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Journal Abstract Search

837 related items for PubMed ID: 30104343

  • 21.
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  • 22. Electrophysiological Alterations of Pyramidal Cells and Interneurons of the CA1 Region of the Hippocampus in a Novel Mouse Model of Dravet Syndrome.
    Dyment DA, Schock SC, Deloughery K, Tran MH, Ure K, Nutter LMJ, Creighton A, Yuan J, Banderali U, Comas T, Baumann E, Jezierski A, Care4Rare Canada Consortium,, Boycott KM, Mackenzie AE, Martina M.
    Genetics; 2020 Aug; 215(4):1055-1066. PubMed ID: 32554600
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  • 23. Preictal dysfunctions of inhibitory interneurons paradoxically lead to their rebound hyperactivity and to low-voltage-fast onset seizures in Dravet syndrome.
    Capitano F, Kuchenbuch M, Lavigne J, Chaptoukaev H, Zuluaga MA, Lorenzi M, Nabbout R, Mantegazza M.
    Proc Natl Acad Sci U S A; 2024 Jun 04; 121(23):e2316364121. PubMed ID: 38809712
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  • 24. Specific deletion of NaV1.1 sodium channels in inhibitory interneurons causes seizures and premature death in a mouse model of Dravet syndrome.
    Cheah CS, Yu FH, Westenbroek RE, Kalume FK, Oakley JC, Potter GB, Rubenstein JL, Catterall WA.
    Proc Natl Acad Sci U S A; 2012 Sep 04; 109(36):14646-51. PubMed ID: 22908258
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  • 27. dCas9-Based Scn1a Gene Activation Restores Inhibitory Interneuron Excitability and Attenuates Seizures in Dravet Syndrome Mice.
    Colasante G, Lignani G, Brusco S, Di Berardino C, Carpenter J, Giannelli S, Valassina N, Bido S, Ricci R, Castoldi V, Marenna S, Church T, Massimino L, Morabito G, Benfenati F, Schorge S, Leocani L, Kullmann DM, Broccoli V.
    Mol Ther; 2020 Jan 08; 28(1):235-253. PubMed ID: 31607539
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  • 28. Corticohippocampal circuit dysfunction in a mouse model of Dravet syndrome.
    Mattis J, Somarowthu A, Goff KM, Jiang E, Yom J, Sotuyo N, Mcgarry LM, Feng H, Kaneko K, Goldberg EM.
    Elife; 2022 Feb 25; 11():. PubMed ID: 35212623
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  • 29. Epilepsy phenotype associated with a chromosome 2q24.3 deletion involving SCN1A: Migrating partial seizures of infancy or atypical Dravet syndrome?
    Lim BC, Hwang H, Kim H, Chae JH, Choi J, Kim KJ, Hwang YS, Yum MS, Ko TS.
    Epilepsy Res; 2015 Jan 25; 109():34-9. PubMed ID: 25524840
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  • 30. Cell-Selective Adeno-Associated Virus-Mediated SCN1A Gene Regulation Therapy Rescues Mortality and Seizure Phenotypes in a Dravet Syndrome Mouse Model and Is Well Tolerated in Nonhuman Primates.
    Tanenhaus A, Stowe T, Young A, McLaughlin J, Aeran R, Lin IW, Li J, Hosur R, Chen M, Leedy J, Chou T, Pillay S, Vila MC, Kearney JA, Moorhead M, Belle A, Tagliatela S.
    Hum Gene Ther; 2022 Jun 25; 33(11-12):579-597. PubMed ID: 35435735
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  • 31. Case studies in neuroscience: a novel amino acid duplication in the NH2-terminus of the brain sodium channel NaV1.1 underlying Dravet syndrome.
    Angus M, Peters CH, Poburko D, Brimble E, Spelbrink EM, Ruben PC.
    J Neurophysiol; 2019 Nov 01; 122(5):1975-1980. PubMed ID: 31533007
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  • 32. Unaltered Network Activity and Interneuronal Firing During Spontaneous Cortical Dynamics In Vivo in a Mouse Model of Severe Myoclonic Epilepsy of Infancy.
    De Stasi AM, Farisello P, Marcon I, Cavallari S, Forli A, Vecchia D, Losi G, Mantegazza M, Panzeri S, Carmignoto G, Bacci A, Fellin T.
    Cereb Cortex; 2016 Apr 01; 26(4):1778-94. PubMed ID: 26819275
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  • 33.
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  • 34. Modeling NaV1.1/SCN1A sodium channel mutations in a microcircuit with realistic ion concentration dynamics suggests differential GABAergic mechanisms leading to hyperexcitability in epilepsy and hemiplegic migraine.
    Lemaire L, Desroches M, Krupa M, Pizzamiglio L, Scalmani P, Mantegazza M.
    PLoS Comput Biol; 2021 Jul 01; 17(7):e1009239. PubMed ID: 34314446
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  • 35. Reduced sodium current in GABAergic interneurons in a mouse model of severe myoclonic epilepsy in infancy.
    Yu FH, Mantegazza M, Westenbroek RE, Robbins CA, Kalume F, Burton KA, Spain WJ, McKnight GS, Scheuer T, Catterall WA.
    Nat Neurosci; 2006 Sep 01; 9(9):1142-9. PubMed ID: 16921370
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  • 36. Unexpected Efficacy of a Novel Sodium Channel Modulator in Dravet Syndrome.
    Anderson LL, Hawkins NA, Thompson CH, Kearney JA, George AL.
    Sci Rep; 2017 May 10; 7(1):1682. PubMed ID: 28490751
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  • 37.
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  • 38. VIP interneuron impairment promotes in vivo circuit dysfunction and autism-related behaviors in Dravet syndrome.
    Goff KM, Liebergall SR, Jiang E, Somarowthu A, Goldberg EM.
    Cell Rep; 2023 Jun 27; 42(6):112628. PubMed ID: 37310860
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  • 39. Neddylation stabilizes Nav1.1 to maintain interneuron excitability and prevent seizures in murine epilepsy models.
    Chen W, Luo B, Gao N, Li H, Wang H, Li L, Cui W, Zhang L, Sun D, Liu F, Dong Z, Ren X, Zhang H, Su H, Xiong WC, Mei L.
    J Clin Invest; 2021 Apr 15; 131(8):. PubMed ID: 33651714
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