Répertoire du corps professoral
Francesca Cicchetti
Professeure titulaire
(418) 525-4444, poste 48853
francesca.cicchetti@fmed.ulaval.ca
Pavillon Ferdinand-Vandry
1050, avenue de la Médecine
Local 4873
Redefining PD pathophysiology mechanisms in the context of heterogeneous substantia nigra neuron subtypes
Programme: ASAP Collaborative Research Network
Organisme(s) subventionnaire(s): Michael J. Fox Foundation for Parkinson's Research
Type de financement: Subvention
Établissement tête: Northwestern University
Du 1 novembre 2024
au 31 octobre 2026
Preventing pathological protein spread in Huntington's disease: relevance to pathology and treatment
Programme: Développement de la recherche (FC)
Organisme(s) subventionnaire(s): CHU de Québec – Université Laval – CHUL
Type de financement: Subvention
Établissement tête: Université Laval
Du 20 décembre 2021
au 19 décembre 2024
Preventing pathological protein spread in Huntington's disease: relevance to pathology and treatment
Programme: Subvention Projet
Organisme(s) subventionnaire(s): Instituts de recherche en santé du Canada
Type de financement: Subvention
Établissement tête: Université Laval
Du 1 avril 2020
au 31 mars 2025
Financements des 2 dernières années
Les effets de la cystéamine chez les patients souffrant de la maladie de Huntington : Analyse des données cliniques
Programme: Développement de la recherche (RFI)
Organisme(s) subventionnaire(s): CHU de Québec – Université Laval – CHUL
Type de financement: Subvention
Établissement tête: Université Laval
Du 1 janvier 2023
au 31 décembre 2023
Premier biomarqueur sanguin de la maladie de Parkinson : de la validation à la commercialisation
Programme: Projets de maturation technologique PSO – volet 2d
Organisme(s) subventionnaire(s): Fondation du CHU de Québec, Synucure Thérapeutique inc., Ministère de l'Économie et de l'Innovation
Type de financement: Subvention
Établissement tête: Université Laval
Du 14 septembre 2022
au 13 septembre 2024
Crosstalk at the blood-brain barrier: new insights into Parkinson's disease
Organisme(s) subventionnaire(s): National Parkinson Foundation
Type de financement: Subvention
Établissement tête: Université Laval
Du 30 juin 2022
au 31 juillet 2023
Redefining PD pathophysiology mechanisms in the context of teterogeneous substantia nigra neuron subtypes
Programme: Target Advancement Program
Organisme(s) subventionnaire(s): Northwestern University
Type de financement: Subvention
Établissement tête: Université Laval
Du 1 septembre 2021
au 31 octobre 2024
Targeting the neurovascular unit to prevent disease dissemination and progression
Programme: Target Advancement Program
Organisme(s) subventionnaire(s): Michael J. Fox Foundation for Parkinson's Research
Type de financement: Subvention
Établissement tête: Université Laval
Du 1 janvier 2021
au 31 mars 2023
Interrogating induced neuronal cells from Huntington’s disease patients to better understand cognitive impairments
Organisme(s) subventionnaire(s): Huntington's Disease Society of America
Type de financement: Subvention
Établissement tête: Université Laval
Du 1 novembre 2019
au 30 juin 2023
Untangling tau contribution to cognitive impairments in Huntington’s disease.
Programme: Subvention Projet
Organisme(s) subventionnaire(s): Instituts de recherche en santé du Canada
Type de financement: Subvention
Établissement tête: Université Laval
Du 1 avril 2019
au 31 mars 2024
Encadrements terminés dans les 5 dernières années
Publications des 5 dernières années
Healthy blood, healthy brain: a window into understanding and treating neurodegenerative diseases Journal of Neurology, 2024/06. Thyago R. Cardim-Pires, Aurélie de Rus Jacquet, Francesca Cicchetti. DOI 10.1007/s00415-024-12337-w
Tau: a biomarker of Huntington’s disease Molecular Psychiatry, 2023/10. Eva Lepinay, Francesca Cicchetti. DOI 10.1038/s41380-023-02230-9
Passive immunization against phosphorylated tau improves features of Huntington's disease pathology Molecular Therapy, 2022/04. Melanie Alpaugh, Maria Masnata, Aurelie de Rus Jacquet, Eva Lepinay, Hélèna L. Denis, Martine Saint-Pierre, Peter Davies, Emmanuel Planel, Francesca Cicchetti. DOI 10.1016/j.ymthe.2022.01.020
Prompting endogenous repair of brain injury: science fiction or reality? Molecular Neurodegeneration, 2022. de Rus Jacquet, A., Cicchetti, F.. DOI 10.1186/s13024-022-00539-7
A light-inducible protein clustering system for in vivo analysis of α-synuclein aggregation in ParkinsonAU disease: PleasenotethatParkinsonsdiseasehasbeen PLoS Biology, 2022. Bérard, M., Sheta, R., Malvaut, S., Rodriguez-Aller, R., Teixeira, M., Idi, W., Turmel, R., Alpaugh, M., Dubois, M., Dahmene, M., Salesse, C., Lamontagne-Proulx, J., St-Pierre, M.-K., Tavassoly, O., Luo, W., Cid-Pellitero, E.D., Qazi, R., Jeong, J.-W., Durcan, T.M., Vallières, L., Tremblay, M.-E., Soulet, D., Lévesque, M., Cicchetti, F., Fon, E.A., Saghatelyan, A., Oueslati, A.. DOI 10.1371/journal.pbio.3001578
Sox6 expression distinguishes dorsally and ventrally biased dopamine neurons in the substantia nigra with distinctive properties and embryonic origins. Cell reports, 2021/11/01. DOI 10.1016/j.celrep.2021.109975
Prion-like properties of the mutant huntingtin protein in living organisms: the evidence and the relevance. Molecular psychiatry, 2021/10/28. DOI 10.1038/s41380-021-01350-4
Clinical perception and management of Parkinson's disease during the COVID-19 pandemic: A Canadian experience. Parkinsonism & related disorders, 2021/09/01. DOI 10.1016/j.parkreldis.2021.08.018
Current and future applications of induced pluripotent stem cell-based models to study pathological proteins in neurodegenerative disorders Molecular Psychiatry, 2021/07. Aurélie de Rus Jacquet, Hélèna L. Denis, Francesca Cicchetti, Melanie Alpaugh. DOI 10.1038/s41380-020-00999-7
Current and future applications of induced pluripotent stem cell-based models to study pathological proteins in neurodegenerative disorders. Molecular psychiatry, 2021/07/01. DOI 10.1038/s41380-021-01055-8
Huntington's disease: lessons from prion disorders. Journal of neurology, 2021/02/24. DOI 10.1007/s00415-021-10418-8
Correction: Shedding a new light on Huntington’s disease: how blood can both propagate and ameliorate disease pathology (Molecular Psychiatry, (2021), 26, 9, (5441-5463), 10.1038/s41380-020-0787-4) Molecular Psychiatry, 2021. Rieux, M., Alpaugh, M., Sciacca, G., Saint-Pierre, M., Masnata, M., Denis, H.L., Lévesque, S.A., Herrmann, F., Bazenet, C., Garneau, A.P., Isenring, P., Truant, R., Oueslati, A., Gould, P.V., Ast, A., Wanker, E.E., Lacroix, S., Cicchetti, F.. DOI 10.1038/s41380-020-0850-1
Targeting Tau to Treat Clinical Features of Huntington's Disease. Frontiers in neurology, 2020/11/19. DOI 10.3389/fneur.2020.580732
Neuronal interleukin-1 receptors mediate pain in chronic inflammatory diseases. The Journal of experimental medicine, 2020/09/01. DOI 10.1084/jem.20191430
Beneficial effects of cysteamine in Thy1-α-Syn mice and induced pluripotent stem cells with a SNCA gene triplication. Neurobiology of disease, 2020/08/13. DOI 10.1016/j.nbd.2020.105042
Shedding a new light on Huntington's disease: how blood can both propagate and ameliorate disease pathology. Molecular psychiatry, 2020/06/08. DOI 10.1038/s41380-020-0787-4
Use of adeno-associated virus-mediated delivery of mutant huntingtin to study the spreading capacity of the protein in mice and non-human primates. Neurobiology of disease, 2020/05/18. DOI 10.1016/j.nbd.2020.104951
Inhibiting cellular uptake of mutant huntingtin using a monoclonal antibody: Implications for the treatment of Huntington's disease. Neurobiology of disease, 2020/05/12. DOI 10.1016/j.nbd.2020.104943
Evidence for the spread of human-derived mutant huntingtin protein in mice and non-human primates. Neurobiology of disease, 2020/05/11. DOI 10.1016/j.nbd.2020.104941
Microglial physiological properties and interactions with synapses are altered at presymptomatic stages in a mouse model of Huntington's disease pathology. Journal of neuroinflammation, 2020/04/02. DOI 10.1186/s12974-020-01782-9
The Quebec Parkinson Network: A Researcher-Patient Matching Platform and Multimodal Biorepository. Journal of Parkinson's disease, 2020/01/01. DOI 10.3233/jpd-191775
Antibody-based therapies for Huntington's disease: current status and future directions. Neurobiology of disease, 2019/08/06. DOI 10.1016/j.nbd.2019.104569
Cysteamine as a novel disease-modifying compound for Parkinson's disease: Over a decade of research supporting a clinical trial. Neurobiology of disease, 2019/07/10. DOI 10.1016/j.nbd.2019.104530
A brief history of antibody-based therapy. Neurobiology of disease, 2019/06/16. DOI 10.1016/j.nbd.2019.104504
A novel wireless brain stimulation device for long-term use in freely moving mice. Scientific reports, 2019/04/23. DOI 10.1038/s41598-019-42910-7
Demonstration of prion-like properties of mutant huntingtin fibrils in both in vitro and in vivo paradigms. Acta neuropathologica, 2019/02/20. DOI 10.1007/s00401-019-01973-6
The troubling story of blood-driven dementias. Molecular psychiatry, 2019/02/01. DOI 10.1038/s41380-018-0225-z
The toxin MPTP generates similar cognitive and locomotor deficits in hTau and tau knock-out mice. Brain research, 2019/01/11. DOI 10.1016/j.brainres.2019.01.016
Optogenetic-Mediated Spatiotemporal Control of α-Synuclein Aggregation Disrupts Nigrostriatal Transmission and Precipitates Neurodegeneration SSRN, 2019. Bérard, M., Sheta, R., Malvaut, S., Turmel, R., Alpaugh, M.J., Dubois, M., Dahmene, M., Salesse, C., Profes, M.S., Lamontagne-Proulx, J., Qazi, R., Tavassoly, O., Soulet, D., Lévesque, M., Jeong, J.-W., Cicchetti, F., Fon, E.A., Saghatelyan, A., Oueslati, A.. DOI 10.2139/ssrn.3416893
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