Mahmoud A. Pouladi
Affiliations: | National University of Singapore, Singapore, Singapore |
Area:
Huntington's disease, Fragile X Syndrome, Multiple SclerosisGoogle:
"Mahmoud Pouladi"Mean distance: (not calculated yet)
Children
Sign in to add trainee| Carola Izabela Radulescu | grad student | 2016-2018 | University of Sheffield |
| Costanza Ferrari Bardile | grad student | 2015-2020 | National University of Singapore |
| Amin Ziaei | grad student | 2015-2020 | National University of Singapore |
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Publications
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| Radulescu CI, Ferrari Bardile C, Garcia-Miralles M, et al. (2023) Environmental Deprivation Effects on Myelin Ultrastructure in Huntington Disease and Wildtype Mice. Molecular Neurobiology |
| Ferrari Bardile C, Radulescu CI, Pouladi MA. (2023) Oligodendrocyte pathology in Huntington's disease: from mechanisms to therapeutics. Trends in Molecular Medicine. 29: 802-816 |
| Ziaei A, Garcia-Miralles M, Radulescu CI, et al. (2022) Ermin deficiency leads to compromised myelin, inflammatory milieu, and susceptibility to demyelinating insult. Brain Pathology (Zurich, Switzerland). e13064 |
| Gabery S, Kwa JE, Cheong RY, et al. (2021) Early white matter pathology in the fornix of the limbic system in Huntington disease. Acta Neuropathologica |
| Lemarié FL, Caron NS, Sanders SS, et al. (2021) Rescue of aberrant huntingtin palmitoylation ameliorates mutant huntingtin-induced toxicity. Neurobiology of Disease. 105479 |
| Ferrari Bardile C, Sidik H, Quek R, et al. (2021) Abnormal Spinal Cord Myelination due to Oligodendrocyte Dysfunction in a Model of Huntington's Disease. Journal of Huntington's Disease |
| Xu X, Ng B, Sim B, et al. (2020) pS421 huntingtin modulates mitochondrial phenotypes and confers neuroprotection in an HD hiPSC model. Cell Death & Disease. 11: 809 |
| Wright GEB, Caron NS, Ng B, et al. (2020) Gene expression profiles complement the analysis of genomic modifiers of the clinical onset of Huntington disease. Human Molecular Genetics |
| Utami KH, Skotte NH, Colaço AR, et al. (2020) Integrative Analysis Identifies Key Molecular Signatures Underlying Neurodevelopmental Deficits in Fragile X Syndrome. Biological Psychiatry |
| Skotte NH, Pouladi MA, Ehrnhoefer DE, et al. (2020) Compromised IGF signaling causes caspase-6 activation in Huntington disease. Experimental Neurology. 113396 |