Hill SF - Search Results

1

Scn8a Antisense Oligonucleotide Is Protective in Mouse Models of SCN8A Encephalopathy and Dravet Syndrome.

Lenk GM, Jafar-Nejad P, Hill SF, Huffman LD, Smolen CE, Wagnon JL, Petit H, Yu W, Ziobro J, Bhatia K, Parent J, Giger RJ, Rigo F, Meisler MH. Lenk GM, et al. Among authors: hill sf. Ann Neurol. 2020 Mar;87(3):339-346. doi: 10.1002/ana.25676. Epub 2020 Feb 6. Ann Neurol. 2020. PMID: 31943325 Free PMC article.

2

Gabra2 is a genetic modifier of Scn8a encephalopathy in the mouse.

Yu W, Hill SF, Xenakis JG, Pardo-Manuel de Villena F, Wagnon JL, Meisler MH. Yu W, et al. Among authors: hill sf. Epilepsia. 2020 Dec;61(12):2847-2856. doi: 10.1111/epi.16741. Epub 2020 Nov 2. Epilepsia. 2020. PMID: 33140451 Free PMC article.

3

Sodium channelopathies in neurodevelopmental disorders.

Meisler MH, Hill SF, Yu W. Meisler MH, et al. Among authors: hill sf. Nat Rev Neurosci. 2021 Mar;22(3):152-166. doi: 10.1038/s41583-020-00418-4. Epub 2021 Feb 2. Nat Rev Neurosci. 2021. PMID: 33531663 Free PMC article. Review.

4

Author Correction: Sodium channelopathies in neurodevelopmental disorders.

Meisler MH, Hill SF, Yu W. Meisler MH, et al. Among authors: hill sf. Nat Rev Neurosci. 2021 Apr;22(4):256. doi: 10.1038/s41583-021-00449-5. Nat Rev Neurosci. 2021. PMID: 33686192 No abstract available.

5

Spontaneous seizures and elevated seizure susceptibility in response to somatic mutation of sodium channel Scn8a in the mouse.

Yu W, Smolen CE, Hill SF, Meisler MH. Yu W, et al. Among authors: hill sf. Hum Mol Genet. 2021 May 29;30(10):902-907. doi: 10.1093/hmg/ddab092. Hum Mol Genet. 2021. PMID: 33822038 Free PMC article.

6

Antisense Oligonucleotide Therapy for Neurodevelopmental Disorders.

Hill SF, Meisler MH. Hill SF, et al. Dev Neurosci. 2021;43(3-4):247-252. doi: 10.1159/000517686. Epub 2021 Aug 5. Dev Neurosci. 2021. PMID: 34412058 Free PMC article. Review.

7

Genetic interaction between Scn8a and potassium channel genes Kcna1 and Kcnq2.

Hill SF, Ziobro JM, Jafar-Nejad P, Rigo F, Meisler MH. Hill SF, et al. Epilepsia. 2022 Oct;63(10):e125-e131. doi: 10.1111/epi.17374. Epub 2022 Aug 11. Epilepsia. 2022. PMID: 35892317 Free PMC article.

8

Reduction of Kcnt1 is therapeutic in mouse models of SCN1A and SCN8A epilepsy.

Hill SF, Jafar-Nejad P, Rigo F, Meisler MH. Hill SF, et al. Front Neurosci. 2023 Oct 13;17:1282201. doi: 10.3389/fnins.2023.1282201. eCollection 2023. Front Neurosci. 2023. PMID: 37901435 Free PMC article.

9

Long-Term Downregulation of the Sodium Channel Gene Scn8a Is Therapeutic in Mouse Models of SCN8A Epilepsy.

Hill SF, Yu W, Ziobro J, Chalasani S, Reger F, Meisler MH. Hill SF, et al. Ann Neurol. 2024 Apr;95(4):754-759. doi: 10.1002/ana.26861. Epub 2024 Jan 6. Ann Neurol. 2024. PMID: 38113311

10

CHD7 promotes neural progenitor differentiation in embryonic stem cells via altered chromatin accessibility and nascent gene expression.

Yao H, Hannum DF, Zhai Y, Hill SF, Albanus RD', Lou W, Skidmore JM, Sanchez G, Saiakhova A, Bielas SL, Scacheri P, Ljungman M, Parker SCJ, Martin DM. Yao H, et al. Among authors: hill sf. Sci Rep. 2020 Oct 15;10(1):17445. doi: 10.1038/s41598-020-74537-4. Sci Rep. 2020. PMID: 33060836 Free PMC article.

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