Jada Lewis
Affiliations: | Neuroscience | University of Florida, Gainesville, Gainesville, FL, United States |
Area:
Aging & Memory Loss,Neurodegeneration,Modeling & Therapeutic Trials for Neurodegenerative Diseases,Alzheimer’s and Parkinson’s Diseases, Frontotemporal Dementia,Amyotrophic Lateral SclerosisGoogle:
"Jada Lewis"Mean distance: 18.66
Parents
Sign in to add mentor| Nobuyo Maeda | grad student | 1992-1996 | UNC Chapel Hill (Cell Biology Tree) | |
| (mentor) | ||||
| Oliver Smithies | grad student | 1992-1996 | UNC Chapel Hill | |
| (co-mentor) | ||||
| Ryzard Kole | post-doc | 1996-1998 | UNC Chapel Hill | |
| Michael Hutton | post-doc | 1998-2001 | Mayo Clinic Jacksonville | |
Children
Sign in to add trainee| Ashley Cannon | grad student | 2007-2010 | Mayo Clinic Jacksonville |
| Rachel Bailey | grad student | 2008-2013 | University of Florida |
| Sruti Rayaprolu | grad student | 2014-2018 | University of Florida |
| Simon D'Alton | post-doc | 2009-2015 | University of Florida |
BETA: Related publications
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Publications
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| Bardai FH, Ordonez DG, Bailey RM, et al. (2018) Lrrk promotes tau neurotoxicity through dysregulation of actin and mitochondrial dynamics. Plos Biology. 16: e2006265 |
| Moloney C, Rayaprolu S, Howard J, et al. (2018) Analysis of spinal and muscle pathology in transgenic mice overexpressing wild-type and ALS-linked mutant MATR3. Acta Neuropathologica Communications. 6: 137 |
| Hamm M, Ladd TB, Levites Y, et al. (2018) Designing antibodies against LRRK2-targeted tau epitopes. Plos One. 13: e0204367 |
| Pace MC, Xu G, Fromholt S, et al. (2018) Changes in proteome solubility indicate widespread proteostatic disruption in mouse models of neurodegenerative disease. Acta Neuropathologica |
| Rayaprolu S, Seven YB, Howard J, et al. (2018) Partial loss of ATP13A2 causes selective gliosis independent of robust lipofuscinosis. Molecular and Cellular Neurosciences |
| Pace MC, Xu G, Fromholt S, et al. (2018) Differential induction of mutant SOD1 misfolding and aggregation by tau and α-synuclein pathology. Molecular Neurodegeneration. 13: 23 |
| Iradi MCG, Triplett JC, Thomas JD, et al. (2018) Characterization of gene regulation and protein interaction networks for Matrin 3 encoding mutations linked to amyotrophic lateral sclerosis and myopathy. Scientific Reports. 8: 4049 |
| Moloney C, Rayaprolu S, Howard J, et al. (2017) Retraction Note: Transgenic mice overexpressing the ALS-linked protein Matrin 3 develop a profound muscle phenotype. Acta Neuropathologica Communications. 5: 97 |
| Khare S, Nick JA, Zhang Y, et al. (2017) A KCNC3 mutation causes a neurodevelopmental, non-progressive SCA13 subtype associated with dominant negative effects and aberrant EGFR trafficking. Plos One. 12: e0173565 |
| Moloney C, Rayaprolu S, Howard J, et al. (2016) Transgenic mice overexpressing the ALS-linked protein Matrin 3 develop a profound muscle phenotype. Acta Neuropathologica Communications. 4: 122 |