Pages that link to "Q74196598"
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The following pages link to Neutral lipid storage disease: a genetic disorder with abnormalities in the regulation of phospholipid metabolism (Q74196598):
Displaying 25 items.
- CGI-58, the causative gene for Chanarin-Dorfman syndrome, mediates acylation of lysophosphatidic acid (Q24310647) (← links)
- Mutations in CGI-58, the gene encoding a new protein of the esterase/lipase/thioesterase subfamily, in Chanarin-Dorfman syndrome (Q24536104) (← links)
- Pathogenesis of permeability barrier abnormalities in the ichthyoses: inherited disorders of lipid metabolism (Q24616344) (← links)
- Lipid droplets at a glance (Q24646389) (← links)
- Comparative gene identification-58 (CGI-58) promotes autophagy as a putative lysophosphatidylglycerol acyltransferase (Q28397954) (← links)
- Triacylglycerol Storage in Lipid Droplets in Procyclic Trypanosoma brucei (Q28542655) (← links)
- CGI-58/ABHD5 is a coenzyme A-dependent lysophosphatidic acid acyltransferase (Q33741180) (← links)
- CGI-58 knockdown in mice causes hepatic steatosis but prevents diet-induced obesity and glucose intolerance (Q34188075) (← links)
- Clinical and genetic characterization of Chanarin-Dorfman syndrome patients: first report of large deletions in the ABHD5 gene. (Q34482020) (← links)
- Lipolysis – A highly regulated multi-enzyme complex mediates the catabolism of cellular fat stores (Q34543395) (← links)
- CGI-58/ABHD5 is phosphorylated on Ser239 by protein kinase A: control of subcellular localization (Q34757325) (← links)
- As the fat flies: The dynamic lipid droplets of Drosophila embryos (Q35893605) (← links)
- Secondary causes of nonalcoholic fatty liver disease (Q35929072) (← links)
- Distinct roles for alpha-beta hydrolase domain 5 (ABHD5/CGI-58) and adipose triglyceride lipase (ATGL/PNPLA2) in lipid metabolism and signaling (Q36382868) (← links)
- Mammalian alpha beta hydrolase domain (ABHD) proteins: Lipid metabolizing enzymes at the interface of cell signaling and energy metabolism (Q36612260) (← links)
- The development of a metabolic disease phenotype in CTP:phosphoethanolamine cytidylyltransferase-deficient mice (Q37377657) (← links)
- PAT proteins, an ancient family of lipid droplet proteins that regulate cellular lipid stores. (Q37435661) (← links)
- Regulation of Hepatic Triacylglycerol Metabolism by CGI-58 Does Not Require ATGL Co-activation (Q37607992) (← links)
- Recent insights into the structure and function of comparative gene identification-58. (Q37865348) (← links)
- Fat in the skin: Triacylglycerol metabolism in keratinocytes and its role in the development of neutral lipid storage disease. (Q37892924) (← links)
- Identification of a novel splicing isoform of murine CGI-58. (Q39827955) (← links)
- CGI-58 is an alpha/beta-hydrolase within lipid transporting lamellar granules of differentiated keratinocytes. (Q42046057) (← links)
- Lipid analysis reveals quiescent and regenerating liver-specific populations of lipid droplets (Q42824343) (← links)
- Alterations of fatty acid metabolism and membrane fluidity in peroxisome-defective mutant ZP102 cells (Q44823090) (← links)
- Neutral Lipid Storage Diseases as Cellular Model to Study Lipid Droplet Function (Q64118342) (← links)