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Nature|June 11, 2015
α-Synuclein strains cause distinct synucleinopathies after local and systemic administrationW Peelaerts, L Bousset, A Van der Perren, et al.
Human Molecular Genetics|March 24, 2017
ATP13A2/PARK9 regulates endo-/lysosomal cargo sorting and proteostasis through a novel PI(3, 5)P2-mediated scaffolding functionS Demirsoy, S Martin, S Motamedi, et al.
Mechanisms of Development|April 5, 2001
Mice with a homozygous gene trap vector insertion in mgcRacGAP die during pre-implantation developmentT Van de Putte, A Zwijsen, O Lonnoy, et al.
Molecular Pharmacology|April 1, 1993
Kinetics of different human immunodeficiency virus type 1 reverse transcriptases resistant to human immunodeficiency virus type 1-specific reverse transcriptase inhibitorsZ Debyser, K De Vreese, P P Knops-Gerrits, et al.
British Journal of Pharmacology|January 12, 2012
A prolyl oligopeptidase inhibitor, KYP-2047, reduces α-synuclein protein levels and aggregates in cellular and animal models of Parkinson's diseaseT T Myöhänen, M J Hannula, R Van Elzen, et al.
Gene Therapy|February 18, 2011
Efficient and stable transduction of dopaminergic neurons in rat substantia nigra by rAAV 2/1, 2/2, 2/5, 2/6.2, 2/7, 2/8 and 2/9A Van der Perren, J Toelen, M Carlon, et al.
Gene Therapy|February 25, 2011
Evaluation of the specificity and sensitivity of ferritin as an MRI reporter gene in the mouse brain using lentiviral and adeno-associated viral vectorsG Vande Velde, J R Rangarajan, J Toelen, et al.
The Journal of Biological Chemistry|February 26, 1999
Early phenotypic changes in transgenic mice that overexpress different mutants of amyloid precursor protein in brainD Moechars, I Dewachter, K Lorent, et al.
Cell Death & Disease|January 18, 2014
Depletion of RIPK3 or MLKL blocks TNF-driven necroptosis and switches towards a delayed RIPK1 kinase-dependent apoptosisQ Remijsen, V Goossens, S Grootjans, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 16, 1999
Presenilin 2 deficiency causes a mild pulmonary phenotype and no changes in amyloid precursor protein processing but enhances the embryonic lethal phenotype of presenilin 1 deficiencyA Herreman, D Hartmann, W Annaert, et al.
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