<p>(A) A model of the human system, which represents a summary of published work relevant to understanding FRG1 and DUX4 in relation to FSHD supplied to aid the reader with context, showing the FSHD-associated human chromosome 4q35 D4Z4 macrosatellite in healthy (upper) and FSHD (lower) subjects. In healthy subjects, the D4Z4 array consists of between 11 and ~120 D4Z4 repeat units (RU) and is epigenetically repressed (black lollipops). FRG1 is ubiquitously expressed, but there is no (or very little) polyadenylated DUX4-fl mRNA expression. In FSHD1 subjects, the D4Z4 array consists of between 1 and 10 D4Z4 RU, is epigenetically derepressed (yellow lollipops), and a significantly higher fraction of cells than in healthy subjects express polya...
Double Homeobox 4, Dux4, is the leading candidate gene for Facioscapulohumeral Dystrophy (FSHD). FSH...
Thesis (Ph.D.)--University of Washington, 2016-12Facioscapulohumeral dystrophy (FSHD) is caused by t...
Skeletal muscle wasting in facioscapulohumeral muscular dystrophy (FSHD) results in substantial morb...
<p>The Chromosome 4 D4Z4 repeats (open triangles) and its homolog on Chromosome 10 (closed triangles...
Facioscapulohumeral muscular dystrophy (FSHD) is typically an adult onset dominant myopathy. Epigene...
FSHD is an autosomal dominant disease that affects 1:20000 individuals. Mapping studies have associ...
Facioscapulohumeral muscular dystrophy (FSHD) is a rare genetic disease and is considered one of the...
Development and application of statistical models for medical scientific researc
Background: Facioscapulohumeral muscular dystrophy (FSHD) is an autosomal dominant neuromuscular dis...
<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...
Facioscapulohumeral muscular dystrophy (FSHD), a prevalent inherited human myopathy, develops follow...
Facioscapulohumeral muscular dystrophy (FSHD) is a progressive muscle-wasting disease that affects a...
Background: Facioscapulohumeral muscular dystrophy (FSHD) is an autosomal dominant neuromuscular dis...
Facioscapulohumeral muscular dystrophy (FSHD) is caused by deletions within the polymorphic DNA tand...
Double Homeobox 4, Dux4, is the leading candidate gene for Facioscapulohumeral Dystrophy (FSHD). FSH...
Thesis (Ph.D.)--University of Washington, 2016-12Facioscapulohumeral dystrophy (FSHD) is caused by t...
Skeletal muscle wasting in facioscapulohumeral muscular dystrophy (FSHD) results in substantial morb...
<p>The Chromosome 4 D4Z4 repeats (open triangles) and its homolog on Chromosome 10 (closed triangles...
Facioscapulohumeral muscular dystrophy (FSHD) is typically an adult onset dominant myopathy. Epigene...
FSHD is an autosomal dominant disease that affects 1:20000 individuals. Mapping studies have associ...
Facioscapulohumeral muscular dystrophy (FSHD) is a rare genetic disease and is considered one of the...
Development and application of statistical models for medical scientific researc
Background: Facioscapulohumeral muscular dystrophy (FSHD) is an autosomal dominant neuromuscular dis...
<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...
Facioscapulohumeral muscular dystrophy (FSHD), a prevalent inherited human myopathy, develops follow...
Facioscapulohumeral muscular dystrophy (FSHD) is a progressive muscle-wasting disease that affects a...
Background: Facioscapulohumeral muscular dystrophy (FSHD) is an autosomal dominant neuromuscular dis...
Facioscapulohumeral muscular dystrophy (FSHD) is caused by deletions within the polymorphic DNA tand...
Double Homeobox 4, Dux4, is the leading candidate gene for Facioscapulohumeral Dystrophy (FSHD). FSH...
Thesis (Ph.D.)--University of Washington, 2016-12Facioscapulohumeral dystrophy (FSHD) is caused by t...
Skeletal muscle wasting in facioscapulohumeral muscular dystrophy (FSHD) results in substantial morb...