed a ≥10% ΔPSI with Stau1 overexpression were selected and identified as either beneficial or detrimental for the DM1 pathology (refer to results). (B) Bar graphs showing the specific ASEs that the overexpression of Stau1-HA under DM1 conditions either returned towards the WT splicing pattern (left bar graph) or continued towards a detrimental effect (right bar graph). (C-E) Comparison of the data obtained from the RT-PCR splicing screen presented here to that of Klinck et al., 2014. The threshold used by Klinck et al., was applied (≥5% PSI) to comp...
Alternative splicing (AS) is a co- or post-transcriptional process by which one gene gives rise to m...
<p>Splicing sensitive microarrays of candidate factors (A) <i>bdf1Δ</i> and <i>bdf2Δ</i>, (B) <i>vps...
Thesis (Ph.D.)--University of Washington, 2020In 2011 Yoshida et al. identified mutations in RNA spl...
Myotonic dystrophy type 1 (DM1) is a neuromuscular disorder caused by an expansion of CUG repeats in...
<p>Total RNA was collected from four GM0 cell lines; WT (GM01653) and DM1 cell lines GM03132 (1700 C...
Background: Pre‐mRNA splicing is a complex process requiring the identification of donor site, accep...
Alternative splicing is a major source of diversity of gene expression. Multiple products, some of w...
DMD is the largest gene in the human genome, spanning over 2.2Mb of the X chromosome, and more than ...
More and more transcription factors and their motifs have been reported and linked to specific gene ...
More and more transcription factors and their motifs have been reported and linked to specific gene ...
<p>(A) pGIPZ (CTRL) or Stau1-HA (Stau1-HA) plasmids were transiently transfected into HeLa cell line...
While it's known that the dysregulation of splicing contributes to disease, identifying specific spl...
Variations in new splicing regulatory elements are difficult to identify exclusively by sequence ins...
<p>(a) Examples of alternative exons (<i>Atl2</i>) or introns (<i>Ttn</i>) spliced normally in the m...
<p>(<b>A–B</b>) <b>A.</b> Ψ values for ten misspliced ASEs are represented as histograms for 4 adult...
Alternative splicing (AS) is a co- or post-transcriptional process by which one gene gives rise to m...
<p>Splicing sensitive microarrays of candidate factors (A) <i>bdf1Δ</i> and <i>bdf2Δ</i>, (B) <i>vps...
Thesis (Ph.D.)--University of Washington, 2020In 2011 Yoshida et al. identified mutations in RNA spl...
Myotonic dystrophy type 1 (DM1) is a neuromuscular disorder caused by an expansion of CUG repeats in...
<p>Total RNA was collected from four GM0 cell lines; WT (GM01653) and DM1 cell lines GM03132 (1700 C...
Background: Pre‐mRNA splicing is a complex process requiring the identification of donor site, accep...
Alternative splicing is a major source of diversity of gene expression. Multiple products, some of w...
DMD is the largest gene in the human genome, spanning over 2.2Mb of the X chromosome, and more than ...
More and more transcription factors and their motifs have been reported and linked to specific gene ...
More and more transcription factors and their motifs have been reported and linked to specific gene ...
<p>(A) pGIPZ (CTRL) or Stau1-HA (Stau1-HA) plasmids were transiently transfected into HeLa cell line...
While it's known that the dysregulation of splicing contributes to disease, identifying specific spl...
Variations in new splicing regulatory elements are difficult to identify exclusively by sequence ins...
<p>(a) Examples of alternative exons (<i>Atl2</i>) or introns (<i>Ttn</i>) spliced normally in the m...
<p>(<b>A–B</b>) <b>A.</b> Ψ values for ten misspliced ASEs are represented as histograms for 4 adult...
Alternative splicing (AS) is a co- or post-transcriptional process by which one gene gives rise to m...
<p>Splicing sensitive microarrays of candidate factors (A) <i>bdf1Δ</i> and <i>bdf2Δ</i>, (B) <i>vps...
Thesis (Ph.D.)--University of Washington, 2020In 2011 Yoshida et al. identified mutations in RNA spl...