501 - 510 of 7877 Results
Title
Year
- LINE-1 retrotransposons drive human neuronal transcriptome complexity and functional diversification2023OPENTitle: LINE-1 retrotransposons drive human neuronal transcriptome complexity and functional diversificationJournal Name: Science AdvancesPublisher: American Association for the Advancement of Science (AAAS)Vol: 9Issue #: 44Start Page:End Page:Publication Date:Open Access(OA) Status: OPENLicense: cc-by-nc, cc-by-nc, cc-by-ncDOI - Digital Object Identifier: 10.1126/sciadv.adh9543Best OA location URL: https://www.science.org/doi/pdf/10.1126/sciadv.adh9543?download=trueCitation Count: 19
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OPENTitle: RTP801 mediates transneuronal toxicity in culture via extracellular vesiclesJournal Name: Journal of Extracellular VesiclesPublisher: WileyVol: 12Issue #: 11Start Page:End Page:Publication Date:Open Access(OA) Status: OPENLicense: cc-by-nc-ndDOI - Digital Object Identifier: 10.1002/jev2.12378Best OA location URL: https://onlinelibrary.wiley.com/doi/pdfdirect/10.1002/jev2.12378Citation Count: 1
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RESTRICTEDTitle: Shifting the trajectory of therapeutic development for neurological and psychiatric disordersJournal Name: Science Translational MedicinePublisher: American Association for the Advancement of Science (AAAS)Vol: 15Issue #: 720Start Page:End Page:Publication Date:Open Access(OA) Status: RESTRICTEDLicense:DOI - Digital Object Identifier: 10.1126/scitranslmed.adg4775Citation Count: 0
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OPENTitle: PFTK1 kinase regulates axogenesis during development via RhoA activationJournal Name: BMC BiologyPublisher: Springer Science and Business Media LLCVol: 21Issue #: 1Start Page:End Page:Publication Date:Open Access(OA) Status: OPENLicense: cc-byDOI - Digital Object Identifier: 10.1186/s12915-023-01732-wBest OA location URL: https://bmcbiol.biomedcentral.com/counter/pdf/10.1186/s12915-023-01732-wCitation Count: 2
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OPENTitle: Free water imaging unravels unique patterns of longitudinal structural brain changes in Parkinson’s disease subtypesJournal Name: Frontiers in NeurologyPublisher: Frontiers Media SAVol: 14Issue #:Start Page:End Page:Publication Date:Open Access(OA) Status: OPENLicense: cc-byDOI - Digital Object Identifier: 10.3389/fneur.2023.1278065Best OA location URL: https://www.frontiersin.org/articles/10.3389/fneur.2023.1278065/pdf?isPublishedV2=FalseCitation Count: 0
- Genetic testing in adults with neurologic disorders: indications, approach, and clinical impacts2023RESTRICTEDTitle: Genetic testing in adults with neurologic disorders: indications, approach, and clinical impactsJournal Name: Journal of NeurologyPublisher: Springer Science and Business Media LLCVol: 271Issue #: 2Start Page: 733End Page: 747Publication Date:Open Access(OA) Status: RESTRICTEDLicense:DOI - Digital Object Identifier: 10.1007/s00415-023-12058-6Citation Count: 1
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OPENTitle: Localization of PPM1H phosphatase tunes Parkinson’s disease-linked LRRK2 kinase-mediated Rab GTPase phosphorylation and ciliogenesisJournal Name: Proceedings of the National Academy of SciencesPublisher: Proceedings of the National Academy of SciencesVol: 120Issue #: 44Start Page:End Page:Publication Date:Open Access(OA) Status: OPENLicense: cc-by, cc-byDOI - Digital Object Identifier: 10.1073/pnas.2315171120Best OA location URL: https://doi.org/10.1073/pnas.2315171120Citation Count: 7
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OPENTitle: Saturation mutagenesis of α-synuclein reveals monomer fold that modulates aggregationJournal Name: Science AdvancesPublisher: American Association for the Advancement of Science (AAAS)Vol: 9Issue #: 43Start Page:End Page:Publication Date:Open Access(OA) Status: OPENLicense: cc-by-ncDOI - Digital Object Identifier: 10.1126/sciadv.adh3457Best OA location URL: https://www.science.org/doi/pdf/10.1126/sciadv.adh3457?download=trueCitation Count: 5
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OPENTitle: The α-synuclein PET tracer [18F] ACI-12589 distinguishes multiple system atrophy from other neurodegenerative diseasesJournal Name: Nature CommunicationsPublisher: Springer Science and Business Media LLCVol: 14Issue #: 1Start Page:End Page:Publication Date:Open Access(OA) Status: OPENLicense: cc-byDOI - Digital Object Identifier: 10.1038/s41467-023-42305-3Best OA location URL: https://www.nature.com/articles/s41467-023-42305-3.pdfCitation Count: 19
- Bi-allelic truncating variants in CASP2 underlie a neurodevelopmental disorder with lissencephaly2023OPENTitle: Bi-allelic truncating variants in CASP2 underlie a neurodevelopmental disorder with lissencephalyJournal Name: European Journal of Human GeneticsPublisher: Springer Science and Business Media LLCVol: 32Issue #: 1Start Page: 52End Page: 60Publication Date:Open Access(OA) Status: OPENLicense: cc-by, cc-byDOI - Digital Object Identifier: 10.1038/s41431-023-01461-2Best OA location URL: https://www.nature.com/articles/s41431-023-01461-2.pdfCitation Count: 4