Gerald W Zamponi, Philippe Lory, Edward Perez-Reyes. Pflugers Arch 2010
Times Cited: 118
Times Cited: 118
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Molecular physiology of low-voltage-activated t-type calcium channels.
Edward Perez-Reyes. Physiol Rev 2003
Edward Perez-Reyes. Physiol Rev 2003
31
Voltage-gated calcium channels and idiopathic generalized epilepsies.
Houman Khosravani, Gerald W Zamponi. Physiol Rev 2006
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Extended spectrum of idiopathic generalized epilepsies associated with CACNA1H functional variants.
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Differential distribution of three members of a gene family encoding low voltage-activated (T-type) calcium channels.
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A Cav3.2 T-type calcium channel point mutation has splice-variant-specific effects on function and segregates with seizure expression in a polygenic rat model of absence epilepsy.
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Gating effects of mutations in the Cav3.2 T-type calcium channel associated with childhood absence epilepsy.
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Genetic enhancement of thalamocortical network activity by elevating alpha 1g-mediated low-voltage-activated calcium current induces pure absence epilepsy.
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Lack of the burst firing of thalamocortical relay neurons and resistance to absence seizures in mice lacking alpha(1G) T-type Ca(2+) channels.
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Silencing of the Cav3.2 T-type calcium channel gene in sensory neurons demonstrates its major role in nociception.
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A Ca(v)3.2/syntaxin-1A signaling complex controls T-type channel activity and low-threshold exocytosis.
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The I-II loop controls plasma membrane expression and gating of Ca(v)3.2 T-type Ca2+ channels: a paradigm for childhood absence epilepsy mutations.
Iuliia Vitko, Isabelle Bidaud, Juan Manuel Arias, Alexandre Mezghrani, Philippe Lory, Edward Perez-Reyes. J Neurosci 2007
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Transcriptional upregulation of Cav3.2 mediates epileptogenesis in the pilocarpine model of epilepsy.
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Presynaptic Cav3.2 channels regulate excitatory neurotransmission in nociceptive dorsal horn neurons.
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Selective increase in T-type calcium conductance of reticular thalamic neurons in a rat model of absence epilepsy.
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Upregulation of the T-type calcium current in small rat sensory neurons after chronic constrictive injury of the sciatic nerve.
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T-type calcium channels contribute to colonic hypersensitivity in a rat model of irritable bowel syndrome.
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Cloning and expression of a novel member of the low voltage-activated T-type calcium channel family.
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Familial hemiplegic migraine and episodic ataxia type-2 are caused by mutations in the Ca2+ channel gene CACNL1A4.
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TTA-P2 is a potent and selective blocker of T-type calcium channels in rat sensory neurons and a novel antinociceptive agent.
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Mechanisms by which a CACNA1H mutation in epilepsy patients increases seizure susceptibility.
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The Physiology, Pathology, and Pharmacology of Voltage-Gated Calcium Channels and Their Future Therapeutic Potential.
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