8371 - 8380 of 9038 Results
Title
Year
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OPENTitle: Mitofusin 2 displays fusion-independent roles in proteostasis surveillanceJournal Name: Nature CommunicationsPublisher: Springer Science and Business Media LLCVol: 16Issue #: 1Start Page: 1501End Page: 1501Publication Date:Open Access(OA) Status: OPENLicense: cc-byDOI - Digital Object Identifier: 10.1038/s41467-025-56673-5Best OA location URL: https://doi.org/10.1038/s41467-025-56673-5Citation Count: 16
- The Amplification of Alpha‐Synuclein Amyloid Fibrils is Suppressed under Fully Quiescent Conditions2024OPENTitle: The Amplification of Alpha‐Synuclein Amyloid Fibrils is Suppressed under Fully Quiescent ConditionsJournal Name: Angewandte Chemie International EditionPublisher: WileyVol: 64Issue #: 7Start Page: e202419173End Page: e202419173Publication Date:Open Access(OA) Status: OPENLicense: cc-by-ncDOI - Digital Object Identifier: 10.1002/anie.202419173Best OA location URL: https://onlinelibrary.wiley.com/doi/pdfdirect/10.1002/anie.202419173Citation Count: 7
- Large-scale validation of skin prion seeding activity as a biomarker for diagnosis of prion diseases2024OPENTitle: Large-scale validation of skin prion seeding activity as a biomarker for diagnosis of prion diseasesJournal Name: Acta NeuropathologicaPublisher: Springer Science and Business Media LLCVol: 147Issue #: 1Start Page: 17End Page: 17Publication Date:Open Access(OA) Status: OPENLicense:DOI - Digital Object Identifier: 10.1007/s00401-023-02661-2Best OA location URL: https://pmc.ncbi.nlm.nih.gov/articles/PMC11812622/pdf/nihms-2035454.pdfCitation Count: 18
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OPENTitle: Endogenous LRRK2 and PINK1 function in a convergent neuroprotective ciliogenesis pathway in the brainJournal Name: Proceedings of the National Academy of SciencesPublisher: National Academy of SciencesVol: 122Issue #: 5Start Page: e2412029122End Page: e2412029122Publication Date:Open Access(OA) Status: OPENLicense: cc-by, cc-byDOI - Digital Object Identifier: 10.1073/pnas.2412029122Best OA location URL: https://doi.org/10.1073/pnas.2412029122Citation Count: 18
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OPENTitle: Bradykinesia and postural instability in a model of prodromal synucleinopathy with α-synuclein aggregation initiated in the gigantocellular nucleiJournal Name: Acta Neuropathologica CommunicationsPublisher: Springer Science and Business Media LLCVol: 13Issue #: 1Start Page: 32End Page: 32Publication Date:Open Access(OA) Status: OPENLicense: cc-by-nc-ndDOI - Digital Object Identifier: 10.1186/s40478-025-01948-7Best OA location URL: https://link.springer.com/content/pdf/10.1186/s40478-025-01948-7.pdfCitation Count: 5
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OPENTitle: Biallelic NDUFA13 variants lead to a neurodevelopmental phenotype with gradual neurological impairmentJournal Name: Brain CommunicationsPublisher: Oxford University Press (OUP)Vol: 7Issue #: 1Start Page: fcae453End Page: fcae453Publication Date:Open Access(OA) Status: OPENLicense: cc-by, cc-byDOI - Digital Object Identifier: 10.1093/braincomms/fcae453Best OA location URL: https://academic.oup.com/braincomms/advance-article-pdf/doi/10.1093/braincomms/fcae453/61218229/fcae453.pdfCitation Count: 3
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OPENTitle: Identification of Parkinson’s disease using MRI and genetic data from the PPMI cohort: an improved machine learning fusion approachJournal Name: Frontiers in Aging NeurosciencePublisher: Frontiers Media SAVol: 17Issue #:Start Page: 1510192End Page: 1510192Publication Date:Open Access(OA) Status: OPENLicense: cc-byDOI - Digital Object Identifier: 10.3389/fnagi.2025.1510192Best OA location URL: https://public-pages-files-2025.frontiersin.org/journals/aging-neuroscience/articles/10.3389/fnagi.2025.1510192/pdfCitation Count: 10
- Updated MDSGene review on the clinical and genetic spectrum of LRRK2 variants in Parkinson´s disease2025OPENTitle: Updated MDSGene review on the clinical and genetic spectrum of LRRK2 variants in Parkinson´s diseaseJournal Name: npj Parkinson's DiseasePublisher: Springer Science and Business Media LLCVol: 11Issue #: 1Start Page: 30End Page: 30Publication Date:Open Access(OA) Status: OPENLicense: cc-byDOI - Digital Object Identifier: 10.1038/s41531-025-00881-9Best OA location URL: https://www.nature.com/articles/s41531-025-00881-9.pdfCitation Count: 31
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OPENTitle: The ZFHX3 GGC Repeat Expansion Underlying Spinocerebellar Ataxia Type 4 has a Common Ancestral FounderJournal Name: Movement DisordersPublisher: WileyVol: 40Issue #: 2Start Page: 363End Page: 369Publication Date:Open Access(OA) Status: OPENLicense: cc-by, cc-byDOI - Digital Object Identifier: 10.1002/mds.30077Best OA location URL: https://onlinelibrary.wiley.com/doi/pdfdirect/10.1002/mds.30077Citation Count: 5
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OPENTitle: Genome Aggregation Database Version 4—Allele Frequency Changes and Impact on Variant Interpretation in DystoniaJournal Name: Movement DisordersPublisher: WileyVol: 40Issue #: 2Start Page: 357End Page: 362Publication Date:Open Access(OA) Status: OPENLicense: cc-by-nc-ndDOI - Digital Object Identifier: 10.1002/mds.30066Best OA location URL: https://onlinelibrary.wiley.com/doi/pdfdirect/10.1002/mds.30066Citation Count: 5