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Methods in Molecular Biology (Clifton, N.J.)|September 2, 2018
Antisense Oligonucleotide Design and Evaluation of Splice-Modulating Properties Using Cell-Based AssaysRalph Slijkerman, Hannie Kremer, Erwin van Wijk
Methods in Molecular Biology (Clifton, N.J.)|February 25, 2022
Generation of Humanized Zebrafish Models for the In Vivo Assessment of Antisense Oligonucleotide-Based Splice Modulation TherapiesRenske Schellens, Erik de Vrieze, Ralph Slijkerman, et al.
Zebrafish|October 4, 2018
Poor Splice-Site Recognition in a Humanized Zebrafish Knockin Model for the Recurrent Deep-Intronic c.7595-2144A>G Mutation in USH2ARalph Slijkerman, Alexander Goloborodko, Sanne Broekman, et al.
Human Molecular Genetics|September 22, 2006
Usher syndrome: molecular links of pathogenesis, proteins and pathwaysHannie Kremer, Erwin van Wijk, Tina Märker, et al.
Cells|June 28, 2023
Generation and Characterization of a Zebrafish Model for ADGRV1-Associated Retinal Dysfunction Using CRISPR/Cas9 Genome Editing TechnologyMerel Stemerdink, Sanne Broekman, Theo Peters, et al.
Biochimica Et Biophysica Acta|July 20, 2011
Direct interaction of the Usher syndrome 1G protein SANS and myomegalin in the retinaNora Overlack, Dilek Kilic, Katharina Bauss, et al.
Experimental Eye Research|May 20, 2018
Usherin defects lead to early-onset retinal dysfunction in zebrafishMargo Dona, Ralph Slijkerman, Kimberly Lerner, et al.
International Journal of Molecular Sciences|September 10, 2021
Efficient Generation of Knock-In Zebrafish Models for Inherited Disorders Using CRISPR-Cas9 Ribonucleoprotein ComplexesErik de Vrieze, Suzanne E de Bruijn, Janine Reurink, et al.
Molecular Therapy. Nucleic Acids|June 14, 2023
A protein domain-oriented approach to expand the opportunities of therapeutic exon skipping for USH2A-associated retinitis pigmentosaRenske T W Schellens, Sanne Broekman, Theo Peters, et al.
Hearing Research|January 23, 2019
Hereditary hearing loss; about the known and the unknownHannie Kremer
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