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 Sclerosis
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"Jada Lewis"
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Parents

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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
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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
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