Bart Dermaut

Affiliations: 
University of Antwerp, Antwerpen, Vlaanderen, Belgium 
Area:
neural development
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"Bart Dermaut"
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Publications

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Marcogliese PC, Shashi V, Spillmann RC, et al. (2018) IRF2BPL Is Associated with Neurological Phenotypes. American Journal of Human Genetics
Malmanche N, Dourlen P, Gistelinck M, et al. (2017) Developmental Expression of 4-Repeat-Tau Induces Neuronal Aneuploidy in Drosophila Tauopathy Models. Scientific Reports. 7: 40764
Letronne F, Laumet G, Ayral AM, et al. (2016) ADAM30 Downregulates APP-Linked Defects Through Cathepsin D Activation in Alzheimer's Disease. Ebiomedicine
Santens P, Van Damme T, Steyaert W, et al. (2015) RNF216 mutations as a novel cause of autosomal recessive Huntington-like disorder. Neurology. 84: 1760-6
Vanden Broeck L, Kleinberger G, Chapuis J, et al. (2015) Functional complementation in Drosophila to predict the pathogenicity of TARDBP variants: evidence for a loss-of-function mechanism. Neurobiology of Aging. 36: 1121-9
Miskiewicz K, Jose LE, Yeshaw WM, et al. (2014) HDAC6 is a Bruchpilot deacetylase that facilitates neurotransmitter release. Cell Reports. 8: 94-102
van der Zee J, Van Langenhove T, Kovacs GG, et al. (2014) Rare mutations in SQSTM1 modify susceptibility to frontotemporal lobar degeneration. Acta Neuropathologica. 128: 397-410
Vanden Broeck L, Callaerts P, Dermaut B. (2014) TDP-43-mediated neurodegeneration: towards a loss-of-function hypothesis? Trends in Molecular Medicine. 20: 66-71
Chapuis J, Hansmannel F, Gistelinck M, et al. (2013) Increased expression of BIN1 mediates Alzheimer genetic risk by modulating tau pathology. Molecular Psychiatry. 18: 1225-34
Vanden Broeck L, Naval-Sánchez M, Adachi Y, et al. (2013) TDP-43 loss-of-function causes neuronal loss due to defective steroid receptor-mediated gene program switching in Drosophila. Cell Reports. 3: 160-72
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