Double Homeobox Protein 4

Known as: DUX4, Double Homeobox Protein 10, Double Homeobox Protein 4/10 
Double homeobox protein 4 (424 aa, ~45 kDa) is encoded by the human DUX4 gene. This protein plays a role in the regulation of transcription.
National Institutes of Health

Papers overview

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2016
2016
Facioscapulohumeral dystrophy (FSHD) is associated with somatic chromatin relaxation of the D4Z4 repeat array and derepression of… (More)
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2015
2015
Facioscapulohumeral muscular dystrophy (FSHD: MIM#158900) is a common myopathy with marked but largely unexplained clinical inter… (More)
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2015
2015
Facioscapulohumeral muscular dystrophy (FSHD) is caused by chromatin relaxation that results in aberrant expression of the… (More)
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2014
2014
Facioscapulohumeral dystrophy (FSHD) is caused by decreased epigenetic repression of the D4Z4 macrosatellite array and recent… (More)
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2014
2014
Facioscapulohumeral muscular dystrophy (FSHD) is linked to epigenetic dysregulation of the chromosome 4q35 D4Z4 macrosatellite… (More)
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2013
2013
Facioscapulohumeral muscular dystrophy (FSHD) is one of the most frequent hereditary muscle disorders. It is linked to… (More)
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2013
2013
The human double-homeodomain retrogene DUX4 is expressed in the testis and epigenetically repressed in somatic tissues… (More)
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Highly Cited
2012
Highly Cited
2012
Primitive round cell sarcomas of childhood and young adults have been problematic to diagnose and classify. Our goal was to… (More)
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2011
2011
Double homeobox 4 (DUX4) is a candidate disease gene for facioscapulohumeral dystrophy (FSHD), one of the most common muscular… (More)
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Highly Cited
1999
Highly Cited
1999
Facioscapulohumeral muscular dystrophy (FSHD) is linked to the polymorphic D4Z4 locus on chromosome 4q35. In non-affected… (More)
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