about
Non-silent story on synonymous sites in voltage-gated ion channel genesMuscle channelopathies and critical points in functional and genetic studies.A C-terminal skeletal muscle sodium channel mutation associated with myotonia disrupts fast inactivationChannelopathiesFunctional properties of a new voltage-dependent calcium channel alpha(2)delta auxiliary subunit gene (CACNA2D2)A missense mutation of the Na+ channel alpha II subunit gene Na(v)1.2 in a patient with febrile and afebrile seizures causes channel dysfunctionMolecular pathophysiology and pharmacology of the voltage-sensing module of neuronal ion channelsCgNa, a type I toxin from the giant Caribbean sea anemone Condylactis gigantea shows structural similarities to both type I and II toxins, as well as distinctive structural and functional properties 1Channelopathies of skeletal muscle excitabilityExcitation-contraction coupling in skeletal muscle of a mouse lacking the dihydropyridine receptor subunit gamma1Mexiletine block of disease-associated mutations in S6 segments of the human skeletal muscle Na(+) channelShock Wave-Induced Damage of a Protein by Void CollapseFunctional imaging in muscular diseasesStructural model of the open-closed-inactivated cycle of prokaryotic voltage-gated sodium channels.Characterization of novel KCNH2 mutations in type 2 long QT syndrome manifesting as seizures.Nicotinic acetylcholine receptor subunit variants are associated with blood pressure; findings in the Old Order Amish and replication in the Framingham Heart Study.Sodium channel biophysics, late sodium current and genetic arrhythmic syndromesDiagnostics and therapy of muscle channelopathies--Guidelines of the Ulm Muscle Centre.Mexiletine is an effective antimyotonia treatment in myotonic dystrophy type 1.Cold-induced defects of sodium channel gating in atypical periodic paralysis plus myotonia.Role of the C-terminal domain in inactivation of brain and cardiac sodium channelsRelationship of common candidate gene variants to electrocardiographic T-wave peak to T-wave end interval and T-wave morphology parameters.Skeletal muscle sodium current is reduced in hypokalemic periodic paralysisIdentifying the subfamilies of voltage-gated potassium channels using feature selection technique.Functional studies of MLC1 mutations in Chinese patients with megalencephalic leukoencephalopathy with subcortical cysts.Voltage-gated sodium channels at 60: structure, function and pathophysiology.The inherited episodic ataxias: how well do we understand the disease mechanisms?First WNK4-hypokalemia animal model identified by genome-wide association in Burmese cats.Regulation of neurovascular coupling in autoimmunity to water and ion channelsIntracellular gold nanoparticles increase neuronal excitability and aggravate seizure activity in the mouse brainMyasthenic syndrome caused by mutation of the SCN4A sodium channelVoltage-sensor sodium channel mutations cause hypokalemic periodic paralysis type 2 by enhanced inactivation and reduced current.Pore stability and gating in voltage-activated calcium channelsNanotechnology for neuronal ion channels.The impact of splice isoforms on voltage-gated calcium channel alpha1 subunits.Estimating the voltage-dependent free energy change of ion channels using the median voltage for activationComputer Simulations of Voltage-Gated Cation ChannelsThree-dimensional reconstruction of the recombinant type 3 ryanodine receptor and localization of its amino terminusPhysiologic and pathophysiologic consequences of altered sialylation and glycosylation on ion channel function.Molecular dynamics simulations of voltage-gated cation channels: insights on voltage-sensor domain function and modulation.
P2860
Q21133912-9985B1DB-FCE0-4591-9DE8-F4E7675169FBQ24532297-05B714B8-FAC8-473F-8C82-09F7E4C2CC43Q24544300-E61AEC7A-AE4F-4612-A007-0579C79C3315Q24601791-F76380B2-F0B5-4109-8619-0A7D65CBBFCFQ24621422-CDA09A60-A32D-4EE1-A3D7-279CE64A8A8FQ24626279-F27C7FC1-E442-4572-9FAA-9B3815CB2DE1Q26800090-6A0D91BF-F741-4327-9467-821E7B518F57Q27644801-37C8E022-4223-474C-ADA4-B72F6A679227Q28082428-53F8D79E-9F2B-4E0C-81F4-1B29F9823708Q28366204-F484B41D-B40C-4622-8219-D59B4EE8E22AQ28366485-3B46BDA1-F57B-4B6A-9A8A-7346A3B0151AQ30366106-B3D4079A-1A11-4F28-941E-E8C56614923DQ30470355-84C4F166-9AE3-41B1-AE55-8DFE4A904E32Q30611726-515BADAA-9C2A-4865-8470-2423804D37F1Q33157691-71984881-DFDE-45CC-81E9-2C080532C720Q33351537-1B662521-7E52-4B67-9B0E-2784AF47F769Q33708707-C4949DE2-B925-47E7-9A7D-CBBE1CC6CB13Q33807683-058AE2CE-2EC1-4E98-8451-28BEC8B8D5B3Q33853335-93BB6588-D8D8-497A-9A9B-DB9C4B1A84C9Q33888835-7D25C485-711D-48A7-BB82-DB26C1841571Q33953193-7EA92A0C-DF76-470E-8736-32BC3F6A811BQ33998438-44461BD9-3DAA-4B9A-82AD-2314AE3312C4Q34011949-E8EB473F-397B-4E3E-A819-C6616B8C3179Q34072558-E9BFEF13-BE0D-4E89-9D8B-8CBB714170F6Q34194967-979B1FDB-30A6-4A9D-9C16-5C0911DEE4D3Q34265707-3FA4B662-BDAC-451B-925A-D18977FB2500Q34326582-AED88067-F822-42FD-9912-3E5E13E9E8C9Q34535055-8319C58D-E4BE-40D0-BDCA-7157A801AD31Q35001946-5E7D452C-FBF2-462B-ADAA-398A2A59D415Q35119975-060E1108-CA19-480F-92A3-FACB201B0F53Q35163768-E8914A23-23C4-4A49-AF8E-DEE404E4FE5FQ35208537-DAD3EE5D-3AE2-4B94-9B39-02653E75686DQ35388651-17249D8B-3A73-45E6-A56E-B3F8DF765858Q35583803-0B725097-1274-4B40-9756-23135F06B384Q35596481-EE269CD8-3367-4E82-92EE-D086A87F181DQ35647374-940A4ED7-EFD7-4275-887B-B775B3745213Q35895884-D9A29FDD-5F81-4225-8B03-2DE092D9205CQ35930374-194BCC97-15F8-4671-9594-DD9A39E7A52FQ35981911-FEF43ACA-0C98-4799-89EC-600F1FDE10AAQ35990363-2B7D4E8D-6D0A-43DA-B215-66697235FC81
P2860
description
1999 nî lūn-bûn
@nan
1999 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած
@hyw
1999 թվականի հոտեմբերին հրատարակված գիտական հոդված
@hy
1999年の論文
@ja
1999年論文
@yue
1999年論文
@zh-hant
1999年論文
@zh-hk
1999年論文
@zh-mo
1999年論文
@zh-tw
1999年论文
@wuu
name
Voltage-gated ion channels and hereditary disease.
@ast
Voltage-gated ion channels and hereditary disease.
@en
type
label
Voltage-gated ion channels and hereditary disease.
@ast
Voltage-gated ion channels and hereditary disease.
@en
prefLabel
Voltage-gated ion channels and hereditary disease.
@ast
Voltage-gated ion channels and hereditary disease.
@en
P1476
Voltage-gated ion channels and hereditary disease.
@en
P2093
Jurkat-Rott K
Lehmann-Horn F
P304
P356
10.1152/PHYSREV.1999.79.4.1317
P577
1999-10-01T00:00:00Z