1476 - 1500 of 8654 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: Computer keyboard interaction as an indicator of early Parkinson’s diseaseJournal Name: Scientific ReportsPublisher: Springer Science and Business Media LLCVol: 6Issue #: 1Start Page:End Page:Publication Date:Open Access(OA) Status: OPENLicense: cc-byDOI - Digital Object Identifier: 10.1038/srep34468Best OA location URL: https://doi.org/10.1038/srep34468Citation Count: 98
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OPENTitle: Structural basis of polyamine transport by human ATP13A2 (PARK9)Journal Name: Molecular CellPublisher: Elsevier BVVol: 81Issue #: 22Start Page: 4635End Page: 4649.e8Publication Date:Open Access(OA) Status: OPENLicense:DOI - Digital Object Identifier: 10.1016/j.molcel.2021.08.017Best OA location URL: https://escholarship.org/content/qt0vq3x5sc/qt0vq3x5sc.pdfCitation Count: 36
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OPENTitle: Reply to: “Overlapping Ranges in Levels Indicate That Hexosylsphingosine Is Not a Clinically Relevant Biomarker for GBA1‐Associated Parkinson's Disease”Journal Name: Movement DisordersPublisher: WileyVol: 37Issue #: 8Start Page: 1781End Page: 1782Publication Date:Open Access(OA) Status: OPENLicense:DOI - Digital Object Identifier: 10.1002/mds.29131Best OA location URL: https://www.ncbi.nlm.nih.gov/pmc/articles/9756875Citation Count: 0
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OPENTitle: No Evidence That Glucosylsphingosine Is a Biomarker for Parkinson's Disease: Statistical Differences Do Not Necessarily Indicate Biological SignificanceJournal Name: Movement DisordersPublisher: WileyVol: 37Issue #: 3Start Page: 653End Page: 653Publication Date:Open Access(OA) Status: OPENLicense:DOI - Digital Object Identifier: 10.1002/mds.28935Best OA location URL: https://www.ncbi.nlm.nih.gov/pmc/articles/8940713Citation Count: 5
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OPENTitle: In silico comparative analysis of LRRK2 interactomes from brain, kidney and lungJournal Name: Brain ResearchPublisher: Elsevier BVVol: 1765Issue #:Start Page: 147503End Page: 147503Publication Date:Open Access(OA) Status: OPENLicense: cc-byDOI - Digital Object Identifier: 10.1016/j.brainres.2021.147503Best OA location URL: https://doi.org/10.1016/j.brainres.2021.147503Citation Count: 7
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OPENTitle: Detecting Motor Impairment in Early Parkinson’s Disease via Natural Typing Interaction With Keyboards: Validation of the neuroQWERTY Approach in an Uncontrolled At-Home SettingJournal Name: Journal of Medical Internet ResearchPublisher: JMIR Publications Inc.Vol: 20Issue #: 3Start Page: e89End Page: e89Publication Date:Open Access(OA) Status: OPENLicense: cc-byDOI - Digital Object Identifier: 10.2196/jmir.9462Best OA location URL: https://doi.org/10.2196/jmir.9462Citation Count: 55
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OPENTitle: Circular RNA expression and regulatory network prediction in posterior cingulate astrocytes in elderly subjectsJournal Name: BMC GenomicsPublisher: Springer Science and Business Media LLCVol: 19Issue #: 1Start Page:End Page:Publication Date:Open Access(OA) Status: OPENLicense: cc-byDOI - Digital Object Identifier: 10.1186/s12864-018-4670-5Best OA location URL: https://bmcgenomics.biomedcentral.com/track/pdf/10.1186/s12864-018-4670-5Citation Count: 34
- A prebiotic diet modulates microglial states and motor deficits in α-synuclein overexpressing mice2022OPENTitle: A prebiotic diet modulates microglial states and motor deficits in α-synuclein overexpressing miceJournal Name: eLifePublisher: eLife Sciences Publications, LtdVol: 11Issue #:Start Page:End Page:Publication Date:Open Access(OA) Status: OPENLicense: cc-by, cc-byDOI - Digital Object Identifier: 10.7554/elife.81453Best OA location URL: https://doi.org/10.7554/elife.81453Citation Count: 54
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OPENTitle: Synaptic location is a determinant of the detrimental effects of α-synuclein pathology to glutamatergic transmission in the basolateral amygdalaJournal Name: eLifePublisher: eLife Sciences Publications, LtdVol: 11Issue #:Start Page:End Page:Publication Date:Open Access(OA) Status: OPENLicense: cc-by, cc-byDOI - Digital Object Identifier: 10.7554/elife.78055Best OA location URL: https://doi.org/10.7554/elife.78055Citation Count: 22
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OPENTitle: Structural basis for membrane recruitment of ATG16L1 by WIPI2 in autophagyJournal Name: eLifePublisher: eLife Sciences Publications, LtdVol: 10Issue #:Start Page:End Page:Publication Date:Open Access(OA) Status: OPENLicense: cc-by, cc-byDOI - Digital Object Identifier: 10.7554/elife.70372Best OA location URL: https://doi.org/10.7554/elife.70372Citation Count: 42
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OPENTitle: Mechanisms controlling selective elimination of damaged lysosomesJournal Name: Current Opinion in PhysiologyPublisher: Elsevier BVVol: 29Issue #:Start Page: 100590End Page: 100590Publication Date:Open Access(OA) Status: OPENLicense: cc-by, cc-byDOI - Digital Object Identifier: 10.1016/j.cophys.2022.100590Best OA location URL: https://doi.org/10.1016/j.cophys.2022.100590Citation Count: 25
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OPENTitle: Spatial snapshots of amyloid precursor protein intramembrane processing via early endosome proteomicsJournal Name: Nature CommunicationsPublisher: Springer Science and Business Media LLCVol: 13Issue #: 1Start Page:End Page:Publication Date:Open Access(OA) Status: OPENLicense: cc-by, cc-byDOI - Digital Object Identifier: 10.1038/s41467-022-33881-xBest OA location URL: https://www.nature.com/articles/s41467-022-33881-x.pdfCitation Count: 35
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OPENTitle: Data-driven models of dominantly-inherited Alzheimer’s disease progressionJournal Name: BrainPublisher: Oxford University Press (OUP)Vol: 141Issue #: 5Start Page: 1529End Page: 1544Publication Date:Open Access(OA) Status: OPENLicense: cc-byDOI - Digital Object Identifier: 10.1093/brain/awy050Best OA location URL: https://academic.oup.com/brain/article-pdf/141/5/1529/25901390/awy050.pdfCitation Count: 123
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OPENTitle: Genetic variants associated with Alzheimer’s disease confer different cerebral cortex cell-type population structureJournal Name: Genome MedicinePublisher: Springer Science and Business Media LLCVol: 10Issue #: 1Start Page:End Page:Publication Date:Open Access(OA) Status: OPENLicense: cc-byDOI - Digital Object Identifier: 10.1186/s13073-018-0551-4Best OA location URL: https://doi.org/10.1186/s13073-018-0551-4Citation Count: 60
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OPENTitle: A Markov random field model-based approach for differentially expressed gene detection from single-cell RNA-seq dataJournal Name: Briefings in BioinformaticsPublisher: Oxford University Press (OUP)Vol: 23Issue #: 5Start Page:End Page:Publication Date:Open Access(OA) Status: OPENLicense: cc-by, cc-byDOI - Digital Object Identifier: 10.1093/bib/bbac166Best OA location URL: https://academic.oup.com/bib/article-pdf/23/5/bbac166/45937268/bbac166.pdfCitation Count: 6
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OPENTitle: Levodopa Responsive Dystonia Parkinsonism, Intellectual Disability, and Optic Atrophy Due to a Heterozygous Missense Variant in AFG3L2Journal Name: Movement Disorders Clinical PracticePublisher: WileyVol: 9Issue #: S2Start Page:End Page:Publication Date:Open Access(OA) Status: OPENLicense: cc-by-nc-ndDOI - Digital Object Identifier: 10.1002/mdc3.13538Best OA location URL: https://onlinelibrary.wiley.com/doi/pdfdirect/10.1002/mdc3.13538Citation Count: 3
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RESTRICTEDTitle: Men with FMR1 premutation alleles of less than 71 CGG repeats have low risk of being affected with fragile X-associated tremor/ataxia syndrome (FXTAS)Journal Name: Journal of Medical GeneticsPublisher: BMJVol: 59Issue #: 7Start Page: 706End Page: 709Publication Date:Open Access(OA) Status: RESTRICTEDLicense:DOI - Digital Object Identifier: 10.1136/jmedgenet-2021-107758Citation Count: 5
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OPENTitle: Faster disease progression in Parkinson’s disease with type 2 diabetes is not associated with increased α‐synuclein, tau, amyloid‐β or vascular pathologyJournal Name: Neuropathology and Applied NeurobiologyPublisher: WileyVol: 47Issue #: 7Start Page: 1080End Page: 1091Publication Date:Open Access(OA) Status: OPENLicense:DOI - Digital Object Identifier: 10.1111/nan.12728Citation Count: 30
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OPENTitle: Altered bile acid profile in mild cognitive impairment and Alzheimer's disease: Relationship to neuroimaging and CSF biomarkersJournal Name: Alzheimer's & DementiaPublisher: WileyVol: 15Issue #: 2Start Page: 232End Page: 244Publication Date:Open Access(OA) Status: OPENLicense:DOI - Digital Object Identifier: 10.1016/j.jalz.2018.08.012Best OA location URL: https://hdl.handle.net/1887/82120Citation Count: 281
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OPENTitle: Virtual house calls for Parkinson disease (Connect.Parkinson): study protocol for a randomized, controlled trialJournal Name: TrialsPublisher: Springer Science and Business Media LLCVol: 15Issue #: 1Start Page:End Page:Publication Date:Open Access(OA) Status: OPENLicense: cc-by, cc-byDOI - Digital Object Identifier: 10.1186/1745-6215-15-465Best OA location URL: https://trialsjournal.biomedcentral.com/counter/pdf/10.1186/1745-6215-15-465Citation Count: 25
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OPENTitle: Group patient visits for Parkinson diseaseJournal Name: NeurologyPublisher: Ovid Technologies (Wolters Kluwer Health)Vol: 76Issue #: 18Start Page: 1542End Page: 1547Publication Date:Open Access(OA) Status: OPENLicense:DOI - Digital Object Identifier: 10.1212/wnl.0b013e3182194badBest OA location URL: https://n.neurology.org/content/neurology/76/18/1542.full.pdfCitation Count: 22
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RESTRICTEDTitle: PINK1 p.Leu347Pro mutations in Malays: Prevalence and illustrative casesJournal Name: Parkinsonism & Related DisordersPublisher: Elsevier BVVol: 79Issue #:Start Page: 34End Page: 39Publication Date:Open Access(OA) Status: RESTRICTEDLicense:DOI - Digital Object Identifier: 10.1016/j.parkreldis.2020.08.015Citation Count: 21
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OPENTitle: Loss‐of‐Function Variants in HOPS Complex Genes VPS16 and VPS41 Cause Early Onset Dystonia Associated with Lysosomal AbnormalitiesJournal Name: Annals of NeurologyPublisher: WileyVol: 88Issue #: 5Start Page: 867End Page: 877Publication Date:Open Access(OA) Status: OPENLicense: cc-by, cc-byDOI - Digital Object Identifier: 10.1002/ana.25879Best OA location URL: https://onlinelibrary.wiley.com/doi/pdfdirect/10.1002/ana.25879Citation Count: 92
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OPENTitle: A novel homozygous KY variant causing a complex neurological disorderJournal Name: European Journal of Medical GeneticsPublisher: Elsevier BVVol: 63Issue #: 11Start Page: 104031End Page: 104031Publication Date:Open Access(OA) Status: OPENLicense:DOI - Digital Object Identifier: 10.1016/j.ejmg.2020.104031Best OA location URL: https://www.ncbi.nlm.nih.gov/pmc/articles/7554104Citation Count: 5