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1 zymes, endothelial nitric oxide synthase and prostacyclin synthase.
2 uced insulin-resistant mice--inactivation of prostacyclin synthase and eNOS was prevented by inhibiti
4 d ELPCs (expressing cyclooxygenase isoform 1-prostacyclin synthase and nuRFP) were tested in rats wit
5 y, we observed that COX-2 deletion decreased prostacyclin synthase and production and peroxisome prol
6 ric oxide synthase-3) nitric oxide synthase, prostacyclin synthase, and constitutive cyclooxygenase (
8 NA and protein levels of cPLA(2), COX-2, and prostacyclin synthase, as well as the promoter and enzym
11 tacyclin) by lung-specific overexpression of prostacyclin synthase decreases lung tumor incidence and
12 HIF-responsive genes (VEGF-A, PPARgamma, and prostacyclin synthase) due to an insufficient increase i
14 ressing a human cyclooxygenase isoform 1 and prostacyclin synthase fusion protein that produces prost
16 ypothesized that pulmonary overexpression of prostacyclin synthase may prevent the development of mur
17 addition of AICAR reduced both O(2).(-) and prostacyclin synthase nitration caused by high glucose,
19 P-2 expression and reduced both O(2).(-) and prostacyclin synthase nitration in diabetic wild-type mi
20 CP-2 significantly ablated both O(2).(-) and prostacyclin synthase nitration triggered by high glucos
22 Transgenic FVB/N mice with lung-specific prostacyclin synthase overexpression were exposed to mai
23 Transgenic mice with selective pulmonary prostacyclin synthase overexpression were exposed to two
25 nes (angiotensin-converting enzyme [ACE] and prostacyclin synthase [PGI2S]) were measured in samples
26 ived from adenoviral cyclo-oxygenase (COX)-1/prostacyclin synthase (PGIS) (Adv-COPI) gene transfer in
28 s to determine whether tyrosine nitration of prostacyclin synthase (PGIS) contributes to retinal cell
34 sis via tyrosine nitration and inhibition of prostacyclin synthase (PGIS), an enzyme with antithrombo
36 ransfected with the cyclooxygenase isoform 1-prostacyclin synthase plasmid and labeled with lentiviru
39 g prostacyclin analogs, we hypothesized that prostacyclin synthase promoter sequence variants associa
42 in reaction approaches were used to genotype prostacyclin synthase promoter variants in more than 300
44 iscovered a significant bias for more active prostacyclin synthase promoter variants in unaffected ca
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