Julie Jacquemyn

Membrane defects and genetic redundancy: Are we at a turning point for DYT1 dystonia?

Rose E Goodchild, R. Goodchild, Ana Cascalho, 2017, Movement disorders : official journal of the Movement Disorder Society.

Molecule-to-Circuit Disease Mechanisms of a Synaptic SNAREopathy

P. Verstreken, R. Praschberger, Julie Jacquemyn, 2021, Neuron.

Parkinsonism mutations in DNAJC6 cause lipid defects and neurodegeneration that are rescued by Synj1

P. Verstreken, Benjamin Pavie, Sabine Kuenen, 2022, bioRxiv.

The ins and outs of endoplasmic reticulum‐controlled lipid biosynthesis

Rose E Goodchild, R. Goodchild, Ana Cascalho, 2017, EMBO reports.

The Mitochondrial m-AAA Protease Prevents Demyelination and Hair Greying

E. Rugarli, T. Langer, P. Martinelli, 2016, PLoS genetics.

Torsin and NEP1R1‐CTDNEP1 phosphatase affect interphase nuclear pore complex insertion by lipid‐dependent and lipid‐independent mechanisms

P. Verstreken, K. Vints, Jef Swerts, 2021, The EMBO journal.

The Torsin/ NEP1R1-CTDNEP1/ Lipin axis regulates nuclear envelope lipid metabolism for nuclear pore complex insertion

P. Verstreken, K. Vints, Jef Swerts, 2020, bioRxiv.

Neuronal AMPK regulates lipid transport to microglia

Julie Jacquemyn, Maria S. Ioannou, Ju-Young Bae, 2024, Trends in Cell Biology.

Tau is required for glial lipid droplet formation and resistance to neuronal oxidative stress.

Oguz Kanca, Julie Jacquemyn, Isha Ralhan, 2024, Nature neuroscience.

Driving factors of neuronal ferroptosis.

Julie Jacquemyn, Isha Ralhan, Maria S. Ioannou, 2024, Trends in cell biology.