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Journal Abstract Search

261 related items for PubMed ID: 31282864

  • 1.
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  • 2. Ndnf Interneuron Excitability Is Spared in a Mouse Model of Dravet Syndrome.
    Liebergall SR, Goldberg EM.
    J Neurosci; 2024 Apr 24; 44(17):. PubMed ID: 38443186
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  • 3. A Transient Developmental Window of Fast-Spiking Interneuron Dysfunction in a Mouse Model of Dravet Syndrome.
    Favero M, Sotuyo NP, Lopez E, Kearney JA, Goldberg EM.
    J Neurosci; 2018 Sep 05; 38(36):7912-7927. PubMed ID: 30104343
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  • 5. Interneuron Desynchronization Precedes Seizures in a Mouse Model of Dravet Syndrome.
    Tran CH, Vaiana M, Nakuci J, Somarowthu A, Goff KM, Goldstein N, Murthy P, Muldoon SF, Goldberg EM.
    J Neurosci; 2020 Mar 25; 40(13):2764-2775. PubMed ID: 32102923
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  • 6. A selective NaV1.1 activator with potential for treatment of Dravet syndrome epilepsy.
    Chow CY, Chin YKY, Ma L, Undheim EAB, Herzig V, King GF.
    Biochem Pharmacol; 2020 Nov 25; 181():113991. PubMed ID: 32335140
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  • 7. Targeted Augmentation of Nuclear Gene Output (TANGO) of Scn1a rescues parvalbumin interneuron excitability and reduces seizures in a mouse model of Dravet Syndrome.
    Wengert ER, Wagley PK, Strohm SM, Reza N, Wenker IC, Gaykema RP, Christiansen A, Liau G, Patel MK.
    Brain Res; 2022 Jan 15; 1775():147743. PubMed ID: 34843701
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  • 8. Impaired excitability of somatostatin- and parvalbumin-expressing cortical interneurons in a mouse model of Dravet syndrome.
    Tai C, Abe Y, Westenbroek RE, Scheuer T, Catterall WA.
    Proc Natl Acad Sci U S A; 2014 Jul 29; 111(30):E3139-48. PubMed ID: 25024183
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  • 11. 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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  • 12. Scn1a gene reactivation after symptom onset rescues pathological phenotypes in a mouse model of Dravet syndrome.
    Valassina N, Brusco S, Salamone A, Serra L, Luoni M, Giannelli S, Bido S, Massimino L, Ungaro F, Mazzara PG, D'Adamo P, Lignani G, Broccoli V, Colasante G.
    Nat Commun; 2022 Jan 10; 13(1):161. PubMed ID: 35013317
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  • 15. Antisense oligonucleotides restore excitability, GABA signalling and sodium current density in a Dravet syndrome model.
    Yuan Y, Lopez-Santiago L, Denomme N, Chen C, O'Malley HA, Hodges SL, Ji S, Han Z, Christiansen A, Isom LL.
    Brain; 2024 Apr 04; 147(4):1231-1246. PubMed ID: 37812817
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  • 16. Genetic background modulates impaired excitability of inhibitory neurons in a mouse model of Dravet syndrome.
    Rubinstein M, Westenbroek RE, Yu FH, Jones CJ, Scheuer T, Catterall WA.
    Neurobiol Dis; 2015 Jan 04; 73():106-17. PubMed ID: 25281316
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  • 19. 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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