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1 ss the GPM as gases and change the pH of the internal solution.
2 t inside-out patches at various pH levels of internal solutions.
3             Application of 20 mM EGTA to the internal solution abolished the slow inward OFF current,
4 as enhanced by inclusion of GTPgammaS in the internal solution and blocked by inclusion of GDPbetaS.
5  peak Na+ current was similar with Ca2+-free internal solution and in 92 nm internal Ca2+, suggesting
6  excised in inside-out mode into a Ca2+-free internal solution and were strongly inhibited by applica
7 ocker dissociation occurs exclusively to the internal solution, and the blocker does not itself enter
8 ients (log KNO,j) for sensors assembled with internal solutions at various pH values range from -0.08
9  that contains a pH electrode immersed in an internal solution behind the GPM.
10 n, however, were prevented by excess PIP2 in internal solutions but not by internal Ca(2+) buffering
11 ngs with 20 mm BAPTA containing postsynaptic internal solution, but a delayed-onset decrease was obse
12              Reduction of the [Cl(-)] in the internal solution caused inwardly directed, but not outw
13                Reduction of the [Cl-] in the internal solution caused inwardly directed, but not outw
14 is was followed by endocytosis only when the internal solution contained a hydrolyzable analog of ATP
15 Vaseline-gap voltage clamp chamber, with the internal solution containing 20 mM EGTA plus 0.4 or 1.8
16  twitch fibers under voltage clamp, with the internal solution containing 20 mM EGTA plus added calci
17 Vaseline-gap voltage-clamp chamber, with the internal solution containing either 0.1 mM EGTA or 20 mM
18      Isolated nuclei were superfused with an internal solution containing the Ca(2+) indicator fluo-4
19 e conventional whole-cell configuration with internal solutions containing 10 mM EGTA to rule out any
20 oduced into the SR by exposing the cells to "internal" solutions containing the buffers.
21 g in myocytes permeabilized with saponin in 'internal' solutions containing: MgATP, EGTA and fluo-3 p
22 mately 2 mM) or spermine (100 microM) in the internal solution counteracted the change in rectificati
23         Calmodulin (0.05-5.0 micro M) in the internal solution (free [Ca(2+)](i) approximately 50-100
24 nase C inhibitor PKC19-36 (20 microM) in the internal solution had little effect on whole-cell curren
25  majority of cells tested with Mg-ATP in the internal solution, IGly induced by 3-10 microM glycine i
26 the protein that bring the extracellular and internal solutions into proximity across a short barrier
27                       The composition of the internal solution is a critical variable when determinin
28 erefore, consideration of the composition of internal solutions is warranted when studying channel ph
29 Inclusion of GTP-gamma-S (500 microM) in the internal solution led to an increase in maximal current
30 cently labeled recombinant calmodulin in the internal solution localized at the Z-line/triad region.
31                        With a chloride-based internal solution, mGluR agonists did not activate inter
32 otoxin, a GABAA blocker, was included in the internal solution of the recording pipette to reduce pos
33                        Suramin, added to the internal solution of voltage-clamped skeletal myotubes,
34 e-cell recording (GDP-beta-S included in the internal solution) on lamina II neurons in rat spinal co
35                        Addition of KF to the internal solution produced a hyperpolarizing shift in th
36  are sensitive to the redox potential of the internal solution, providing evidence for their physical
37 ines by washout or by omitting them from the internal solution results in a loss of the facilitatory
38                         Because of different internal solutions that are used in voltage-clamp and cu
39 e solutions have been assembled using acidic internal solutions that inhibit the formation of a dense
40                Using a Cs(+)-gluconate-based internal solution, the leptin-activated current reversed
41 ordings obtained with methanesulfonate-based internal solutions, we found an mGluR-activated current
42 ation or in inside-out patches with ATP-free internal solution were compared with sarcolemmal KATP ch
43                                        In an internal solution with 0.4 mM [Mg2+], sparks (989 events

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