Properties of lamin A mutants found in Emery-Dreifuss muscular dystrophy, cardiomyopathy and Dunnigan-type partial lipodystrophy

Journal of Cell Science

Volumn 114, Issue 24, 2001, Pages 4435-4445

  Östlund, Cecilia ^a   Bonne, Giséle ^a   Schwartz, Ketty ^a   Worman, Howard J ^a  

^a New York Presbyterian Columbia University Medical Center   (United States)

Author keywords

Cardiomyopathy; Intermediate filaments; Lamins; Lipodystrophy; Muscular dystrophy; Nuclear envelope

Indexed keywords

COMPLEMENTARY DNA; EMERIN; LAMIN A; LAMIN B; LAMIN C; MUTANT PROTEIN;

ANIMAL CELL; ARTICLE; CELL NUCLEUS; CELL NUCLEUS MEMBRANE; CELL STRAIN; CELLULAR DISTRIBUTION; CONTROLLED STUDY; CYTOPATHOLOGY; DNA TRANSFECTION; EMERY DREIFUSS MUSCULAR DYSTROPHY; GENE LOCATION; GENE MUTATION; GENETIC CODE; HEART DILATATION; IMMUNOFLUORESCENCE MICROSCOPY; LIPODYSTROPHY; MOUSE; MYOBLAST; NONHUMAN; PATHOGENESIS; PRIORITY JOURNAL; PROTEIN EXPRESSION; PROTEIN LOCALIZATION; PROTEIN PROTEIN INTERACTION; PROTEIN STABILITY; TWO HYBRID SYSTEM; WILD TYPE; YEAST;

ANIMALS; CARDIOMYOPATHY, DILATED; CELL NUCLEUS; CELLS, CULTURED; COS CELLS; FLUORESCENT ANTIBODY TECHNIQUE; HUMANS; LAMIN TYPE A; LAMIN TYPE B; LAMINS; LIPODYSTROPHY; MICE; MUSCULAR DYSTROPHY, EMERY-DREIFUSS; MUTAGENESIS, SITE-DIRECTED; MUTATION; NUCLEAR PROTEINS; PROTEIN PRECURSORS; TRANSFECTION; TWO-HYBRID SYSTEM TECHNIQUES;

ANIMALIA;

EID: 0035697055     PISSN: 00219533     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (55)

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