6391 - 6400 of 6440 Results
Title
Year
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OPENTitle: LRRK2: an éminence grise of Wnt-mediated neurogenesis?Journal Name: Frontiers in Cellular NeurosciencePublisher: Frontiers Media SAVol: 7Issue #:Start Page:End Page:Publication Date:Open Access(OA) Status: OPENLicense: cc-by, cc-byDOI - Digital Object Identifier: 10.3389/fncel.2013.00082Best OA location URL: https://www.frontiersin.org/articles/10.3389/fncel.2013.00082/pdfCitation Count: 31
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OPENTitle: Distinct spatiotemporal atrophy patterns in corticobasal syndrome are associated with different underlying pathologiesJournal Name: Brain CommunicationsPublisher: Oxford University Press (OUP)Vol: 7Issue #: 2Start Page: fcaf066End Page: fcaf066Publication Date:Open Access(OA) Status: OPENLicense: cc-by, cc-byDOI - Digital Object Identifier: 10.1093/braincomms/fcaf066Best OA location URL: https://doi.org/10.1093/braincomms/fcaf066Citation Count: 1
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OPENTitle: Major Shifts in Glial Regional Identity Are a Transcriptional Hallmark of Human Brain AgingJournal Name: Cell ReportsPublisher: Elsevier BVVol: 18Issue #: 2Start Page: 557End Page: 570Publication Date:Open Access(OA) Status: OPENLicense: cc-by, cc-byDOI - Digital Object Identifier: 10.1016/j.celrep.2016.12.011Best OA location URL: http://www.cell.com/article/S2211124716316849/pdfCitation Count: 425
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OPENTitle: Structural determinants for ERK5 (MAPK7) and leucine rich repeat kinase 2 activities of benzo[e]pyrimido-[5,4-b]diazepine-6(11H)-onesJournal Name: European Journal of Medicinal ChemistryPublisher: Elsevier BVVol: 70Issue #:Start Page: 758End Page: 767Publication Date:Open Access(OA) Status: OPENLicense: cc-by, cc-byDOI - Digital Object Identifier: 10.1016/j.ejmech.2013.10.052Best OA location URL: https://doi.org/10.1016/j.ejmech.2013.10.052Citation Count: 48
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OPENTitle: A data-driven model of brain volume changes in progressive supranuclear palsyJournal Name: Brain CommunicationsPublisher: Oxford University Press (OUP)Vol: 4Issue #: 3Start Page: fcac098End Page: fcac098Publication Date:Open Access(OA) Status: OPENLicense: cc-by, cc-byDOI - Digital Object Identifier: 10.1093/braincomms/fcac098Best OA location URL: https://academic.oup.com/braincomms/article-pdf/4/3/fcac098/44351975/fcac098.pdfCitation Count: 24
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OPENTitle: Clinical and neuroradiological spectrum of biallelic variants in NOTCH3Journal Name: eBioMedicinePublisher: Elsevier BVVol: 107Issue #:Start Page: 105297End Page: 105297Publication Date:Open Access(OA) Status: OPENLicense: cc-byDOI - Digital Object Identifier: 10.1016/j.ebiom.2024.105297Best OA location URL: https://doi.org/10.1016/j.ebiom.2024.105297Citation Count: 11
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OPENTitle: Biallelic LGI1 and ADAM23 variants cause hippocampal epileptic encephalopathy via the LGI1–ADAM22/23 pathwayJournal Name: BrainPublisher: Oxford University Press (OUP)Vol: 148Issue #: 10Start Page: 3514End Page: 3522Publication Date:Open Access(OA) Status: OPENLicense: cc-by, cc-byDOI - Digital Object Identifier: 10.1093/brain/awaf202Best OA location URL: https://academic.oup.com/brain/advance-article-pdf/doi/10.1093/brain/awaf202/63419094/awaf202.pdfCitation Count: 2
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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: 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: Additional rare variant analysis in Parkinson’s disease cases with and without known pathogenic mutations: evidence for oligogenic inheritanceJournal Name: Human Molecular GeneticsPublisher: Oxford University Press (OUP)Vol:Issue #:Start Page: ddw348End Page: ddw348Publication Date:Open Access(OA) Status: OPENLicense: cc-by, cc-byDOI - Digital Object Identifier: 10.1093/hmg/ddw348Best OA location URL: https://academic.oup.com/hmg/article-pdf/25/24/5483/10408585/ddw348.pdfCitation Count: 59