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1 he rate of conversion of arachidonic acid to prostaglandin H2.
2  catalyze formation of an identical product, prostaglandin H2.
3 oxidase reaction reduces prostaglandin G2 to prostaglandin H2.
4 rostaglandin biosynthesis, the generation of prostaglandin H(2).
5 rome P450 that catalyzes an isomerization of prostaglandin H(2), an endoperoxide, to prostacyclin.
6 shifts the dose response curve for U46619, a prostaglandin H2 analogue, to the right.
7 9) inhibited platelet aggregation induced by prostaglandin H2 and the conversion of prostaglandin H2
8 ne synthase using the cyclooxygenase product prostaglandin H(2) as the substrate.
9  of the cyclooxygenase-derived endoperoxide, prostaglandin H2, avidly binds to proteins.
10 nd platelet aggregation, is synthesized from prostaglandin H(2) by thromboxane synthase (TXAS).
11                                 Synthesis of prostaglandin H2 by prostaglandin H synthase (PHS) resul
12     The cyclooxygenase-derived endoperoxide, prostaglandin H2, can undergo rearrangement to highly re
13  In addition, synthetic levuglandin E(2) and prostaglandin H(2)-derived levuglandins produced pyrrole
14 cts formed by synthetic levuglandin E(2) and prostaglandin H(2)-derived levuglandins with lysine.
15 the ability of COX-2 to efficiently generate prostaglandin H(2) ethanolamide.
16 e (AEA) and 2-arachidonylglycerol (2-AG), to prostaglandin-H2-ethanolamide (PGH2-EA) and -glycerol es
17 e cyclooxygenases (COX-1 and COX-2) generate prostaglandin H(2) from arachidonic acid (AA).
18 ted heme-containing homodimers that generate prostaglandin H(2) from arachidonic acid (AA).
19 d 2-AG oxygenation provides the novel lipid, prostaglandin H(2) glycerol ester (PGH(2)-G), in vitro a
20 the ability of COX-2 to efficiently generate prostaglandin H(2) glycerol ester, explaining, in part,
21 n the presence of U46619, a stable analog of prostaglandin H(2) Half-maximal effective potential (V(0
22                                              Prostaglandin H(2) has been demonstrated to rearrange to
23 ucible nitric oxide synthase), production of prostaglandin H(2) (i.e., cyclooxygenase 2), and regulat
24 ermal sheets identified diminished levels of prostaglandin H2 in Tgfa(-/-) mice.
25  (PGHSs) 1 and 2 convert arachidonic acid to prostaglandin H2 in the committed step of prostanoid bio
26  rate of conversion from arachidonic acid to prostaglandin H2 in the PR pathway.
27 her enhancing or suppressing the activity of prostaglandin H(2) isoforms (PGHS-1 and PGHS-2).
28 sed to determine the docking of a substrate (prostaglandin H2) mimic (U46619) to the engineered prost
29  a good electrochemical sensing platform for prostaglandin H(2) (PGH(2)) as the basis for quantitatio
30                                              Prostaglandin H(2) (PGH(2)) formed from arachidonic acid
31                                              Prostaglandin H(2) (PGH(2)) formed from arachidonic acid
32 oxygenases, convert arachidonic acid (AA) to prostaglandin H(2) (PGH(2)) in the committed step of pro
33                        The product of COX-2, prostaglandin H(2) (PGH(2)), can undergo spontaneous rea
34  (PGHS-1 and -2) convert arachidonic acid to prostaglandin H(2) (PGH(2)), the committed step in prost
35  oxygenate arachidonic acid (AA) to generate Prostaglandin H(2) (PGH(2)), the precursor to prostaglan
36 ), respectively, convert the same substrate, prostaglandin H(2) (PGH(2)), to thromboxane A(2) and pro
37 cid by the prostaglandin H synthases (PGHS), prostaglandin H(2) (PGH(2)), undergoes rearrangement to
38 the conversion of arachidonic acid (AA) into prostaglandin H(2) (PGH(2)).
39                       The first COX product, prostaglandin H2 (PGH2) is also a command substrate for
40 everal prostaglandin E synthases involved in prostaglandin H2 (PGH2) metabolism.
41 the dioxygenase and peroxidase activities of prostaglandin H2 (PGH2) synthase I and II were monitored
42 for a reductase or molecular oxygen, it uses prostaglandin H2 (PGH2) to catalyze either an isomerizat
43                           TBXAS1 metabolizes prostaglandin H2 (PGH2), a cyclooxygenase (COX) product
44 he formation of prostaglandin E2 (PGE2) from prostaglandin H2 (PGH2).
45 the conversion of arachidonic acid (AA) into prostaglandin H2 (PGH2).
46            However, neither a thromboxane A2/prostaglandin H2 receptor antagonist SQ29548 and a throm
47       Furthermore, SQ29548, a thromboxane A2/prostaglandin H2 receptor antagonist, significantly redu
48 -dependent PGIS nitration and thromboxane A2/prostaglandin H2 receptor stimulation.
49 OX-2) (indomethacin or celecoxib) or of TXA2/prostaglandin H2 receptors (SQ-29548).
50 ly, as the conversion of arachidonic acid to prostaglandin H(2) requires two oxygenation and two cycl
51 y prostaglandin synthases of the accumulated prostaglandin H(2) substrate.
52                  It has been shown to target prostaglandin H(2) synthase (COX)-1 and COX-2, which cat
53  block prostanoid biosynthesis by inhibiting prostaglandin H(2) synthase (EC 1.14.99.1).
54 have been shown to both activate and inhibit prostaglandin H(2) synthase 1 (PGHS-1).
55        We present here crystal structures of prostaglandin H(2) synthase-1 in complex with the inhibi
56 The response of the inducible isoform of the prostaglandin H2 synthase (COX-2) and the c-Jun N-termin
57                                              Prostaglandin H2 synthase (EC 1.14.99.1) is an integral
58 looxygenase activity of the membrane protein prostaglandin H2 synthase isoform 1 (PGHS-1) is the targ
59  resolution X-ray crystal structure of ovine prostaglandin H2 synthase-1 in complex with alpha-methyl
60                                              Prostaglandin H(2) synthesis by prostaglandin endoperoxi
61 talyze the conversion of arachidonic acid to prostaglandin H(2), the committed step in prostanoid syn
62 Cox-1) and Cox-2 convert arachidonic acid to prostaglandin H(2), the precursor of other prostaglandin
63            Free arachidonate is converted to prostaglandin H2, the common precursor to all prostanoid
64 sozymes produce the same precursor compound, prostaglandin H(2), they have distinct functions based o
65                  The conversion of exogenous prostaglandin H2 to prostaglandin E2 was only modestly i
66  these cells efficiently converted exogenous prostaglandin H2 to prostaglandin E2.
67 ed by prostaglandin H2 and the conversion of prostaglandin H2 to thromboxane A2 in intact platelets.
68 e enzyme that catalyzes the isomerization of prostaglandin H2 to thromboxane A2.
69 ificantly alter beta 2-AR and thromboxane A2/prostaglandin H2 (TP) receptor affinity.
70 c (S > > R) and antagonism at thromboxane A2/prostaglandin H2 (TP; R > > S) receptors.
71 can also activate cyclooxygenases to produce prostaglandin H(2), which can form two specific isomers
72 genase-2 (COX-2) convert arachidonic acid to prostaglandin H(2), which has proinflammatory effects.
73 enase-2, both metabolize arachidonic acid to prostaglandin H2, which is subsequently processed by dow