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Methods in Molecular Biology (Clifton, N.J.)|February 25, 2022
Delivery of Antisense Oligonucleotides to the Mouse Brain by Intracerebroventricular InjectionsTom Metz, Elsa C Kuijper, Willeke M C van Roon-MomJournal of Inherited Metabolic Disease|May 12, 2020
Opportunities and challenges for antisense oligonucleotide therapiesElsa C Kuijper, Atze J Bergsma, W W M Pim Pijnappel, et al.Molecular Neurobiology|January 29, 2022
Huntington Disease Gene Expression Signatures in Blood Compared to Brain of YAC128 Mice as Candidates for Monitoring of PathologyElsa C Kuijper, Lodewijk J A Toonen, Maurice Overzier, et al.Biomedicines|September 28, 2024
Calcium-Enhanced Medium-Based Delivery of Splice Modulating Antisense Oligonucleotides in 2D and 3D hiPSC-Derived Neuronal ModelsRonald A M Buijsen, Linda M van der Graaf, Elsa C Kuijper, et al.Scientific Reports|January 9, 2025
A collaborative network analysis for the interpretation of transcriptomics data in Huntington's diseaseOzan Ozisik, Nazli Sila Kara, Tooba Abbassi-Daloii, et al.Neurobiology of Disease|December 1, 2023
Antisense oligonucleotide-mediated disruption of HTT caspase-6 cleavage site ameliorates the phenotype of YAC128 Huntington disease miceElsa C Kuijper, Maurice Overzier, Ernst Suidgeest, et al.Human Molecular Genetics|October 9, 2025
Determining off-target effects of splice-switching antisense oligonucleotides using short read RNAseq in neuronally differentiated human induced pluripotent stem cellsElsa C Kuijper, Linda van der Graaf, Barry A Pepers, et al.Nature Communications|March 2, 2018
FcαRI co-stimulation converts human intestinal CD103+ dendritic cells into pro-inflammatory cells through glycolytic reprogrammingIvo S Hansen, Lisette Krabbendam, Jochem H Bernink, et al.Pageof 1