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Article

Diot, A., Agnew, T., Sanderson, J. et al. (16 more authors) (2018) Validating the RedMIT/GFP-LC3 Mouse Model by Studying Mitophagy in Autosomal Dominant Optic Atrophy Due to the OPA1Q285STOP Mutation. Frontiers in Cell and Developmental Biology, 6. 103.

Southam, H.M., Smith, T.W., Lyon, R.L. et al. (10 more authors) (2018) A thiol-reactive Ru(II) ion, not CO release, underlies the potent antimicrobial and cytotoxic properties of CO-releasing molecule-3. Redox Biology, 18. pp. 114-123.

Liao, C., Beveridge, R., Hudson, J.J.R. et al. (7 more authors) (2018) UCHL3 Regulates Topoisomerase-Induced Chromosomal Break Repair by Controlling TDP1 Proteostasis. Cell Reports, 23 (11). pp. 3352-3365. ISSN 2211-1247

Walker, C., Herranz-Martin, S., Karyka, E. et al. (19 more authors) (2017) C9orf72 Expansion Disrupts ATM-mediated Chromosomal Break Repair. Nature Neuroscience. ISSN 1097-6256

Meisenberg, C., Ashour, M.E., El-Shafie, L. et al. (7 more authors) (2017) Epigenetic changes in histone acetylation underpin resistance to the topoisomerase I inhibitor irinotecan. Nucleic Acids Research, 45 (3). pp. 1159-1176. ISSN 0305-1048

Liao, C., Ashley, N., Diot, A. et al. (30 more authors) (2017) Dysregulated mitophagy and mitochondrial organization in optic atrophy due to OPA1 mutations. Neurology, 88 (2). pp. 131-142. ISSN 0028-3878

Dombi, E., Diot, A., Morten, K. et al. (16 more authors) (2016) The m.13051G>A mitochondrial DNA mutation results in variable neurology and activated mitophagy. Neurology, 86 (20). pp. 1921-1923. ISSN 0028-3878

This list was generated on Sun Oct 13 08:15:09 2019 BST.