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1 ith the expected field, temperature and gate voltage dependencies.
2 channels characterized by positively shifted voltage dependencies and very fast deactivation rates.
3 junctional hemichannels that display altered voltage dependency and reduced permeability, and which c
4                           We showed that the voltage dependency and slope factors of NLC and motility
5                 We subsequently compared the voltage dependency and the values of slope factor of NLC
6  a mechanism underlying the diverse BacNa(V) voltage dependencies, and demonstrate that a discrete do
7 n the physiological voltage range, and their voltage dependencies are of opposite signs.
8 C1, which had a similar channel activity and voltage dependency as full-length, was hypoxia-inducible
9                                  The derived voltage dependency does not require any physical, molecu
10 reaks down without electrical coupling; NMDA voltage-dependency doubles the range of synaptic feedbac
11 me constant of inactivation (tauh) derives a voltage dependency from coupling to voltage-dependent ac
12 ocytes had smaller Na+ currents with altered voltage dependencies of activation and inactivation and
13 be composed of two components with differing voltage dependencies of activation.
14                                          The voltage dependencies of steady-state activation and inac
15 rent using protocols employing the different voltage dependencies of the channel types and their diff
16 ximal current and by positively shifting the voltage dependency of gating.
17 alian cells, induced a positive shift in the voltage dependency of K(+) current activation, and slowe
18                                The different voltage dependency of LTP induction is thought to be med
19            This hyperpolarizing shift in the voltage dependency of LTS amplitude is best explained by
20 nally, the beta3 subunit alters the rate and voltage dependency of relief of the inhibition produced
21 nnel activation and inactivation in that the voltage dependency of tauh is substantially reduced whil
22 ome independent, parallel processes, and any voltage dependency of tauh is then entirely intrinsic to
23 te constant of zero also removes the derived voltage dependency of tauh, but activation and inactivat
24 plitude of the delay process and the derived voltage dependency of tauh.
25 ICa as manifested by flattened and broadened voltage dependency of the amplitude of cytosolic Ca2+ tr
26 f I(Ca)- induced Ca transients (at 0 mV) but voltage dependency of the Ca transients was markedly wid
27 e (I/V) data that may be used to measure the voltage dependency of the membrane conductance.
28  manner: (1) by providing the driving force (voltage dependency of the transport itself) and (2) by l
29                                     The weak voltage dependency of the VIC channel (and its lack of m
30  a depolarizing prepulse and also shifts the voltage dependency of this relief to more hyperpolarized
31  channel CCA-1 and symmetrically re-tune its voltage-dependencies of activation and inactivation towa
32                                The different voltage-dependencies of the two modes of action of these
33 the second and third resting states, and the voltage-dependency of forward transitions through restin
34                                This shift in voltage dependency strongly and specifically bypasses th
35 gh Cav1 channels of lymphocytes retain their voltage dependency, T cell receptor stimulation dramatic
36 e that accompanies electromotility imparts a voltage dependency to the membrane capacitance.
37 d inactivation curves showed no shift in the voltage dependency under the inhibition by oxo-M.
38 fold to fourfold by 50 microm NEM, and their voltage dependencies were negatively shifted by 10-20 mV
39 different time-dependent characteristics and voltage dependencies, which interact with each other and

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