Publications by authors named "Remko Goossens"

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antisense oligonucleotide mediated exon skipping efficiency correlates with flanking intron retention time and target position within the exon.
Remko Goossens, Nisha Verwey, Yavuz Ariyurek, Fred Schnell, Annemieke Aartsma-Rus

RNA Biol· January 2023

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Histone deacetylase inhibitors improve antisense-mediated exon-skipping efficacy in mice.
Flavien Bizot, Remko Goossens, Thomas Tensorer, Sergei Dmitriev, Luis Garcia

Mol Ther Nucleic Acids· December 2022

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In Vitro Delivery of PMOs in Myoblasts by Electroporation.
Remko Goossens, Annemieke Aartsma-Rus

Methods Mol Biol· March 2022

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A proteomics study identifying interactors of the FSHD2 gene product SMCHD1 reveals RUVBL1-dependent DUX4 repression.
Remko Goossens, Mara S Tihaya, Anita van den Heuvel, Klorane Tabot-Ndip, Iris M Willemsen

Sci Rep· December 2021

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Consequences of epigenetic derepression in facioscapulohumeral muscular dystrophy.
Anna Greco, Remko Goossens, Baziel van Engelen, Silvère M van der Maarel

Clin Genet· June 2020

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Homozygous nonsense variant in associated with facioscapulohumeral muscular dystrophy.
Kohei Hamanaka, Darina Šikrová, Satomi Mitsuhashi, Hiroki Masuda, Yukari Sekiguchi, Remko Goossens

Neurology· June 2020

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Intronic variants in FSHD: testing the potential for CRISPR-Cas9 genome editing.
Remko Goossens, Marlinde L van den Boogaard, Richard J L F Lemmers, Judit Balog, Patrick J van der Vliet

J Med Genet· December 2019

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Monosomy 18p is a risk factor for facioscapulohumeral dystrophy.
Judit Balog, Remko Goossens, Richard J L F Lemmers, Kirsten R Straasheijm, Patrick J van der Vliet

J Med Genet· July 2018

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