Publications by authors named "Wout Weuring"

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Increased prime edit rates in KCNQ2 and SCN1A via single nicking all-in-one plasmids.
N Dirkx, Wout J Weuring, E De Vriendt, N Smal, J van de Vondervoort

BMC Biol· July 2023

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Genetic and Functional Differences between Duplicated Zebrafish Genes for Human .
Wout J Weuring, Jos W Hoekman, Kees P J Braun, Bobby P C Koeleman

Cells· January 2022

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Gene Therapies for Monogenic Autism Spectrum Disorders.
Wout Weuring, Jeroen Geerligs, Bobby P C Koeleman

Genes (Basel)· October 2021

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CRISPRa-Mediated Upregulation of During Early Development Causes Epileptiform Activity and dCas9-Associated Toxicity.
Wout J Weuring, Ivana Dilevska, Jos Hoekman, Joep van de Vondervoort, Martijn Koetsier

CRISPR J· August 2021

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NaV1.1 and NaV1.6 selective compounds reduce the behavior phenotype and epileptiform activity in a novel zebrafish model for Dravet Syndrome.
Wout J Weuring, Sakshi Singh, Linda Volkers, Martin B Rook, Ruben H van 't Slot

PLoS One· May 2021

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Influence of common SCN1A promoter variants on the severity of SCN1A-related phenotypes.
Iris M de Lange, Wout Weuring, Ruben van 't Slot, Boudewijn Gunning, Anja C M Sonsma

Mol Genet Genomic Med· July 2019

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