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1 no effect on the expression of the cytosolic PGE synthase.
2 etermined using mice deficient in microsomal PGE synthase 1 (mPGES-1) and in the receptors for PGI2.
3 ination a mouse line deficient in microsomal PGE synthase 1 (mPGES1) on the inbred DBA/1lacJ backgrou
4 onses, we infected macrophages from membrane PGE synthase 1 knockout mice (mPGES1(-/-)) that cannot p
5 natants from F. tularensis-infected membrane PGE synthase 1(-/-) macrophages did not inhibit T cell p
6 ghts the role of cyclooxygenase-2/microsomal PGE synthase 1/PGE2 signaling in hypertension and diabet
9 cence, we detected both COX-2 and microsomal PGE synthase-1 (mPGES-1) but not COX-1 in the Golgi appa
12 PS exposure induced expression of microsomal PGE synthase-1 (mPGES-1), a key enzyme in PGE2 biosynthe
20 -HSL induction of Cox-2, membrane-associated PGE synthase, and PGE(2) likely contributes to the infla
22 wly discovered inducible membrane-associated PGE synthase but had no effect on the expression of the
23 tation sites where Ptgs2 and microsomal type PGE synthases but not PGI synthases are co-expressed.
26 2) synthesis in inflammation suggests that a PGE synthase may be linked to an inducible pathway for P
27 of the recently cloned inducible microsomal PGE synthase (mPGES) in synoviocytes from patients with
30 re synthesized by the prostanoid isomerases, PGE synthases (PGES) and PGD synthases (PGDS), respectiv
35 udy the physiological role of the individual PGE synthases, we have generated by targeted homologous
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