Laetitia Francelle
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NeurosciencesGoogle:
"Laetitia Francelle"Mean distance: (not calculated yet)
Parents
Sign in to add mentor| Emmanuel Brouillet | grad student | 2011-2014 | |
| Vance Lemmon | post-doc | 2019-2019 |
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Publications
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| Francelle L, Mazzulli JR. (2022) Neuroinflammation in Gaucher disease, neuronal ceroid lipofuscinosis, and commonalities with Parkinson's disease. Brain Research. 1780: 147798 |
| Francelle L, Outeiro TF, Rappold GA. (2020) Inhibition of HDAC6 activity protects dopaminergic neurons from alpha-synuclein toxicity. Scientific Reports. 10: 6064 |
| Galvan L, Francelle L, Gaillard MC, et al. (2018) The striatal kinase DCLK3 produces neuroprotection against mutant huntingtin. Brain : a Journal of Neurology |
| de Oliveira RM, Vicente Miranda H, Francelle L, et al. (2017) The mechanism of sirtuin 2-mediated exacerbation of alpha-synuclein toxicity in models of Parkinson disease. Plos Biology. 15: e2000374 |
| Francelle L, Lotz C, Outeiro T, et al. (2017) Contribution of Neuroepigenetics to Huntington's Disease. Frontiers in Human Neuroscience. 11: 17 |
| Pardo J, Abba M, Lacunza E, et al. (2017) Identification of a conserved gene signature associated with an exacerbated inflammatory environment in the hippocampus of aging rats. Hippocampus |
| Pépin J, Francelle L, Carrillo-de Sauvage MA, et al. (2016) In vivo imaging of brain glutamate defects in a knock-in mouse model of Huntington's disease. Neuroimage. 139: 53-64 |
| Flament J, Pépin J, Francelle L, et al. (2016) B40 In vivo imaging of brain glutamate defects in a knock-in mouse model of huntington’s disease Journal of Neurology, Neurosurgery, and Psychiatry. 87 |
| Francelle L, Galvan L, Gaillard MC, et al. (2015) The striatal long noncoding RNA Abhd11os is neuroprotective against an N-terminal fragment of mutant huntingtin in vivo. Neurobiology of Aging. 36: 1601.e7-16 |
| Francelle L, Galvan L, Gaillard MC, et al. (2015) Loss of the thyroid hormone-binding protein Crym renders striatal neurons more vulnerable to mutant huntingtin in Huntington's disease. Human Molecular Genetics. 24: 1563-73 |