<div><p>The <i>DUX4</i> gene, encoded within D4Z4 repeats on human chromosome 4q35, has recently emerged as a key factor in the pathogenic mechanisms underlying Facioscapulohumeral muscular dystrophy (FSHD). This recognition prompted development of animal models expressing the <i>DUX4</i> open reading frame (ORF) alone or embedded within D4Z4 repeats. In the first published model, we used adeno-associated viral vectors (AAV) and strong viral control elements (CMV promoter, SV40 poly A) to demonstrate that the <i>DUX4</i> cDNA caused dose-dependent toxicity in mouse muscles. As a follow-up, we designed a second generation of <i>DUX4</i>-expressing AAV vectors to more faithfully genocopy the FSHD-permissive D4Z4 repeat region located at 4q35....
Facioscapulohumeral muscular dystrophy (FSHD) is a common form of muscular dystrophy in adults that ...
The Double homeobox 4 (DUX4) gene is an important regulator of early human development and its aberr...
Facioscapulohumeral muscular dystrophy (FSHD) is caused by incomplete epigenetic repression of the D...
The DUX4 gene, encoded within D4Z4 repeats on human chromosome 4q35, has recently emerged as a key f...
<p>A: <i>Top</i> shows the exon-intron structure of the DUX4 gene arising from the distal D4Z4 unit,...
<div><p>Facioscapulohumeral dystrophy (FSHD) is a progressive muscular dystrophy caused by decreased...
Facioscapulohumeral dystrophy (FSHD) is a progressive muscular dystrophy caused by decreased epigene...
Thesis (Ph.D.)--University of Washington, 2016-12Facioscapulohumeral dystrophy (FSHD) is caused by t...
Facioscapulohumeral muscular dystrophy is the most common inherited muscular dystrophy though no tre...
Facioscapulohumeral muscular dystrophy (FSHD) is linked to deletions in 4q35 within the D4Z4 repeat ...
Facioscapulohumeral muscular dystrophy (FSHD), a prevalent inherited human myopathy, develops follow...
Facioscapulohumeral muscular dystrophy (FSHD) is an autosomal dominant neuromuscular disorder that i...
Item does not contain fulltextFacioscapulohumeral muscular dystrophy (FSHD) is a common form of musc...
SummaryFacioscapulohumeral muscular dystrophy (FSHD) is an enigmatic disease associated with epigene...
Facioscapulohumeral muscular dystrophy (FSHD) is an autosomal dominant neuromuscular disorder that i...
Facioscapulohumeral muscular dystrophy (FSHD) is a common form of muscular dystrophy in adults that ...
The Double homeobox 4 (DUX4) gene is an important regulator of early human development and its aberr...
Facioscapulohumeral muscular dystrophy (FSHD) is caused by incomplete epigenetic repression of the D...
The DUX4 gene, encoded within D4Z4 repeats on human chromosome 4q35, has recently emerged as a key f...
<p>A: <i>Top</i> shows the exon-intron structure of the DUX4 gene arising from the distal D4Z4 unit,...
<div><p>Facioscapulohumeral dystrophy (FSHD) is a progressive muscular dystrophy caused by decreased...
Facioscapulohumeral dystrophy (FSHD) is a progressive muscular dystrophy caused by decreased epigene...
Thesis (Ph.D.)--University of Washington, 2016-12Facioscapulohumeral dystrophy (FSHD) is caused by t...
Facioscapulohumeral muscular dystrophy is the most common inherited muscular dystrophy though no tre...
Facioscapulohumeral muscular dystrophy (FSHD) is linked to deletions in 4q35 within the D4Z4 repeat ...
Facioscapulohumeral muscular dystrophy (FSHD), a prevalent inherited human myopathy, develops follow...
Facioscapulohumeral muscular dystrophy (FSHD) is an autosomal dominant neuromuscular disorder that i...
Item does not contain fulltextFacioscapulohumeral muscular dystrophy (FSHD) is a common form of musc...
SummaryFacioscapulohumeral muscular dystrophy (FSHD) is an enigmatic disease associated with epigene...
Facioscapulohumeral muscular dystrophy (FSHD) is an autosomal dominant neuromuscular disorder that i...
Facioscapulohumeral muscular dystrophy (FSHD) is a common form of muscular dystrophy in adults that ...
The Double homeobox 4 (DUX4) gene is an important regulator of early human development and its aberr...
Facioscapulohumeral muscular dystrophy (FSHD) is caused by incomplete epigenetic repression of the D...