3991 - 4000 of 5832 Results
Title
Year
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OPENTitle: The human brainome: network analysis identifies HSPA2 as a novel Alzheimer’s disease targetJournal Name: BrainPublisher: Oxford University Press (OUP)Vol:Issue #:Start Page:End Page:Publication Date:Open Access(OA) Status: OPENLicense: cc-by-ncDOI - Digital Object Identifier: 10.1093/brain/awy215Best OA location URL: https://academic.oup.com/brain/article-pdf/141/9/2721/25590456/awy215.pdfCitation Count: 39
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OPENTitle: Functional Connectivity-Based Modelling Simulates Subject-Specific Network Spreading Effects of Focal Brain StimulationJournal Name: Neuroscience BulletinPublisher: Springer Science and Business Media LLCVol: 34Issue #: 6Start Page: 921End Page: 938Publication Date:Open Access(OA) Status: OPENLicense: cc-byDOI - Digital Object Identifier: 10.1007/s12264-018-0256-0Best OA location URL: https://link.springer.com/content/pdf/10.1007/s12264-018-0256-0.pdfCitation Count: 13
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OPENTitle: Proteasome-targeted nanobodies alleviate pathology and functional decline in an α-synuclein-based Parkinson’s disease modelJournal Name: npj Parkinson's DiseasePublisher: Springer Science and Business Media LLCVol: 4Issue #: 1Start Page:End Page:Publication Date:Open Access(OA) Status: OPENLicense: cc-byDOI - Digital Object Identifier: 10.1038/s41531-018-0062-4Best OA location URL: https://www.nature.com/articles/s41531-018-0062-4.pdfCitation Count: 78
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OPENTitle: The G2019S mutation in LRRK2 imparts resiliency to kinase inhibitionJournal Name: Experimental NeurologyPublisher: Elsevier BVVol: 309Issue #:Start Page: 1End Page: 13Publication Date:Open Access(OA) Status: OPENLicense: cc-byDOI - Digital Object Identifier: 10.1016/j.expneurol.2018.07.012Best OA location URL: https://doi.org/10.1016/j.expneurol.2018.07.012Citation Count: 44
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OPENTitle: Endoplasmic reticulum stress leads to accumulation of wild-type SOD1 aggregates associated with sporadic amyotrophic lateral sclerosisJournal Name: Proceedings of the National Academy of SciencesPublisher: Proceedings of the National Academy of SciencesVol: 115Issue #: 32Start Page: 8209End Page: 8214Publication Date:Open Access(OA) Status: OPENLicense:DOI - Digital Object Identifier: 10.1073/pnas.1801109115Best OA location URL: https://www.pnas.org/content/pnas/115/32/8209.full.pdfCitation Count: 94
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OPENTitle: Combined accelerometer and genetic analysis to differentiate essential tremor from Parkinson’s diseaseJournal Name: PeerJPublisher: PeerJVol: 6Issue #:Start Page: e5308End Page: e5308Publication Date:Open Access(OA) Status: OPENLicense: cc-byDOI - Digital Object Identifier: 10.7717/peerj.5308Best OA location URL: https://peerj.com/articles/5308.pdfCitation Count: 11
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OPENTitle: NLRP3 expression in mesencephalic neurons and characterization of a rare NLRP3 polymorphism associated with decreased risk of Parkinson’s diseaseJournal Name: npj Parkinson's DiseasePublisher: Springer Science and Business Media LLCVol: 4Issue #: 1Start Page:End Page:Publication Date:Open Access(OA) Status: OPENLicense: cc-byDOI - Digital Object Identifier: 10.1038/s41531-018-0061-5Best OA location URL: https://www.nature.com/articles/s41531-018-0061-5.pdfCitation Count: 134
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OPENTitle: The GBA p.Trp378Gly mutation is a probable French‐Canadian founder mutation causing Gaucher disease and synucleinopathiesJournal Name: Clinical GeneticsPublisher: WileyVol: 94Issue #: 3-4Start Page: 339End Page: 345Publication Date:Open Access(OA) Status: OPENLicense:DOI - Digital Object Identifier: 10.1111/cge.13405Best OA location URL: https://zenodo.org/record/3911322Citation Count: 9
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OPENTitle: Mitochondrial Stasis Reveals p62-Mediated Ubiquitination in Parkin-Independent Mitophagy and Mitigates Nonalcoholic Fatty Liver DiseaseJournal Name: Cell MetabolismPublisher: Elsevier BVVol: 28Issue #: 4Start Page: 588End Page: 604.e5Publication Date:Open Access(OA) Status: OPENLicense: publisher-specific-oaDOI - Digital Object Identifier: 10.1016/j.cmet.2018.06.014Best OA location URL: http://www.cell.com/article/S1550413118303966/pdfCitation Count: 226
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OPENTitle: Loss of Sarm1 does not suppress motor neuron degeneration in the SOD1G93A mouse model of amyotrophic lateral sclerosisJournal Name: Human Molecular GeneticsPublisher: Oxford University Press (OUP)Vol: 27Issue #: 21Start Page: 3761End Page: 3771Publication Date:Open Access(OA) Status: OPENLicense: cc-by, cc-byDOI - Digital Object Identifier: 10.1093/hmg/ddy260Best OA location URL: https://academic.oup.com/hmg/article-pdf/27/21/3761/26127115/ddy260.pdfCitation Count: 50