The sjögren-larsson syndrome gene encodes a hexadecenal dehydrogenase of the sphingosine 1-phosphate degradation pathway.
Reactive oxygen species facilitate translocation of hormone sensitive lipase to the lipid droplet during lipolysis in human differentiated adipocytes.
Glucose-6-phosphate isomerase deficiency results in mTOR activation, failed translocation of lipin 1a to the nucleus and hypersensitivity to glucose: Implications for the inherited glycolytic disease.
Chlorinated lipid species in activated human neutrophils: lipid metabolites of 2-chlorohexadecanal.
Isolation of novel animal cell lines defective in glycerolipid biosynthesis reveals mutations in glucose-6-phosphate isomerase.
On the importance of plasmalogen status in stimulated arachidonic acid release in the macrophage cell line RAW 264.7.
Synthesis and biological properties of the fluorescent ether lipid precursor 1-O-[9'-(1''-pyrenyl)]nonyl-sn-glycerol.
Role of dihydroxyacetonephosphate acyltransferase in the biosynthesis of plasmalogens and nonether glycerolipids.
Deficiency in ethanolamine plasmalogen leads to altered cholesterol transport.
Increasing plasmalogen levels protects human endothelial cells during hypoxia.
Plasmalogens: biosynthesis and functions.
Incorporation of polyunsaturated fatty acids into CT-26, a transplantable murine colonic adenocarcinoma.
Plasmalogens as endogenous antioxidants: somatic cell mutants reveal the importance of the vinyl ether.
Plasmalogen status influences docosahexaenoic acid levels in a macrophage cell line. Insights using ether lipid-deficient variants.
Isolation of a Chinese hamster fibroblast variant defective in dihydroxyacetonephosphate acyltransferase activity and plasmalogen biosynthesis: use of a novel two-step selection protocol.
Isolation of animal cell mutants defective in long-chain fatty aldehyde dehydrogenase. Sensitivity to fatty aldehydes and Schiff's base modification of phospholipids: implications for Sj-ogren-Larsson syndrome.
An animal cell mutant with a deficiency in acyl/alkyl-dihydroxyacetone-phosphate reductase activity. Effects on the biosynthesis of ether-linked and diacyl glycerolipids.
A fibroblast cell line defective in alkyl-dihydroxyacetone phosphate synthase: a novel defect in plasmalogen biosynthesis.
Animal cell mutants unable to take up biologically active glycerophospholipids.
Fatty acid desaturation in an animal cell mutant defective in plasmanylethanolamine desaturase.
Addition of lipid substituents of mammalian protein glycosylphosphoinositol anchors.
Surface expression of human CD14 in Chinese hamster ovary fibroblasts imparts macrophage-like responsiveness to bacterial endotoxin.
Mutants in a macrophage-like cell line are defective in plasmalogen biosynthesis, but contain functional peroxisomes.
Strategies for isolating somatic cell mutants defective in lipid biosynthesis.
Hydroxyeicosatetraenoic acid oxidation in Chinese hamster ovary cells: a peroxisomal metabolic pathway.
Isolation and characterization of a Chinese hamster ovary cell line deficient in fatty alcohol:NAD+ oxidoreductase activity.
A rapid selection for animal cell mutants with defective peroxisomes.
Chinese hamster ovary cell mutants defective in peroxisome biogenesis. Comparison to Zellweger syndrome.
Disappearance of plasmalogens from membranes of animal cells subjected to photosensitized oxidation.
A possible role for plasmalogens in protecting animal cells against photosensitized killing.
Accumulation of lysophosphatidylinositol in RAW 264.7 macrophage tumor cells stimulated by lipid A precursors.
Isolation of animal cell mutants deficient in plasmalogen biosynthesis and peroxisome assembly.
The importance of the stearoyl-CoA desaturase system in octadecenoate metabolism in the Morris hepatoma 7288C.
Effects of cyclopropene fatty acids on the lipid composition of the Morris hepatoma 7288C.
Analysis of the stearoyl-CoA desaturase system in the Morris hepatoma 7288C and 7288CTC.