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The Journal of Cell Biology|November 26, 2014
Reduced synaptic vesicle protein degradation at lysosomes curbs TBC1D24/sky-induced neurodegenerationAna Clara Fernandes, Valerie Uytterhoeven, Sabine Kuenen, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|November 25, 2003
Endophilin promotes a late step in endocytosis at glial invaginations in Drosophila photoreceptor terminalsRuth Fabian-Fine, Patrik Verstreken, P Robin Hiesinger, et al.
Nature Structural & Molecular Biology|November 5, 2016
Skywalker-TBC1D24 has a lipid-binding pocket mutated in epilepsy and required for synaptic functionBaptiste Fischer, Kevin Lüthy, Jone Paesmans, et al.
The Journal of Cell Biology|December 26, 2007
Huntingtin-interacting protein 14, a palmitoyl transferase required for exocytosis and targeting of CSP to synaptic vesiclesTomoko Ohyama, Patrik Verstreken, Cindy V Ly, et al.
Proceedings of the National Academy of Sciences of the United States of America|November 2, 2022
Nano-positioning and tubulin conformation contribute to axonal transport regulation of mitochondria along microtubulesValérie Van Steenbergen, Flavie Lavoie-Cardinal, Youcef Kazwiny, et al.
Frontiers in Neural Circuits|September 26, 2013
Mushroom body miscellanea: transgenic Drosophila strains expressing anatomical and physiological sensor proteins in Kenyon cellsUlrike Pech, Shubham Dipt, Jonas Barth, et al.
Elife|December 22, 2020
A structure of substrate-bound Synaptojanin1 provides new insights in its mechanism and the effect of disease mutationsJone Paesmans, Ella Martin, Babette Deckers, et al.
ACS Pharmacology & Translational Science|September 19, 2025
Discovery and Characterization of a Selective Inhibitor of Synaptojanin1 5‑Phosphatase ActivityElla Martin, Danaë Giakoumakis, Jone Paesmans, et al.
Human Molecular Genetics|March 9, 2012
Alternative oxidase rescues mitochondria-mediated dopaminergic cell loss in DrosophilaDickon M Humphrey, Richard B Parsons, Zoe N Ludlow, et al.
NPJ Parkinson'S Disease|February 4, 2023
Parkinsonism mutations in DNAJC6 cause lipid defects and neurodegeneration that are rescued by Synj1Julie Jacquemyn, Sabine Kuenen, Jef Swerts, et al.
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