Familial hemiplegic migraine mutations change alpha1A Ca2+ channel kinetics
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Spinocerebellar ataxia type 6 mutation alters P-type calcium channel functionMuscle channelopathies and critical points in functional and genetic studies.Complete loss of P/Q calcium channel activity caused by a CACNA1A missense mutation carried by patients with episodic ataxia type 2Familial hemiplegic migraine mutations increase Ca(2+) influx through single human CaV2.1 channels and decrease maximal CaV2.1 current density in neurons.Recurrence of the T666M calcium channel CACNA1A gene mutation in familial hemiplegic migraine with progressive cerebellar ataxia.Effects of familial hemiplegic migraine type 1 mutations on neuronal P/Q-type Ca2+ channel activity and inhibitory synaptic transmissionThe familial hemiplegic migraine mutation R192Q reduces G-protein-mediated inhibition of P/Q-type (Ca(V)2.1) calcium channels expressed in human embryonic kidney cellsThe role of distal S6 hydrophobic residues in the voltage-dependent gating of CaV2.3 channels.A Single Amino Acid Deletion (ΔF1502) in the S6 Segment of CaV2.1 Domain III Associated with Congenital Ataxia Increases Channel Activity and Promotes Ca2+ InfluxThree new familial hemiplegic migraine mutants affect P/Q-type Ca(2+) channel kineticsDelayed cerebral edema and fatal coma after minor head trauma: role of the CACNA1A calcium channel subunit gene and relationship with familial hemiplegic migraineSpecific kinetic alterations of human CaV2.1 calcium channels produced by mutation S218L causing familial hemiplegic migraine and delayed cerebral edema and coma after minor head traumaGating deficiency in a familial hemiplegic migraine type 1 mutant P/Q-type calcium channelFamilial hemiplegic migraine type 1 mutations K1336E, W1684R, and V1696I alter Cav2.1 Ca2+ channel gating: evidence for beta-subunit isoform-specific effectsEffects of congenital stationary night blindness type 2 mutations R508Q and L1364H on Cav1.4 L-type Ca2+ channel function and expressionFGF14 regulates presynaptic Ca2+ channels and synaptic transmissionAltered expression and assembly of N-type calcium channel alpha1B and beta subunits in epileptic lethargic (lh/lh) mouseAblation of P/Q-type Ca(2+) channel currents, altered synaptic transmission, and progressive ataxia in mice lacking the alpha(1A)-subunitCooperative activation of the T-type CaV3.2 channel: interaction between Domains II and III.Migraine: new molecular mechanisms.Familial hemiplegic migraine.Molecular endpoints of Ca2+/calmodulin- and voltage-dependent inactivation of Ca(v)1.3 channelsA mutation in the first intracellular loop of CACNA1A prevents P/Q channel modulation by SNARE proteins and lowers exocytosis.Calcium channels and synaptic transmission in familial hemiplegic migraine type 1 animal models.Voltage-dependent calcium channel mutations in neurological disease.Mouse models of spike-wave epilepsy.Neurological channelopathies: diagnosis and therapy in the new millennium.Molecular genetics of migraine headaches: a review.Gain of function in FHM-1 Cav2.1 knock-in mice is related to the shape of the action potential.Channelopathies: ion channel defects linked to heritable clinical disorders.Molecular determinants of inactivation in voltage-gated Ca2+ channels.Contribution of calcium-dependent facilitation to synaptic plasticity revealed by migraine mutations in the P/Q-type calcium channel.The inherited episodic ataxias: how well do we understand the disease mechanisms?Genetic analysis of a synaptic calcium channel in Drosophila: intragenic modifiers of a temperature-sensitive paralytic mutant of cacophonyThe neuronal channelopathies.Genetics of migraine: possible links to neurophysiological abnormalities.Functional roles of cytoplasmic loops and pore lining transmembrane helices in the voltage-dependent inactivation of HVA calcium channels.A single amino acid mutation attenuates rundown of voltage-gated calcium channels.Pore stability and gating in voltage-activated calcium channelsMolecular dynamics and mutational analysis of a channelopathy mutation in the IIS6 helix of Ca V 1.2.
P2860
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P2860
Familial hemiplegic migraine mutations change alpha1A Ca2+ channel kinetics
description
1998 nî lūn-bûn
@nan
1998 թուականի Մարտին հրատարակուած գիտական յօդուած
@hyw
1998 թվականի մարտին հրատարակված գիտական հոդված
@hy
1998年の論文
@ja
1998年論文
@yue
1998年論文
@zh-hant
1998年論文
@zh-hk
1998年論文
@zh-mo
1998年論文
@zh-tw
1998年论文
@wuu
name
Familial hemiplegic migraine mutations change alpha1A Ca2+ channel kinetics
@ast
Familial hemiplegic migraine mutations change alpha1A Ca2+ channel kinetics
@en
Familial hemiplegic migraine mutations change alpha1A Ca2+ channel kinetics
@nl
type
label
Familial hemiplegic migraine mutations change alpha1A Ca2+ channel kinetics
@ast
Familial hemiplegic migraine mutations change alpha1A Ca2+ channel kinetics
@en
Familial hemiplegic migraine mutations change alpha1A Ca2+ channel kinetics
@nl
prefLabel
Familial hemiplegic migraine mutations change alpha1A Ca2+ channel kinetics
@ast
Familial hemiplegic migraine mutations change alpha1A Ca2+ channel kinetics
@en
Familial hemiplegic migraine mutations change alpha1A Ca2+ channel kinetics
@nl
P2093
P2860
P356
P1476
Familial hemiplegic migraine mutations change alpha1A Ca2+ channel kinetics
@en
P2093
H Glossmann
J Striessnig
M J Sinnegger
P2860
P304
P356
10.1074/JBC.273.10.5586
P407
P577
1998-03-06T00:00:00Z