DUX4 gene

Known as: DOUBLE HOMEOBOX PROTEIN 4, DUX4, Double Homeobox 4 Gene 
This gene plays a role in transcriptional regulation.
National Institutes of Health

Papers overview

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Highly Cited
2012
Highly Cited
2012
Facioscapulohumeral dystrophy (FSHD) is one of the most common inherited muscular dystrophies. The causative gene remains… (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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Highly Cited
2012
Highly Cited
2012
Facioscapulohumeral muscular dystrophy (FSHD), the most prevalent myopathy afflicting both children and adults, is predominantly… (More)
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Highly Cited
2012
Highly Cited
2012
Facioscapulohumeral dystrophy (FSHD) is characterized by chromatin relaxation of the D4Z4 macrosatellite array on chromosome 4… (More)
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Highly Cited
2011
Highly Cited
2011
OBJECTIVE Facioscapulohumeral muscular dystrophy (FSHD) is associated with D4Z4 repeat contraction on human chromosome 4q35. This… (More)
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Highly Cited
2010
Highly Cited
2010
Each unit of the D4Z4 macrosatellite repeat contains a retrotransposed gene encoding the DUX4 double-homeobox transcription… (More)
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Highly Cited
2010
Highly Cited
2010
Facioscapulohumeral muscular dystrophy (FSHD) is a common form of muscular dystrophy in adults that is foremost characterized by… (More)
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Highly Cited
2007
Highly Cited
2007
Facioscapulohumeral muscular dystrophy (FSHD) patients carry contractions of the D4Z4-tandem repeat array on chromosome 4q35… (More)
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Highly Cited
2007
Highly Cited
2007
Facioscapulohumeral muscular dystrophy (FSHD) is an autosomal dominant disorder linked to contractions of the D4Z4 repeat array… (More)
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Highly Cited
2006
Highly Cited
2006
Ewing's family tumors (EFTs) are highly malignant tumors arising from bone and soft tissues that exhibit EWS-FLI1 or variant EWS… (More)
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