Bart Dermaut

University of Antwerp, Antwerpen, Vlaanderen, Belgium 
neural development
"Bart Dermaut"
BETA: Related publications


You can help our author matching system! If you notice any publications incorrectly attributed to this author, please sign in and mark matches as correct or incorrect.

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
See more...