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1 to HCMV infection, identifying IE2 as an IFN-beta antagonist.
2 exposure and were also inhibited by PKCalpha/beta antagonist.
3 with carvedilol and metoprolol, a selective beta-antagonist.
4 tions as an alpha/beta interferon (IFN-alpha/beta) antagonist.
5 could the synergism be blocked by alpha1- or beta-antagonists.
6 nced (P < 0.01) by propranolol (nonselective beta antagonist; -53 +/- 6%), CGP-20,712A (selective bet
7 where classic agonists (catecholamines) and beta-antagonists act, and 2) where CGP 12177 is an agoni
10 nd is also found in neurite plaques, the TGF-beta antagonist and partial agonist activities of Abeta
11 ovide insights into developing effective TGF-beta antagonists and biomarkers for patient selection an
12 ers and Abeta aggregates may function as TGF-beta antagonists and partial agonists, analogous to prev
13 ells, and this activation was prevented by a beta-antagonist and by protein kinase A inhibitors but n
14 adrenergic agents propranolol (non-selective beta-antagonist) and salbutamol (beta(2)-agonist), which
15 t-derived growth factor receptor-beta (PDGFr-beta) antagonist, and the tumor-seeking radiolabeled ant
16 rus-encoded alpha/beta interferon (IFN-alpha/beta) antagonist, appears to be a key regulator of prote
18 virus is an alpha/beta interferon (IFN-alpha/beta) antagonist, both in vitro and in experimental anim
19 tions as an interferon alpha/beta (IFN-alpha/beta) antagonist by preventing the synthesis of IFN duri
20 de evidence that therapeutic dosing of a TGF-beta antagonist can diminish and potentially reverse hep
21 viously shown that high molecular weight TGF-beta antagonists can suppress metastasis without the pre
23 gated whether microiontophoretic ejection of beta antagonists could inhibit thalamocortical activity
24 pothesis that the transforming growth factor-beta antagonist decorin has therapeutic potential for re
26 hat the ability of BF-1 to function as a TGF-beta antagonist does not require its DNA binding activit
27 n, and reperfusion and that the short-acting beta-antagonist esmolol administered at reperfusion woul
28 ividual components of an investigational non-beta-antagonist fixed combination of brinzolamide, 1%, a
29 ify the transforming growth factor beta (TGF-beta) antagonist follistatin (Fst) as a key mediator of
31 Several compounds described previously as beta-antagonists have agonist properties at the beta3-ad
32 that can be mitigated by treatment with TGF-beta antagonists, including angiotensin II-receptor bloc
33 raventricular administration of propranolol (beta antagonist) initiated a significant increase in pro
34 The Dan family of transforming growth factor beta antagonists is a large, evolutionarily conserved fa
37 ed TGF-beta genes Nv-dpp, Nv-BMP5-8, six TGF-beta antagonists (NvChordin, NvNoggin1, NvNoggin2, NvGre
38 e developed transgenic mice expressing a TGF-beta antagonist of the soluble type II TGF-beta receptor
40 ment of rats with TbetaRII/Fc chimera, a TGF-beta antagonist, or U0126, a specific MEK inhibitor, cou
42 , and treatment of stressed animals with the beta-antagonist propranolol reversed the stress-induced
45 emia in P. falciparum cultures in vitro, and beta-antagonists reduced parasitemia of P. berghei infec
47 F-beta signaling and can be prevented by TGF-beta antagonists such as TGF-beta-neutralizing antibody
49 ral, but not unilateral, MS infusions of the beta-antagonist timolol (3.75 microg, 8.7 nmol) decrease
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