calcium voltage-gated channel subunit alpha1 S ; Homo sapiens






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1 1656465 Identification of 1,4-dihydropyridine binding regions within the alpha 1 subunit of skeletal muscle Ca2+ channels by photoaffinity labeling with diazipine. Proc Natl Acad Sci U S A 1991 Oct 15 1
2 1666652 Differential effects of ryanodine and tetracaine on charge movement and calcium transients in frog skeletal muscle. J Physiol 1991 1
3 1716078 Effects of calcium-free solution, calcium antagonists, and the calcium agonist BAY K 8644 on mechanical responses of skeletal muscle from patients susceptible to malignant hyperthermia. Anesthesiology 1991 Sep 2
4 2348398 The effect of phenylglyoxal on contraction and intramembrane charge movement in frog skeletal muscle. J Physiol 1990 Feb 1
5 2408616 Nitrendipine potentiates Bay k 8644-induced contraction of isolated porcine coronary artery: evidence for functionally distinct dihydropyridine receptor subtypes. Biochem Biophys Res Commun 1985 May 16 2
6 2436829 Excitation-contraction coupling in cardiac and vascular smooth muscle: modification by calcium-entry blockade. Circulation 1987 Jun 2
7 2455516 Voltage-dependence of nitrendipine provides direct evidence for dihydropyridine receptor coupling to calcium channels in intact cat adrenals. Biochem Biophys Res Commun 1988 Jun 30 1
8 2545137 32,000-Dalton subunit of the 1,4-dihydropyridine receptor. Ann N Y Acad Sci 1989 1
9 3706782 Immunohistochemical localization of the MHS-5 antigen in principal cells of human seminal vesicle epithelium. Anat Rec 1986 Apr 2
10 7629172 Phosphorylation of dihydropyridine receptor II-III loop peptide regulates skeletal muscle calcium release channel function. Evidence for an essential role of the beta-OH group of Ser687. J Biol Chem 1995 Aug 4 2
11 7777513 Full-length myotonin protein kinase (72 kDa) displays serine kinase activity. Proc Natl Acad Sci U S A 1995 Jun 6 1
12 7847370 Hypokalemic periodic paralysis and the dihydropyridine receptor (CACNL1A3): genotype/phenotype correlations for two predominant mutations and evidence for the absence of a founder effect in 16 caucasian families. Am J Hum Genet 1995 Feb 3
13 7865878 Molecular organization of transverse tubule/sarcoplasmic reticulum junctions during development of excitation-contraction coupling in skeletal muscle. Mol Biol Cell 1994 Oct 2
14 7916735 Assignment of the human gene for the alpha 1 subunit of the skeletal muscle DHP-sensitive Ca2+ channel (CACNL1A3) to chromosome 1q31-q32. Genomics 1993 Jan 1
15 7959693 Genetic heterogeneity in hypokalemic periodic paralysis (hypoPP). Hum Genet 1994 Nov 2
16 8004673 Dihydropyridine receptor mutations cause hypokalemic periodic paralysis. Cell 1994 Jun 17 3
17 8012389 Mapping of the hypokalaemic periodic paralysis (HypoPP) locus to chromosome 1q31-32 in three European families. Nat Genet 1994 Mar 1
18 8169595 Relationship of calcium transients to calcium currents and charge movements in myotubes expressing skeletal and cardiac dihydropyridine receptors. J Gen Physiol 1994 Jan 7
19 8188298 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. Genomics 1994 Feb 2
20 8838325 The structure of the gene encoding the human skeletal muscle alpha 1 subunit of the dihydropyridine-sensitive L-type calcium channel (CACNL1A3). Genomics 1996 Feb 1 1
21 9199552 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. Am J Hum Genet 1997 Jun 2
22 9514900 Fluorescent probing with felodipine of the dihydropyridine receptor and its interaction with the ryanodine receptor calcium release channel. Biochem Biophys Res Commun 1998 Mar 17 15
23 9737952 Localization in the II-III loop of the dihydropyridine receptor of a sequence critical for excitation-contraction coupling. J Biol Chem 1998 Sep 25 1
24 9769415 The influence of caffeine on intramembrane charge movements in intact frog striated muscle. J Physiol 1998 Nov 1 2
25 9852570 Gating of the L-type Ca channel in human skeletal myotubes: an activation defect caused by the hypokalemic periodic paralysis mutation R528H. J Neurosci 1998 Dec 15 1
26 10427100 Three-dimensional location of the imperatoxin A binding site on the ryanodine receptor. J Cell Biol 1999 Jul 26 4
27 10550622 Relocalization of the calcium gradient and a dihydropyridine receptor is involved in upward bending by bulging of Chara protonemata, but not in downward bending by bowing of Chara rhizoids. Planta 1999 Oct 3
28 10599760 A novel sodium channel mutation in a family with hypokalemic periodic paralysis. Neurology 1999 Dec 10 2
29 11102465 The human skeletal muscle Na channel mutation R669H associated with hypokalemic periodic paralysis enhances slow inactivation. J Neurosci 2000 Dec 1 3
30 11353725 Hypokalaemic periodic paralysis type 2 caused by mutations at codon 672 in the muscle sodium channel gene SCN4A. Brain 2001 Jun 2
31 11361129 Structure and targeting of RyR1: implications from fusion of green fluorescent protein at the amino-terminal. Arch Biochem Biophys 2001 Apr 1 2
32 11600671 Calcium waves induced by hypertonic solutions in intact frog skeletal muscle fibres. J Physiol 2001 Oct 15 6
33 12037132 A mechanism for both capacitative Ca(2+) entry and excitation-contraction coupled Ca(2+) release by the sarcoplasmic reticulum of skeletal muscle cells. Exp Biol Med (Maywood) 2002 Jun 1
34 12736539 Clinical and molecular analysis of chinese patients with thyrotoxic periodic paralysis. Eur Neurol 2003 3
35 13679303 Conformational coupling of DHPR and RyR1 in skeletal myotubes is influenced by long-range allosterism: evidence for a negative regulatory module. Am J Physiol Cell Physiol 2004 Jan 1
36 15098604 A family of hypokalemic periodic paralysis with CACNA1S gene mutation showing incomplete penetrance in women. Intern Med 2004 Mar 1
37 15185439 [From gene to diseases; hypokalemic periodic paralysis]. Ned Tijdschr Geneeskd 2004 May 22 3
38 15507442 The C-terminal residues in the alpha-interacting domain (AID) helix anchor CaV beta subunit interaction and modulation of CaV2.3 channels. J Biol Chem 2005 Jan 7 6
39 15530142 Regulation of skeletal ryanodine receptors by dihydropyridine receptor II-III loop C-region peptides: relief of Mg2+ inhibition. Biochem J 2005 Apr 15 1
40 15596759 New mutations of SCN4A cause a potassium-sensitive normokalemic periodic paralysis. Neurology 2004 Dec 14 1
41 15726306 Novel CACNA1S mutation causes autosomal dominant hypokalemic periodic paralysis in a Chinese family. J Mol Med (Berl) 2005 Mar 1
42 15793008 Sites of proteolytic processing and noncovalent association of the distal C-terminal domain of CaV1.1 channels in skeletal muscle. Proc Natl Acad Sci U S A 2005 Apr 5 1
43 16120606 Ryanodine receptor type 1 (RyR1) mutations C4958S and C4961S reveal excitation-coupled calcium entry (ECCE) is independent of sarcoplasmic reticulum store depletion. J Biol Chem 2005 Nov 4 1
44 16675661 Allosteric interactions required for high-affinity binding of dihydropyridine antagonists to Ca(V)1.1 Channels are modulated by calcium in the pore. Mol Pharmacol 2006 Aug 2
45 16767662 [R1239H mutation of CACNA1S gene in a Chinese family with hypokalaemic periodic paralysis]. Zhonghua Yi Xue Yi Chuan Xue Za Zhi 2006 Jun 1
46 17042924 Structural and functional characterization of interactions between the dihydropyridine receptor II-III loop and the ryanodine receptor. Clin Exp Pharmacol Physiol 2006 Nov 1
47 17556873 Hypokalemic periodic paralysis in a patient with acquired growth hormone deficiency. J Endocrinol Invest 2007 Apr 3
48 17587224 Progressive muscle atrophy with hypokalemic periodic paralysis and calcium channel mutation. Muscle Nerve 2008 Jan 1
49 17591984 A Na+ channel mutation linked to hypokalemic periodic paralysis exposes a proton-selective gating pore. J Gen Physiol 2007 Jul 1
50 18162704 The genotype and clinical phenotype of Korean patients with familial hypokalemic periodic paralysis. J Korean Med Sci 2007 Dec 1