An acid amidase hydrolyzing anandamide as an endogenous ligand for cannabinoid receptors.
about
N-acyl-dopamines: novel synthetic CB(1) cannabinoid-receptor ligands and inhibitors of anandamide inactivation with cannabimimetic activity in vitro and in vivoSupersensitivity to anandamide and enhanced endogenous cannabinoid signaling in mice lacking fatty acid amide hydrolasePalmitoylethanolamide inhibits the expression of fatty acid amide hydrolase and enhances the anti-proliferative effect of anandamide in human breast cancer cellsInhibitory effect of palmitoylethanolamide on gastrointestinal motility in miceEffects of pH on the inhibition of fatty acid amidohydrolase by ibuprofenEndogenous molecules stimulating N-acylethanolamine-hydrolyzing acid amidase (NAAA).Metabolism of endocannabinoids and related N-acylethanolamines: canonical and alternative pathways.Functional disassociation of the central and peripheral fatty acid amide signaling systems.Evidence for bidirectional endocannabinoid transport across cell membranesMicroglia produce and hydrolyze palmitoylethanolamide.Proteomics of the lysosome.PUFA-derived endocannabinoids: an overview.Macrophage-derived lipid agonists of PPAR-α as intrinsic controllers of inflammation.Interactions between the endocannabinoid and nicotinic cholinergic systems: preclinical evidence and therapeutic perspectives.Expression and secretion of N-acylethanolamine-hydrolysing acid amidase in human prostate cancer cells.N-cyclohexanecarbonylpentadecylamine: a selective inhibitor of the acid amidase hydrolysing N-acylethanolamines, as a tool to distinguish acid amidase from fatty acid amide hydrolase.Human mast cells take up and hydrolyze anandamide under the control of 5-lipoxygenase and do not express cannabinoid receptors.Mammalian cells stably overexpressing N-acylphosphatidylethanolamine-hydrolysing phospholipase D exhibit significantly decreased levels of N-acylphosphatidylethanolamines.Differences in the pharmacological properties of rat and chicken brain fatty acid amidohydrolase.The cellular uptake of anandamide is coupled to its breakdown by fatty-acid amide hydrolase.
P2860
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P2860
An acid amidase hydrolyzing anandamide as an endogenous ligand for cannabinoid receptors.
description
1999 nî lūn-bûn
@nan
1999年の論文
@ja
1999年論文
@yue
1999年論文
@zh-hant
1999年論文
@zh-hk
1999年論文
@zh-mo
1999年論文
@zh-tw
1999年论文
@wuu
1999年论文
@zh
1999年论文
@zh-cn
name
An acid amidase hydrolyzing anandamide as an endogenous ligand for cannabinoid receptors.
@en
type
label
An acid amidase hydrolyzing anandamide as an endogenous ligand for cannabinoid receptors.
@en
prefLabel
An acid amidase hydrolyzing anandamide as an endogenous ligand for cannabinoid receptors.
@en
P2093
P2860
P921
P1433
P1476
An acid amidase hydrolyzing anandamide as an endogenous ligand for cannabinoid receptors.
@en
P2093
P2860
P304
P356
10.1016/S0014-5793(99)00820-0
P407
P577
1999-07-01T00:00:00Z