(Q37371706)

20 August 2017

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title

Alternative splicing of voltage-gated calcium channels: from molecular biology to disease (English)

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alternative mRNA splicing, via spliceosome

20 August 2017

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Ping Liao

1

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20 August 2017

Heng Yu Zhang

series ordinal

2

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20 August 2017

Tuck Wah Soong

series ordinal

3

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20 August 2017

publication date

17 January 2009

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20 August 2017

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20 August 2017

volume

458

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20 August 2017

issue

3

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20 August 2017

page(s)

481-487

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Calcium channel blockers and pain therapy

20 August 2017

cites work

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FS00424-009-0635-5

Alternatively spliced IS6 segments of the alpha 1C gene determine the tissue-specific dihydropyridine sensitivity of cardiac and vascular smooth muscle L-type Ca2+ channels

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FS00424-009-0635-5

Differential role of N-type calcium channel splice isoforms in pain.

21 January 2018

1 reference

12 December 2020

Silencing of the Cav3.2 T-type calcium channel gene in sensory neurons demonstrates its major role in nociception.

1 reference

12 December 2020

Functional embryonic cardiomyocytes after disruption of the L-type alpha1C (Cav1.2) calcium channel gene in the mouse.

1 reference

12 December 2020

Direct binding of G-protein betagamma complex to voltage-dependent calcium channels

1 reference

12 December 2020

Thalamic Control of Visceral Nociception Mediated by T-Type Ca 2+ Channels

1 reference

12 December 2020

Crosstalk between G proteins and protein kinase C mediated by the calcium channel alpha1 subunit.

1 reference

12 December 2020

Attenuated neuropathic pain in Cav3.1 null mice.

1 reference

12 December 2020

Structure and functional expression of a member of the low voltage-activated calcium channel family

1 reference

12 December 2020

Cell-type-specific alternative splicing in spinocerebellar ataxia type 6.

1 reference

12 December 2020

Structure and alternative splicing of the gene encoding alpha1G, a human brain T calcium channel alpha1 subunit

1 reference

12 December 2020

Voltage window for sustained elevation of cytosolic calcium in smooth muscle cells

1 reference

12 December 2020

Autosomal dominant cerebellar ataxia (SCA6) associated with small polyglutamine expansions in the alpha 1A-voltage-dependent calcium channel

1 reference

12 December 2020

A profile of alternative RNA splicing and transcript variation of CACNA1H, a human T-channel gene candidate for idiopathic generalized epilepsies

1 reference

12 December 2020

Molecular analysis and functional expression of the human type E neuronal Ca2+ channel alpha 1 subunit

1 reference

12 December 2020

Splicing for alternative structures of Cav1.2 Ca2+ channels in cardiac and smooth muscles

1 reference

12 December 2020

Atherosclerosis-related molecular alteration of the human CaV1.2 calcium channel alpha1C subunit

1 reference

12 December 2020

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

1 reference

12 December 2020

A summary of 20 CACNA1F mutations identified in 36 families with incomplete X-linked congenital stationary night blindness, and characterization of splice variants

1 reference

12 December 2020

Transcript scanning reveals novel and extensive splice variations in human l-type voltage-gated calcium channel, Cav1.2 alpha1 subunit.

1 reference

12 December 2020

CACNA1H mutations in autism spectrum disorders.

1 reference

12 December 2020

Novel molecular mechanism involving alpha1D (Cav1.3) L-type calcium channel in autoimmune-associated sinus bradycardia.

1 reference

12 December 2020

Structure and alternative splicing of the gene encoding alpha1I, a human brain T calcium channel alpha1 subunit

1 reference

12 December 2020

Genomic structure of human L-type Ca2+ channel

1 reference

12 December 2020

Mutually exclusive exon splicing of the cardiac calcium channel alpha 1 subunit gene generates developmentally regulated isoforms in the rat heart

1 reference

12 December 2020

Abnormal coronary function in mice deficient in alpha1H T-type Ca2+ channels

1 reference

12 December 2020

Familial hemiplegic migraine and episodic ataxia type-2 are caused by mutations in the Ca2+ channel gene CACNL1A4

1 reference

12 December 2020

Molecular basis of Ca(v)2.3 calcium channels in rat nociceptive neurons

1 reference

12 December 2020

L-type Ca2+ channel alpha 1c subunit isoform switching in failing human ventricular myocardium

1 reference

12 December 2020

Systematic identification of splice variants in human P/Q-type channel alpha1(2.1) subunits: implications for current density and Ca2+-dependent inactivation

1 reference

12 December 2020

Altered pain responses in mice lacking alpha 1E subunit of the voltage-dependent Ca2+ channel.

1 reference

12 December 2020

G protein-gated inhibitory module of N-type (ca(v)2.2) ca2+ channels

1 reference

12 December 2020

Differential splicing patterns of L-type calcium channel Cav1.2 subunit in hearts of Spontaneously Hypertensive Rats and Wistar Kyoto Rats

1 reference

12 December 2020

Congenital deafness and sinoatrial node dysfunction in mice lacking class D L-type Ca2+ channels

1 reference

12 December 2020

Loss-of-function mutations in a calcium-channel alpha1-subunit gene in Xp11.23 cause incomplete X-linked congenital stationary night blindness

1 reference

12 December 2020

Japanese families with autosomal dominant pure cerebellar ataxia map to chromosome 19p13.1-p13.2 and are strongly associated with mild CAG expansions in the spinocerebellar ataxia type 6 gene in chromosome 19p13.1

1 reference

12 December 2020

A novel Ca(V)1.2 N terminus expressed in smooth muscle cells of resistance size arteries modifies channel regulation by auxiliary subunits

1 reference

12 December 2020

A mechanism for exon skipping caused by nonsense or missense mutations in BRCA1 and other genes

1 reference

12 December 2020

Alternative splicing controls G protein-dependent inhibition of N-type calcium channels in nociceptors

1 reference

12 December 2020

Mapping of the hypokalaemic periodic paralysis (HypoPP) locus to chromosome 1q31-32 in three European families

1 reference

12 December 2020

Cell-specific alternative splicing increases calcium channel current density in the pain pathway

1 reference

12 December 2020

Reemergence of the fetal pattern of L-type calcium channel gene expression in non infarcted myocardium during left ventricular remodeling

1 reference

12 December 2020

Alternative splicing as a molecular switch for Ca2+/calmodulin-dependent facilitation of P/Q-type Ca2+ channels.

1 reference

12 December 2020

Smooth muscle-selective alternatively spliced exon generates functional variation in Cav1.2 calcium channels

1 reference

12 December 2020

Alternative splicing of the rat Ca(v)3.3 T-type calcium channel gene produces variants with distinct functional properties(1).

1 reference

12 December 2020

Structure-functional diversity of human L-type Ca2+ channel: perspectives for new pharmacological targets

1 reference

12 December 2020

Association between genetic variation of CACNA1H and childhood absence epilepsy

1 reference

12 December 2020

Regulation of calcium channel alpha(1A) subunit splice variant mRNAs in kainate-induced temporal lobe epilepsy

1 reference

12 December 2020

A smooth muscle Cav1.2 calcium channel splice variant underlies hyperpolarized window current and enhanced state-dependent inhibition by nifedipine

1 reference

12 December 2020

X linked cone-rod dystrophy, CORDX3, is caused by a mutation in the CACNA1F gene

1 reference

12 December 2020

Profiling the array of Ca(v)3.1 variants from the human T-type calcium channel gene CACNA1G: alternative structures, developmental expression, and biophysical variations

1 reference

12 December 2020

Dihydropyridine receptor mutations cause hypokalemic periodic paralysis

1 reference

12 December 2020

Hair cell-specific splicing of mRNA for the alpha1D subunit of voltage-gated Ca2+ channels in the chicken's cochlea

1 reference

12 December 2020

Alternative splicing of the Ca(v)1.3 channel IQ domain, a molecular switch for Ca2+-dependent inactivation within auditory hair cells

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

Functional impact of alternative splicing of human T-type Cav3.3 calcium channels

1 reference

12 December 2020

Dynamic remodeling of K+ and Ca2+ currents in cells that survived in the epicardial border zone of canine healed infarcted heart

1 reference

12 December 2020

Sensory neuron N-type calcium currents are inhibited by both voltage-dependent and -independent mechanisms

1 reference

12 December 2020

Substance P and somatostatin inhibit calcium channels in rat sympathetic neurons via different G protein pathwavs

1 reference

12 December 2020

Bradycardia and slowing of the atrioventricular conduction in mice lacking CaV3.1/alpha1G T-type calcium channels

1 reference

12 December 2020

An L-type calcium-channel gene mutated in incomplete X-linked congenital stationary night blindness

1 reference

12 December 2020

10.1007/S00424-009-0635-5

Identifiers

DOI

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20 August 2017

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