Expression of lamin a mutated in the carboxyl-terminal tail generates an aberrant nuclear phenotype similar to that observed in cells from patients with dunnigan-type partial lipodystrophy and Emery-Dreifuss muscular dystrophy

Experimental Cell Research

Volumn 282, Issue 1, 2003, Pages 14-23

  Favreau, Catherine ^a   Dubosclard, Emmanuelle ^b   Östlund, Cecilia ^c   Vigouroux, Corinne ^b   Capeau, Jacqueline ^b   Wehnert, Manfred ^d   Higuet, Dominique ^a   Worman, Howard J ^c   Courvalin, Jean Claude ^a   Buendia, Brigitte ^a  

^a INSTITUT JACQUES MONOD   (France)

^b INSERM   (France)

^c Columbia University ^*  (United States)

^d UNIVERSITY OF GREIFSWALD   (Germany)

Author keywords

Human diseases; Lamins; Mouse cell lines; Mutations; Nuclear envelope

Indexed keywords

EMERIN; LAMIN A;

ANIMAL CELL; ARTICLE; CARBOXY TERMINAL SEQUENCE; CELL ASSAY; CELL LINE; CELL NUCLEUS MEMBRANE; CHROMATIN; CONTROLLED STUDY; CORRELATION ANALYSIS; EMERY DREIFUSS MUSCULAR DYSTROPHY; FIBROBLAST; GENETIC TRANSFECTION; HUMAN; HUMAN CELL; LIPODYSTROPHY; MOUSE; MUTATION; MYOBLAST; NONHUMAN; PHENOTYPE; PRIORITY JOURNAL; PROADIPOCYTE; PROTEIN CONTENT; PROTEIN EXPRESSION;

EID: 0037225049     PISSN: 00144827     EISSN: None     Source Type: Journal    
DOI: 10.1006/excr.2002.5669     Document Type: Article

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