Items where authors include "Liao, C."
Up a levelArticle
Liao, C., Wu, J., Wayne, S.J. et al. (2 more authors) (2024) It’s Unexpected, but Good: Leader Traditionality Fuels Greater Follower Reciprocation to Servant Leadership. Journal of Management. ISSN 0149-2063
Ray, S., Abugable, A.A., Parker, J. et al. (8 more authors) (2022) A mechanism for oxidative damage repair at gene regulatory elements. Nature, 609 (7929). pp. 1038-1047. ISSN 0028-0836
Lyon, R.F., Southam, H.M., Trevitt, C.R. et al. (4 more authors) (2022) CORM-3 induces DNA damage through Ru(II) binding to DNA. Biochemical Journal, 479 (13). pp. 1429-1439. ISSN 0264-6021
Palminha, N.M., Dos Santos Souza, C. orcid.org/0000-0001-5314-6263, Griffin, J. orcid.org/0000-0003-3969-7637 et al. (3 more authors) (2022) Defective repair of topoisomerase I induced chromosomal damage in Huntington’s disease. Cellular and Molecular Life Sciences, 79 (3). 160. ISSN 1420-682X
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, 20 (9). pp. 1225-1235. 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