Brent Ryan
Departmental Research Lecturer
I joined the University of Oxford in 2010 investigating animal and iPSC models of Parkinson's. Since becoming a Departmental Lecturer in 2021, my work has focused on combining new approaches such as post-translational proteomics, Crispr and high-throughput biology to identify new drugs and drug targets for Parkinson’s disease, with a focus on mitochondrial biology and quality control. My team has successfully identified novel targets for Parkinson’s using engineered and patient-derived iPSCs differentiated into dopaminergic neurons using novel post-translational and standard proteomics platforms. My team has also established phenotypic screening platforms in mature patient iPSC-derived neurons, primary rodent neurons and neuroblastoma to exploit proteomics targets and identify novel targets and chemical series’, some of which are being progressed into animal models.
Recent publications
-
TFEB and TFE3 have cell-type specific expression in the brain and divergent roles in neurons
Preprint
McGuinness W. et al, (2025)
-
Heritable maintenance of chromatin modifications confers transcriptional memory of interferon-γ signaling
Journal article
Mikulski P. et al, (2025), Nature Structural & Molecular Biology
-
USP30 inhibition improves mitochondrial health through both PINK1-dependent and independent mechanisms
Preprint
Williamson MG. et al, (2025)
-
CRISPRi: a way to integrate iPSC-derived neuronal models
Journal article
Franks SNJ. et al, (2024), Biochemical Society Transactions, 52, 539 - 551
-
Transcriptional memory is conferred by combined heritable maintenance and local removal of selective chromatin modifications
Preprint
Mikulski P. et al, (2023)