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

por Hill, Sophie F., Jafar-Nejad, Paymaan, Rigo, Frank, Meisler, Miriam H.
Publicado 2023

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

por Yu, Wenxi, Smolen, Corrine E, Hill, Sophie F, Meisler, Miriam H
Publicado 2021

Genetic interaction between Scn8a and potassium channel genes Kcna1 and Kcnq2

por Hill, Sophie F., Ziobro, Julie M., Jafar‐Nejad, Paymaan, Rigo, Frank, Meisler, Miriam H.
Publicado 2022

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

por Yu, Wenxi, Hill, Sophie F., Xenakis, James G., Pardo‐Manuel de Villena, Fernando, Wagnon, Jacy L., Meisler, Miriam H.
Publicado 2020

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

por Lenk, Guy M., Jafar‐Nejad, Paymaan, Hill, Sophie F., Huffman, Lucas D., Smolen, Corrine E., Wagnon, Jacy L., Petit, Hayley, Yu, Wenxi, Ziobro, Julie, Bhatia, Kritika, Parent, Jack, Giger, Roman J., Rigo, Frank, Meisler, Miriam H.
Publicado 2020

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

por Yao, Hui, Hannum, Douglas F., Zhai, Yiwen, Hill, Sophie F., Albanus, Ricardo D.’Oliveira, Lou, Wenjia, Skidmore, Jennifer M., Sanchez, Gilson, Saiakhova, Alina, Bielas, Stephanie L., Scacheri, Peter, Ljungman, Mats, Parker, Stephen C. J., Martin, Donna M.
Publicado 2020