Expression of the myodystrophic R453W mutation of lamin A in C2C12 myoblasts causes promoter-specific and global epigenetic defects

Experimental Cell Research

Volumn 314, Issue 8, 2008, Pages 1869-1880

  Håkelien, Anne Mari ^a   Delbarre, Erwan ^a   Gaustad, Kristine G ^a   Buendia, Brigitte ^b   Collas, Philippe ^a  

^a UNIVERSITY OF OSLO   (Norway)

^b INSTITUT JACQUES MONOD   (France)

Author keywords

Chromatin; Differentiation; Histone modification; Lamin A mutation; Myoblast

Indexed keywords

LAMIN A; LYSINE;

ANIMAL CELL; ARTICLE; AUTOSOMAL DOMINANT DISORDER; CELL DIFFERENTIATION; CLONE; CONTROLLED STUDY; EMERY DREIFUSS MUSCULAR DYSTROPHY; EPIGENETICS; GENE; GENE ACTIVATION; GENE EXPRESSION; GENE MUTATION; GENE OVEREXPRESSION; GENOME; HETEROCHROMATIN; LIPODYSTROPHY; LMNA GENE; METHYLATION; MUSCLE ATROPHY; MUSCULAR DYSTROPHY; MYOBLAST; MYOG GENE; NONHUMAN; PRIORITY JOURNAL; PROMOTER REGION; PROTEIN EXPRESSION; TRANSCRIPTION REGULATION;

EID: 43249124368     PISSN: 00144827     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.yexcr.2008.02.018     Document Type: Article

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