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1 tion of the spread, as did the ATP-activated potassium channel blocker.
2 l fluid containing 4-aminopyridine (4-AP), a potassium channel blocker.
3 could be abolished by barium, a non-specific potassium channel blocker.
4 mol/L) plus glibenclamide (10 micromol/L), a potassium channel blocker.
5 monly used symptomatic treatment option is a potassium channel blocker [3,4-diaminopyridine (3,4-DAP)
6 l of central hyperexcitability that uses the potassium channel blocker 4-aminopyridine (4-AP) to indu
7 ves a 48-hour preconditioning step using the potassium channel blocker 4-aminopyridine (4-AP), at a l
8 affected by spike broadening produced by the potassium channel blocker 4-aminopyridine (4-AP).
9 pioid inhibition was reduced by 65% with the potassium channel blocker 4-aminopyridine (4-AP; 100 mic
10 s of mutant Shaker IR channels and using the potassium channel blocker 4-aminopyridine (4AP).
11 t hippocampal slices by superfusion with the potassium channel blocker 4-aminopyridine in Mg(2+)-free
12                                          The potassium channel blocker 4-aminopyridine reliably induc
13 s and the isolated guinea pig brain with the potassium channel blocker 4-aminopyridine.
14 n mouse thalamocortical slices in vitro, the potassium channel blocker 4-AP and GABAA receptor antago
15  in EPSCs induced by either serotonin or the potassium channel blockers 4-aminopyridine (4-AP) or alp
16 ctural similarity to cone snail and scorpion potassium channel blockers, a mutant molecule, Tk-hefu,
17 WIN 55,212-2 was also investigated using the potassium channel blockers barium and 4-aminopyridine.
18 s virtually eliminated with the nonselective potassium channel blockers barium and cesium.
19 ections to probe interactions of an exemplar potassium channel blocker, barium, with the inward recti
20 ations to IAA-94 and DIDS were unaffected by potassium channel blockers, but were prevented by elevat
21 hich resulted in differential sensitivity to potassium channel blockers (cesium and barium) and sudde
22                   A selective Ca2+-activated potassium channel blocker charybdotoxin (CTX) significan
23 r, SKF525A, but not by the calcium-activated potassium channel blocker, charybdotoxin, indicating a m
24           The prophylactic use of a specific potassium-channel blocker does not reduce mortality, and
25 ed by exposure to four concentrations of the potassium channel blocker dofetilide.
26                             More recently, a potassium channel-blocker for Kv1.3 has been shown to do
27                                 ShK toxin, a potassium channel blocker from the sea anemone Stichodac
28                                          The potassium channel blockers glibenclamide (10 microM), 4-
29 sensitivity to the BK-type calcium-activated potassium channel blocker iberiotoxin.
30 efficacy of adenosine triphosphate-sensitive potassium channel blockers in human septic shock.
31 mall-conductance (SK-type) calcium-activated potassium channel blockers in normally innervated cells
32                We used a recently identified potassium channel blocker, kappa-conotoxin PVIIA, to stu
33          Other studies have suggested that a potassium-channel blocker might reduce this risk with mi
34 lucidates some recent advances in the use of potassium channel-blockers of Kv1.3 and IKCa1 to amelior
35 cium-dependent (KCa) or ATP-sensitive (KATP) potassium channel blockers on pial arteriolar CO2 reacti
36 vide a mechanism for the variable effects of potassium channel blockers on transmitter release magnit
37                                              Potassium channel blockers or high K+ medium, but not Ca
38 sion of cesium acetate (CsAc) and the sodium/potassium channel blocker, QX314, each blocked the effec
39 h this idea, administration of voltage-gated potassium channel blockers restores conduction and resul
40                                              Potassium channel blockers, such as 4-aminopyridine, ind
41 g electrical stimulation and exposure to the potassium channel blocker tetraethyl ammonium chloride (
42  pathway inhibitor PD98059, the nonselective potassium channel blocker tetraethylammonium (TEA), and
43 2 receptor antagonist cimetidine or with the potassium channel blocker tetraethylammonium chloride.
44 c channels are inhibited by the nonselective potassium channel blockers tetraethylammonium and barium
45                          Local delivery of a potassium-channel blocker to the ventromedial hypothalam
46                  By comparing DTX with other potassium channel blockers, we found that the ability to
47  (Na(+))-channel blocker, and d,l-sotalol, a potassium channel blocker, were studied in littermate mi
48 e treat embryonic chick cardiac cells with a potassium channel blocker, which leads to the initiation
49    We investigated whether d-sotalol, a pure potassium-channel blocker with no clinically significant

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