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CACNA1S gene

Known as: CACNL1A3, calcium voltage-gated channel subunit alpha1 S, CALCIUM CHANNEL, SKELETAL MUSCLE DIHYDROPYRIDINE-SENSITIVE, ALPHA-1 SUBUNIT 
National Institutes of Health

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CACNA1E gene

Papers overview

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2014
2014
Hot on the trail of "I know it when I see it!".
• Volume 118 • Number 2 www.anesthesia-analgesia.org 243 Copyright © 2014 International Anesthesia Research Society DOI: 10.1213… 
2008
2008
An Arg1239His mutation of the CACNL1A3 gene in a Korean family with hypokalemic periodic paralysis
= Abstract = Familial hypokalemic periodic paralysis (hypoPP is a rare inherited channelopathy that often presents with episodic… 
2007
2007
Gating of the HypoPP-1 mutations: II. Effects of a calcium-channel agonist BayK 8644
L-type calcium-channel mutations causing hypokalemic periodic paralysis type 1 (HypoPP-1) have pronounced “loss-of-function… 
2002
2002
Association Of Snp Of Dihydropyridine Receptor Gene (cacnl1a3) With Thyrotoxic Periodic Paralysis (tpp)
1996
1996
The structure of the gene encoding the human skeletal muscle alpha 1 subunit of the dihydropyridine-sensitive L-type calcium channel (CACNL1A3).
The structure of the gene encoding the human skeletal muscle alpha 1 subunit (CACNL1A3) of the dihydropyridine-sensitive voltage… 
1996
1996
Fine mapping of the autosomal recessive retinitis pigmentosa locus (RP12) on chromosome 1q; exclusion of the phosducin gene (PDC).
In a previous study on a large pedigree from a genetically isolated population in the Netherlands, we localized a gene for… 
1994
1994
Cloning of the human skeletal muscle alpha 1 subunit of the dihydropyridine-sensitive L-type calcium channel (CACNL1A3).
Skeletal muscle contraction is initiated by release of calcium stored in the sarcoplasmic reticulum in response to membrane… 
1994
1994
Refined localization of the alpha 1-subunit of the skeletal muscle L-type voltage-dependent calcium channel (CACNL1A3) to human chromosome 1q32 by in situ hybridization.
We isolated and partially sequenced a cosmid clone containing the human skeletal muscle L-type voltage-dependent calcium channel… 
1994
1994
Confirmation of linkage of Hypokalemic periodic paralysis to chromosome 1q31-32: Further evidence supporting CACNL1A3 as a candidate gene
Hypokalemic periodic paralysis (HOKPP; MIM 170400) is one entity of a series of periodic paralyses characterized by episodic… 
1993
1993
Assignment of the human gene for the alpha 1 subunit of the skeletal muscle DHP-sensitive Ca2+ channel (CACNL1A3) to chromosome 1q31-q32.
A human clone corresponding to the gene encoding the alpha 1 subunit of the skeletal muscle dihydropyridine-sensitive calcium… 
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