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My research group investigates how dysfunctional transport between the nucleus and cytoplasm (nucleocytoplasmic transport) can initiate neurodegeneration in frontotemporal dementia (FTD) and amyotrophic lateral sclerosis (ALS). We are particularly interested in the most common genetic mutation in these diseases – C9orf72, and the most common protein found in aggregates in these diseases (and across many dementias) TDP-43. We investigate this using quantitative microscopy techniques, developing novel super-resolution methodologies for monitoring single molecule nucleocytoplasmic transport and assessing the phase transitioning properties of the nuclear pore. Much of this work is associated with my role as a Programme Leader at the UK Dementia Research Institute and I also participate in undergraduate/postgraduate teaching and co-lead a module in an online distance learning MSc.
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Brain : a journal of neurology (2024)
ACTA NEUROPATHOLOGICAno. 1 (2024)
Acta Neuropathologicano. 1 (2024): 1-14
Niamh O’Brien,Sarah Mizielinska
Science (New York, N.Y.)no. 6637 (2023): 1090-1091
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