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Statement of Research Interest

1. Understanding the role of abnormal protein aggregates in the pathogenesis of MND

2. Using zebrafish to visualise neuron‐glia interactions underlying MND disease mechanisms

3. Nanoparticle‐based theranostics for MND and other neurodegenerative diseases

Lab Members

Zebrafish Publications of lab members

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• Rayner, S.L., Hogan, A., Davidson, J.M., Chapman, T., Cheng, F., Luu, L., Wu, S., Zhang, S., Yang, S., Blair, I., Morsch, M., Chung, R., Lee, A. (2024) Cyclin F can alter the turnover of TDP-43. Neurobiology of disease. 192:106421
• Fu, L., Shi, B., Wen, S., Morsch, M., Wang, G., Zhou, Z., Mi, C., Sadraeian, M., Lin, G., Lu, Y., Jin, D., Chung, R. (2022) Aspect Ratio of PEGylated Upconversion Nanocrystals Affects the Cellular Uptake In Vitro and In Vivo. Acta biomaterialia. 147:403-413
• Cheng, F., De Luca, A., Hogan, A.L., Rayner, S.L., Davidson, J.M., Watchon, M., Stevens, C.H., Muñoz, S.S., Ooi, L., Yerbury, J.J., Don, E.K., Fifita, J.A., Villalva, M.D., Suddull, H., Chapman, T.R., Hedl, T.J., Walker, A.K., Yang, S., Morsch, M., Shi, B., Blair, I.P., Laird, A.S., Chung, R.S., Lee, A. (2021) Unbiased Label-Free Quantitative Proteomics of Cells Expressing Amyotrophic Lateral Sclerosis (ALS) Mutations in CCNF Reveals Activation of the Apoptosis Pathway: A Workflow to Screen Pathogenic Gene Mutations. Frontiers in molecular neuroscience. 14:627740
• Don, E.K., Maschirow, A., Radford, R.A.W., Scherer, N.M., Vidal-Itriago, A., Hogan, A., Maurel, C., Formella, I., Stoddart, J.J., Hall, T.E., Lee, A., Shi, B., Cole, N.J., Laird, A.S., Badrock, A.P., Chung, R.S., Morsch, M. (2021) In vivo Validation of Bimolecular Fluorescence Complementation (BiFC) to Investigate Aggregate Formation in Amyotrophic Lateral Sclerosis (ALS). Molecular neurobiology. 58(5):2061-2074
• Watchon, M., Luu, L., Robinson, K.J., Yuan, K.C., De Luca, A., Suddull, H.J., Tym, M.C., Guillemin, G.J., Cole, N.J., Nicholson, G.A., Chung, R.S., Lee, A., Laird, A.S. (2021) Sodium valproate increases activity of the sirtuin pathway resulting in beneficial effects for spinocerebellar ataxia-3 in vivo. Molecular brain. 14:128
• Cheng, D., Morsch, M., Shami, G.J., Chung, R.S., Braet, F. (2020) Observation and characterisation of macrophages in zebrafish liver. Micron (Oxford, England : 1993). 132:102851
• Wang, G., Zhao, X., Wu, H., Lovejoy, D.B., Zheng, M., Lee, A., Fu, L., Miao, K., An, Y., Sayyadi, N., Ding, K., Chung, R.S., Lu, Y., Li, J., Morsch, M., Shi, B. (2020) A Robust Intrinsically Green Fluorescent Poly(Amidoamine) Dendrimer for Imaging and Traceable Central Nervous System Delivery in Zebrafish. Small (Weinheim an der Bergstrasse, Germany). 16(39):e2003654
• Aksoy, Y.A., Nguyen, D.T., Chow, S., Chung, R.S., Guillemin, G.J., Cole, N.J., Hesselson, D. (2019) Chemical reprogramming enhances homology-directed genome editing in zebrafish embryos. Communications biology. 2:198
• Fu, L., Chung, R., Shi, B. (2019) Upconversion Nanoparticle-Based Strategy for Crossing the Blood-Brain Barrier to Treat the Central Nervous System Disease. Methods in molecular biology (Clifton, N.J.). 2054:263-282
• Cheng, D., Morsch, M., Shami, G.J., Chung, R.S., Braet, F. (2018) Albumin uptake and distribution in the zebrafish liver as observed via correlative imaging. Experimental cell research. 374(1):162-171

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