Joel C. Watts

Affiliations: 
2003-2008 Centre for Research in Neurodegenerative Diseases University of Toronto, Toronto, ON, Canada 
 2008-2014 Institute for Neurodegenerative Diseases, Department of Neurology University of California, San Francisco, San Francisco, CA 
 2014- Tanz Centre for Research in Neurodegenerative Diseases, Department of Biochemistry University of Toronto, Toronto, ON, Canada 
Website:
http://biochemistry.utoronto.ca/person/joel-c-watts/
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Walsh DJ, Rees JR, Mehra S, et al. (2023) Anti-prion drugs do not improve survival in knock-in models of inherited prion disease. Biorxiv : the Preprint Server For Biology
Lau HHC, Martinez-Valbuena I, So RWL, et al. (2023) The G51D SNCA mutation generates a slowly progressive α-synuclein strain in early-onset Parkinson's disease. Acta Neuropathologica Communications. 11: 72
So RWL, Watts JC. (2023) α-Synuclein Conformational Strains as Drivers of Phenotypic Heterogeneity in Neurodegenerative Diseases. Journal of Molecular Biology. 168011
Williams D, Yan BQ, Wang H, et al. (2023) Somatostatin slows Aβ plaque deposition in aged APP mice by blocking Aβ aggregation. Scientific Reports. 13: 2337
Arshad H, Patel Z, Amano G, et al. (2022) A Single Protective Polymorphism in the Prion Protein Blocks Cross-Species Prion Replication in Cultured Cells. Journal of Neurochemistry
Arshad H, Watts JC. (2022) Genetically engineered cellular models of prion propagation. Cell and Tissue Research
Williams D, Mehrabian M, Arshad H, et al. (2021) The cellular prion protein interacts with and promotes the activity of Na,K-ATPases. Plos One. 16: e0258682
Arshad H, Patel Z, Mehrabian M, et al. (2021) The aminoglycoside G418 hinders de novo prion infection in cultured cells. The Journal of Biological Chemistry. 101073
Ruiz-Riquelme A, Mao A, Barghash MM, et al. (2021) Aβ43 aggregates exhibit enhanced prion-like seeding activity in mice. Acta Neuropathologica Communications. 9: 83
Bélondrade M, Nicot S, Mayran C, et al. (2021) Sensitive protein misfolding cyclic amplification of sporadic Creutzfeldt-Jakob disease prions is strongly seed and substrate dependent. Scientific Reports. 11: 4058
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