Elias Adriaenssens
Affiliations: | 2016-2020 | Receptor Biology Lab | University of Antwerp, Antwerpen, Vlaanderen, Belgium |
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| Tedesco B, Vendredy L, Adriaenssens E, et al. (2023) HSPB8 frameshift mutant aggregates weaken chaperone-assisted selective autophagy in neuromyopathies. Autophagy. 1-23 |
| Van Lent J, Verstraelen P, Asselbergh B, et al. (2021) Induced pluripotent stem cell-derived motor neurons of CMT type 2 patients reveal progressive mitochondrial dysfunction. Brain : a Journal of Neurology |
| Reid Alderson T, Adriaenssens E, Asselbergh B, et al. (2021) A weakened interface in the P182L variant of HSP27 associated with severe Charcot-Marie-Tooth neuropathy causes aberrant binding to interacting proteins. The Embo Journal. e103811 |
| Adriaenssens E, Tedesco B, Mediani L, et al. (2020) BAG3 Pro209 mutants associated with myopathy and neuropathy relocate chaperones of the CASA-complex to aggresomes. Scientific Reports. 10: 8755 |
| Vendredy L, Adriaenssens E, Timmerman V. (2020) Small heat shock proteins in neurodegenerative diseases. Cell Stress & Chaperones |
| Siekierska A, Stamberger H, Deconinck T, et al. (2019) Biallelic VARS variants cause developmental encephalopathy with microcephaly that is recapitulated in vars knockout zebrafish. Nature Communications. 10: 708 |
| Haidar M, Asselbergh B, Adriaenssens E, et al. (2019) Neuropathy-causing mutations in HSPB1 impair autophagy by disturbing the formation of SQSTM1/p62 bodies. Autophagy. 1-18 |
| Adriaenssens E, Geuens T, Baets J, et al. (2017) Novel insights in the disease biology of mutant small heat shock proteins in neuromuscular diseases. Brain : a Journal of Neurology. 140: 2541-2549 |
| Echaniz-Laguna A, Geuens T, Petiot P, et al. (2017) Axonal Neuropathies due to Mutations in Small Heat Shock Proteins: Clinical, Genetic and Functional Insights into Novel Mutations. Human Mutation |
| Capponi S, Geuens T, Geroldi A, et al. (2016) Molecular Chaperones in the Pathogenesis of Amyotrophic Lateral Sclerosis: the role of HSPB1. Human Mutation |