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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
5                                              Diacylglycerol lipase a (DAGLa), a major biosynthetic en
6 sustained rise in intracellular calcium, and diacylglycerol lipase activity.
7                                         sn-1-Diacylglycerol lipase alpha (DAGL-alpha) is the main enz
8 s the role of the main 2-AG producing enzyme diacylglycerol lipase alpha (DAGL-alpha).
9                                         Both diacylglycerol lipase alpha (DAGLalpha) and DAGLbeta can
10 e Sprague-Dawley rats were injected with the diacylglycerol lipase alpha (DAGLalpha) inhibitor LEI-10
11                    The administration of the diacylglycerol lipase alpha (DAGLalpha) inhibitor LEI-10
12                                              Diacylglycerol lipase alpha (DAGLalpha) is responsible f
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
17 rade signal 2-arachidonoylglycerol (2-AG) by diacylglycerol lipase alpha (DGLalpha).
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
22                                Expression of diacylglycerol lipase alpha mRNA, which is not altered i
23 c glutamate receptor 5a (mGluR5a), Homer 2b, diacylglycerol lipase alpha, and CB(1)R.
24 d proteins involved in eCB signaling such as diacylglycerol lipase alpha, N-acyl-phosphatidylethanola
25 d by inhibiting the 2-AG-synthesizing enzyme diacylglycerol lipase alpha.
26 etic deletion or pharmacologic inhibition of diacylglycerol lipase-alpha (DAGL-alpha) impairs hippoca
27                                              Diacylglycerol lipase-alpha (DAGL-alpha), the principal
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
32             Here we show the localization of diacylglycerol lipase-alpha and -beta (DGLalpha/beta), i
33 of 2-AG is calcium-dependent and mediated by diacylglycerol lipase and COX-2.
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
38                                              Diacylglycerol lipase-beta (DAGLbeta) serves as a princi
39 embers of this large enzyme class, including diacylglycerol lipase-beta (DAGLbeta), a principal biosy
40                      Here we identify DAGLB (diacylglycerol lipase-beta), a key enzyme for generation
41 s), type 1 cannabinoid receptors (CB1Rs) and diacylglycerol lipase (DAGL) in the VTA.
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),
44                                              Diacylglycerol lipase (DAGL)-alpha and -beta are enzymes
45 eaving group of triazole urea derivatives as diacylglycerol lipase (DAGL)-alpha inhibitors.
46  to selectively inhibit 2-AG biosynthesis by diacylglycerol lipase (DAGL).
47  the enzyme responsible for 2-AG generation, diacylglycerol lipase (DAGL).
48 ), an inhibitor of the 2-AG synthesis enzyme diacylglycerol lipase (DAGL).
49                                              Diacylglycerol lipases (DAGLalpha and DAGLbeta) convert
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
58 mediated by 2-AG since it was blocked by the diacylglycerol lipase inhibitor DO34.
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
61 lglycerol synthesis that is inhibited by the diacylglycerol lipase inhibitor, DO34.
62 of either the CB1R antagonist, AM251, or the diacylglycerol lipase inhibitor, DO34.
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
65 ction via the phosphatidate phosphohydrolase/diacylglycerol lipase pathway.
66     Our findings suggest Vaha functions as a diacylglycerol lipase physiologically, by being a molecu
67                                Inhibitors of diacylglycerol lipase (RHC 80267), cyclooxygenase (indom
68 phatidate phosphohydrolase (propranolol) and diacylglycerol lipase (RHC-80267), attenuated ET-1-induc
69                              An inhibitor of diacylglycerol lipase, RHC-80267, inhibited AVP-evoked S
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