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