Complementation of the metabolic defect in CTP: Phosphoethanolamine cytidylyltransferase (Pcyt2)-deficient primary hepatocytes

Metabolism: Clinical and Experimental

Volumn 59, Issue 12, 2010, Pages 1691-1700

  Fullerton, Morgan D ^a   Bakovic, Marica ^a  

^a UNIVERSITY OF GUELPH   (Canada)

Author keywords

[No Author keywords available]

Indexed keywords

ACETIC ACID; COMPLEMENTARY DNA; DIACYLGLYCEROL; ETHANOLAMINE; GLYCEROL; MYC PROTEIN; PHOSPHATIDYLETHANOLAMINE; TRIACYLGLYCEROL;

ANIMAL CELL; ARTICLE; CATALYSIS; CTP:PHOSPHOETHANOLAMINE CYTIDYLYLTRANSFERASE GENE; FATTY ACID SYNTHESIS; FATTY LIVER; GENE; GENE EXPRESSION; GENE OVEREXPRESSION; ISOTOPE LABELING; LIPOGENESIS; LIVER CELL; METABOLIC DISORDER; MOUSE; NONHUMAN; PRIORITY JOURNAL; PROTEIN EXPRESSION;

AMINO ACID SEQUENCE; ANIMALS; CELLS, CULTURED; CERCOPITHECUS AETHIOPS; CLONING, MOLECULAR; COS CELLS; DNA, COMPLEMENTARY; GENETIC COMPLEMENTATION TEST; HEPATOCYTES; LIPOGENESIS; MICE; MOLECULAR SEQUENCE DATA; MUTATION; RNA NUCLEOTIDYLTRANSFERASES; TRIGLYCERIDES;

EID: 78549234648     PISSN: 00260495     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.metabol.2010.03.022     Document Type: Article

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