International audienceFacioscapulohumeral muscular dystrophy (FSHD) patients carry contractions of the D4Z4-tandem repeat array on chromosome 4q35. Decrease in D4Z4 copy number is thought to alter a chromatin structure and activate expression of neighboring genes. D4Z4 contains a putative double-homeobox gene called DUX4. We identified DUX4 mRNAs in cells transfected with genomic fragments containing the DUX4 gene. Using RT-PCR we also recognized expressed DUX4 mRNAs in primary FSHD myoblasts. Polyclonal antibodies raised against specific DUX4 peptides detected the DUX4 protein in cells transfected with D4Z4 elements. DUX4 localizes in the nucleus of cells transfected with CMV–DUX4 expression vectors. A DUX4-related protein is endogenously ...
International audienceFacioscapulohumeral muscular dystrophy (FSHD) is a dominant disease linked to ...
Aberrant expression of the full-length isoform of DUX4 (DUX4-FL) appears to underlie pathogenesis in...
Facioscapulohumeral muscular dystrophy (FSHD) is a dominant disease linked to contractions of the D4...
Facioscapulohumeral muscular dystrophy (FSHD) patients carry contractions of the D4Z4-tandem repeat ...
Facioscapulohumeral muscular dystrophy (FSHD) is linked to deletions in 4q35 within the D4Z4 repeat ...
Facioscapulohumeral muscular dystrophy (FSHD) is a muscle degenerative disease that disproportionall...
Facioscapulohumeral muscular dystrophy (FSHD) is linked to the deletion of the D4Z4 arrays at chromo...
DUX4 is a double homeodomain gene embedded within D4Z4 macrosatellite repeats on chromosome 4. Evide...
DUX4 (Double Homeobox Protein 4) is a nuclear transcription factor encoded at each D4Z4 unit of a ta...
Facioscapulohumeral muscular dystrophy (FSHD) is caused by an unusual deletion with neomorphic activ...
Facioscapulohumeral muscular dystrophy (FSHD), a prevalent inherited human myopathy, develops follow...
Facioscapulohumeral muscular dystrophy (FSHD) is linked to the deletion of the D4Z4 arrays at chromo...
Facioscapulohumeral muscular dystrophy (FSHD) is neuromuscular disorder connected with deletion of D...
<div><p>Facioscapulohumeral muscular dystrophy (FSHD) is linked to the deletion of the D4Z4 arrays a...
DUX4 (Double Homeobox Protein 4) is a nuclear transcription factor encoded at each D4Z4 unit of a ta...
International audienceFacioscapulohumeral muscular dystrophy (FSHD) is a dominant disease linked to ...
Aberrant expression of the full-length isoform of DUX4 (DUX4-FL) appears to underlie pathogenesis in...
Facioscapulohumeral muscular dystrophy (FSHD) is a dominant disease linked to contractions of the D4...
Facioscapulohumeral muscular dystrophy (FSHD) patients carry contractions of the D4Z4-tandem repeat ...
Facioscapulohumeral muscular dystrophy (FSHD) is linked to deletions in 4q35 within the D4Z4 repeat ...
Facioscapulohumeral muscular dystrophy (FSHD) is a muscle degenerative disease that disproportionall...
Facioscapulohumeral muscular dystrophy (FSHD) is linked to the deletion of the D4Z4 arrays at chromo...
DUX4 is a double homeodomain gene embedded within D4Z4 macrosatellite repeats on chromosome 4. Evide...
DUX4 (Double Homeobox Protein 4) is a nuclear transcription factor encoded at each D4Z4 unit of a ta...
Facioscapulohumeral muscular dystrophy (FSHD) is caused by an unusual deletion with neomorphic activ...
Facioscapulohumeral muscular dystrophy (FSHD), a prevalent inherited human myopathy, develops follow...
Facioscapulohumeral muscular dystrophy (FSHD) is linked to the deletion of the D4Z4 arrays at chromo...
Facioscapulohumeral muscular dystrophy (FSHD) is neuromuscular disorder connected with deletion of D...
<div><p>Facioscapulohumeral muscular dystrophy (FSHD) is linked to the deletion of the D4Z4 arrays a...
DUX4 (Double Homeobox Protein 4) is a nuclear transcription factor encoded at each D4Z4 unit of a ta...
International audienceFacioscapulohumeral muscular dystrophy (FSHD) is a dominant disease linked to ...
Aberrant expression of the full-length isoform of DUX4 (DUX4-FL) appears to underlie pathogenesis in...
Facioscapulohumeral muscular dystrophy (FSHD) is a dominant disease linked to contractions of the D4...