5561 - 5570 of 6568 Results
Title
Year
- Creation of an Open-Access, Mutation-Defined Fibroblast Resource for Neurological Disease Research2012OPENTitle: Creation of an Open-Access, Mutation-Defined Fibroblast Resource for Neurological Disease ResearchJournal Name: PLoS ONEPublisher: Public Library of Science (PLoS)Vol: 7Issue #: 8Start Page: e43099End Page: e43099Publication Date:Open Access(OA) Status: OPENLicense: cc0, cc0DOI - Digital Object Identifier: 10.1371/journal.pone.0043099Best OA location URL: https://escholarship.org/uc/item/0hr9m7btCitation Count: 141
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OPENTitle: Genetics and Pathophysiology of Neurodegeneration with Brain Iron Accumulation (NBIA)Journal Name: Current NeuropharmacologyPublisher: Bentham Science Publishers Ltd.Vol: 11Issue #: 1Start Page: 59End Page: 79Publication Date:Open Access(OA) Status: OPENLicense:DOI - Digital Object Identifier: 10.2174/157015913804999469Best OA location URL: http://europepmc.org/articles/PMC3580793Citation Count: 127
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OPENTitle: A Tangled Web – Tau and Sporadic Parkinson's DiseaseJournal Name: Frontiers in PsychiatryPublisher: Frontiers Media SAVol: 1Issue #:Start Page: 150End Page: 150Publication Date:Open Access(OA) Status: OPENLicense: cc-by, cc-byDOI - Digital Object Identifier: 10.3389/fpsyt.2010.00150Best OA location URL: https://www.frontiersin.org/articles/10.3389/fpsyt.2010.00150/pdfCitation Count: 32
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OPENTitle: CAG repeat expansion in Huntington disease determines age at onset in a fully dominant fashionJournal Name: NeurologyPublisher: Ovid Technologies (Wolters Kluwer Health)Vol: 78Issue #: 10Start Page: 690End Page: 695Publication Date:Open Access(OA) Status: OPENLicense:DOI - Digital Object Identifier: 10.1212/wnl.0b013e318249f683Best OA location URL: https://hdl.handle.net/2108/99911Citation Count: 391
- LRRK2 functions as a Wnt signaling scaffold, bridging cytosolic proteins and membrane-localized LRP62012OPENTitle: LRRK2 functions as a Wnt signaling scaffold, bridging cytosolic proteins and membrane-localized LRP6Journal Name: Human Molecular GeneticsPublisher: Oxford University Press (OUP)Vol: 21Issue #: 22Start Page: 4966End Page: 4979Publication Date:Open Access(OA) Status: OPENLicense: other-oa, other-oaDOI - Digital Object Identifier: 10.1093/hmg/dds342Best OA location URL: https://academic.oup.com/hmg/article-pdf/21/22/4966/17257652/dds342.pdfCitation Count: 103
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OPENTitle: Divergent α-synuclein solubility and aggregation properties in G2019S LRRK2 Parkinson's disease brains with Lewy Body pathology compared to idiopathic casesJournal Name: Neurobiology of DiseasePublisher: Elsevier BVVol: 58Issue #:Start Page: 183End Page: 190Publication Date:Open Access(OA) Status: OPENLicense: cc-by-nc-nd, cc-by-nc-ndDOI - Digital Object Identifier: 10.1016/j.nbd.2013.05.017Best OA location URL: http://infoscience.epfl.ch/record/189244Citation Count: 59
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OPENTitle: Analysis of macroautophagy related proteins in G2019S LRRK2 Parkinson’s disease brains with Lewy body pathologyJournal Name: Brain ResearchPublisher: Elsevier BVVol: 1701Issue #:Start Page: 75End Page: 84Publication Date:Open Access(OA) Status: OPENLicense: cc-by, cc-byDOI - Digital Object Identifier: 10.1016/j.brainres.2018.07.023Best OA location URL: https://doi.org/10.1016/j.brainres.2018.07.023Citation Count: 41
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OPENTitle: A multi-ancestry genome-wide study incorporating gene–smoking interactions identifies multiple new loci for pulse pressure and mean arterial pressureJournal Name: Human Molecular GeneticsPublisher: Oxford University Press (OUP)Vol: 28Issue #: 15Start Page: 2615End Page: 2633Publication Date:Open Access(OA) Status: OPENLicense:DOI - Digital Object Identifier: 10.1093/hmg/ddz070Best OA location URL: https://academic.oup.com/hmg/article-pdf/28/15/2615/28936234/ddz070.pdfCitation Count: 48
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OPENTitle: Clinical and demographic characteristics related to onset site and spread of cervical dystoniaJournal Name: Movement DisordersPublisher: WileyVol: 31Issue #: 12Start Page: 1874End Page: 1882Publication Date:Open Access(OA) Status: OPENLicense:DOI - Digital Object Identifier: 10.1002/mds.26817Best OA location URL: http://doi.org/10.1002/mds.26817Citation Count: 47
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OPENTitle: A NAC domain mutation (E83Q) unlocks the pathogenicity of human alpha-synuclein and recapitulates its pathological diversityJournal Name: Science AdvancesPublisher: American Association for the Advancement of Science (AAAS)Vol: 8Issue #: 17Start Page: eabn0044End Page: eabn0044Publication Date:Open Access(OA) Status: OPENLicense:DOI - Digital Object Identifier: 10.1126/sciadv.abn0044Best OA location URL: https://www.science.org/doi/pdf/10.1126/sciadv.abn0044?download=trueCitation Count: 48