Research groups
Colleges
Rachel Heon-Roberts
DPhil Student
Research Project
Mitochondrial dysfunction and impairment of the autophagy-lysosomal system have emerged as common mechanisms that characterise several neurodegenerative diseases, Parkinson’s disease and Alzheimer’s disease in particular. Using high-throughput imaging, electron microscopy and the CRISPRi system, my research investigates these mechanisms in the context of dementia, focussing on the impact of protein aggregation on these critical cellular systems.
Background
Whilst completing my undergraduate degree in Anatomy and Cell Biology at McGill University, I became interested in neurodegenerative diseases through my time as a research student in the lab of Alexey Pshezhetsky, investigating genetically-inherited neurological lysosomal storage disorders.
After graduating from my undergraduate degree in 2019, I spent a year as a research assistant working on mitochondrial dysfunction in the context of Parkinson’s disease with the Wade-Martins group before starting my DPhil.
Recent publications
CRISPRi: a way to integrate iPSC-derived neuronal models.
Journal article
Franks SNJ. et al, (2024), Biochem Soc Trans, 52, 539 - 551
Mitochondrial dysfunction and mitophagy defects in LRRK2-R1441C Parkinson's disease models.
Journal article
Williamson MG. et al, (2023), Hum Mol Genet, 32, 2808 - 2821
Post-translational proteomics platform identifies neurite outgrowth impairments in Parkinson's disease GBA-N370S dopamine neurons.
Journal article
Bogetofte H. et al, (2023), Cell Rep, 42
Glucosamine amends CNS pathology in mucopolysaccharidosis IIIC mouse expressing misfolded HGSNAT.
Journal article
Pan X. et al, (2022), J Exp Med, 219

