Sarat C Vatsavayai
Affiliations: | The Open University, Kents Hill, England, United Kingdom |
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| Vatsavayai SC, Nana AL, Yokoyama JS, et al. (2018) C9orf72-FTD/ALS pathogenesis: evidence from human neuropathological studies. Acta Neuropathologica |
| Celona B, von Dollen J, Vatsavayai SC, et al. (2017) Suppression of C9orf72 RNA repeat-induced neurotoxicity by the ALS-associated RNA-binding protein Zfp106. Elife. 6 |
| Vatsavayai SC, Yoon SJ, Gardner RC, et al. (2016) Timing and significance of pathological features in C9orf72 expansion-associated frontotemporal dementia. Brain : a Journal of Neurology |
| Dallérac GM, Levasseur G, Vatsavayai SC, et al. (2015) Dysfunctional Dopaminergic Neurones in Mouse Models of Huntington's Disease: A Role for SK3 Channels. Neuro-Degenerative Diseases. 15: 93-108 |
| Murphy K, Dallerac G, Milnerwood A, et al. (2012) B24 Dysfunctional dopaminergic neurones and biphasic activity-dependent dopamine release in mouse models of Huntington's disease Journal of Neurology, Neurosurgery, and Psychiatry. 83 |
| Hirst M, Vatsavayai S, Dallerac G, et al. (2012) B05 CAG profiling in R6/1 89Q indicates early and progressive expansion in critical neuronal populations and expansion and changes in surrounding glial cell populations Journal of Neurology, Neurosurgery & Psychiatry. 83: A7.1-A7 |
| Dallérac GM, Vatsavayai SC, Cummings DM, et al. (2011) Impaired long-term potentiation in the prefrontal cortex of Huntington's disease mouse models: rescue by D1 dopamine receptor activation. Neuro-Degenerative Diseases. 8: 230-9 |
| Cummings DM, Milnerwood AJ, Dallérac GM, et al. (2007) Abnormal cortical synaptic plasticity in a mouse model of Huntington's disease. Brain Research Bulletin. 72: 103-7 |
| Vatsavayai SC, Dallérac GM, Milnerwood AJ, et al. (2007) Progressive CAG expansion in the brain of a novel R6/1-89Q mouse model of Huntington's disease with delayed phenotypic onset. Brain Research Bulletin. 72: 98-102 |
| Cummings DM, Milnerwood AJ, Dallérac GM, et al. (2006) Aberrant cortical synaptic plasticity and dopaminergic dysfunction in a mouse model of Huntington's disease. Human Molecular Genetics. 15: 2856-68 |