Items where authors include "Poulton, J."

Article

Harvey, C., Weinreich, M. orcid.org/0009-0003-1576-3385, Lee, J.A.K. orcid.org/0000-0001-9843-6475 et al. (22 more authors) (2024) Rare and common genetic determinants of mitochondrial function determine severity but not risk of amyotrophic lateral sclerosis. Heliyon, 10 (3). e24975. ISSN 2405-8440

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.

Dombi, E., Mortiboys, H. and Poulton, J. (2018) Modulating mitophagy in mitochondrial disease. Current Medicinal Chemistry, 25 (40). pp. 5597-5612. ISSN 0929-8673

McRae, J.F., Clayton, S., Fitzgerald, T.W. et al. (299 more authors) (2017) Prevalence and architecture of de novo mutations in developmental disorders. Nature, 542 (7642). pp. 433-438. ISSN 0028-0836

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

Poulton, J., Bentham, C. orcid.org/0000-0003-0698-0161, George, S.P. et al. (1 more author) (2014) Monte Carlo simulations for Ising spins with spin greater than 1/2 applied to the square and triangular lattices with antiferromagnetic interactions and comparing results using Kawasaki and Glauber dynamics. arXiv. (Unpublished)