Voltage-gated calcium channels (VGCC) are key to many biological functions. Entry of Ca2+ into cells is essential for initiating or modulating important processes such as secretion, cell motility, and gene transcription. In the retina and other neural tissues, one of the major roles of Ca2+-entry is to stimulate or regulate exocytosis of synaptic vesicles, without which synaptic transmission is impaired. This review will address the special properties of one L-type VGCC, CaV1.4, with particular emphasis on its role in transmission of visual signals from rod and cone photoreceptors (hereafter called “photoreceptors,” to the exclusion of intrinsically photoreceptive retinal ganglion cells) to the second-order retinal neurons, and the patholog...
Light-dependent conductance changes of voltage-gated Cav1.4 channels regulate neurotransmitter relea...
Retinal signal transmission depends on the activity of high voltage–gated l-type calcium channels in...
Unidentified pathogenetic mechanisms and genetic and clinical heterogeneity represent critical facto...
L-type voltage-gated calcium channels (LTCCs) regulate tonic neurotransmitter release from sensory n...
Several studies have shown the importance of calcium channels in the development and/or maturation o...
α2δ-4 is an auxiliary subunit of voltage-gated Cav1.4 L-type channels that regulate the development ...
α2δ-4 is an auxiliary subunit of voltage-gated Cav1.4 L-type channels that regulate the development ...
α2δ-4 is an auxiliary subunit of voltage-gated Cav1.4 L-type channels that regulate the development ...
The Cacna1f gene encodes the α1F subunit of an L-type voltage-gated calcium channel, Cav1.4. In phot...
Incomplete X-linked congenital stationary night blind-ness (CSNB2) is a recessive, nonprogressive vi...
Neural circuit wiring relies on selective synapse formation whereby a presynaptic release apparatus ...
Retinitis pigmentosa is an inherited blinding disorder characterized by progressive degeneration and...
PURPOSE: In a spontaneous mutant substrain of C57BL/10 mice, severely affected retinal ribbon-type s...
Light-dependent conductance changes of voltage-gated Cav1.4 channels regulate neurotransmitter relea...
This study provides novel insights to the function and regulation of Cav1.4 LTCCs. In the first par...
Light-dependent conductance changes of voltage-gated Cav1.4 channels regulate neurotransmitter relea...
Retinal signal transmission depends on the activity of high voltage–gated l-type calcium channels in...
Unidentified pathogenetic mechanisms and genetic and clinical heterogeneity represent critical facto...
L-type voltage-gated calcium channels (LTCCs) regulate tonic neurotransmitter release from sensory n...
Several studies have shown the importance of calcium channels in the development and/or maturation o...
α2δ-4 is an auxiliary subunit of voltage-gated Cav1.4 L-type channels that regulate the development ...
α2δ-4 is an auxiliary subunit of voltage-gated Cav1.4 L-type channels that regulate the development ...
α2δ-4 is an auxiliary subunit of voltage-gated Cav1.4 L-type channels that regulate the development ...
The Cacna1f gene encodes the α1F subunit of an L-type voltage-gated calcium channel, Cav1.4. In phot...
Incomplete X-linked congenital stationary night blind-ness (CSNB2) is a recessive, nonprogressive vi...
Neural circuit wiring relies on selective synapse formation whereby a presynaptic release apparatus ...
Retinitis pigmentosa is an inherited blinding disorder characterized by progressive degeneration and...
PURPOSE: In a spontaneous mutant substrain of C57BL/10 mice, severely affected retinal ribbon-type s...
Light-dependent conductance changes of voltage-gated Cav1.4 channels regulate neurotransmitter relea...
This study provides novel insights to the function and regulation of Cav1.4 LTCCs. In the first par...
Light-dependent conductance changes of voltage-gated Cav1.4 channels regulate neurotransmitter relea...
Retinal signal transmission depends on the activity of high voltage–gated l-type calcium channels in...
Unidentified pathogenetic mechanisms and genetic and clinical heterogeneity represent critical facto...