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1 for moxonidine versus -13.5+/-1.9 mm Hg for guanabenz).
2 e also excited by norepinephrine (50 ng) and guanabenz (10 microg) but not by clonidine (3 microg) or
4 gically Active Compounds and discovered that Guanabenz acetate (Wytensin), an FDA-approved drug forme
5 , experimental autoimmune encephalomyelitis, guanabenz alleviates clinical symptoms, which correlates
8 in vivo, we have investigated the effects of guanabenz and N(G)-nitro-L-arginine in HEK 293 cells sta
9 have used two mechanism-based inactivators, guanabenz and NG-amino-L-arginine, to alter the heme/sub
10 The [(o-chlorobenzylidene)amino]guanidines (Guanabenz and Sephin1) have been proposed to exert prote
11 ee specific compounds, namely valproic acid, guanabenz, and a specific Caspase12 inhibitor, achieved
12 the alpha2-adrenoceptor (alpha2-AR) agonist guanabenz, but not by the Ih-imidazoline receptor agonis
14 ver pure alpha(2)-adrenergic agonists (i.e., guanabenz) due to its lowered incidence of sedative side
16 stress response using the FDA-approved drug guanabenz increases oligodendrocyte survival in culture
17 ompared to saline-injected controls; whereas guanabenz induced only dose-responsive sedative-like beh
18 complex and constitutive protein synthesis, guanabenz prolonged eIF2alpha phosphorylation in human s
19 by inhibition of Gadd34-PP1 phosphatase with guanabenz protects oligodendrocytes and partially rescue
21 er signaling cascade, it was possible to use guanabenz to dose-dependently control expression of GLP-
23 AR involvement, the sedative-like effects of guanabenz were completely blocked by pretreatment with t
24 he clinically licensed antihypertensive drug guanabenz (Wytensin) activates a synthetic signal cascad
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