Channelopathies in Cav1.1, Cav1.3, and Cav1.4 voltage-gated L-type Ca2+ channels. - Wikidata - wikimedia - TriplyDB

Channelopathies in Cav1.1, Cav1.3, and Cav1.4 voltage-gated L-type Ca2+ channels.

Channelopathies in Cav1.1, Cav1.3, and Cav1.4 voltage-gated L-type Ca2+ channels.

http://www.wikidata.org/entity/Q37705122

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Ca2+-dependent modulation of voltage-gated Ca2+ channels Loss of Ca(v)1.3 (CACNA1D) function in a human channelopathy with bradycardia and congenital deafness Ion channels and transporters in lymphocyte function and immunity The dynamic architecture of photoreceptor ribbon synapses: cytoskeletal, extracellular matrix, and intramembrane proteins Towards a Unified Theory of Calmodulin Regulation (Calmodulation) of Voltage-Gated Calcium and Sodium Channels CaV channels and cancer: canonical functions indicate benefits of repurposed drugs as cancer therapeutics Decreased temporal precision of neuronal signaling as a candidate mechanism of auditory processing disorder Voltage-Gated Cav1 Channels in Disorders of Vision and Hearing Voltage-gated calcium channels Emerging evidence for specific neuronal functions of auxiliary calcium channel α₂δ subunits.Dysregulation of Ca(v)1.4 channels disrupts the maturation of photoreceptor synaptic ribbons in congenital stationary night blindness type 2 Age-related homeostatic midchannel proteolysis of neuronal L-type voltage-gated Ca²⁺ channels.Spectrum of Cav1.4 dysfunction in congenital stationary night blindness type 2 L-type calcium channels play a critical role in maintaining lens transparency by regulating phosphorylation of aquaporin-0 and myosin light chain and expression of connexins Channelopathies: summary of the hot topic keynotes session Functional properties of a newly identified C-terminal splice variant of Cav1.3 L-type Ca2+ channels Calcium channel blocking as a therapeutic strategy for Alzheimer's disease: the case for isradipine.Calcineurin Controls Voltage-Dependent-Inactivation (VDI) of the Normal and Timothy Cardiac Channels.Levels of Ca(V)1.2 L-Type Ca(2+) Channels Peak in the First Two Weeks in Rat Hippocampus Whereas Ca(V)1.3 Channels Steadily Increase through Development.The expression of whirlin and Cav1.3α₁ is mutually independent in photoreceptors.Ion channels in innate and adaptive immunity GDF-15 enhances intracellular Ca2+ by increasing Cav1.3 expression in rat cerebellar granule neurons.What can naturally occurring mutations tell us about Ca(v)1.x channel function?A naturally occurring truncated Cav1.2 α1-subunit inhibits Ca2+ current in A7r5 cells.Orais and STIMs: physiological mechanisms and disease Photoreceptor degeneration in two mouse models for congenital stationary night blindness type 2 Presynaptic [Ca(2+)] and GCAPs: aspects on the structure and function of photoreceptor ribbon synapses.How voltage-gated calcium channels gate forms of homeostatic synaptic plasticity Signaling complexes of voltage-gated calcium channels Novel insights into the pathomechanisms of skeletal muscle channelopathies.Neuronal P/Q-type calcium channel dysfunction in inherited disorders of the CNS.EF hand-mediated Ca- and cGMP-signaling in photoreceptor synaptic terminals.L-type CaV1.2 calcium channels: from in vitro findings to in vivo function.Biophysics, pathophysiology, and pharmacology of ion channel gating pores.Muscle weakness in myotonic dystrophy associated with misregulated splicing and altered gating of Ca(V)1.1 calcium channel.Decalmodulation of Cav1 channels by CaBPs.C-terminal modulatory domain controls coupling of voltage-sensing to pore opening in Cav1.3 L-type Ca(2+) channels.Transcriptional regulation of voltage-gated Ca2+ channels.Retinal characteristics of the congenital disorder of glycosylation PMM2-CDG.Homeostatic synaptic depression is achieved through a regulated decrease in presynaptic calcium channel abundance.

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Channelopathies in Cav1.1, Cav1.3, and Cav1.4 voltage-gated L-type Ca2+ channels.

http://www.wikidata.org/entity/Q37705122

description

article científic

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article scientifique

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articolo scientifico

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artigo científico

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bilimsel makale

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scientific article published on 07 March 2010

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vedecký článok

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vetenskaplig artikel

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videnskabelig artikel

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vědecký článek

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name

Channelopathies in Cav1.1, Cav1.3, and Cav1.4 voltage-gated L-type Ca2+ channels.

@en

Channelopathies in Cav1.1, Cav1.3, and Cav1.4 voltage-gated L-type Ca2+ channels.

@nl

type

label

Channelopathies in Cav1.1, Cav1.3, and Cav1.4 voltage-gated L-type Ca2+ channels.

@en

Channelopathies in Cav1.1, Cav1.3, and Cav1.4 voltage-gated L-type Ca2+ channels.

@nl

prefLabel

Channelopathies in Cav1.1, Cav1.3, and Cav1.4 voltage-gated L-type Ca2+ channels.

@en

Channelopathies in Cav1.1, Cav1.3, and Cav1.4 voltage-gated L-type Ca2+ channels.

@nl

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Pfluegers Archiv

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Channelopathies in Cav1.1, Cav1.3, and Cav1.4 voltage-gated L-type Ca2+ channels.

@en

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Alexandra Koschak

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Jörg Striessnig

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P2860

A CACNA1F mutation identified in an X-linked retinal disorder shifts the voltage dependence of Cav1.4 channel activation.

Essential role of Ca2+-binding protein 4, a Cav1.4 channel regulator, in photoreceptor synaptic function.

Mutation in the auxiliary calcium-channel subunit CACNA2D4 causes autosomal recessive cone dystrophy

The electroretinographic diagnosis of the incomplete form of congenital stationary night blindness

Severe arrhythmia disorder caused by cardiac L-type calcium channel mutations

Muscle channelopathies and critical points in functional and genetic studies.

Malignant-hyperthermia susceptibility is associated with a mutation of the alpha 1-subunit of the human dihydropyridine-sensitive L-type voltage-dependent calcium-channel receptor in skeletal muscle

Ca(V)1.2 calcium channel dysfunction causes a multisystem disorder including arrhythmia and autism

Clinical variability among patients with incomplete X-linked congenital stationary night blindness and a founder mutation in CACNA1F

Cav1.4alpha1 subunits can form slowly inactivating dihydropyridine-sensitive L-type Ca2+ channels lacking Ca2+-dependent inactivation

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361-374

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10.1007/S00424-010-0800-X

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Hanno Jörn Bolz

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2010-03-07T00:00:00Z

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2010-07-01T00:00:00Z

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