Edinburgh Research Explorer

Anna Williams

Personal chair of Regenerative neurology

  1. Comparative assessment of phototherapy protocols for reduction of oxidative stress in partially transected spinal cord slices undergoing secondary degeneration

    Ashworth, B. E., Stephens, E., Bartlett, C. A., Serghiou, S., Giacci, M. K., Williams, A., Hart, N. S. & Fitzgerald, M., 18 May 2016, In: BMC Neuroscience.

    Research output: Contribution to journalArticlepeer-review

  2. Association between endothelial cell stabilizing medication and small vessel disease stroke: a case-control study

    Becker, C. E., Quinn, T. & Williams, A., 25 Sep 2019, In: Frontiers in Neurology.

    Research output: Contribution to journalArticlepeer-review

  3. Correlated Heterospectral Lipidomics for Biomolecular Profiling of Remyelination in Multiple Sclerosis

    Bergholt, M. S., Serio, A., McKenzie, J. S., Boyd, A., Soares, R. F., Tillner, J., Chiappini, C., Wu, V., Dannhorn, A., Takats, Z., Williams, A. & Stevens, M. M., 27 Dec 2017, In: ACS Central Science. 4, 1, p. 39-51 13 p.

    Research output: Contribution to journalArticlepeer-review

  4. Insufficient OPC migration into demyelinated lesions is a cause of poor remyelination in MS and mouse models

    Boyd, A., Zhang, H. & Williams, A., Jun 2013, In: Acta Neuropathologica. p. 1-19 19 p.

    Research output: Contribution to journalArticlepeer-review

  5. A systematic approach to selecting licensed drugs for repurposing in the treatment of progressive multiple sclerosis

    Cunniffe, N., Vuong, K. A., Ainslie, D., Baker, D., Beveridge, J., Bickley, S. R. B., Camilleri, P., Craner, M., Fitzgerald, D. C., De La Fuente, A. G., Giovannoni, G., Gray, E., Hazlehurst, L., Kapoor, R., Kaur, R., Kozlowski, D., Lumicisi, B., Mahad, D., Neumann, B., Palmer, A. & 9 others, Peruzzotti-Jametti, L., Pluchino, S., Robertson, J., Rothaul, A., Shellard, L., Smith, K. J., Wilkins, A., Williams, A. C. & Coles, A. J., 12 Nov 2020, In: Journal of Neurology, Neurosurgery & Psychiatry.

    Research output: Contribution to journalArticlepeer-review

  6. Activin receptors regulate the oligodendrocyte lineage in health and disease

    Dillenburg, A., Ireland, G., Holloway, R. K., Davies, C. L., Evans, F. L., Swire, M., Bechler, M. E., Soong, D., Yuen, T. J., Su, G. H., Becher, J-C., Smith, C., Williams, A. & Miron, V. E., 30 Jun 2018, In: Acta Neuropathologica. 135, 6, p. 887–906 20 p.

    Research output: Contribution to journalArticlepeer-review

  7. Regulatory T cells promote myelin regeneration in the central nervous system

    Dombrowski, Y., O'Hagan, T., Dittmer, M., Penalva, R., Mayoral, S. R., Bankhead, P., Fleville, S., Eleftheriadis, G., Zhao, C., Naughton, M., Hassan, R., Moffat, J., Falconer, J., Boyd, A., Hamilton, P., Allen, I. V., Kissenpfennig, A., Moynagh, P. N., Evergren, E., Perbal, B. & 5 others, Williams, A. C., Ingram, R. J., Chan, J. R., Franklin, R. J. M. & Fitzgerald, D. C., May 2017, In: Nature Neuroscience. 20, 5, p. 674-680 7 p.

    Research output: Contribution to journalArticlepeer-review

  8. Cryogel scaffolds for regionally constrained delivery of lysophosphatidylcholine to central nervous system slice cultures: a model of focal demyelination for multiple sclerosis research

    Eigel, D., Zoupi, L., Sekizar, S., Welzel, P., Werner, C., Williams, A. & Newland, B., Oct 2019, In: Acta Biomaterialia.

    Research output: Contribution to journalArticlepeer-review

  9. Intrinsic mutant HTT-mediated defects in oligodendroglia cause myelination deficits and behavioral abnormalities in Huntington disease

    Ferrari Bardile, C., Garcia-Miralles, M., Caron, N. S., Rayan, N. A., Langley, S. R., Harmston, N., Rondelli, A. M., Teo, R. T. Y., Waltl, S., Anderson, L. M., Bae, H-G., Jung, S., Williams, A., Prabhakar, S., Petretto, E., Hayden, M. R. & Pouladi, M. A., 7 May 2019, In: Proceedings of the National Academy of Sciences of the United States of America.

    Research output: Contribution to journalArticlepeer-review

  10. A mutation in periaxin is responsible for CMT4F, an autosomal recessive form of Charcot-Marie-Tooth disease

    Guilbot, A., Williams, A., Ravisé, N., Verny, C., Brice, A., Sherman, D. L., Brophy, P. J., LeGuern, E., Delague, V., Bareil, C., Mégarbané, A. & Claustres, M., 15 Feb 2001, In: Human Molecular Genetics. 10, 4, p. 415-21 7 p.

    Research output: Contribution to journalArticlepeer-review

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