dCas9-Based Scn1a Gene Activation Restores Inhibitory Interneuron Excitability and Attenuates Seizures in Dravet Syndrome Mice

Dravet syndrome (DS) is a severe epileptic encephalopathy caused mainly by heterozygous loss-of-function mutations of the SCN1A gene, indicating haploinsufficiency as the pathogenic mechanism. Here we tested whether catalytically dead Cas9 (dCas9)-mediated Scn1a gene activation can rescue Scn1a hapl...

पूर्ण विवरण

में बचाया:
ग्रंथसूची विवरण
में प्रकाशित:Mol Ther
मुख्य लेखकों: Colasante, Gaia, Lignani, Gabriele, Brusco, Simone, Di Berardino, Claudia, Carpenter, Jenna, Giannelli, Serena, Valassina, Nicholas, Bido, Simone, Ricci, Raffaele, Castoldi, Valerio, Marenna, Silvia, Church, Timothy, Massimino, Luca, Morabito, Giuseppe, Benfenati, Fabio, Schorge, Stephanie, Leocani, Letizia, Kullmann, Dimitri M., Broccoli, Vania
स्वरूप: Artigo
भाषा:Inglês
प्रकाशित: American Society of Gene & Cell Therapy 2020
विषय:
Original Article
ऑनलाइन पहुंच:https://ncbi.nlm.nih.gov/pmc/articles/PMC6952031/
https://ncbi.nlm.nih.gov/pubmed/31607539
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.ymthe.2019.08.018
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