Mahmoud A. Pouladi

National University of Singapore, Singapore, Singapore 
Huntington's disease, Fragile X Syndrome, Multiple Sclerosis
"Mahmoud Pouladi"
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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
Utami KH, Yusof NABM, Kwa JE, et al. (2020) Elevated de novo protein synthesis in FMRP-deficient human neurons and its correction by metformin treatment. Molecular Autism. 11: 41
Laroche M, Lessard-Beaudoin M, Garcia-Miralles M, et al. (2020) Early deficits in olfaction are associated with structural and molecular alterations in the olfactory system of a Huntington disease mouse model. Human Molecular Genetics
Takata K, Kozaki T, Lee CZW, et al. (2020) Induced-Pluripotent-Stem-Cell-Derived Primitive Macrophages Provide a Platform for Modeling Tissue-Resident Macrophage Differentiation and Function. Immunity. 52: 417-418
Hengel H, Bosso-Lefèvre C, Grady G, et al. (2020) Loss-of-function mutations in UDP-Glucose 6-Dehydrogenase cause recessive developmental epileptic encephalopathy. Nature Communications. 11: 595
Radulescu CI, Garcia-Miralles M, Sidik H, et al. (2020) Reprint of: Manipulation of microbiota reveals altered callosal myelination and white matter plasticity in a model of Huntington disease. Neurobiology of Disease. 104744
Sidik H, Ang CJ, Pouladi MA. (2019) Huntingtin confers fitness but is not embryonically essential in zebrafish development. Developmental Biology
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