sodium voltage-gated channel alpha subunit 4 ; Homo sapiens






216 Article(s)
Download
PMID
Title
Journal
Pub. Date
#Total Relationship(s)
51 15072700 Absence of ion channels CACN1AS and SCN4A mutations in thyrotoxic hypokalemic periodic paralysis. Thyroid 2004 Mar 1
52 15185439 [From gene to diseases; hypokalemic periodic paralysis]. Ned Tijdschr Geneeskd 2004 May 22 3
53 15498118 [Effect of sodium butyrate in combination with ATRA on the proliferation/differentiation of MDS cell line SKM-1]. Zhongguo Shi Yan Xue Ye Xue Za Zhi 2004 Oct 4
54 15557532 SCN4A-associated hypokalemic periodic paralysis merits a trial of acetazolamide. Neurology 2004 Nov 23 1
55 15562257 State-dependent mibefradil block of Na+ channels. Mol Pharmacol 2004 Dec 1
56 15587392 The effect of sodium butyrate in combination with ATRA on the proliferation/differentiation of SKM-1. J Huazhong Univ Sci Technolog Med Sci 2004 3
57 15596759 New mutations of SCN4A cause a potassium-sensitive normokalemic periodic paralysis. Neurology 2004 Dec 14 3
58 15642860 Familial periodic paralysis and Charcot-Marie-Tooth disease in a 7-generation family. Arch Neurol 2005 Jan 1
59 15864116 Preferred mexiletine block of human sodium channels with IVS4 mutations and its pH-dependence. Pharmacogenet Genomics 2005 Apr 1
60 16174788 Molecular modeling of local anesthetic drug binding by voltage-gated sodium channels. Mol Pharmacol 2005 Dec 2
61 16713241 Recombinant human voltage-gated skeletal muscle sodium channels are pharmacologically functional in planar lipid bilayers. Biosens Bioelectron 2007 Jan 15 7
62 16800929 [ERK pathway change in the differentiation of human MDS cell lines SKM-1 induced by sodium butyrate]. Zhongguo Shi Yan Xue Ye Xue Za Zhi 2006 Jun 12
63 17237232 A cation-pi interaction discriminates among sodium channels that are either sensitive or resistant to tetrodotoxin block. J Biol Chem 2007 Mar 16 1
64 17638382 Individual variation and hormonal modulation of a sodium channel beta subunit in the electric organ correlate with variation in a social signal. Dev Neurobiol 2007 Sep 1 1
65 18079277 State- and use-dependent block of muscle Nav1.4 and neuronal Nav1.7 voltage-gated Na+ channel isoforms by ranolazine. Mol Pharmacol 2008 Mar 6
66 18162704 The genotype and clinical phenotype of Korean patients with familial hypokalemic periodic paralysis. J Korean Med Sci 2007 Dec 1
67 18203179 Severe neonatal non-dystrophic myotonia secondary to a novel mutation of the voltage-gated sodium channel (SCN4A) gene. Am J Med Genet A 2008 Feb 1 3
68 18718068 [Effect of decitabine combined with Trichostatin A on MDS cell line SKM-1 in vitro]. Zhongguo Shi Yan Xue Ye Xue Za Zhi 2008 Aug 8
69 19876661 Isolated eyelid closure myotonia in two families with sodium channel myotonia. Neurogenetics 2010 May 1
70 20038812 Human voltage-gated sodium channel mutations that cause inherited neuronal and muscle channelopathies increase resurgent sodium currents. J Clin Invest 2010 Jan 4
71 20445432 A case of paramyotonia congenita without periodic paralysis: electrophysiological and molecular genetic studies. Neurologist 2010 May 2
72 20580661 Effects of a new potent analog of tocainide on hNav1.7 sodium channels and in vivo neuropathic pain models. Neuroscience 2010 Aug 25 1
73 20590641 Molecular determinants of state-dependent block of voltage-gated sodium channels by pilsicainide. Br J Pharmacol 2010 Jul 3
74 20634695 Skeletal muscle channelopathies: nondystrophic myotonias and periodic paralysis. Curr Opin Neurol 2010 Oct 1
75 20693878 Block of neuronal Na+ channels by antidepressant duloxetine in a state-dependent manner. Anesthesiology 2010 Sep 1
76 21081490 Possible roles of exceptionally conserved residues around the selectivity filters of sodium and calcium channels. J Biol Chem 2011 Jan 28 1
77 21176362 [Effect of sodium valproate on human myelodysplastic syndrome cell line SKM-1 and its mechanism]. Zhongguo Shi Yan Xue Ye Xue Za Zhi 2010 Dec 3
78 21204798 Myotonia congenita and myotonic dystrophy in the same family: coexistence of a CLCN1 mutation and expansion in the CNBP (ZNF9) gene. Clin Genet 2011 Dec 2
79 21317558 Ranolazine block of human Na v 1.4 sodium channels and paramyotonia congenita mutants. Channels (Austin) 2011 Mar-Apr 1
80 21654192 Azacitidine-resistant SKM1 myeloid cells are defective for AZA-induced mitochondrial apoptosis and autophagy. Cell Cycle 2011 Jul 15 5
81 21802953 Searching for novel anti-myotonic agents: pharmacophore requirement for use-dependent block of skeletal muscle sodium channels by N-benzylated cyclic derivatives of tocainide. Neuromuscul Disord 2012 Jan 4
82 22033299 Enhancing effects of salicylate on quinidine-induced block of human wild type and LQT3 related mutant cardiac Na+ channels. Biomed Res 2011 Oct 2
83 22250216 Biophysical characterization of M1476I, a sodium channel founder mutation associated with cold-induced myotonia in French Canadians. J Physiol 2012 Jun 1 1
84 22253645 Hypokalemic periodic paralysis; two different genes responsible for similar clinical manifestations. Korean J Pediatr 2011 Nov 1
85 22399596 Antiproliferative and antitumor effects of azacitidine against the human myelodysplastic syndrome cell line SKM-1. Anticancer Res 2012 Mar 6
86 22403541 Molecular Insights into the Local Anesthetic Receptor within Voltage-Gated Sodium Channels Using Hydroxylated Analogs of Mexiletine. Front Pharmacol 2012 1
87 22522923 Sensitivity of cloned muscle, heart and neuronal voltage-gated sodium channels to block by polyamines: a possible basis for modulation of excitability in vivo. Channels (Austin) 2012 Jan-Feb 4
88 22577154 BCL2L10 is a predictive factor for resistance to azacitidine in MDS and AML patients. Oncotarget 2012 Apr 4
89 22617007 A sodium channel myotonia due to a novel SCN4A mutation accompanied by acquired autoimmune myasthenia gravis. Neurosci Lett 2012 Jun 21 3
90 22849704 An improved synthesis of m-hydroxymexiletine, a potent mexiletine metabolite. Drug Metab Lett 2012 Jun 1 3
91 22967374 [Establishment of human homoharringtonine-resistant SKM-1 cell line and its biological characteristics]. Zhonghua Xue Ye Xue Za Zhi 2012 Jun 5
92 23093371 Methylation of Wnt antagonist genes: a useful prognostic marker for myelodysplastic syndrome. Ann Hematol 2013 Jan 2
93 23417379 Double trouble in a patient with myotonia. BMJ Case Rep 2013 Feb 14 1
94 23821303 Voltage-gated sodium channel polymorphisms play a pivotal role in the development of oxaliplatin-induced peripheral neurotoxicity: results from a prospective multicenter study. Cancer 2013 Oct 1 2
95 24302985 Direct evidence that scorpion α-toxins (site-3) modulate sodium channel inactivation by hindrance of voltage-sensor movements. PLoS One 2013 4
96 24607901 Mechanism of tetrodotoxin block and resistance in sodium channels. Biochem Biophys Res Commun 2014 Mar 28 6
97 24608798 Reversal of bortezomib resistance in myelodysplastic syndrome cells by MAPK inhibitors. PLoS One 2014 3
98 24704559 Artesunate induces apoptosis through caspase-dependent and -independent mitochondrial pathways in human myelodysplastic syndrome SKM-1 cells. Chem Biol Interact 2014 Aug 5 1
99 24939454 Focal and abnormally persistent paralysis associated with congenital paramyotonia. BMJ Case Rep 2014 Jun 17 2
100 24943082 [Normokalemic periodic paralysis lasting for two weeks: a severe form of sodium channelopathy with M1592V mutation]. Rinsho Shinkeigaku 2014 2