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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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
Diaper DC, Adachi Y, Sutcliffe B, et al. (2013) Loss and gain of Drosophila TDP-43 impair synaptic efficacy and motor control leading to age-related neurodegeneration by loss-of-function phenotypes. Human Molecular Genetics. 22: 1539-57
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