2611 - 2620 of 6466 Results
Title
Year
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OPENTitle: Autoantibodies against α-synuclein inhibit its aggregation and cytotoxicityJournal Name: Journal of AutoimmunityPublisher: Elsevier BVVol: 152Issue #:Start Page: 103390End Page: 103390Publication Date:Open Access(OA) Status: OPENLicense: cc-byDOI - Digital Object Identifier: 10.1016/j.jaut.2025.103390Best OA location URL: https://doi.org/10.1016/j.jaut.2025.103390Citation Count: 6
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OPENTitle: Pathogenic Mechanisms of Cytosolic and Membrane-Enriched α-Synuclein Converge on Fatty Acid HomeostasisJournal Name: The Journal of NeurosciencePublisher: Society for NeuroscienceVol: 42Issue #: 10Start Page: 2116End Page: 2130Publication Date:Open Access(OA) Status: OPENLicense: cc-by-nc-saDOI - Digital Object Identifier: 10.1523/jneurosci.1881-21.2022Best OA location URL: https://www.jneurosci.org/content/jneuro/42/10/2116.full.pdfCitation Count: 26
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OPENTitle: Chemical proteomics reveals human liver fatty acid binding protein as a predominant and selective target of triphenyl phosphateJournal Name: Environmental Science: Processes & ImpactsPublisher: Royal Society of Chemistry (RSC)Vol: 27Issue #: 9Start Page: 2865End Page: 2874Publication Date:Open Access(OA) Status: OPENLicense: cc-by-ncDOI - Digital Object Identifier: 10.1039/d5em00327jBest OA location URL: https://pubs.rsc.org/en/content/articlepdf/2025/em/d5em00327jCitation Count: 1
- Increased Menopausal Age Reduces the Risk of Parkinson's Disease: A Mendelian Randomization Approach2021OPENTitle: Increased Menopausal Age Reduces the Risk of Parkinson's Disease: A Mendelian Randomization ApproachJournal Name: Movement DisordersPublisher: WileyVol: 36Issue #: 10Start Page: 2264End Page: 2272Publication Date:Open Access(OA) Status: OPENLicense:DOI - Digital Object Identifier: 10.1002/mds.28760Best OA location URL: https://www.ncbi.nlm.nih.gov/pmc/articles/8530889Citation Count: 46
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OPENTitle: A study of RNA splicing and protein expression in the living human brainJournal Name: PLOS OnePublisher: Public Library of Science (PLoS)Vol: 20Issue #: 10Start Page: e0332651End Page: e0332651Publication Date:Open Access(OA) Status: OPENLicense: cc-byDOI - Digital Object Identifier: 10.1371/journal.pone.0332651Best OA location URL: https://doi.org/10.1371/journal.pone.0332651Citation Count: 1
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OPENTitle: Dynamics of PARKIN-Dependent Mitochondrial Ubiquitylation in Induced Neurons and Model Systems Revealed by Digital Snapshot ProteomicsJournal Name: Molecular CellPublisher: Elsevier BVVol: 70Issue #: 2Start Page: 211End Page: 227.e8Publication Date:Open Access(OA) Status: OPENLicense:DOI - Digital Object Identifier: 10.1016/j.molcel.2018.03.012Best OA location URL: http://www.cell.com/article/S1097276518302156/pdfCitation Count: 196
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OPENTitle: LRRK2 p.G2385R and p.R1628P variants in a multi-ethnic Asian Parkinson’s Cohort: epidemiology and clinical insightsJournal Name: npj Parkinson's DiseasePublisher: Springer Science and Business Media LLCVol: 11Issue #: 1Start Page: 320End Page: 320Publication Date:Open Access(OA) Status: OPENLicense:DOI - Digital Object Identifier: 10.1038/s41531-025-01166-xBest OA location URL: https://www.nature.com/articles/s41531-025-01166-x.pdfCitation Count: 2
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OPENTitle: Familial knockin mutation of LRRK2 causes lysosomal dysfunction and accumulation of endogenous insoluble α-synuclein in neuronsJournal Name: Neurobiology of DiseasePublisher: Elsevier BVVol: 111Issue #:Start Page: 26End Page: 35Publication Date:Open Access(OA) Status: OPENLicense:DOI - Digital Object Identifier: 10.1016/j.nbd.2017.12.005Best OA location URL: https://doaj.org/article/fd9888c9cbe94f60a22d9ed0b3ff97d3Citation Count: 143
- RAB7L1-Mediated Relocalization of LRRK2 to the Golgi Complex Causes Centrosomal Deficits via RAB8A2018OPENTitle: RAB7L1-Mediated Relocalization of LRRK2 to the Golgi Complex Causes Centrosomal Deficits via RAB8AJournal Name: Frontiers in Molecular NeurosciencePublisher: Frontiers Media SAVol: 11Issue #:Start Page: 417End Page: 417Publication Date:Open Access(OA) Status: OPENLicense: cc-byDOI - Digital Object Identifier: 10.3389/fnmol.2018.00417Best OA location URL: https://www.frontiersin.org/articles/10.3389/fnmol.2018.00417/pdfCitation Count: 46
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OPENTitle: Black and African American Connections to Parkinson's Disease Study: Addressing Missing Diversity in Parkinson's Disease GeneticsJournal Name: Movement DisordersPublisher: WileyVol: 37Issue #: 7Start Page: 1559End Page: 1561Publication Date:Open Access(OA) Status: OPENLicense: cc-byDOI - Digital Object Identifier: 10.1002/mds.29042Best OA location URL: https://doi.org/10.1002/mds.29042Citation Count: 12