Detalhe da pesquisa
1.
Increased prime edit rates in KCNQ2 and SCN1A via single nicking all-in-one plasmids.
BMC Biol
; 21(1): 156, 2023 07 13.
Artigo
Inglês
| MEDLINE | ID: mdl-37443005
2.
Genetic and Functional Differences between Duplicated Zebrafish Genes for Human SCN1A.
Cells
; 11(3)2022 01 28.
Artigo
Inglês
| MEDLINE | ID: mdl-35159264
3.
Gene Therapies for Monogenic Autism Spectrum Disorders.
Genes (Basel)
; 12(11)2021 10 22.
Artigo
Inglês
| MEDLINE | ID: mdl-34828273
4.
CRISPRa-Mediated Upregulation of scn1laa During Early Development Causes Epileptiform Activity and dCas9-Associated Toxicity.
CRISPR J
; 4(4): 575-582, 2021 08.
Artigo
Inglês
| MEDLINE | ID: mdl-34406040
5.
NaV1.1 and NaV1.6 selective compounds reduce the behavior phenotype and epileptiform activity in a novel zebrafish model for Dravet Syndrome.
PLoS One
; 15(3): e0219106, 2020.
Artigo
Inglês
| MEDLINE | ID: mdl-32134913
6.
Influence of common SCN1A promoter variants on the severity of SCN1A-related phenotypes.
Mol Genet Genomic Med
; 7(7): e00727, 2019 07.
Artigo
Inglês
| MEDLINE | ID: mdl-31144463