4621 - 4630 of 7915 Results
Title
Year
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OPENTitle: APOE genotype regulates pathology and disease progression in synucleinopathyJournal Name: Science Translational MedicinePublisher: American Association for the Advancement of Science (AAAS)Vol: 12Issue #: 529Start Page:End Page:Publication Date:Open Access(OA) Status: OPENLicense:DOI - Digital Object Identifier: 10.1126/scitranslmed.aay3069Best OA location URL: https://stm.sciencemag.org/content/scitransmed/12/529/eaay3069.full.pdfCitation Count: 120
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OPENTitle: Discriminating α-synuclein strains in Parkinson’s disease and multiple system atrophyJournal Name: NaturePublisher: Springer Science and Business Media LLCVol: 578Issue #: 7794Start Page: 273End Page: 277Publication Date:Open Access(OA) Status: OPENLicense:DOI - Digital Object Identifier: 10.1038/s41586-020-1984-7Best OA location URL: https://europepmc.org/articles/pmc7066875?pdf=renderCitation Count: 540
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OPENTitle: The parkin-coregulated gene product PACRG promotes TNF signaling by stabilizing LUBACJournal Name: Science SignalingPublisher: American Association for the Advancement of Science (AAAS)Vol: 13Issue #: 617Start Page:End Page:Publication Date:Open Access(OA) Status: OPENLicense:DOI - Digital Object Identifier: 10.1126/scisignal.aav1256Best OA location URL: https://stke.sciencemag.org/content/sigtrans/13/617/eaav1256.full.pdfCitation Count: 18
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OPENTitle: Exceptionally low likelihood of Alzheimer’s dementia in APOE2 homozygotes from a 5,000-person neuropathological studyJournal Name: Nature CommunicationsPublisher: Springer Science and Business Media LLCVol: 11Issue #: 1Start Page:End Page:Publication Date:Open Access(OA) Status: OPENLicense: cc-byDOI - Digital Object Identifier: 10.1038/s41467-019-14279-8Best OA location URL: https://www.nature.com/articles/s41467-019-14279-8.pdfCitation Count: 306
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RESTRICTEDTitle: Practical Evaluation and Management of Insomnia in Parkinson's Disease: A ReviewJournal Name: Movement Disorders Clinical PracticePublisher: WileyVol: 7Issue #: 3Start Page: 250End Page: 266Publication Date:Open Access(OA) Status: RESTRICTEDLicense: cc-by-ncDOI - Digital Object Identifier: 10.1002/mdc3.12899Best OA location URL: https://doi.org/10.1002/mdc3.12899Citation Count: 21
- RGS Proteins as Critical Regulators of Motor Function and Their Implications in Parkinson’s Disease2020RESTRICTEDTitle: RGS Proteins as Critical Regulators of Motor Function and Their Implications in Parkinson’s DiseaseJournal Name: Molecular PharmacologyPublisher: American Society for Pharmacology & Experimental Therapeutics (ASPET)Vol: 98Issue #: 6Start Page: 730End Page: 738Publication Date:Open Access(OA) Status: RESTRICTEDLicense:DOI - Digital Object Identifier: 10.1124/mol.119.118836Best OA location URL: https://molpharm.aspetjournals.org/content/molpharm/98/6/730.full.pdfCitation Count: 12
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OPENTitle: Structural Basis for Rab8a Recruitment of RILPL2 via LRRK2 Phosphorylation of Switch 2Journal Name: StructurePublisher: Elsevier BVVol: 28Issue #: 4Start Page: 406End Page: 417.e6Publication Date:Open Access(OA) Status: OPENLicense: cc-byDOI - Digital Object Identifier: 10.1016/j.str.2020.01.005Best OA location URL: http://www.cell.com/article/S0969212620300058/pdfCitation Count: 67
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OPENTitle: Tensor decomposition of stimulated monocyte and macrophage gene expression profiles identifies neurodegenerative disease-specific trans-eQTLsJournal Name: PLOS GeneticsPublisher: Public Library of Science (PLoS)Vol: 16Issue #: 2Start Page: e1008549End Page: e1008549Publication Date:Open Access(OA) Status: OPENLicense: cc-byDOI - Digital Object Identifier: 10.1371/journal.pgen.1008549Best OA location URL: https://journals.plos.org/plosgenetics/article/file?id=10.1371/journal.pgen.1008549&type=printableCitation Count: 21
- Abstracts2020OPENTitle: AbstractsJournal Name: Movement Disorders Clinical PracticePublisher: WileyVol: 7Issue #: S1Start Page:End Page:Publication Date:Open Access(OA) Status: OPENLicense:DOI - Digital Object Identifier: 10.1002/mdc3.12905Best OA location URL: https://onlinelibrary.wiley.com/doi/pdfdirect/10.1002/mdc3.12905Citation Count: 2
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OPENTitle: Analysis of common and rare VPS13C variants in late-onset Parkinson diseaseJournal Name: Neurology GeneticsPublisher: Ovid Technologies (Wolters Kluwer Health)Vol: 6Issue #: 1Start Page:End Page:Publication Date:Open Access(OA) Status: OPENLicense: cc-by-nc-ndDOI - Digital Object Identifier: 10.1212/nxg.0000000000000385Best OA location URL: https://ng.neurology.org/content/nng/6/1/385.full.pdfCitation Count: 19