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Differential modulation of Ca(v)2.1 channels by calmodulin and Ca2+-binding protein 1Complete loss of P/Q calcium channel activity caused by a CACNA1A missense mutation carried by patients with episodic ataxia type 2PICK1 is required for the control of synaptic transmission by the metabotropic glutamate receptor 7Familial hemiplegic migraine mutations increase Ca(2+) influx through single human CaV2.1 channels and decrease maximal CaV2.1 current density in neurons.Effects of familial hemiplegic migraine type 1 mutations on neuronal P/Q-type Ca2+ channel activity and inhibitory synaptic transmissionA blocker of N- and T-type voltage-gated calcium channels attenuates ethanol-induced intoxication, place preference, self-administration, and reinstatementSynaptic targeting of N-type calcium channels in hippocampal neuronsThe cerebellum and migraineDirect interaction of gbetagamma with a C-terminal gbetagamma-binding domain of the Ca2+ channel alpha1 subunit is responsible for channel inhibition by G protein-coupled receptorsThe 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 cellsElementary mechanisms producing facilitation of Cav2.1 (P/Q-type) channelsRegulatory role of E-NTPase/E-NTPDase in Ca2+/Mg2+ transport via gated channel'Medusa head ataxia': the expanding spectrum of Purkinje cell antibodies in autoimmune cerebellar ataxia. Part 2: Anti-PKC-gamma, anti-GluR-delta2, anti-Ca/ARHGAP26 and anti-VGCCModal gating of human CaV2.1 (P/Q-type) calcium channels: I. The slow and the fast gating modes and their modulation by beta subunitsREM sleep and its Loss-Associated Epigenetic Regulation with Reference to Noradrenaline in ParticularSpecific 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 channelVoltage-gated calcium channelsA single Gbeta subunit locus controls cross-talk between protein kinase C and G protein regulation of N-type calcium channelsGabapentin inhibits high-threshold calcium channel currents in cultured rat dorsal root ganglion neuronesDifferential regulation of GABA release and neuronal excitability mediated by neuropeptide Y1 and Y2 receptors in rat thalamic neuronsChick cochlear hair cell exocytosis mediated by dihydropyridine-sensitive calcium channelsNicotine facilitates glycine release in the rat spinal dorsal hornOxytocin retrogradely inhibits evoked, but not miniature, EPSCs in the rat supraoptic nucleus: role of N- and P/Q-type calcium channelsPharmacological discrimination between effects of carbamazepine on hippocampal basal, Ca(2+)- and K(+)-evoked serotonin releaseThe neuronal beta 4 subunit increases the unitary conductance of L-type voltage-gated calcium channels in PC12 cellsTetanic depression is overcome by tonic adenosine A(2A) receptor facilitation of L-type Ca(2+) influx into rat motor nerve terminalsCa1.2 and CaV1.3 neuronal L-type calcium channels: differential targeting and signaling to pCREBClass A calcium channel variants in pancreatic islets and their role in insulin secretionNovel Cav2.1 splice variants isolated from Purkinje cells do not generate P-type Ca2+ currentAblation of P/Q-type Ca(2+) channel currents, altered synaptic transmission, and progressive ataxia in mice lacking the alpha(1A)-subunitAltered properties of quantal neurotransmitter release at endplates of mice lacking P/Q-type Ca2+ channelsThe VGL-Chanome: A Protein Superfamily Specialized for Electrical Signaling and Ionic HomeostasisA relationship between bruxism and orofacial-dystonia? A trigeminal electrophysiological approach in a case report of pineal cavernoma.Ablation of Ca2+ channel beta3 subunit leads to enhanced N-methyl-D-aspartate receptor-dependent long term potentiation and improved long term memoryCourtship and visual defects of cacophony mutants reveal functional complexity of a calcium-channel alpha1 subunit in DrosophilaDelayed postnatal loss of P/Q-type calcium channels recapitulates the absence epilepsy, dyskinesia, and ataxia phenotypes of genomic Cacna1a mutations.Targeting chronic and neuropathic pain: the N-type calcium channel comes of age.Calcium currents in hair cells isolated from semicircular canals of the frog.Developmental alterations in the biophysical properties of Ca(v) 1.3 Ca(2+) channels in mouse inner hair cells.
P2860
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P2860
description
1995 nî lūn-bûn
@nan
1995 թուականի Փետրուարին հրատարակուած գիտական յօդուած
@hyw
1995 թվականի փետրվարին հրատարակված գիտական հոդված
@hy
1995年の論文
@ja
1995年論文
@yue
1995年論文
@zh-hant
1995年論文
@zh-hk
1995年論文
@zh-mo
1995年論文
@zh-tw
1995年论文
@wuu
name
Exocytotic Ca2+ channels in mammalian central neurons.
@ast
Exocytotic Ca2+ channels in mammalian central neurons.
@en
Exocytotic Ca2+ channels in mammalian central neurons.
@nl
type
label
Exocytotic Ca2+ channels in mammalian central neurons.
@ast
Exocytotic Ca2+ channels in mammalian central neurons.
@en
Exocytotic Ca2+ channels in mammalian central neurons.
@nl
prefLabel
Exocytotic Ca2+ channels in mammalian central neurons.
@ast
Exocytotic Ca2+ channels in mammalian central neurons.
@en
Exocytotic Ca2+ channels in mammalian central neurons.
@nl
P2093
P1476
Exocytotic Ca2+ channels in mammalian central neurons.
@en
P2093
P356
10.1016/0166-2236(95)93882-X
P577
1995-02-01T00:00:00Z