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1 , which is co-localized presynaptically with diacylglycerol lipase.
2 ntial activities of phosphoinositidase C and diacylglycerol lipase.
3 mediated by the enzymes phospholipase C and diacylglycerol lipase.
4 he sequential activities of phospholipase C, diacylglycerol lipase, 5-lipo-oxygenease, and leukotrien
10 e Sprague-Dawley rats were injected with the diacylglycerol lipase alpha (DAGLalpha) inhibitor LEI-10
13 nced expression of a biosynthesizing enzyme (diacylglycerol lipase alpha (DAGLalpha)) of 2-AG in tast
14 e expression of the 2-AG-synthesizing enzyme diacylglycerol lipase alpha (DGLalpha) from ventral tegm
15 t mice in which the 2-AG-synthesizing enzyme diacylglycerol lipase alpha (DGLalpha) was deleted in dM
16 cy by deleting its primary synthetic enzyme, diacylglycerol lipase alpha (DGLalpha), from dopamine D1
18 ybridization, we measured CB1R, GAD(67), and diacylglycerol lipase alpha (the synthesizing enzyme for
19 lethanolamine phospholipase D [NAPE-PLD] and diacylglycerol lipase alpha [DAGLalpha]) in the spinal c
20 pocampal protein concentrations for the sn-1-diacylglycerol lipase alpha and beta isoforms, synthesiz
21 hosphoinositide-specific phospholipase C and diacylglycerol lipase alpha is known, alternative pathwa
24 d proteins involved in eCB signaling such as diacylglycerol lipase alpha, N-acyl-phosphatidylethanola
26 etic deletion or pharmacologic inhibition of diacylglycerol lipase-alpha (DAGL-alpha) impairs hippoca
28 f endocannabinoid (eCB) biosynthetic enzymes diacylglycerol lipase-alpha (DAGLalpha) and -beta (DAGLb
29 1a))-positive GABAergic interneurons express diacylglycerol lipase-alpha (DGL-alpha), a synthesizing
30 nteraction between the 2-AG synthetic enzyme diacylglycerol lipase-alpha (DGLalpha) and calcium/calmo
31 2-arachidonoyl-sn-glycerol-producing enzyme, diacylglycerol lipase-alpha (endocannabinoid signalosome
34 can be inferred in part through measures of diacylglycerol lipase and monoglyceride lipase, which sy
35 ne cells of the pars tuberalis and coexpress diacylglycerol lipase B - an endocannabinoid biosyntheti
36 loss-of-function mutations in 2-AG synthase diacylglycerol lipase beta (DAGLB) to an early onset aut
37 heimer's (Braak stage VI), with ectopic sn-1-diacylglycerol lipase beta expression found in microglia
39 embers of this large enzyme class, including diacylglycerol lipase-beta (DAGLbeta), a principal biosy
42 f inhibitors of the 2-AG-synthesizing enzyme diacylglycerol lipase (DAGL) or the 2-AG-degrading enzym
43 tidylethanolaminephospholipase D (NAPE-PLD), diacylglycerol lipase (DAGL), or phospholipase C (PLC),
50 t as selective and CNS-active inhibitors for diacylglycerol lipases (DAGLs), enzymes responsible for
51 a mechanism dependent upon both postsynaptic diacylglycerol lipase (DGL) activity, which releases 2-A
52 aptic response was blocked by inhibitors for diacylglycerol lipase (DGL), which biosynthesizes 2-AG,
53 cerol, suggesting that SMc01003 also acts as diacylglycerol lipase (DglA) in its native background.
54 ease in 2-LG amounts depended on the PLC and diacylglycerol lipase encoded by norpA and inaE, respect
55 d 2-arachidonylglycerol 1) is synthesized by diacylglycerol lipase in pyramidal neurons; 2) travels r
56 xygenases), LOXs (lipooxygenases), and DGLs (diacylglycerol lipases), indicating the involvement of a
57 ited by antibodies to the FGF receptor and a diacylglycerol lipase inhibitor (RHC80267) that blocks t
59 in iron-overloaded NRVMs was reduced by the diacylglycerol lipase inhibitor RHC80267 but was largely
60 e phospholipase C inhibitor U-73122, and the diacylglycerol lipase inhibitor tetrahydrolipstatin (THL
63 bition of the major 2-AG synthesizing enzyme diacylglycerol lipase or blockade of CB1 receptors aboli
64 main containing 4 protein, cyclooxygenase 2, diacylglycerol lipase paralogs (DAGLalpha, DAGLbeta), fa
66 Our findings suggest Vaha functions as a diacylglycerol lipase physiologically, by being a molecu
68 phatidate phosphohydrolase (propranolol) and diacylglycerol lipase (RHC-80267), attenuated ET-1-induc
70 : cytosolic phospholipase A(2) (cPLA(2)) and diacylglycerol lipase; the former cascade is responsible
71 the postsynaptic membrane-associated lipase, diacylglycerol lipase type-alpha (DGL-alpha), in mGlu re
72 B(1)R (SR141716 and AM251) and inhibition of diacylglycerol lipase using tetrahydrolipstatin also aug
73 concentrations of the 2-AG synthetic enzyme diacylglycerol lipase were not affected by PLX treatment
74 rs, we demonstrated that phospholipase D and diacylglycerol lipase were required for providing AA for