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1 te, we measured [Mg(2+)](i) using mag-indo-1 microfluorometry.
2 ame time period with the use of quantitative microfluorometry.
3 ould not be detected in the chamber by using microfluorometry.
4 ation and HCO3 (-)transport were assessed by microfluorometry.
5   [Ca2+]i transients were characterized with microfluorometry.
6 chemically and by patch clamp recordings and microfluorometry.
7 ls (OECs) was performed using Indo-1 calcium microfluorometry.
8 diabetic fatty rat islets by digital imaging microfluorometry.
9                                 Using indo-1 microfluorometry and a specific inhibitor of the mitocho
10 ellular free Ca2+ (measured by use of fura-2 microfluorometry and Ca(2+)-dependent 42K+ efflux) in sm
11 ells were compared using simultaneous indo-1 microfluorometry and constant potential amperometry.
12 rgy transfer (RET) imaging, quantitative RET microfluorometry, and single-cell imaging spectrophotome
13 novial fluid was isolated and quantitated by microfluorometry, and the oligonucleosomal fraction was
14 d trigeminal ganglion cultures using calcium microfluorometry, and we assessed the sensitivity to cap
15 xperiments, membrane potential measurements, microfluorometry, contractility measurements, and in viv
16 minal Cl- concentration was also measured by microfluorometry following microinjection of the dextran
17     We further showed, using a dual emission microfluorometry in a calcium-free medium, that the 17be
18                          Using dual emission microfluorometry in a calcium-free medium, the 17beta-es
19  Na+ concentration ([Na+]i) were measured by microfluorometry in duct cells loaded with either the pH
20                           Using quantitative microfluorometry, neutrophil-mediated extracellular puls
21 ane Cl(-)/HCO(3)(-) exchange was measured by microfluorometry of intracellular pH in intact villous e
22 ography and intracellular TPT levels by flow microfluorometry revealed that CI1033 increased the stea
23                                              Microfluorometry showed that the HAT-7 cells were polari
24 further showed with the use of dual emission microfluorometry that 17beta-estradiol-stimulated releas
25 in an in vitro slice preparation with Ca(2+) microfluorometry to detect single inspiratory neuron som
26                      We have used multicolor microfluorometry to enumerate DC1 and DC2 in the periphe
27 ue was used in combination with Indo-1-based microfluorometry to record Ca2+ current and [Ca2+]i simu
28 rements were used in combination with fura-2 microfluorometry under whole-cell patch clamp recording
29                                     Confocal microfluorometry was used to study the effects of tetrac
30         In separate experiments using fura-2 microfluorometry, we measured depolarization-induced (80

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