1641 - 1650 of 6509 Results
Title
Year
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OPENTitle: The Roc domain of LRRK2 as a hub for protein-protein interactions: a focus on PAK6 and its impact on RAB phosphorylationJournal Name: Brain ResearchPublisher: Elsevier BVVol: 1778Issue #:Start Page: 147781End Page: 147781Publication Date:Open Access(OA) Status: OPENLicense:DOI - Digital Object Identifier: 10.1016/j.brainres.2022.147781Best OA location URL: https://ars.els-cdn.com/content/image/1-s2.0-S0006899322000051-ga1_lrg.jpgCitation Count: 21
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OPENTitle: The misallocation of climate research fundingJournal Name: Energy Research & Social SciencePublisher: Elsevier BVVol: 62Issue #:Start Page: 101349End Page: 101349Publication Date:Open Access(OA) Status: OPENLicense: cc-by, cc-byDOI - Digital Object Identifier: 10.1016/j.erss.2019.101349Best OA location URL: https://doi.org/10.1016/j.erss.2019.101349Citation Count: 284
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OPENTitle: Genome sequencing analysis identifies new loci associated with Lewy body dementia and provides insights into its genetic architectureJournal Name: Nature GeneticsPublisher: Springer Science and Business Media LLCVol: 53Issue #: 3Start Page: 294End Page: 303Publication Date:Open Access(OA) Status: OPENLicense:DOI - Digital Object Identifier: 10.1038/s41588-021-00785-3Best OA location URL: https://escholarship.org/uc/item/7qn6v913Citation Count: 469
- Contingent negative variation: a biomarker of abnormal attention in functional movement disorders2020OPENTitle: Contingent negative variation: a biomarker of abnormal attention in functional movement disordersJournal Name: European Journal of NeurologyPublisher: WileyVol: 27Issue #: 6Start Page: 985End Page: 994Publication Date:Open Access(OA) Status: OPENLicense: cc-by, cc-byDOI - Digital Object Identifier: 10.1111/ene.14189Best OA location URL: https://escholarship.org/uc/item/4kw389mzCitation Count: 23
- Genetic determinants of survival in progressive supranuclear palsy: a genome-wide association study2020OPENTitle: Genetic determinants of survival in progressive supranuclear palsy: a genome-wide association studyJournal Name: The Lancet NeurologyPublisher: Elsevier BVVol: 20Issue #: 2Start Page: 107End Page: 116Publication Date:Open Access(OA) Status: OPENLicense:DOI - Digital Object Identifier: 10.1016/s1474-4422(20)30394-xBest OA location URL: http://hdl.handle.net/10044/1/85602Citation Count: 117
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OPENTitle: Tossing and Turning in Bed: Nocturnal Movements in Parkinson's DiseaseJournal Name: Movement DisordersPublisher: WileyVol: 35Issue #: 6Start Page: 959End Page: 968Publication Date:Open Access(OA) Status: OPENLicense:DOI - Digital Object Identifier: 10.1002/mds.28006Best OA location URL: https://onlinelibrary.wiley.com/doi/pdfdirect/10.1002/mds.28006Citation Count: 62
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OPENTitle: Normative vs. patient-specific brain connectivity in deep brain stimulationJournal Name: NeuroImagePublisher: Elsevier BVVol: 224Issue #:Start Page: 117307End Page: 117307Publication Date:Open Access(OA) Status: OPENLicense: cc-by, cc-byDOI - Digital Object Identifier: 10.1016/j.neuroimage.2020.117307Best OA location URL: https://doi.org/10.1016/j.neuroimage.2020.117307Citation Count: 131
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OPENTitle: GTP binding controls complex formation by the human ROCO protein MASL1Journal Name: The FEBS JournalPublisher: WileyVol: 281Issue #: 1Start Page: 261End Page: 274Publication Date:Open Access(OA) Status: OPENLicense: cc-byDOI - Digital Object Identifier: 10.1111/febs.12593Best OA location URL: https://onlinelibrary.wiley.com/doi/pdfdirect/10.1111/febs.12593Citation Count: 13
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OPENTitle: The novel MAPT mutation K298E: mechanisms of mutant tau toxicity, brain pathology and tau expression in induced fibroblast-derived neuronsJournal Name: Acta NeuropathologicaPublisher: Springer Science and Business Media LLCVol: 127Issue #: 2Start Page: 283End Page: 295Publication Date:Open Access(OA) Status: OPENLicense: cc-byDOI - Digital Object Identifier: 10.1007/s00401-013-1219-1Best OA location URL: https://link.springer.com/content/pdf/10.1007/s00401-013-1219-1.pdfCitation Count: 34
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OPENTitle: Mild dopa-responsive dystonia in heterozygous tyrosine hydroxylase mutation carrier: Evidence of symptomatic enzyme deficiency?Journal Name: Parkinsonism & Related DisordersPublisher: Elsevier BVVol: 71Issue #:Start Page: 44End Page: 45Publication Date:Open Access(OA) Status: OPENLicense: cc-by, cc-byDOI - Digital Object Identifier: 10.1016/j.parkreldis.2020.01.017Best OA location URL: http://www.prd-journal.com/article/S1353802020300237/pdfCitation Count: 8
