コーパス検索結果 (１語後でソート)
通し番号をクリックするとPubMedの該当ページを表示します
1 ucible nitric oxide synthase), production of prostaglandin H(2) (i.e., cyclooxygenase 2), and regulat
2 a good electrochemical sensing platform for prostaglandin H(2) (PGH(2)) as the basis for quantitatio
5 oxygenases, convert arachidonic acid (AA) to prostaglandin H(2) (PGH(2)) in the committed step of pro
7 (PGHS-1 and -2) convert arachidonic acid to prostaglandin H(2) (PGH(2)), the committed step in prost
8 oxygenate arachidonic acid (AA) to generate Prostaglandin H(2) (PGH(2)), the precursor to prostaglan
9 ), respectively, convert the same substrate, prostaglandin H(2) (PGH(2)), to thromboxane A(2) and pro
10 cid by the prostaglandin H synthases (PGHS), prostaglandin H(2) (PGH(2)), undergoes rearrangement to
17 d 2-AG oxygenation provides the novel lipid, prostaglandin H(2) glycerol ester (PGH(2)-G), in vitro a
18 the ability of COX-2 to efficiently generate prostaglandin H(2) glycerol ester, explaining, in part,
19 n the presence of U46619, a stable analog of prostaglandin H(2) Half-maximal effective potential (V(0
22 ly, as the conversion of arachidonic acid to prostaglandin H(2) requires two oxygenation and two cycl
29 rome P450 that catalyzes an isomerization of prostaglandin H(2), an endoperoxide, to prostacyclin.
30 talyze the conversion of arachidonic acid to prostaglandin H(2), the committed step in prostanoid syn
31 Cox-1) and Cox-2 convert arachidonic acid to prostaglandin H(2), the precursor of other prostaglandin
32 sozymes produce the same precursor compound, prostaglandin H(2), they have distinct functions based o
33 can also activate cyclooxygenases to produce prostaglandin H(2), which can form two specific isomers
34 genase-2 (COX-2) convert arachidonic acid to prostaglandin H(2), which has proinflammatory effects.
35 In addition, synthetic levuglandin E(2) and prostaglandin H(2)-derived levuglandins produced pyrrole
36 cts formed by synthetic levuglandin E(2) and prostaglandin H(2)-derived levuglandins with lysine.
38 sing specific antibodies for human 15-Lox-1, prostaglandin H synthase (also called cyclooxygenase, Co
42 mmalian tissues is regulated at the level of prostaglandin H synthase (PGHS) cyclooxygenase catalysis
43 nt techniques to examine the distribution of prostaglandin H synthase (PGHS) in ovine astrocyte-enric
48 Peroxide-generated tyrosyl radicals in both prostaglandin H synthase (PGHS) isozymes have been demon
49 in hours after infection, and is mediated by prostaglandin H synthase (PGHS) products in animal model
54 dal antiinflammatory drugs and inhibitors of prostaglandin H synthase (PGHS)-2 by exhibiting little e
60 with both native and indomethacin-pretreated prostaglandin H synthase 1 (PGHS-1) were examined by low
61 e monotopic lumenal enzyme cyclooxygenase 1 (prostaglandin H synthase 1) that share this mechanism of
62 ucible cyclooxygenase (Cox-2), also known as prostaglandin H synthase 2 (PGH-2) is a key enzyme in th
63 d the hypothesis that abnormal expression of prostaglandin H synthase 2 (PHS-2), which can be induced
64 that C. parvum infection directly activates prostaglandin H synthase 2 expression and prostaglandin
73 nce electron reactions in enzymes, including prostaglandin H synthase, galactose oxidase, ribonucleot
74 ooxygenase (COX)-2, the inducible isoform of prostaglandin H synthase, has been implicated in the gro
75 -oxygenase 2 (COX2), an inducible isoform of prostaglandin H synthase, which mediates prostaglandin s
76 peroxidase and cyclooxygenase activities of prostaglandin H synthase-1 (PGHS-1) both become irrevers
77 radical generated in the peroxidase cycle of prostaglandin H synthase-1 (PGHS-1) can serve as the ini
78 cosubstrates for the peroxidase activity of prostaglandin H synthase-1 (PGHS-1) have been reported t
81 l middle dot)NO is catalytically consumed by prostaglandin H synthase-1 (PGHS-1) through acting as a
83 The method was successfully used to detect prostaglandin H synthase-1 and -2 (PGHS-1 and -2) in nor
86 Peroxides also induce radical formation in prostaglandin H synthase-2 (PGHS-2) and in PGHS-1 recons
87 t redox characteristics on the modulation of prostaglandin H synthase-2 (PGHS-2) in primary mouse cor
89 lted in a significant inhibition of monocyte prostaglandin H synthase-2 (PGHS-2), a pivotal enzyme in
91 e drugs block the cyclooxygenase activity of prostaglandin H synthase-2 (PGHS2), but do not affect th
93 gonucleotide or when the early response gene prostaglandin H synthase-2 mRNA was measured over the ti
94 radicals detected in the photosystem II and prostaglandin H synthase-2 systems strongly suggest a me
99 ct of oxygenation of arachidonic acid by the prostaglandin H synthases (PGHS), prostaglandin H(2) (PG
101 prostanoids is regulated by cyclooxygenases (prostaglandin H synthases), which catalyze the conversio
102 the covalent binding of reactive products of prostaglandin H-synthases (PGHSs) to the enzyme and to o