Defective GM3 synthesis in Cog2 null mutant CHO cells associates to mislocalization of lactosylceramide sialyltransferase in the golgi complex

Neurochemical Research

Volumn 35, Issue 12, 2010, Pages 2161-2167

  Spessott, Waldo ^a   Uliana, Andrea ^a   MacCioni, Hugo J F ^a  

^a UNIVERSIDAD NACIONAL DE CÓRDOBA   (Argentina)

Author keywords

COG complex; Glycolipids Sialyltransferase; Glycosiltransferases; Golgi

Indexed keywords

CELL PROTEIN; GANGLIOSIDE GM3; GLYCOSYLTRANSFERASE; LACTOSYLCERAMIDE SIALYLTRANSFERASE; PROTEIN COG1; PROTEIN COG2; PROTEIN SIALT1; SIALYLTRANSFERASE; UNCLASSIFIED DRUG;

ANIMAL CELL; ARTICLE; CELL MUTANT; CHO CELL; CONSERVED OLIGOMERIC GOLGI COMPLEX; CONTROLLED STUDY; ENZYME ACTIVITY; ENZYME LOCALIZATION; FEMALE; GOLGI COMPLEX; IMMUNOCYTOCHEMISTRY; IMMUNOPRECIPITATION; LIPID COMPOSITION; LIPOGENESIS; NONHUMAN; NULL CELL; PRIORITY JOURNAL; PROTEIN PROTEIN INTERACTION; PROTEIN TRANSPORT;

ANIMALS; CHO CELLS; CRICETINAE; CRICETULUS; G(M3) GANGLIOSIDE; GOLGI APPARATUS; MICROSCOPY, FLUORESCENCE; MUTATION; PROTEIN BINDING; SIALYLTRANSFERASES;

EID: 78651310761     PISSN: 03643190     EISSN: None     Source Type: Journal    
DOI: 10.1007/s11064-010-0319-8     Document Type: Article

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