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1 ulators of RNA splicing, such as digoxin and digitoxin.
2 he direct synthesis of digitoxin and C1'-epi-digitoxin.
3 - and disaccharide analogues of digoxose and digitoxin.
8 n-approved, small-molecule compounds such as digitoxin and digoxin have been in clinical usage for co
9 that multiple cardiac glycosides, including digitoxin and digoxin, are significantly more toxic to h
10 an assay was developed for quantification of digitoxin and its metabolites from human serum samples a
11 ative analysis of the cardiac glycoside drug digitoxin and its three main metabolites digitoxigenin-b
12 annels may be part of the mechanism by which digitoxin and other active cardiac glycosides, such as d
18 eroids already in use in humans, digoxin and digitoxin, are potent inhibitors of multiple adenovirus
19 These agents included acetyldigitoxin and digitoxin as probes for the digitoxin site, phenol red a
24 We interpret this result to suggest that digitoxin can also partially mimic the genomic consequen
25 try of the lipid affects the kinetics of the digitoxin channel activity, but not the cation selectivi
29 In isolated rat ventricular myocytes, the CG digitoxin (DGT) increased the incidence of arrhythmogeni
30 utants were analyzed for binding to digoxin, digitoxin, digoxigenin, and ouabain resulting in the gen
31 inhibitor reduces ERK phosphorylation, while digitoxin disrupts ion gradients, altering plasma membra
37 anding the mechanism(s) by which digoxin and digitoxin inhibit adenovirus replication will guide the
38 occurring class of cardiac glycosides (CG); digitoxin is clinically approved for heart failure and k
39 ctivation is used, the glycorandomization of digitoxin leads to analogs that display significantly en
46 and prior to genome replication, digoxin and digitoxin show potential as antiviral agents for treatme
47 tyldigitoxin and digitoxin as probes for the digitoxin site, phenol red as a probe for the bilirubin
48 ction combinatorial relations we showed that digitoxin targets cancer cells in a time and dose-depend
50 glycoside family, ouabain, gitoxigenin, and digitoxin, that inhibit placental sFlt1 production at na
51 additively or synergistically combined with digitoxin to induce cell death, inhibiting growth of pat
53 een successfully applied to the synthesis of digitoxin trisaccharide glycal for the direct synthesis
54 19 total steps from achiral 2-acylfuran, and digitoxin was fashioned in 15 steps starting from digito
56 ac glycosides, such as ouabain, digoxin, and digitoxin, which is highly conserved among species rangi
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