5251 - 5260 of 6509 Results
Title
Year
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OPENTitle: Understanding what aspects of Parkinson’s disease matter most to patients and familiesJournal Name: Scientific ReportsPublisher: Springer Science and Business Media LLCVol: 14Issue #: 1Start Page: 21171End Page: 21171Publication Date:Open Access(OA) Status: OPENLicense:DOI - Digital Object Identifier: 10.1038/s41598-024-71555-4Best OA location URL: https://www.nature.com/articles/s41598-024-71555-4.pdfCitation Count: 12
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OPENTitle: An Inducible Luminescent System to Explore Parkinson’s Disease-Associated GenesJournal Name: International Journal of Molecular SciencesPublisher: MDPI AGVol: 25Issue #: 17Start Page: 9493End Page: 9493Publication Date:Open Access(OA) Status: OPENLicense:DOI - Digital Object Identifier: 10.3390/ijms25179493Best OA location URL: https://doi.org/10.3390/ijms25179493Citation Count: 1
- The clinical and genetic spectrum of inherited glycosylphosphatidylinositol deficiency disorders2024OPENTitle: The clinical and genetic spectrum of inherited glycosylphosphatidylinositol deficiency disordersJournal Name: BrainPublisher: Oxford University Press (OUP)Vol: 147Issue #: 8Start Page: 2775End Page: 2790Publication Date:Open Access(OA) Status: OPENLicense: cc-byDOI - Digital Object Identifier: 10.1093/brain/awae056Best OA location URL: https://academic.oup.com/brain/advance-article-pdf/doi/10.1093/brain/awae056/56907442/awae056.pdfCitation Count: 13
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OPENTitle: [3H]-NFPS binding to the glycine transporter 1 in the hemi-parkinsonian rat brainJournal Name: Experimental Brain ResearchPublisher: Springer Science and Business Media LLCVol: 242Issue #: 5Start Page: 1203End Page: 1214Publication Date:Open Access(OA) Status: OPENLicense:DOI - Digital Object Identifier: 10.1007/s00221-024-06815-wBest OA location URL: https://link.springer.com/content/pdf/10.1007/s00221-024-06815-w.pdfCitation Count: 4
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OPENTitle: Parkinson’s-linked LRRK2-G2019S derails AMPAR trafficking, mobility, and composition in striatum with cell-type and subunit specificityJournal Name: Proceedings of the National Academy of SciencesPublisher: Proceedings of the National Academy of SciencesVol: 121Issue #: 28Start Page: e2317833121End Page: e2317833121Publication Date:Open Access(OA) Status: OPENLicense:DOI - Digital Object Identifier: 10.1073/pnas.2317833121Best OA location URL: https://www.pnas.org/doi/pdf/10.1073/pnas.2317833121Citation Count: 6
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OPENTitle: Development and characterization of phospho-ubiquitin antibodies to monitor PINK1-PRKN signaling in cells and tissueJournal Name: AutophagyPublisher: Informa UK LimitedVol: 20Issue #: 9Start Page: 2076End Page: 2091Publication Date:Open Access(OA) Status: OPENLicense: cc-byDOI - Digital Object Identifier: 10.1080/15548627.2024.2356490Best OA location URL: https://www.tandfonline.com/doi/pdf/10.1080/15548627.2024.2356490?needAccess=trueCitation Count: 9
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OPENTitle: Activation of parkin by a molecular glueJournal Name: Nature CommunicationsPublisher: Springer Science and Business Media LLCVol: 15Issue #: 1Start Page: 7707End Page: 7707Publication Date:Open Access(OA) Status: OPENLicense:DOI - Digital Object Identifier: 10.1038/s41467-024-51889-3Best OA location URL: https://www.nature.com/articles/s41467-024-51889-3.pdfCitation Count: 40
- Novel tools to quantify total, phospho-Ser129 and aggregated alpha-synuclein in the mouse brain2024OPENTitle: Novel tools to quantify total, phospho-Ser129 and aggregated alpha-synuclein in the mouse brainJournal Name: npj Parkinson's DiseasePublisher: Springer Science and Business Media LLCVol: 10Issue #: 1Start Page: 217End Page: 217Publication Date:Open Access(OA) Status: OPENLicense:DOI - Digital Object Identifier: 10.1038/s41531-024-00830-yBest OA location URL: https://www.nature.com/articles/s41531-024-00830-y.pdfCitation Count: 8
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OPENTitle: Autosomal recessive VWA1-related disorder: comprehensive analysis of phenotypic variability and genetic mutationsJournal Name: Brain CommunicationsPublisher: Oxford University Press (OUP)Vol: 6Issue #: 6Start Page: fcae377End Page: fcae377Publication Date:Open Access(OA) Status: OPENLicense: cc-byDOI - Digital Object Identifier: 10.1093/braincomms/fcae377Best OA location URL: https://doi.org/10.1093/braincomms/fcae377Citation Count: 6
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OPENTitle: The p.Gly2019Ser is a common LRRK2 pathogenic variant among Egyptians with familial and sporadic Parkinson’s diseaseJournal Name: npj Parkinson's DiseasePublisher: Springer Science and Business Media LLCVol: 10Issue #: 1Start Page: 215End Page: 215Publication Date:Open Access(OA) Status: OPENLicense:DOI - Digital Object Identifier: 10.1038/s41531-024-00826-8Best OA location URL: https://www.nature.com/articles/s41531-024-00826-8.pdfCitation Count: 7