3551 - 3575 of 6255 Results
Title
Year
- Application of the Movement Disorder Society prodromal criteria in healthy G2019S‐LRRK2 carriers2018OPENTitle: Application of the Movement Disorder Society prodromal criteria in healthy G2019S‐LRRK2 carriersJournal Name: Movement DisordersPublisher: WileyVol: 33Issue #: 6Start Page: 966End Page: 973Publication Date:Open Access(OA) Status: OPENLicense:DOI - Digital Object Identifier: 10.1002/mds.27342Best OA location URL: https://www.ncbi.nlm.nih.gov/pmc/articles/6105406Citation Count: 50
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OPENTitle: α‐synuclein genetic variability: A biomarker for dementia in Parkinson diseaseJournal Name: Annals of NeurologyPublisher: WileyVol: 79Issue #: 6Start Page: 991End Page: 999Publication Date:Open Access(OA) Status: OPENLicense:DOI - Digital Object Identifier: 10.1002/ana.24664Best OA location URL: http://hdl.handle.net/10044/1/61098Citation Count: 93
- Neuronal BAG3 attenuates tau hyperphosphorylation, synaptic dysfunction, and cognitive deficits induced by traumatic brain injury via the regulation of autophagy-lysosome pathway2024OPENTitle: Neuronal BAG3 attenuates tau hyperphosphorylation, synaptic dysfunction, and cognitive deficits induced by traumatic brain injury via the regulation of autophagy-lysosome pathwayJournal Name: Acta NeuropathologicaPublisher: Springer Science and Business Media LLCVol: 148Issue #: 1Start Page:End Page:Publication Date:Open Access(OA) Status: OPENLicense: cc-byDOI - Digital Object Identifier: 10.1007/s00401-024-02810-1Best OA location URL: https://doi.org/10.1007/s00401-024-02810-1Citation Count: 3
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OPENTitle: Reconstitution of cargo-induced LC3 lipidation in mammalian selective autophagyJournal Name: Science AdvancesPublisher: American Association for the Advancement of Science (AAAS)Vol: 7Issue #: 17Start Page:End Page:Publication Date:Open Access(OA) Status: OPENLicense: cc-by-nc, cc-byDOI - Digital Object Identifier: 10.1126/sciadv.abg4922Best OA location URL: https://doi.org/10.1126/sciadv.abg4922Citation Count: 43
- Mitochondrial DNA deletions in the cerebrospinal fluid of patients with idiopathic REM sleep behaviour disorder2024OPENTitle: Mitochondrial DNA deletions in the cerebrospinal fluid of patients with idiopathic REM sleep behaviour disorderJournal Name: eBioMedicinePublisher: Elsevier BVVol: 102Issue #:Start Page: 105065End Page: 105065Publication Date:Open Access(OA) Status: OPENLicense: cc-by-ncDOI - Digital Object Identifier: 10.1016/j.ebiom.2024.105065Best OA location URL: http://www.thelancet.com/article/S2352396424001002/pdfCitation Count: 6
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OPENTitle: Early-stage idiopathic Parkinson’s disease is associated with reduced circular RNA expressionJournal Name: npj Parkinson's DiseasePublisher: Springer Science and Business Media LLCVol: 10Issue #: 1Start Page:End Page:Publication Date:Open Access(OA) Status: OPENLicense: cc-by, cc-byDOI - Digital Object Identifier: 10.1038/s41531-024-00636-yBest OA location URL: https://www.nature.com/articles/s41531-024-00636-y.pdfCitation Count: 12
- DaT-SPECT assessment depicts dopamine depletion among asymptomatic G2019S LRRK2 mutation carriers2017OPENTitle: DaT-SPECT assessment depicts dopamine depletion among asymptomatic G2019S LRRK2 mutation carriersJournal Name: PLOS ONEPublisher: Public Library of Science (PLoS)Vol: 12Issue #: 4Start Page: e0175424End Page: e0175424Publication Date:Open Access(OA) Status: OPENLicense: cc-byDOI - Digital Object Identifier: 10.1371/journal.pone.0175424Best OA location URL: https://journals.plos.org/plosone/article/file?id=10.1371/journal.pone.0175424&type=printableCitation Count: 33
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OPENTitle: Parkinson’s Disease Drug Therapies in the Clinical Trial Pipeline: 2023 UpdateJournal Name: Journal of Parkinson’s DiseasePublisher: SAGE PublicationsVol: 13Issue #: 4Start Page: 427End Page: 439Publication Date:Open Access(OA) Status: OPENLicense: cc-by-ncDOI - Digital Object Identifier: 10.3233/jpd-239901Best OA location URL: https://content.iospress.com:443/download/journal-of-parkinsons-disease/jpd239901?id=journal-of-parkinsons-disease%2Fjpd239901Citation Count: 62
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OPENTitle: Investigation of the genetic aetiology of Lewy body diseases with and without dementiaJournal Name: Brain CommunicationsPublisher: Oxford University Press (OUP)Vol: 6Issue #: 4Start Page:End Page:Publication Date:Open Access(OA) Status: OPENLicense: cc-by, cc-by, cc-byDOI - Digital Object Identifier: 10.1093/braincomms/fcae190Best OA location URL: https://academic.oup.com/braincomms/advance-article-pdf/doi/10.1093/braincomms/fcae190/58033276/fcae190.pdfCitation Count: 3
- Leveraging sex-genetic interactions to understand brain disorders: recent advances and current gaps2024OPENTitle: Leveraging sex-genetic interactions to understand brain disorders: recent advances and current gapsJournal Name: Brain CommunicationsPublisher: Oxford University Press (OUP)Vol: 6Issue #: 3Start Page:End Page:Publication Date:Open Access(OA) Status: OPENLicense: cc-by, cc-byDOI - Digital Object Identifier: 10.1093/braincomms/fcae192Best OA location URL: https://doi.org/10.1093/braincomms/fcae192Citation Count: 0
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OPENTitle: Inhaling xenon ameliorates l‐dopa‐induced dyskinesia in experimental parkinsonismJournal Name: Movement DisordersPublisher: WileyVol: 33Issue #: 10Start Page: 1632End Page: 1642Publication Date:Open Access(OA) Status: OPENLicense: cc-by-nc-ndDOI - Digital Object Identifier: 10.1002/mds.27404Best OA location URL: https://onlinelibrary.wiley.com/doi/pdfdirect/10.1002/mds.27404Citation Count: 15
- SNCAandmTORPathway Single Nucleotide Polymorphisms Interact to Modulate the Age at Onset of Parkinson's Disease2019OPENTitle: SNCAandmTORPathway Single Nucleotide Polymorphisms Interact to Modulate the Age at Onset of Parkinson's DiseaseJournal Name: Movement DisordersPublisher: WileyVol: 34Issue #: 9Start Page: 1333End Page: 1344Publication Date:Open Access(OA) Status: OPENLicense:DOI - Digital Object Identifier: 10.1002/mds.27770Best OA location URL: http://hdl.handle.net/10668/14165Citation Count: 24
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OPENTitle: hipFG: high-throughput harmonization and integration pipeline for functional genomics dataJournal Name: BioinformaticsPublisher: Oxford University Press (OUP)Vol: 39Issue #: 11Start Page:End Page:Publication Date:Open Access(OA) Status: OPENLicense: cc-byDOI - Digital Object Identifier: 10.1093/bioinformatics/btad673Best OA location URL: https://academic.oup.com/bioinformatics/advance-article-pdf/doi/10.1093/bioinformatics/btad673/53050063/btad673.pdfCitation Count: 2
- Human LRRK2 G2019S mutation represses post-synaptic protein PSD95 and causes cognitive impairment in transgenic mice2017OPENTitle: Human LRRK2 G2019S mutation represses post-synaptic protein PSD95 and causes cognitive impairment in transgenic miceJournal Name: Neurobiology of Learning and MemoryPublisher: Elsevier BVVol: 142Issue #:Start Page: 182End Page: 189Publication Date:Open Access(OA) Status: OPENLicense:DOI - Digital Object Identifier: 10.1016/j.nlm.2017.05.001Citation Count: 13
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OPENTitle: Neurogenesis in Cancun: where science meets the seaJournal Name: DevelopmentPublisher: The Company of BiologistsVol: 143Issue #: 10Start Page: 1649End Page: 1654Publication Date:Open Access(OA) Status: OPENLicense:DOI - Digital Object Identifier: 10.1242/dev.138412Best OA location URL: https://journals.biologists.com/dev/article-pdf/143/10/1649/1842172/dev138412.pdfCitation Count: 0
- Rational design of structure‐based vaccines targeting misfolded alpha‐synuclein conformers of Parkinson's disease and related disorders2024OPENTitle: Rational design of structure‐based vaccines targeting misfolded alpha‐synuclein conformers of Parkinson's disease and related disordersJournal Name: Bioengineering & Translational MedicinePublisher: WileyVol: 9Issue #: 4Start Page:End Page:Publication Date:Open Access(OA) Status: OPENLicense: cc-byDOI - Digital Object Identifier: 10.1002/btm2.10665Best OA location URL: https://doi.org/10.1002/btm2.10665Citation Count: 0
- Movement disorders rounds: A case of missing pathology in a patient with LRRK2 Parkinson's disease2019OPENTitle: Movement disorders rounds: A case of missing pathology in a patient with LRRK2 Parkinson's diseaseJournal Name: Parkinsonism & Related DisordersPublisher: Elsevier BVVol: 74Issue #:Start Page: 76End Page: 77Publication Date:Open Access(OA) Status: OPENLicense:DOI - Digital Object Identifier: 10.1016/j.parkreldis.2019.11.006Best OA location URL: https://www.ncbi.nlm.nih.gov/pmc/articles/7374981Citation Count: 14
- Characterization of intracellular elevation of glutathione (GSH) with glutathione monoethyl ester and GSH in brain and neuronal cultures: Relevance to Parkinson's disease2006OPENTitle: Characterization of intracellular elevation of glutathione (GSH) with glutathione monoethyl ester and GSH in brain and neuronal cultures: Relevance to Parkinson's diseaseJournal Name: Experimental NeurologyPublisher: Elsevier BVVol: 203Issue #: 2Start Page: 512End Page: 520Publication Date:Open Access(OA) Status: OPENLicense:DOI - Digital Object Identifier: 10.1016/j.expneurol.2006.09.004Best OA location URL: http://doi.org/10.1016/j.expneurol.2006.09.004Citation Count: 97
- Proteome wide association studies of LRRK2 variants identify novel causal and druggable proteins for Parkinson’s disease2023OPENTitle: Proteome wide association studies of LRRK2 variants identify novel causal and druggable proteins for Parkinson’s diseaseJournal Name: npj Parkinson's DiseasePublisher: Springer Science and Business Media LLCVol: 9Issue #: 1Start Page:End Page:Publication Date:Open Access(OA) Status: OPENLicense: cc-byDOI - Digital Object Identifier: 10.1038/s41531-023-00555-4Best OA location URL: https://www.nature.com/articles/s41531-023-00555-4.pdfCitation Count: 16
- DNA methylome study of human cerebellar tissues identified genes and pathways possibly involved in essential tremor2019OPENTitle: DNA methylome study of human cerebellar tissues identified genes and pathways possibly involved in essential tremorJournal Name: Precision Clinical MedicinePublisher: Oxford University Press (OUP)Vol: 2Issue #: 4Start Page: 221End Page: 234Publication Date:Open Access(OA) Status: OPENLicense: cc-by-ncDOI - Digital Object Identifier: 10.1093/pcmedi/pbz028Citation Count: 5
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OPENTitle: The vermiform appendix impacts the risk of developing Parkinson’s diseaseJournal Name: Science Translational MedicinePublisher: American Association for the Advancement of Science (AAAS)Vol: 10Issue #: 465Start Page:End Page:Publication Date:Open Access(OA) Status: OPENLicense:DOI - Digital Object Identifier: 10.1126/scitranslmed.aar5280Best OA location URL: https://hal.science/hal-04247698Citation Count: 249
- Pathogenetic Contributions and Therapeutic Implications of Transglutaminase 2 in Neurodegenerative Diseases2024OPENTitle: Pathogenetic Contributions and Therapeutic Implications of Transglutaminase 2 in Neurodegenerative DiseasesJournal Name: International Journal of Molecular SciencesPublisher: MDPI AGVol: 25Issue #: 4Start Page: 2364End Page: 2364Publication Date:Open Access(OA) Status: OPENLicense: cc-byDOI - Digital Object Identifier: 10.3390/ijms25042364Best OA location URL: https://www.mdpi.com/1422-0067/25/4/2364/pdf?version=1708157539Citation Count: 3
- Multiscale Analysis of Independent Alzheimer’s Cohorts Finds Disruption of Molecular, Genetic, and Clinical Networks by Human Herpesvirus2018OPENTitle: Multiscale Analysis of Independent Alzheimer’s Cohorts Finds Disruption of Molecular, Genetic, and Clinical Networks by Human HerpesvirusJournal Name: NeuronPublisher: Elsevier BVVol: 99Issue #: 1Start Page: 64End Page: 82.e7Publication Date:Open Access(OA) Status: OPENLicense:DOI - Digital Object Identifier: 10.1016/j.neuron.2018.05.023Best OA location URL: http://www.cell.com/article/S0896627318304215/pdfCitation Count: 645
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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: 381
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OPENTitle: Systematic Functional Analysis of PINK1 and PRKN Coding VariantsJournal Name: CellsPublisher: MDPI AGVol: 11Issue #: 15Start Page: 2426End Page: 2426Publication Date:Open Access(OA) Status: OPENLicense: cc-byDOI - Digital Object Identifier: 10.3390/cells11152426Best OA location URL: https://www.mdpi.com/2073-4409/11/15/2426/pdf?version=1659696395Citation Count: 18