戻る
「早戻しボタン」を押すと検索画面に戻ります。 [閉じる]

コーパス検索結果 (１語後でソート)

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