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Journal Abstract Search

185 related items for PubMed ID: 37812817

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  • 2. 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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  • 4. Dravet Syndrome: A Developmental and Epileptic Encephalopathy.
    Lopez-Santiago L, Isom LL.
    Epilepsy Curr; 2019 Jan 15; 19(1):51-53. PubMed ID: 30838929
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  • 6. Antisense oligonucleotides increase Scn1a expression and reduce seizures and SUDEP incidence in a mouse model of Dravet syndrome.
    Han Z, Chen C, Christiansen A, Ji S, Lin Q, Anumonwo C, Liu C, Leiser SC, Meena, Aznarez I, Liau G, Isom LL.
    Sci Transl Med; 2020 Aug 26; 12(558):. PubMed ID: 32848094
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  • 8. Strain- and age-dependent hippocampal neuron sodium currents correlate with epilepsy severity in Dravet syndrome mice.
    Mistry AM, Thompson CH, Miller AR, Vanoye CG, George AL, Kearney JA.
    Neurobiol Dis; 2014 May 26; 65():1-11. PubMed ID: 24434335
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  • 9. 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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  • 10. 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 08; 73():106-17. PubMed ID: 25281316
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  • 13. 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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  • 15. Upregulation of Haploinsufficient Gene Expression in the Brain by Targeting a Long Non-coding RNA Improves Seizure Phenotype in a Model of Dravet Syndrome.
    Hsiao J, Yuan TY, Tsai MS, Lu CY, Lin YC, Lee ML, Lin SW, Chang FC, Liu Pimentel H, Olive C, Coito C, Shen G, Young M, Thorne T, Lawrence M, Magistri M, Faghihi MA, Khorkova O, Wahlestedt C.
    EBioMedicine; 2016 Jul 24; 9():257-277. PubMed ID: 27333023
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  • 16. Dissecting the phenotypes of Dravet syndrome by gene deletion.
    Rubinstein M, Han S, Tai C, Westenbroek RE, Hunker A, Scheuer T, Catterall WA.
    Brain; 2015 Aug 24; 138(Pt 8):2219-33. PubMed ID: 26017580
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  • 17. 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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