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EW

E. van der Wal

Pompe diseaseastro-ph.IMcell biologyexon inclusionlysosomal storage diseaselysosomal storage disorderpre-mRNA splicingskeletal muscleskeletal muscle differentiation3D-tissue engineering

On Valency

published · living versions
W_hfxes35b·v1 · currentpublished
LOFAR: The LOw-Frequency ARray
with M. P. van Haarlem, M. W. Wise, A. W. Gunst, G. Heald +195
1 version

Preprints & journals

18 papers in the corpus · 2011–2025
Three-dimensional tissue engineered skeletal muscle modelling facioscapulohumeral muscular dystrophy.39556762 · Franken, Marnix, van der Wal, Erik, Zheng, Dongxu et al.2025 · 11 citationsBrain : a journal of neurology. 2025;148(5):1723-1739
Highly contractile 3D tissue engineered skeletal muscles from human iPSCs reveal similarities with primary myoblast-derived tissues.37774701 · van der Wal, Erik, Iuliano, Alessandro, In 't Groen, Stijn L M et al.2023 · 44 citationsStem cell reports. 2023;18(10):1954-1971
USP18 is an essential regulator of muscle cell differentiation and maturation.37002195 · Olie, Cyriel Sebastiaan, Pinto-Fernández, Adán, Damianou, Andreas et al.2023 · 22 citationsCell death & disease. 2023;14(3):231
Author Correction: Cytoskeletal disorganization underlies PABPN1-mediated myogenic disability.33723339 · Olie, Cyriel Sebastiaan, van der Wal, Erik, Cikes, Domagoj et al.2025 · 1 citationScientific reports. 2021;11(1):6429
Cytoskeletal disorganization underlies PABPN1-mediated myogenic disability.33077830 · Olie, Cyriel Sebastiaan, van der Wal, Erik, Cikes, Domagoj et al.2021 · 11 citationsScientific reports. 2020;10(1):17621
Generation of genetically matched hiPSC lines from two mosaic facioscapulohumeral dystrophy type 1 patients.31518905 · van der Wal, Erik, den Hamer, Bianca, van der Vliet, Patrick J et al.2020 · 7 citationsStem cell research. 2019;40:101560
Large-Scale Expansion of Human iPSC-Derived Skeletal Muscle Cells for Disease Modeling and Cell-Based Therapeutic Strategies.29731431 · van der Wal, Erik, Herrero-Hernandez, Pablo, Wan, Raymond et al.2019 · 117 citationsStem cell reports. 2018;10(6):1975-1990
Alternative Splicing in Genetic Diseases: Improved Diagnosis and Novel Treatment Options.29305015 · Bergsma, Atze J, van der Wal, Erik, Broeders, Mike et al.2018 · 36 citationsInternational review of cell and molecular biology. 2018;335:85-141
GAA Deficiency in Pompe Disease Is Alleviated by Exon Inclusion in iPSC-Derived Skeletal Muscle Cells.28624186 · van der Wal, Erik, Bergsma, Atze J, van Gestel, Tom J M et al.2020 · 65 citationsMolecular therapy. Nucleic acids. 2017;7:101-115
Antisense Oligonucleotides Promote Exon Inclusion and Correct the Common c.-32-13T>G GAA Splicing Variant in Pompe Disease.28624228 · van der Wal, Erik, Bergsma, Atze J, Pijnenburg, Joon M et al.2020 · 68 citationsMolecular therapy. Nucleic acids. 2017;7:90-100
Epigenetic characterization of the FMR1 promoter in induced pluripotent stem cells from human fibroblasts carrying an unmethylated full mutation.25358783 · de Esch, Celine E F, Ghazvini, Mehrnaz, Loos, Friedemann et al.2015 · 58 citationsStem cell reports. 2014;3(4):548-55
LOFAR: The LOw-Frequency ARray1305.3550v2 · M. P. van Haarlem, M. W. Wise, A. W. Gunst et al.2013 · 2,662 citationsarXivon Valency
A central role for TFIID in the pluripotent transcription circuitry.23503660 · Pijnappel, W W M Pim, Esch, Daniel, Baltissen, Marijke P A et al.2013 · 88 citationsNature. 2013;495(7442):516-9
Dual function of Pin1 in NR4A nuclear receptor activation: enhanced activity of NR4As and increased Nur77 protein stability.22789442 · van Tiel, Claudia M, Kurakula, Kondababu, Koenis, Duco S et al.2012 · 32 citationsBiochimica et biophysica acta. 2012;1823(10):1894-904
FHL2 protein is a novel co-repressor of nuclear receptor Nur77.22049082 · Kurakula, Kondababu, van der Wal, Erik, Geerts, Dirk et al.2012 · 45 citationsThe Journal of biological chemistry. 2011;286(52):44336-43
Optimized Trigger for Ultra-High-Energy Cosmic-Ray and Neutrino Observations with the Low Frequency Radio Array1108.5745v1 · K. Singh, M. Mevius, O. Scholten et al.2011 · 17 citationsNucl. Inst. and Meth. 664 (2012) 171-185
Modeling oculopharyngeal muscular dystrophy in myotube cultures reveals reduced accumulation of soluble mutant PABPN1 protein.21854744 · Raz, Vered, Routledge, Samantha, Venema, Andrea et al.2012 · 44 citationsThe American journal of pathology. 2011;179(4):1988-2000
Career total: 40 works. 18 are in this corpus.

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