Folgen
Femke M.S. de Vrij
Femke M.S. de Vrij
Department of Psychiatry, Erasmus MC, Rotterdam, The Netherlands
Bestätigte E-Mail-Adresse bei erasmusmc.nl
Titel
Zitiert von
Zitiert von
Jahr
Rescue of behavioral phenotype and neuronal protrusion morphology in Fmr1 KO mice
FMS de Vrij, J Levenga, HC Van der Linde, SK Koekkoek, CI De Zeeuw, ...
Neurobiology of disease 31 (1), 127-132, 2008
3512008
Activity-based protein profiling reveals off-target proteins of the FAAH inhibitor BIA 10-2474
ACM van Esbroeck, APA Janssen, AB Cognetta, D Ogasawara, G Shpak, ...
Science 356 (6342), 1084-1087, 2017
3132017
Mutant ubiquitin found in neurodegenerative disorders is a ubiquitin fusion degradation substrate that blocks proteasomal degradation
K Lindsten, FMS de Vrij, LGGC Verhoef, DF Fischer, FW van Leeuwen, ...
The Journal of cell biology 157 (3), 417-427, 2002
2592002
A simplified protocol for differentiation of electrophysiologically mature neuronal networks from human induced pluripotent stem cells
N Gunhanlar, G Shpak, M Van Der Kroeg, LA Gouty-Colomer, ST Munshi, ...
Molecular Psychiatry, 2017
2112017
The SAC1 domain in synaptojanin is required for autophagosome maturation at presynaptic terminals
R Vanhauwaert, S Kuenen, R Masius, A Bademosi, J Manetsberger, ...
The EMBO journal 36 (10), 1392-1411, 2017
1942017
Mutant ubiquitin expressed in Alzheimer’s disease causes neuronal death1
FMS De Vrij, JA Sluijs, L Gregori, DF Fischer, WT Hermens, D Goldgaber, ...
The FASEB Journal 15 (14), 2680-2688, 2001
1582001
The neuroinvasiveness, neurotropism, and neurovirulence of SARS-CoV-2
L Bauer, BM Laksono, FMS de Vrij, SA Kushner, O Harschnitz, D van Riel
Trends in Neurosciences, 2022
1422022
Disease-specific accumulation of mutant ubiquitin as a marker for proteasomal dysfunction in the brain
DF FISCHER, ROBAI DE VOS, R VAN DIJK, FMS DE VRIJ, EA PROPER, ...
The FASEB Journal 17 (14), 2014-2024, 2003
1422003
AFQ056, a new mGluR5 antagonist for treatment of fragile X syndrome
J Levenga, S Hayashi, FMS de Vrij, SK Koekkoek, HC van der Linde, ...
Neurobiology of disease 42 (3), 311-317, 2011
1362011
Hepatitis E virus infects neurons and brains
X Zhou, F Huang, L Xu, Z Lin, F de Vrij, AC Ayo-Martin, M van der Kroeg, ...
The Journal of Infectious Diseases 215 (8), 1197-1206, 2017
1192017
Potential therapeutic interventions for fragile X syndrome
J Levenga, FMS de Vrij, BA Oostra, R Willemsen
Trends in molecular medicine 16 (11), 516-527, 2010
1102010
Dose-dependent inhibition of proteasome activity by a mutant ubiquitin associated with neurodegenerative disease
P van Tijn, FMS de Vrij, KG Schuurman, NP Dantuma, DF Fischer, ...
Journal of cell science 120 (9), 1615-1623, 2007
1072007
SOX10 Single Transcription Factor-Based Fast and Efficient Generation of Oligodendrocytes from Human Pluripotent Stem Cells
JA García-León, M Kumar, R Boon, D Chau, E Wolfs, K Eggermont, ...
Stem cell reports 10 (2), 655-672, 2018
1012018
Phenotypic differences between Asian and African lineage Zika viruses in human neural progenitor cells
F Anfasa, JY Siegers, M van der Kroeg, N Mumtaz, VS Raj, FMS de Vrij, ...
MSphere 2 (4), 2017
852017
Loss of nuclear UBE3A causes electrophysiological and behavioral deficits in mice and is associated with Angelman syndrome
R Avagliano Trezza, M Sonzogni, SNV Bossuyt, FI Zampeta, AM Punt, ...
Nature Neuroscience, 2019
772019
Novel genetic loci affecting facial shape variation in humans
Z Xiong, G Dankova, LJ Howe, MK Lee, PG Hysi, MA de Jong, G Zhu, ...
Elife 8, e49898, 2019
702019
Novel genetic loci affecting facial shape variation in humans
Z Xiong, G Dankova, LJ Howe, MK Lee, PG Hysi, MA de Jong, G Zhu, ...
Elife 8, e49898, 2019
702019
Candidate CSPG4 mutations and induced pluripotent stem cell modeling implicate oligodendrocyte progenitor cell dysfunction in familial schizophrenia
FM de Vrij, CG Bouwkamp, N Gunhanlar, G Shpak, B Lendemeijer, ...
Molecular psychiatry 24 (5), 757-771, 2019
662019
Epigenetic characterization of the FMR1 promoter in induced pluripotent stem cells from human fibroblasts carrying an unmethylated full mutation
CEF de Esch, M Ghazvini, F Loos, N Schelling-Kazaryan, W Widagdo, ...
Stem cell reports 3 (4), 548-555, 2014
642014
Subregion-specific dendritic spine abnormalities in the hippocampus of Fmr1 KO mice
J Levenga, FMS de Vrij, RAM Buijsen, T Li, IM Nieuwenhuizen, A Pop, ...
Neurobiology of learning and memory 95 (4), 467-472, 2011
632011
Das System kann den Vorgang jetzt nicht ausführen. Versuchen Sie es später erneut.
Artikel 1–20