Cohen syndrome-associated protein, COH1, is a novel, giant Golgi matrix protein required for Golgi integrity

Journal of Biological Chemistry

Volumn 286, Issue 43, 2011, Pages 37665-37675

  Seifert, Wenke ^a,b   Kühnisch, Jirko ^b,c   Maritzen, Tanja ^b   Horn, Denise ^b   Haucke, Volker ^b   Hennies, Hans Christian ^a,d  

^a UNIVERSITY OF COLOGNE   (Germany)

^b CHARITÉ UNIVERSITÄTSMEDIZIN BERLIN   (Germany)

^c MAX PLANCK INSTITUTE FOR MOLECULAR GENETICS   (Germany)

^d UNIVERSITY OF COLOGNE   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

CELLULAR DISTRIBUTIONS; ENCODED PROTEINS; GOLGI MEMBRANE; GOLGI ORGANIZATION; MAMMALIAN PROTEINS; MATRIX PROTEINS; SUBCELLULAR LOCALIZATIONS;

AMINO ACIDS; BIOLOGICAL MEMBRANES; CELL CULTURE; DISTRIBUTION FUNCTIONS; GENES; MAMMALS;

PROTEINS;

COHEN SYNDROME ASSOCIATED PROTEIN 1; GOLGI MATRIX PROTEIN; MATRIX PROTEIN; NUCLEAR MATRIX PROTEIN; PROTEIN GM130; UNCLASSIFIED DRUG;

ARTICLE; AUTOSOMAL RECESSIVE DISORDER; CELL FUNCTION; CELLULAR DISTRIBUTION; COH1 GENE; COHEN SYNDROME; CONTROLLED STUDY; DNA FRAGMENTATION; FIBROBLAST; GENE; GENETIC ORGANIZATION; GOLGI COMPLEX; HUMAN; HUMAN CELL; NUCLEOTIDE SEQUENCE; PATHOGENESIS; PRIORITY JOURNAL; PROTEIN DEPLETION; RNA INTERFERENCE; SEQUENCE HOMOLOGY;

DEVELOPMENTAL DISABILITIES; FINGERS; GENE DELETION; GOLGI APPARATUS; HEK293 CELLS; HELA CELLS; HUMANS; INTELLECTUAL DISABILITY; INTRACELLULAR MEMBRANES; MICROCEPHALY; MUSCLE HYPOTONIA; MUTATION; MYOPIA; OBESITY; VESICULAR TRANSPORT PROTEINS;

MAMMALIA;

EID: 80054805821     PISSN: 00219258     EISSN: 1083351X     Source Type: Journal    
DOI: 10.1074/jbc.M111.267971     Document Type: Article

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