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Labro, Alain
One or more keywords matched the following items that are connected to Labro, Alain
Item TypeName
Concept Potassium Channels
Concept Shaker Superfamily of Potassium Channels
Concept Ether-A-Go-Go Potassium Channels
Concept Potassium Channels, Inwardly Rectifying
Concept Shaw Potassium Channels
Concept Potassium Channels, Voltage-Gated
Concept Shab Potassium Channels
Academic Article Gating of shaker-type channels requires the flexibility of S6 caused by prolines.
Academic Article Coupling of voltage sensing to channel opening reflects intrasubunit interactions in kv channels.
Academic Article Modulation of HERG gating by a charge cluster in the N-terminal proximal domain.
Academic Article A polyether biotoxin binding site on the lipid-exposed face of the pore domain of Kv channels revealed by the marine toxin gambierol.
Academic Article Conserved negative charges in the N-terminal tetramerization domain mediate efficient assembly of Kv2.1 and Kv2.1/Kv6.4 channels.
Academic Article KCNQ1 channels voltage dependence through a voltage-dependent binding of the S4-S5 linker to the pore domain.
Academic Article The electrically silent Kv6.4 subunit confers hyperpolarized gating charge movement in Kv2.1/Kv6.4 heterotetrameric channels.
Academic Article Quantitative single-cell ion-channel gene expression profiling through an improved qRT-PCR technique combined with whole cell patch clamp.
Academic Article Being flexible: the voltage-controllable activation gate of kv channels.
Academic Article Kv channel gating requires a compatible S4-S5 linker and bottom part of S6, constrained by non-interacting residues.
Academic Article Phosphatidylinositol-4,5-bisphosphate (PIP(2)) stabilizes the open pore conformation of the Kv11.1 (hERG) channel.
Academic Article The S4-S5 linker of KCNQ1 channels forms a structural scaffold with the S6 segment controlling gate closure.
Academic Article Dual effect of phosphatidylinositol (4,5)-bisphosphate PIP(2) on Shaker K(+) [corrected] channels.
Academic Article Properties of deactivation gating currents in Shaker channels.
Academic Article The ladder-shaped polyether toxin gambierol anchors the gating machinery of Kv3.1 channels in the resting state.
Academic Article Mutations in the S6 gate isolate a late step in the activation pathway and reduce 4-AP sensitivity in shaker K(v) channel.
Academic Article Modulation of Closed-State Inactivation in Kv2.1/Kv6.4 Heterotetramers as Mechanism for 4-AP Induced Potentiation.
Academic Article Alkanols inhibit voltage-gated K(+) channels via a distinct gating modifying mechanism that prevents gate opening.
Academic Article Kv3.1 uses a timely resurgent K(+) current to secure action potential repolarization.
Academic Article Voltage-sensor conformation shapes the intra-membrane drug binding site that determines gambierol affinity in Kv channels.
Academic Article Gambierol and n-alkanols inhibit Shaker Kv channel via distinct binding sites outside the K(+) pore.
Academic Article Dromedary immune response and specific Kv2.1 antibody generation using a specific immunization approach.
Academic Article Inverted allosteric coupling between activation and inactivation gates in K+ channels.
Academic Article Determining the correct stoichiometry of Kv2.1/Kv6.4 heterotetramers, functional in multiple stoichiometrical configurations.
Academic Article The Selectivity Filter Is Involved in the U-Type Inactivation Process of Kv2.1 and Kv3.1 Channels.
Academic Article Hydrophobic Drug/Toxin Binding Sites in Voltage-Dependent K+ and Na+ Channels.
Academic Article Impaired cytoplasmic domain interactions cause co-assembly defect and loss of function in the p.Glu293Lys KNCJ2 variant isolated from an Andersen-Tawil syndrome patient.
Academic Article The resting membrane potential of hSC-CM in a syncytium is more hyperpolarised than that of isolated cells.
Academic Article The nonconducting W434F mutant adopts upon membrane depolarization an inactivated-like state that differs from wild-type Shaker-IR potassium channels.
Academic Article Immunosuppressive effects of new thiophene-based KV1.3 inhibitors.
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  • Hyperpolarization Activated Cyclic Nucleotide Gated Channels