Neutral lipid storage disease: A genetic disorder with abnormalities in the regulation of phospholipid metabolism

Journal of Lipid Research

Volumn 39, Issue 1, 1998, Pages 31-43

  Igal, R Ariel ^a   Coleman, Rosalind A ^a  

^a UNIVERSITY OF NORTH CAROLINA SCHOOL OF MEDICINE   (United States)

Author keywords

Glycerolipids; Lipid droplets; Neutral lipid storage disease; Phospholipid synthesis; Triacsin C

Indexed keywords

PHOSPHATIDYLCHOLINE; PHOSPHATIDYLETHANOLAMINE; PHOSPHATIDYLSERINE; SPHINGOMYELIN; TRIACYLGLYCEROL;

ARTICLE; CELL COMPOSITION; CELL LEVEL; FIBROBLAST; GENETIC LINKAGE; HUMAN; HUMAN CELL; LIPID COMPOSITION; LIPID STORAGE; LIPIDOSIS; PATHOGENESIS; PHOSPHOLIPID SYNTHESIS; PRIORITY JOURNAL;

CELLS, CULTURED; CHOLINE; CYTIDINE DIPHOSPHATE; CYTIDINE DIPHOSPHATE CHOLINE; DIGLYCERIDES; ETHANOLAMINE; ETHANOLAMINES; FIBROBLASTS; GLYCEROL; HOMEOSTASIS; HUMANS; LIPID METABOLISM, INBORN ERRORS; OLEIC ACID; PHOSPHATIDYLCHOLINES; PHOSPHATIDYLINOSITOLS; PHOSPHATIDYLSERINES; PHOSPHOLIPIDS; SPHINGOMYELINS; TRIGLYCERIDES;

EID: 0031883290     PISSN: 00222275     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

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