The R482Q lamin A/C mutation that causes lipodystrophy does not prevent nuclear targeting of lamin A in adipocytes or its interaction with emerin

European Journal of Human Genetics

Volumn 9, Issue 3, 2001, Pages 204-208

  Holt, Ian ^a   Clements, Lisa ^a   Manilal, Sushila ^a   Brown, Susan C ^b   Morris, Glenn E ^a  

^a GLYNDWR UNIVERSITY   (United Kingdom)

^b HAMMERSMITH HOSPITAL   (United Kingdom)

Author keywords

BIAcore; Dilated cardiomyopathy; Emery Dreifuss muscular dystrophy; In vitro mutagenesis; Myoblast; Nuclear lamina

Indexed keywords

EMERIN; LAMIN A; LAMIN C; MEMBRANE PROTEIN;

ADIPOCYTE; ANIMAL CELL; ARTICLE; BIOSENSOR; CELL CULTURE; CELL DIFFERENTIATION; CELL NUCLEUS; CELL STRAIN COS1; CONTROLLED STUDY; FAMILIAL DISEASE; GENE FUNCTION; GENE LOSS; GENE MUTATION; GENE TARGETING; GENETIC TRANSFECTION; HUMAN; HUMAN CELL; IN VITRO STUDY; LIPODYSTROPHY; MOUSE; MUSCLE CELL; MUTAGENESIS; NONHUMAN; PRIORITY JOURNAL; PROTEIN PROTEIN INTERACTION; SKELETAL MUSCLE;

ADIPOCYTES; ANIMALS; BASE SEQUENCE; CARDIOMYOPATHY, DILATED; CELL NUCLEUS; COS CELLS; DNA PRIMERS; LAMIN TYPE A; LAMINS; LIPODYSTROPHY; MEMBRANE PROTEINS; MUSCULAR DYSTROPHIES; MUTATION; NUCLEAR PROTEINS; THYMOPOIETINS;

ANIMALIA;

EID: 0035084090     PISSN: 10184813     EISSN: None     Source Type: Journal    
DOI: 10.1038/sj.ejhg.5200609     Document Type: Article

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