about
Multiple sodium channel isoforms mediate the pathological effects of Pacific ciguatoxin-1.The activation mechanism of alpha1beta2gamma2S and alpha3beta3gamma2S GABAA receptors.Structure-Function Analysis of the GlyR α2 Subunit Autism Mutation p.R323L Reveals a Gain-of-Functionγ1-Containing GABA-A Receptors Cluster at Synapses Where they Mediate Slower Synaptic Currents than γ2-Containing GABA-A Receptors.Correlating structural and energetic changes in glycine receptor activation.Ligand-gated ion channels: mechanisms underlying ion selectivity.Zolpidem and eszopiclone prime α1β2γ2 GABAA receptors for longer duration of activity.Single channel analysis of conductance and rectification in cation-selective, mutant glycine receptor channelsCation-selective mutations in the M2 domain of the inhibitory glycine receptor channel reveal determinants of ion-charge selectivity.Novel missense mutations in the glycine receptor β subunit gene (GLRB) in startle diseaseInvestigating the Mechanism by Which Gain-of-function Mutations to the α1 Glycine Receptor Cause Hyperekplexia.The Free Zinc Concentration in the Synaptic Cleft of Artificial Glycinergic Synapses Rises to At least 1 μMNew hyperekplexia mutations provide insight into glycine receptor assembly, trafficking, and activation mechanisms.An outline of desensitization in pentameric ligand-gated ion channel receptors.Physiological and pharmacological properties of inhibitory postsynaptic currents mediated by α5β1γ2, α5β2γ2 and α5β3γ2 GABAA receptors.Agonist-dependent single channel current and gating in alpha4beta2delta and alpha1beta2gamma2S GABAA receptorsTaurine is a potent activator of extrasynaptic GABA(A) receptors in the thalamus.Potent neuroprotection after stroke afforded by a double-knot spider-venom peptide that inhibits acid-sensing ion channel 1a.GABAA receptor α and γ subunits shape synaptic currents via different mechanisms.Effects of glutamate and ivermectin on single glutamate-gated chloride channels of the parasitic nematode H. contortus.The contribution of proline 250 (P-2') to pore diameter and ion selectivity in the human glycine receptor channel.Identification of molluscan nicotinic acetylcholine receptor (nAChR) subunits involved in formation of cation- and anion-selective nAChRs.Inhibitory synapse deficits caused by familial α1 GABAA receptor mutations in epilepsy.Probing the Structural Mechanism of Partial Agonism in Glycine Receptors Using the Fluorescent Artificial Amino Acid, ANAP.Functional reconstitution of glycinergic synapses incorporating defined glycine receptor subunit combinations.Ivermectin-Activated, Cation-Permeable Glycine Receptors for the Chemogenetic Control of Neuronal Excitation.Structure/Function Studies of the α4 Subunit Reveal Evolutionary Loss of a GlyR Subtype Involved in Startle and Escape Responses.SAHA (Vorinostat) Corrects Inhibitory Synaptic Deficits Caused by Missense Epilepsy Mutations to the GABAA Receptor γ2 Subunit.GluClR-mediated inhibitory postsynaptic currents reveal targets for ivermectin and potential mechanisms of ivermectin resistanceMeasurement of the limiting equivalent conductivities and mobilities of the most prevalent ionic species of EGTA (EGTA2- and EGTA3-) for use in electrophysiological experimentsThe effects of insecticides on two splice variants of the glutamate-gated chloride channel receptor of the major malaria vector, Anopheles gambiaeA novel glycine receptor variant with startle disease affects syndapin I and glycinergic inhibition
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Q30839530-B1FA4C26-5951-4006-91FA-83DD04068999Q33590305-D943DAB5-C74E-40FA-AAD5-384DBE9BEE59Q33715197-7155A230-5C9C-4919-999C-9DAFCAE6B71BQ33774539-01FE50DA-32C3-403B-A6D0-57781CEC60E0Q35126661-02E8D3C8-FA9D-488A-B802-44B683D0AEDCQ35853354-87CD04CE-4B42-416B-929B-391F72A75E1CQ35865429-F060F2FA-3A4E-4976-9F12-1469F86EB467Q36445134-BDC83FBD-3081-4950-8696-DABE49A7613BQ36445140-77A4B867-4B97-4592-BC9F-6136BDABE0ECQ36636926-05186EEE-FF6B-4D9F-9D52-D021CEAE315BQ37098960-11A860C4-0361-4188-88C4-9E3E31A749ABQ37273287-61310ECA-3223-4530-B109-E4E291979C90Q37333728-304FDFBB-C4F4-4DDB-9934-AE6336079765Q38039375-D7E3A79D-D056-4459-8978-CD77A6DD6B3DQ38649703-08FB4DBF-5256-4EFB-B05F-64F664216AC2Q40019623-7A0161F5-5726-4BD1-9A2E-F5A81012E271Q40028844-295B66ED-1BA4-4639-A9BB-93CBC119DD79Q41929851-7DE82781-B2B6-4B55-B8EE-EDF8A4FF652BQ41984180-4672FEE9-1BC8-4BE6-A0B5-0A2A273DB2B3Q42703040-1026132B-07A8-4647-B2C1-CF4BD9817F35Q44659054-1EB69526-CC8A-4D52-B629-0B9E9F6B8A71Q46807864-664041A2-F59B-42F1-872C-8C1341D6B02BQ48127416-834B43FA-9EE5-482B-8944-3F1B7BBAB70EQ48313698-4994B2AD-0CA0-4454-BF93-2D8D9EF4F912Q48438645-7E079FCE-7CA9-4C1B-8F19-4EFED45C9836Q48521885-0AA7A5DB-F2A8-458D-ACC1-F8E4B4726046Q49489241-28FC4859-4B10-4BC5-A1DA-64E5F9A9229BQ52599717-0DA4AD2E-5C3F-4A78-978B-5F8E136C0EFDQ64215129-2EEF4ED7-BBA5-4D82-9FB6-CF5D0182DA05Q78221361-3415C443-338F-4A6C-B42A-7674410F6AECQ93074285-159CDF21-5168-4804-B7EB-49AFB4F8B411Q94473302-FE70BF82-82DB-45A3-BB9A-8DEF63B69130
P50
description
hulumtues
@sq
researcher
@en
wetenschapper
@nl
հետազոտող
@hy
name
Angelo Keramidas
@ast
Angelo Keramidas
@en
Angelo Keramidas
@es
Angelo Keramidas
@nl
Angelo Keramidas
@sl
type
label
Angelo Keramidas
@ast
Angelo Keramidas
@en
Angelo Keramidas
@es
Angelo Keramidas
@nl
Angelo Keramidas
@sl
prefLabel
Angelo Keramidas
@ast
Angelo Keramidas
@en
Angelo Keramidas
@es
Angelo Keramidas
@nl
Angelo Keramidas
@sl
P1053
I-1704-2013
P106
P21
P2798
P31
P3829
P496
0000-0003-2846-052X