{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2024,3,28]],"date-time":"2024-03-28T14:06:05Z","timestamp":1711634765348},"reference-count":32,"publisher":"Springer Science and Business Media LLC","issue":"5","license":[{"start":{"date-parts":[[2014,3,29]],"date-time":"2014-03-29T00:00:00Z","timestamp":1396051200000},"content-version":"tdm","delay-in-days":0,"URL":"http:\/\/www.springer.com\/tdm"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Cell Mol Neurobiol"],"published-print":{"date-parts":[[2014,7]]},"DOI":"10.1007\/s10571-014-0052-y","type":"journal-article","created":{"date-parts":[[2014,3,28]],"date-time":"2014-03-28T20:19:59Z","timestamp":1396037999000},"page":"707-714","source":"Crossref","is-referenced-by-count":7,"title":["Enhanced Slow Inactivation of the Human Skeletal Muscle Sodium Channel Causing Normokalemic Periodic Paralysis"],"prefix":"10.1007","volume":"34","author":[{"given":"Lei","family":"Wu","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Baorong","family":"Zhang","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Ying","family":"Kang","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Weiping","family":"Wu","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"297","published-online":{"date-parts":[[2014,3,29]]},"reference":[{"issue":"1","key":"52_CR1","doi-asserted-by":"crossref","first-page":"148","DOI":"10.1021\/bp049830x","volume":"21","author":"L Baldi","year":"2005","unstructured":"Baldi L, Muller N, Picasso S, Jacquet R, Girard P, Thanh HP, Derow E, Wurm FM (2005) Transient gene expression in suspension HEK-293 cells: application to large-scale protein production. Biotechnol Prog 21(1):148\u2013153. doi: 10.1021\/bp049830x","journal-title":"Biotechnol Prog"},{"issue":"12","key":"52_CR2","doi-asserted-by":"crossref","first-page":"4762","DOI":"10.1523\/JNEUROSCI.19-12-04762.1999","volume":"19","author":"S Bendahhou","year":"1999","unstructured":"Bendahhou S, Cummins TR, Tawil R, Waxman SG, Ptacek LJ (1999) Activation and inactivation of the voltage-gated sodium channel: role of segment S5 revealed by a novel hyperkalemic periodic paralysis mutation. The Journal of neuroscience : the official journal of the Society for Neuroscience 19(12):4762\u20134771","journal-title":"J Neurosci: Off J Soc Neurosci"},{"issue":"3","key":"52_CR3","doi-asserted-by":"crossref","first-page":"431","DOI":"10.1172\/JCI9654","volume":"106","author":"S Bendahhou","year":"2000","unstructured":"Bendahhou S, Cummins TR, Hahn AF, Langlois S, Waxman SG, Ptacek LJ (2000) A double mutation in families with periodic paralysis defines new aspects of sodium channel slow inactivation. J Clin Investig 106(3):431\u2013438","journal-title":"J Clin Investig"},{"issue":"12","key":"52_CR4","doi-asserted-by":"crossref","first-page":"e81063","DOI":"10.1371\/journal.pone.0081063","volume":"8","author":"S Biswas","year":"2013","unstructured":"Biswas S, Disilvestre DA, Dong P, Tomaselli GF (2013) Mechanisms of a Human Skeletal Myotonia Produced by Mutation in the C-Terminus of NaV1.4: is Ca(2\u00a0+) Regulation Defective? PLoS ONE 8(12):e81063","journal-title":"PLoS ONE"},{"issue":"4","key":"52_CR5","doi-asserted-by":"crossref","first-page":"241","DOI":"10.1016\/S0960-8966(97)00430-6","volume":"7","author":"SC Cannon","year":"1997","unstructured":"Cannon SC (1997) From mutation to myotonia in sodium channel disorders. Neuromuscular disorders : NMD 7(4):241\u2013249","journal-title":"Neuromuscul Disord: NMD"},{"issue":"2","key":"52_CR6","doi-asserted-by":"crossref","first-page":"317","DOI":"10.1016\/0896-6273(93)90321-H","volume":"10","author":"SC Cannon","year":"1993","unstructured":"Cannon SC, Strittmatter SM (1993) Functional expression of sodium channel mutations identified in families with periodic paralysis. Neuron 10(2):317\u2013326","journal-title":"Neuron"},{"issue":"1","key":"52_CR7","doi-asserted-by":"crossref","first-page":"270","DOI":"10.1016\/S0006-3495(93)81045-2","volume":"65","author":"SC Cannon","year":"1993","unstructured":"Cannon SC, Brown RH Jr, Corey DP (1993) Theoretical reconstruction of myotonia and paralysis caused by incomplete inactivation of sodium channels. Biophys J 65(1):270\u2013288","journal-title":"Biophys J"},{"issue":"1\u20132","key":"52_CR8","doi-asserted-by":"crossref","first-page":"136","DOI":"10.1007\/BF00585952","volume":"427","author":"M Chahine","year":"1994","unstructured":"Chahine M, Bennett PB, George AL Jr, Horn R (1994) Functional expression and properties of the human skeletal muscle sodium channel. Pflugers Arch 427(1\u20132):136\u2013142","journal-title":"Pflugers Arch"},{"issue":"2","key":"52_CR9","doi-asserted-by":"crossref","first-page":"251","DOI":"10.1002\/ana.10257","volume":"52","author":"PF Chinnery","year":"2002","unstructured":"Chinnery PF, Walls TJ, Hanna MG, Bates D, Fawcett PR (2002) Normokalemic periodic paralysis revisited: does it exist? Annals of neurology 52(2):251\u2013252","journal-title":"Ann Neurol"},{"issue":"1","key":"52_CR10","doi-asserted-by":"crossref","first-page":"227","DOI":"10.1016\/S0006-3495(96)79219-6","volume":"71","author":"TR Cummins","year":"1996","unstructured":"Cummins TR, Sigworth FJ (1996) Impaired slow inactivation in mutant sodium channels. Biophys J 71(1):227\u2013236","journal-title":"Biophys J"},{"issue":"3","key":"52_CR11","first-page":"199","volume":"37","author":"XH Guo","year":"2004","unstructured":"Guo XH, Wu WP, Zhang YH, Zhu K (2004) The detection of a novel mutation by screening SCN4A gene in normokalemic periodic paralysis(write in Chinese). Chin J Neurol 37(3):199\u2013202","journal-title":"Chin J Neurol"},{"issue":"5","key":"52_CR12","doi-asserted-by":"crossref","first-page":"559","DOI":"10.1085\/jgp.107.5.559","volume":"107","author":"LJ Hayward","year":"1996","unstructured":"Hayward LJ, Brown RH Jr, Cannon SC (1996) Inactivation defects caused by myotonia-associated mutations in the sodium channel III-IV linker. J Gen Physiol 107(5):559\u2013576","journal-title":"J Gen Physiol"},{"issue":"3","key":"52_CR13","doi-asserted-by":"crossref","first-page":"1204","DOI":"10.1016\/S0006-3495(97)78768-X","volume":"72","author":"LJ Hayward","year":"1997","unstructured":"Hayward LJ, Brown RH Jr, Cannon SC (1997) Slow inactivation differs among mutant Na channels associated with myotonia and periodic paralysis. Biophys J 72(3):1204\u20131219","journal-title":"Biophys J"},{"issue":"7","key":"52_CR14","doi-asserted-by":"crossref","first-page":"1447","DOI":"10.1212\/WNL.52.7.1447","volume":"52","author":"LJ Hayward","year":"1999","unstructured":"Hayward LJ, Sandoval GM, Cannon SC (1999) Defective slow inactivation of sodium channels contributes to familial periodic paralysis. Neurology 52(7):1447\u20131453","journal-title":"Neurology"},{"issue":"17","key":"52_CR15","doi-asserted-by":"crossref","first-page":"9549","DOI":"10.1073\/pnas.97.17.9549","volume":"97","author":"K Jurkat-Rott","year":"2000","unstructured":"Jurkat-Rott K, Mitrovic N, Hang C, Kouzmekine A, Iaizzo P, Herzog J, Lerche H, Nicole S, Vale-Santos J, Chauveau D, Fontaine B, Lehmann-Horn F (2000) Voltage-sensor sodium channel mutations cause hypokalemic periodic paralysis type 2 by enhanced inactivation and reduced current. Proc Natl Acad Sci USA 97(17):9549\u20139554","journal-title":"Proc Natl Acad Sci USA"},{"issue":"4","key":"52_CR16","doi-asserted-by":"crossref","first-page":"403","DOI":"10.1085\/jgp.110.4.403","volume":"110","author":"KJ Kontis","year":"1997","unstructured":"Kontis KJ, Goldin AL (1997) Sodium channel inactivation is altered by substitution of voltage sensor positive charges. The Journal of general physiology 110(4):403\u2013413","journal-title":"J Gen Physiol"},{"issue":"Pt 4","key":"52_CR17","doi-asserted-by":"crossref","first-page":"835","DOI":"10.1093\/brain\/awf071","volume":"125","author":"A Kuzmenkin","year":"2002","unstructured":"Kuzmenkin A, Muncan V, Jurkat-Rott K, Hang C, Lerche H, Lehmann-Horn F, Mitrovic N (2002) Enhanced inactivation and pH sensitivity of Na(+) channel mutations causing hypokalemic periodic paralysis type II. Brain : a journal of neurology 125(Pt 4):835\u2013843","journal-title":"Brain : J Neurol"},{"issue":"4","key":"52_CR18","doi-asserted-by":"crossref","first-page":"1317","DOI":"10.1152\/physrev.1999.79.4.1317","volume":"79","author":"F Lehmann-Horn","year":"1999","unstructured":"Lehmann-Horn F, Jurkat-Rott K (1999) Voltage-gated ion channels and hereditary disease. Physiol Rev 79(4):1317\u20131372","journal-title":"Physiol Rev"},{"key":"52_CR19","doi-asserted-by":"crossref","unstructured":"Lehmann-Horn F, Rudel R, Ricker K (1993) Non-dystrophic myotonias and periodic paralyses. A European Neuromuscular Center Workshop held 4-6 October 1992, Ulm, Germany. Neuromuscular disorders : NMD 3 (2):161\u2013168","DOI":"10.1016\/0960-8966(93)90009-9"},{"issue":"22","key":"52_CR20","doi-asserted-by":"crossref","first-page":"10905","DOI":"10.1073\/pnas.89.22.10905","volume":"89","author":"DE Patton","year":"1992","unstructured":"Patton DE, West JW, Catterall WA, Goldin AL (1992) Amino acid residues required for fast Na(+)-channel inactivation: charge neutralizations and deletions in the III-IV linker. Proc Natl Acad Sci USA 89(22):10905\u201310909","journal-title":"Proc Natl Acad Sci USA"},{"key":"52_CR21","doi-asserted-by":"crossref","first-page":"328","DOI":"10.1016\/0002-9343(61)90122-X","volume":"31","author":"DC Poskanzer","year":"1961","unstructured":"Poskanzer DC, Kerr DN (1961) A third type of periodic paralysis, with normokalemia and favourable response to sodium chloride. The American journal of medicine 31:328\u2013342","journal-title":"Am J Med"},{"key":"52_CR22","first-page":"604","volume-title":"Disorders of voluntary muscle","author":"LJBS Ptacek","year":"2001","unstructured":"Ptacek LJBS (2001) Ion channel disorders of muscle. In: Karpati GH-JD, Griggs RC (eds) Disorders of voluntary muscle, 7th edn. Cambridge University Press, Cambridge, pp 604\u2013635","edition":"7"},{"issue":"2 Pt 1","key":"52_CR23","doi-asserted-by":"crossref","first-page":"542","DOI":"10.1016\/S0006-3495(94)80807-0","volume":"66","author":"RL Ruff","year":"1994","unstructured":"Ruff RL (1994) Slow Na\u00a0+\u00a0channel inactivation must be disrupted to evoke prolonged depolarization-induced paralysis. Biophys J 66(2 Pt 1):542","journal-title":"Biophys J"},{"issue":"5","key":"52_CR24","doi-asserted-by":"crossref","first-page":"502","DOI":"10.1002\/mus.880110514","volume":"11","author":"RL Ruff","year":"1988","unstructured":"Ruff RL, Simoncini L, Stuhmer W (1988) Slow sodium channel inactivation in mammalian muscle: a possible role in regulating excitability. Muscle Nerve 11(5):502\u2013510","journal-title":"Muscle Nerve"},{"issue":"50","key":"52_CR25","doi-asserted-by":"crossref","first-page":"19980","DOI":"10.1073\/pnas.0810562105","volume":"105","author":"S Sokolov","year":"2008","unstructured":"Sokolov S, Scheuer T, Catterall WA (2008) Depolarization-activated gating pore current conducted by mutant sodium channels in potassium-sensitive normokalemic periodic paralysis. Proc Natl Acad Sci USA 105(50):19980\u201319985","journal-title":"Proc Natl Acad Sci USA"},{"issue":"23","key":"52_CR26","doi-asserted-by":"crossref","first-page":"8610","DOI":"10.1523\/JNEUROSCI.20-23-08610.2000","volume":"20","author":"AF Struyk","year":"2000","unstructured":"Struyk AF, Scoggan KA, Bulman DE, Cannon SC (2000) The human skeletal muscle Na channel mutation R669H associated with hypokalemic periodic paralysis enhances slow inactivation. The Journal of neuroscience : the official journal of the Society for Neuroscience 20(23):8610\u20138617","journal-title":"J Neurosci: Off J Soc Neurosci"},{"issue":"4","key":"52_CR27","doi-asserted-by":"crossref","first-page":"447","DOI":"10.1085\/jgp.200809967","volume":"132","author":"AF Struyk","year":"2008","unstructured":"Struyk AF, Markin VS, Francis D, Cannon SC (2008) Gating pore currents in DIIS4 mutations of NaV1.4 associated with periodic paralysis: saturation of ion flux and implications for disease pathogenesis. The Journal of general physiology 132(4):447\u2013464","journal-title":"J Gen Physiol"},{"issue":"11","key":"52_CR28","doi-asserted-by":"crossref","first-page":"2120","DOI":"10.1212\/01.WNL.0000145768.09934.EC","volume":"63","author":"S Vicart","year":"2004","unstructured":"Vicart S, Sternberg D, Fournier E, Ochsner F, Laforet P, Kuntzer T, Eymard B, Hainque B, Fontaine B (2004) New mutations of SCN4A cause a potassium-sensitive normokalemic periodic paralysis. Neurology 63(11):2120\u20132127","journal-title":"Neurology"},{"issue":"4","key":"52_CR29","doi-asserted-by":"crossref","first-page":"1633","DOI":"10.1016\/S0006-3495(97)78809-X","volume":"72","author":"SY Wang","year":"1997","unstructured":"Wang SY, Wang GK (1997) A mutation in segment I-S6 alters slow inactivation of sodium channels. Biophys J 72(4):1633\u20131640","journal-title":"Biophys J"},{"issue":"22","key":"52_CR30","doi-asserted-by":"crossref","first-page":"10910","DOI":"10.1073\/pnas.89.22.10910","volume":"89","author":"JW West","year":"1992","unstructured":"West JW, Patton DE, Scheuer T, Wang Y, Goldin AL, Catterall WA (1992) A cluster of hydrophobic amino acid residues required for fast Na(+)-channel inactivation. Proc Natl Acad Sci USA 89(22):10910\u201310914","journal-title":"Proc Natl Acad Sci USA"},{"issue":"2","key":"52_CR31","doi-asserted-by":"crossref","first-page":"65","DOI":"10.1016\/S1056-8719(03)00041-8","volume":"48","author":"HJ Witchel","year":"2002","unstructured":"Witchel HJ, Milnes JT, Mitcheson JS, Hancox JC (2002) Troubleshooting problems with in vitro screening of drugs for QT interval prolongation using HERG K\u00a0+\u00a0channels expressed in mammalian cell lines and Xenopus oocytes. J Pharmacol Toxicol Methods 48(2):65\u201380","journal-title":"J Pharmacol Toxicol Methods"},{"issue":"5","key":"52_CR32","doi-asserted-by":"crossref","first-page":"653","DOI":"10.1007\/s10571-007-9231-4","volume":"28","author":"G Xiuhai","year":"2008","unstructured":"Xiuhai G, Weiping W, Ke Z, Hongbin W, Yiling S, MaoYanling (2008) Mutations of sodium channel alpha-subunit genes in Chinese patients with normokalemic periodic paralysis. Cell Mol Neurobiol 28(5):653\u2013661","journal-title":"Cell Mol Neurobiol"}],"container-title":["Cellular and Molecular Neurobiology"],"original-title":[],"language":"en","link":[{"URL":"http:\/\/link.springer.com\/content\/pdf\/10.1007\/s10571-014-0052-y.pdf","content-type":"application\/pdf","content-version":"vor","intended-application":"text-mining"},{"URL":"http:\/\/link.springer.com\/article\/10.1007\/s10571-014-0052-y\/fulltext.html","content-type":"text\/html","content-version":"vor","intended-application":"text-mining"},{"URL":"http:\/\/link.springer.com\/content\/pdf\/10.1007\/s10571-014-0052-y","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2019,8,8]],"date-time":"2019-08-08T21:27:35Z","timestamp":1565299655000},"score":1,"resource":{"primary":{"URL":"http:\/\/link.springer.com\/10.1007\/s10571-014-0052-y"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2014,3,29]]},"references-count":32,"journal-issue":{"issue":"5","published-print":{"date-parts":[[2014,7]]}},"alternative-id":["52"],"URL":"https:\/\/doi.org\/10.1007\/s10571-014-0052-y","relation":{},"ISSN":["0272-4340","1573-6830"],"issn-type":[{"value":"0272-4340","type":"print"},{"value":"1573-6830","type":"electronic"}],"subject":[],"published":{"date-parts":[[2014,3,29]]}}}