<p>(A) DUX4-bound regions show correlated activation levels in FSHD patient myotubes and in our <i>DUX4</i>-transduced myoblast experimental system. We show log2-activation levels in each system, counting RNA-seq reads within an arbitrary 1 kb of DUX4-bound regions as for <a href="http://www.plosgenetics.org/article/info:doi/10.1371/journal.pgen.1003947#pgen-1003947-g003" target="_blank">Figure 3A</a>. “+” symbols show bound repetitive elements and dot symbols are unique regions. Green symbols show regions that reach statistical significance in only the <i>DUX4</i>-transduced myoblasts, blue symbols are significant in only the FSHD myotubes, and red symbols are significant in both comparisons. The dotted line is a regression line (slope 0.2...
Advances in understanding the pathophysiology of facioscapulohumeral dystrophy (FSHD) have led to th...
Facioscapulohumeral muscular dystrophy (FSHD) is caused by an unusual deletion with neomorphic activ...
<p>(A) Example RNA-seq track showing reads at the MYC locus in MB135-DUX4i cells +/- doxycyline for ...
Facioscapulohumeral dystrophy (FSHD) is associated with the upregulation of the DUX4 transcription f...
FSHD is characterized by the misexpression of DUX4 in skeletal muscle. Although DUX4 upregulation is...
<p>(A) ∼1% of DUX4-bound regions show statistically-significant activation in response to DUX4 in ou...
Facioscapulohumeral muscular dystrophy (FSHD) is a dominant disease linked to contractions of the D4...
International audienceFacioscapulohumeral muscular dystrophy (FSHD) is a dominant disease linked to ...
Additional file 1: Figure S1. Quantification of DUX4 expression in FSHD cell cultures. Flow cytometr...
Item does not contain fulltextFacioscapulohumeral muscular dystrophy (FSHD) is characterized by spor...
Abstract Background Facioscapulohumeral muscular dystrophy (FSHD) is most commonly inherited in an a...
Facioscapulohumeral muscular dystrophy (FSHD) is linked to deletions in 4q35 within the D4Z4 repeat ...
The aim of our study was to identify relationships between epigenetic parameters correlating with a ...
International audience: Facioscapulohumeral muscular dystrophy (FSHD) is one of the most prevalent a...
Facioscapulohumeral muscular dystrophy (FSHD) is a rare disease with characteristic weakness in faci...
Advances in understanding the pathophysiology of facioscapulohumeral dystrophy (FSHD) have led to th...
Facioscapulohumeral muscular dystrophy (FSHD) is caused by an unusual deletion with neomorphic activ...
<p>(A) Example RNA-seq track showing reads at the MYC locus in MB135-DUX4i cells +/- doxycyline for ...
Facioscapulohumeral dystrophy (FSHD) is associated with the upregulation of the DUX4 transcription f...
FSHD is characterized by the misexpression of DUX4 in skeletal muscle. Although DUX4 upregulation is...
<p>(A) ∼1% of DUX4-bound regions show statistically-significant activation in response to DUX4 in ou...
Facioscapulohumeral muscular dystrophy (FSHD) is a dominant disease linked to contractions of the D4...
International audienceFacioscapulohumeral muscular dystrophy (FSHD) is a dominant disease linked to ...
Additional file 1: Figure S1. Quantification of DUX4 expression in FSHD cell cultures. Flow cytometr...
Item does not contain fulltextFacioscapulohumeral muscular dystrophy (FSHD) is characterized by spor...
Abstract Background Facioscapulohumeral muscular dystrophy (FSHD) is most commonly inherited in an a...
Facioscapulohumeral muscular dystrophy (FSHD) is linked to deletions in 4q35 within the D4Z4 repeat ...
The aim of our study was to identify relationships between epigenetic parameters correlating with a ...
International audience: Facioscapulohumeral muscular dystrophy (FSHD) is one of the most prevalent a...
Facioscapulohumeral muscular dystrophy (FSHD) is a rare disease with characteristic weakness in faci...
Advances in understanding the pathophysiology of facioscapulohumeral dystrophy (FSHD) have led to th...
Facioscapulohumeral muscular dystrophy (FSHD) is caused by an unusual deletion with neomorphic activ...
<p>(A) Example RNA-seq track showing reads at the MYC locus in MB135-DUX4i cells +/- doxycyline for ...