3481 - 3490 of 6570 Results
Title
Year
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OPENTitle: Optical Structural Analysis of Individual α‐Synuclein OligomersJournal Name: Angewandte Chemie International EditionPublisher: WileyVol: 57Issue #: 18Start Page: 4886End Page: 4890Publication Date:Open Access(OA) Status: OPENLicense: cc-by, cc-byDOI - Digital Object Identifier: 10.1002/anie.201710779Best OA location URL: https://onlinelibrary.wiley.com/doi/pdfdirect/10.1002/anie.201710779Citation Count: 48
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OPENTitle: Alzheimer's disease pathology explains association between dementia with Lewy bodies and APOE‐ε4/TOMM40 long poly‐T repeat allele variantsJournal Name: Alzheimer's & Dementia: Translational Research & Clinical InterventionsPublisher: WileyVol: 5Issue #: 1Start Page: 814End Page: 824Publication Date:Open Access(OA) Status: OPENLicense: cc-by-nc-nd, cc-by-nc-ndDOI - Digital Object Identifier: 10.1016/j.trci.2019.08.005Best OA location URL: https://onlinelibrary.wiley.com/doi/pdfdirect/10.1016/j.trci.2019.08.005Citation Count: 22
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OPENTitle: Falls Risk in Relation to Activity Exposure in High-Risk Older AdultsJournal Name: The Journals of Gerontology: Series APublisher: Oxford University Press (OUP)Vol: 75Issue #: 6Start Page: 1198End Page: 1205Publication Date:Open Access(OA) Status: OPENLicense: cc-by, cc-byDOI - Digital Object Identifier: 10.1093/gerona/glaa007Best OA location URL: https://academic.oup.com/biomedgerontology/article-pdf/75/6/1198/33283332/glaa007.pdfCitation Count: 86
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OPENTitle: Genetic analysis implicates APOE, SNCA and suggests lysosomal dysfunction in the etiology of dementia with Lewy bodiesJournal Name: Human Molecular GeneticsPublisher: Oxford University Press (OUP)Vol: 23Issue #: 23Start Page: 6139End Page: 6146Publication Date:Open Access(OA) Status: OPENLicense:DOI - Digital Object Identifier: 10.1093/hmg/ddu334Best OA location URL: http://doi.org/10.1093/hmg/ddu334Citation Count: 241
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OPENTitle: Enhanced ubiquitin-dependent degradation by Nedd4 protects against α-synuclein accumulation and toxicity in animal models of Parkinson's diseaseJournal Name: Neurobiology of DiseasePublisher: Elsevier BVVol: 64Issue #:Start Page: 79End Page: 87Publication Date:Open Access(OA) Status: OPENLicense: cc-by, cc-byDOI - Digital Object Identifier: 10.1016/j.nbd.2013.12.011Best OA location URL: https://doi.org/10.1016/j.nbd.2013.12.011Citation Count: 88
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OPENTitle: Parkinson’s disease in GTP cyclohydrolase 1 mutation carriersJournal Name: BrainPublisher: Oxford University Press (OUP)Vol: 137Issue #: 9Start Page: 2480End Page: 2492Publication Date:Open Access(OA) Status: OPENLicense:DOI - Digital Object Identifier: 10.1093/brain/awu179Best OA location URL: https://academic.oup.com/brain/article-pdf/137/9/2480/13798270/awu179.pdfCitation Count: 200
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OPENTitle: The LRRK2 G2019S variant rewires Rab GTPase phosphorylation after lysosomal damage and promotes cell death in human macrophagesJournal Name: Journal of Cell SciencePublisher: The Company of BiologistsVol: 139Issue #: 14Start Page:End Page:Publication Date:Open Access(OA) Status: OPENLicense: cc-by, cc-byDOI - Digital Object Identifier: 10.1242/jcs.265083Best OA location URL: https://doi.org/10.1242/jcs.265083Citation Count: 1
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OPENTitle: Variations in Cardiovascular Structure, Function, and Geometry in Midlife Associated With a History of Hypertensive PregnancyJournal Name: HypertensionPublisher: Ovid Technologies (Wolters Kluwer Health)Vol: 75Issue #: 6Start Page: 1542End Page: 1550Publication Date:Open Access(OA) Status: OPENLicense: cc-by, cc-byDOI - Digital Object Identifier: 10.1161/hypertensionaha.119.14530Best OA location URL: https://www.ahajournals.org/doi/pdf/10.1161/HYPERTENSIONAHA.119.14530Citation Count: 65
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OPENTitle: Distinct clinical and neuropathological features of G51D SNCA mutation cases compared with SNCA duplication and H50Q mutationJournal Name: Molecular NeurodegenerationPublisher: Springer Science and Business Media LLCVol: 10Issue #: 1Start Page: 41End Page: 41Publication Date:Open Access(OA) Status: OPENLicense: cc-by, cc-byDOI - Digital Object Identifier: 10.1186/s13024-015-0038-3Best OA location URL: https://molecularneurodegeneration.biomedcentral.com/counter/pdf/10.1186/s13024-015-0038-3Citation Count: 125
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OPENTitle: Dysregulation of glucose metabolism is an early event in sporadic Parkinson's diseaseJournal Name: Neurobiology of AgingPublisher: Elsevier BVVol: 35Issue #: 5Start Page: 1111End Page: 1115Publication Date:Open Access(OA) Status: OPENLicense: cc-by-nc-nd, cc-by-nc-ndDOI - Digital Object Identifier: 10.1016/j.neurobiolaging.2013.11.001Best OA location URL: https://doi.org/10.1016/j.neurobiolaging.2013.11.001Citation Count: 258