Sruti Rayaprolu, Ph.D.
Affiliations: | Neurology | Emory University School of Medicine, Atlanta, GA, United States |
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Parents
Sign in to add mentor| Jada Lewis | grad student | 2014-2018 | UF Gainesville |
| Allan I. Levey | post-doc | 2018- | Emory University School of Medicine |
| Thomas N. Seyfried | post-doc | 2018- | Emory University School of Medicine |
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Publications
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| Wynne ME, Ogunbona O, Lane AR, et al. (2023) APOE expression and secretion are modulated by mitochondrial dysfunction. Elife. 12 |
| Rayaprolu S, Bitarafan S, Santiago JV, et al. (2022) Cell type-specific biotin labeling in vivo resolves regional neuronal and astrocyte proteomic differences in mouse brain. Nature Communications. 13: 2927 |
| Ramesha S, Rayaprolu S, Bowen CA, et al. (2021) Unique molecular characteristics and microglial origin of Kv1.3 channel-positive brain myeloid cells in Alzheimer's disease. Proceedings of the National Academy of Sciences of the United States of America. 118 |
| Rayaprolu S, Higginbotham L, Bagchi P, et al. (2020) Systems-based proteomics to resolve the biology of Alzheimer's disease beyond amyloid and tau. Neuropsychopharmacology : Official Publication of the American College of Neuropsychopharmacology |
| Rayaprolu S, Gao T, Xiao H, et al. (2020) Flow-cytometric microglial sorting coupled with quantitative proteomics identifies moesin as a highly-abundant microglial protein with relevance to Alzheimer's disease. Molecular Neurodegeneration. 15: 28 |
| 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 |
| Rayaprolu S, Seven YB, Howard J, et al. (2018) Partial loss of ATP13A2 causes selective gliosis independent of robust lipofuscinosis. Molecular and Cellular Neurosciences |
| 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 |