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The Physiology, Pathology, and Pharmacology of Voltage-Gated Calcium Channels and Their Future Therapeutic PotentialSignal processing by T-type calcium channel interactions in the cerebellumActivity-dependent subcellular cotrafficking of the small GTPase Rem2 and Ca2+/CaM-dependent protein kinase IIαProtein interactome mining defines melatonin MT1 receptors as integral component of presynaptic protein complexes of neuronsBlock of voltage-dependent calcium channel by the green mamba toxin calcicludineGating effects of mutations in the Cav3.2 T-type calcium channel associated with childhood absence epilepsyThe CACNA1F gene encodes an L-type calcium channel with unique biophysical properties and tissue distributionThe alpha2delta auxiliary subunit reduces affinity of omega-conotoxins for recombinant N-type (Cav2.2) calcium channelsIntegrin receptor activation triggers converging regulation of Cav1.2 calcium channels by c-Src and protein kinase A pathwaysCa(V)3 T-type calcium channel isoforms differentially distribute to somatic and dendritic compartments in rat central neuronsProtease-activated receptor-4: a novel mechanism of inflammatory pain modulationExpression of voltage-gated Ca2+ channel subtypes in cultured astrocytesRole of voltage-gated calcium channels in epilepsy.Role of voltage-gated calcium channels in ascending pain pathwaysPrion protein attenuates excitotoxicity by inhibiting NMDA receptorsCharacterization of novel cannabinoid based T-type calcium channel blockers with analgesic effects.1,4-Dihydropyridine derivatives with T-type calcium channel blocking activity attenuate inflammatory and neuropathic pain.Amino acid residues outside of the pore region contribute to N-type calcium channel permeation.Glutamate receptors on myelinated spinal cord axons: I. GluR6 kainate receptorsA role for transient receptor potential vanilloid 4 in tonicity-induced neurogenic inflammation.Fast lidocaine block of cardiac and skeletal muscle sodium channels: one site with two routes of access.Dissecting lidocaine action: diethylamide and phenol mimic separate modes of lidocaine block of sodium channels from heart and skeletal muscleA novel slow-inactivation-specific ion channel modulator attenuates neuropathic pain.In vivo expression of G-protein beta1gamma2 dimer in adult mouse skeletal muscle alters L-type calcium current and excitation-contraction coupling.Kainate receptor activation induces glycine receptor endocytosis through PKC deSUMOylationCav1.4 encodes a calcium channel with low open probability and unitary conductance.Interactions between presynaptic Ca2+ channels, cytoplasmic messengers and proteins of the synaptic vesicle release complex.Glycerotoxin from Glycera convoluta stimulates neurosecretion by up-regulating N-type Ca2+ channel activityVoltage-dependent calcium channels--beyond dihydropyridine antagonists.The immediately releasable pool of mouse chromaffin cell vesicles is coupled to P/Q-type calcium channels via the synaptic protein interaction site.Specific T-type calcium channel isoforms are associated with distinct burst phenotypes in deep cerebellar nuclear neurons.Extended spectrum of idiopathic generalized epilepsies associated with CACNA1H functional variants.Spatial association of the Cav1.2 calcium channel with α5β1-integrin.NMP-7 inhibits chronic inflammatory and neuropathic pain via block of Cav3.2 T-type calcium channels and activation of CB2 receptors.Functional roles of cytoplasmic loops and pore lining transmembrane helices in the voltage-dependent inactivation of HVA calcium channels.Functional interactions between presynaptic calcium channels and the neurotransmitter release machinery.Small organic molecule disruptors of Cav3.2 - USP5 interactions reverse inflammatory and neuropathic pain.Calmodulin lobotomized: novel insights into calcium regulation of voltage-gated calcium channels.Neuroprotection against traumatic brain injury by a peptide derived from the collapsin response mediator protein 2 (CRMP2)Solution NMR and calorimetric analysis of Rem2 binding to the Ca2+ channel β4 subunit: a low affinity interaction is required for inhibition of Cav2.1 Ca2+ currents
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