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2023 Journal Article 3D in vitro modelling of human patient microglia: A focus on clinical translation and drug development in neurodegenerative diseasesCuní-López, Carla, Stewart, Romal, White, Anthony R. and Quek, Hazel (2023). 3D in vitro modelling of human patient microglia: A focus on clinical translation and drug development in neurodegenerative diseases. Journal of Neuroimmunology, 375 578017, 578017. doi: 10.1016/j.jneuroim.2023.578017 |
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2022 Journal Article Recent advances in microglia modelling to address translational outcomes in neurodegenerative diseasesCuní-López, Carla, Stewart, Romal, Quek, Hazel and White, Anthony R. (2022). Recent advances in microglia modelling to address translational outcomes in neurodegenerative diseases. Cells, 11 (10) 1662, 1-23. doi: 10.3390/cells11101662 |
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2019 Other Outputs A neuronal model to investigate the human genetic disorder Ataxia-TelangiectasiaStewart, Romal (2019). A neuronal model to investigate the human genetic disorder Ataxia-Telangiectasia. PhD Thesis, Faculty of Medicine, The University of Queensland. doi: 10.14264/uql.2019.371 |
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2017 Book Chapter A patient-specific stem cell model to investigate the neurological phenotype observed in ataxia-telangiectasiaStewart, Romal, Wali, Gautam, Perry, Chris, Lavin, Martin F., Féron, Francois, Mackay-Sim, Alan and Sutharsan, Ratneswary (2017). A patient-specific stem cell model to investigate the neurological phenotype observed in ataxia-telangiectasia. ATM kinase: methods and protocols. (pp. 391-400) New York, NY, United States: Humana Press. doi: 10.1007/978-1-4939-6955-5_28 |
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2016 Journal Article Mechanism of impaired microtubule-dependent peroxisome trafficking and oxidative stress in SPAST-mutated cells from patients with Hereditary Spastic ParaplegiaWali, Gautam, Sutharsan, Ratneswary, Fan, Yongjun, Stewart, Romal, Velasquez, Johana Tello, Sue, Carolyn M., Crane, Denis I. and Mackay-Sim, Alan (2016). Mechanism of impaired microtubule-dependent peroxisome trafficking and oxidative stress in SPAST-mutated cells from patients with Hereditary Spastic Paraplegia. Scientific Reports, 6 (27004) 27004, 27004. doi: 10.1038/srep27004 |
