Mutational analysis of ion conduction and drug binding sites in the inner mouth of voltage-gated K+ channels.
about
The pore-lining region of shaker voltage-gated potassium channels: comparison of beta-barrel and alpha-helix bundle modelsContributions of a negatively charged residue in the hydrophobic domain of the IRK1 inwardly rectifying K+ channel to K(+)-selective permeation.Multiple residues specify external tetraethylammonium blockade in voltage-gated potassium channels.Glutamate substitution in repeat IV alters divalent and monovalent cation permeation in the heart Ca2+ channel.Control of ion conduction in L-type Ca2+ channels by the concerted action of S5-6 regions.Fluorescent system based on bacterial expression of hybrid KcsA channels designed for Kv1.3 ligand screening and study.Elucidating the molecular basis of action of a classic drug: guanidine compounds as inhibitors of voltage-gated potassium channels.Variability of Potassium Channel Blockers in Mesobuthus eupeus Scorpion Venom with Focus on Kv1.1: AN INTEGRATED TRANSCRIPTOMIC AND PROTEOMIC STUDY.Mechanisms involved in the vasorelaxant effects produced by the acute application of amfepramone in vitro to rat aortic ringsModulation of Closed-State Inactivation in Kv2.1/Kv6.4 Heterotetramers as Mechanism for 4-AP Induced Potentiation.Pharmacological characterization of mechanisms involved in the vasorelaxation produced by rosuvastatin in aortic rings from rats with a cafeteria-style diet.Alkanols inhibit voltage-gated K(+) channels via a distinct gating modifying mechanism that prevents gate opening.Role of transmembrane segment S5 on gating of voltage-dependent K+ channels.Inactivation gating of Kv4 potassium channels: molecular interactions involving the inner vestibule of the pore.Pharmacological study of the mechanisms involved in the vasodilator effect produced by the acute application of triiodothyronine to rat aortic ringsMutations in the S6 gate isolate a late step in the activation pathway and reduce 4-AP sensitivity in shaker K(v) channel.Being flexible: the voltage-controllable activation gate of kv channels.Nonspecific block of voltage-gated potassium channels has greater effect on distal schaffer collaterals than proximal schaffer collaterals during periods of high activity.Molecular determinants of high affinity phenylalkylamine block of L-type calcium channels.Possible mechanisms involved in the vasorelaxant effect produced by clobenzorex in aortic segments of rats.A single residue contributes to the difference between Kir4.1 and Kir1.1 channels in pH sensitivity, rectification and single channel conductance.Receptors and channels regulating acrosome reactions.
P2860
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P2860
Mutational analysis of ion conduction and drug binding sites in the inner mouth of voltage-gated K+ channels.
description
1994 nî lūn-bûn
@nan
1994 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած
@hyw
1994 թվականի դեկտեմբերին հրատարակված գիտական հոդված
@hy
1994年の論文
@ja
1994年学术文章
@wuu
1994年学术文章
@zh-cn
1994年学术文章
@zh-hans
1994年学术文章
@zh-my
1994年学术文章
@zh-sg
1994年學術文章
@yue
name
Mutational analysis of ion con ...... of voltage-gated K+ channels.
@ast
Mutational analysis of ion con ...... of voltage-gated K+ channels.
@en
Mutational analysis of ion con ...... of voltage-gated K+ channels.
@nl
type
label
Mutational analysis of ion con ...... of voltage-gated K+ channels.
@ast
Mutational analysis of ion con ...... of voltage-gated K+ channels.
@en
Mutational analysis of ion con ...... of voltage-gated K+ channels.
@nl
prefLabel
Mutational analysis of ion con ...... of voltage-gated K+ channels.
@ast
Mutational analysis of ion con ...... of voltage-gated K+ channels.
@en
Mutational analysis of ion con ...... of voltage-gated K+ channels.
@nl
P2860
P1433
P1476
Mutational analysis of ion con ...... of voltage-gated K+ channels.
@en
P2093
P2860
P304
P356
10.1016/S0006-3495(94)80718-0
P407
P577
1994-12-01T00:00:00Z