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1 gatively charged subnanometer-sized confined ionic channels.
2 and CCK-8, which operate through independent ionic channels.
3 ake, but may be due to a secondary effect on ionic channels.
4 ndent properties in two molecularly distinct ionic channels.
5 those of gating current records reported for ionic channels.
6 to variability in the types and densities of ionic channels.
7 5 other G-protein-coupled receptors or on 15 ionic channels.
9 n translocation into liposomes and to elicit ionic channel activity at the phospholipids low affinity
10 h-clamped, providing the first recordings of ionic channel activity, synaptic vesicle release, and ga
11 fabricating angstrom-scale artificial solid ionic channels aiming to replicate the biological ion ch
12 ese operations, involving synapses, membrane ionic channels and changes in membrane potential, are th
14 des a handle for optimization of radical and ionic channels and yields accelerations up to 1 order of
15 teins, including receptors, transporters and ionic channels, and to be active mostly as a homodimer.
17 reproducible conductance levels expected for ionic channels, Bax, but not Bcl-xL, created arbitrary a
18 nd lipid uptake through a temporarily stable ionic channel) become dominant in model liposome systems
19 nlinear DeltaV(m), we studied the effects of ionic channel blockers on DeltaV(m) in geometrically def
20 in cell cultures by measuring the effects of ionic channel blockers on DeltaVm and measuring uptake o
21 models with many compartments and dozens of ionic channels can account for this Ca(2+) spike-depende
22 n with the rapid movement of calcium through ionic channels can cause large external calcium fluctuat
23 changes include alterations at the levels of ionic channels, cellular energy balance, neurohormonal e
24 We incorporated these parameters into a nine ionic channel conductance model to obtain completed mode
25 h as adenosine)-mediated response and not in ionic channel coupled receptor (such as GABA(A))-mediate
26 tal data sets on AF-induced changes of major ionic channel currents (ICaL, IKur, Ito, IK1, IKs, INaCa
27 duced in the model by inhibiting appropriate ionic channel currents according to experimentally repor
28 ctifier potassium current) or block multiple ionic channels (e.g., ibutilide and azimilide) in order
29 lity of SOICs such as three-dimensional (3D) ionic channels, excellent thermal stability, dual functi
30 systems, suggesting that the coregulation of ionic channel expression, by thus linking their variabil
35 ionic transport through porous membranes and ionic channels is important in numerous applications ran
38 In this review, we focus on the principal ionic channels (KATP, Nav, and Cav channels) involved in
39 he dynamic clamp and voltage-gated potassium ionic channels (Kv1.3) expressed in Xenopus oocytes.
40 Additional experiments examined the membrane ionic channels mediating these GluR activation effects.
41 biological "fusion pores" can be as small as ionic channels or gap junctions, one model posits a prot
42 altered current density primarily impact the ionic channel pore and those associated with altered res
43 hy causes remodelling, leading to changes in ionic channel, pump and exchanger densities and kinetics
44 t the cellular scale this remodelling of the ionic channels, pumps and exchangers gives rise to chang
46 or agents that are neuroprotective or affect ionic channels; straightforward transduction of gene exp
47 expressed in a "retrograde" manner with the ionic channel that is modulated appearing early in devel
48 lyamine macromolecules, forming a network of ionic channels that exhibit regulated permeability of wa