Neurotransmitter release, neuronal excitation, and a whole variety of other neuronal functions are controlled by the intralextra cellular ca2+ gradient. The major pathway for entry of ca2+ into the excitable cells is mediated by voltage-gated ca2+ channels. Several functional subclasses of voltage-dependent ca2+ channels have been identified, based on their pharmacological, biophysical properties, and molecular cloning. Recently, three human diseases (familial hemiplegic migraine, episodic ataxia type 2, and spinocerebellar ataxia 6) were added to the growing list of ion-channel disorders, all caused by different mutations in the P/Qtype ca2+ channel α1 subunit. Molecular analysis of the ca2+ channelopathies will provide new insights into t...
<div><p>Mutations in the <i>CACNA1A</i> gene, encoding the pore-forming Ca<sub>V</sub>2.1 (P/Q-type)...
This thesis describes clinical, molecular genetic and electrophysiological studies in two dominantly...
One of the outstanding developments in clinical neurology has been the identification of ion channel...
AbstractVoltage-gated calcium channels (VGCCs) mediate calcium entry into excitable cells in respons...
AbstractVoltage-gated Ca2+ channels allow for Ca2+-dependent intracellular signaling by directly med...
Mutations in the CACNA1A gene that encodes the pore-forming alpha(1) subunit of human voltage-gated ...
Studies on the genetic forms of epilepsy, chronic pain, and migraine caused by mutations in ion chan...
International audienceVoltage-dependent calcium channels constitute one of the main pathways of calc...
Several inherited human neurological disorders can be caused by mutations in genes encoding Ca2+ cha...
Mutations in the CACNA1A gene, encoding the pore-forming CaV2.1 (P/Q-type) channel α1A subunit, resu...
Mutations in the CACNA1A gene, encoding the pore-forming Ca2.1 (P/Q-type) channel α subunit, result ...
In the past few years several spontaneous or engineered mouse models with mutations in Ca2+ channel ...
In the last decade, advances in molecular genetics and cellular electrophysiology have increased our...
Studies of genetic forms of epilepsy, chronic pain, and migraine caused by mutations in ion channels...
P/Q-type voltage-gated calcium channels are essential for Ca2+ influx and neurotransmitter release i...
<div><p>Mutations in the <i>CACNA1A</i> gene, encoding the pore-forming Ca<sub>V</sub>2.1 (P/Q-type)...
This thesis describes clinical, molecular genetic and electrophysiological studies in two dominantly...
One of the outstanding developments in clinical neurology has been the identification of ion channel...
AbstractVoltage-gated calcium channels (VGCCs) mediate calcium entry into excitable cells in respons...
AbstractVoltage-gated Ca2+ channels allow for Ca2+-dependent intracellular signaling by directly med...
Mutations in the CACNA1A gene that encodes the pore-forming alpha(1) subunit of human voltage-gated ...
Studies on the genetic forms of epilepsy, chronic pain, and migraine caused by mutations in ion chan...
International audienceVoltage-dependent calcium channels constitute one of the main pathways of calc...
Several inherited human neurological disorders can be caused by mutations in genes encoding Ca2+ cha...
Mutations in the CACNA1A gene, encoding the pore-forming CaV2.1 (P/Q-type) channel α1A subunit, resu...
Mutations in the CACNA1A gene, encoding the pore-forming Ca2.1 (P/Q-type) channel α subunit, result ...
In the past few years several spontaneous or engineered mouse models with mutations in Ca2+ channel ...
In the last decade, advances in molecular genetics and cellular electrophysiology have increased our...
Studies of genetic forms of epilepsy, chronic pain, and migraine caused by mutations in ion channels...
P/Q-type voltage-gated calcium channels are essential for Ca2+ influx and neurotransmitter release i...
<div><p>Mutations in the <i>CACNA1A</i> gene, encoding the pore-forming Ca<sub>V</sub>2.1 (P/Q-type)...
This thesis describes clinical, molecular genetic and electrophysiological studies in two dominantly...
One of the outstanding developments in clinical neurology has been the identification of ion channel...