Jacob Ayers
Affiliations: | Neuroscience | University of Florida, Gainesville, Gainesville, FL, United States |
Area:
Aging & Memory Loss,NeurodegenerationGoogle:
"Jacob Ayers"Mean distance: 106866
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Publications
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Ayers JI, Lee J, Monteiro O, et al. (2022) Different α-synuclein prion strains cause dementia with Lewy bodies and multiple system atrophy. Proceedings of the National Academy of Sciences of the United States of America. 119 |
Ayers JI, Borchelt DR. (2020) Phenotypic diversity in ALS and the role of poly-conformational protein misfolding. Acta Neuropathologica |
Ayers JI, Paras NA, Prusiner SB. (2020) Expanding spectrum of prion diseases. Emerging Topics in Life Sciences. 4: 155-167 |
Ayers JI, Prusiner SB. (2020) Prion protein - mediator of toxicity in multiple proteinopathies. Nature Reviews. Neurology |
Crown A, McAlary L, Fagerli E, et al. (2020) Tryptophan residue 32 in human Cu-Zn superoxide dismutase modulates prion-like propagation and strain selection. Plos One. 15: e0227655 |
Crown AM, Roberts BL, Crosby K, et al. (2019) Experimental Mutations in Superoxide Dismutase 1 Provide Insight into Potential Mechanisms Involved in Aberrant Aggregation in Familial Amyotrophic Lateral Sclerosis. G3 (Bethesda, Md.) |
Crosby K, Crown AM, Roberts BL, et al. (2018) Loss of charge mutations in solvent exposed Lys residues of superoxide dismutase 1 do not induce inclusion formation in cultured cell models. Plos One. 13: e0206751 |
Ayers JI, Riffe CJ, Sorrentino ZA, et al. (2018) Localized induction of wild-type and mutant alpha-synuclein aggregation reveals propagation along neuroanatomical tracts. Journal of Virology |
Ayers JI, McMahon B, Gill S, et al. (2016) Relationship between mutant SOD1 maturation and inclusion formation in cell models. Journal of Neurochemistry |
Ayers JI, Diamond J, Sari A, et al. (2016) Distinct conformers of transmissible misfolded SOD1 distinguish human SOD1-FALS from other forms of familial and sporadic ALS. Acta Neuropathologica |