2001 - 2025 of 6514 Results
Title
Year
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OPENTitle: Molecular Mechanisms of Cationic Fusogenic Liposome Interactions with Bacterial EnvelopesJournal Name: Journal of the American Chemical SocietyPublisher: American Chemical Society (ACS)Vol: 145Issue #: 51Start Page: 28240End Page: 28250Publication Date:Open Access(OA) Status: OPENLicense: cc-by, cc-byDOI - Digital Object Identifier: 10.1021/jacs.3c11463Best OA location URL: https://doi.org/10.1021/jacs.3c11463Citation Count: 48
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OPENTitle: Post-mortem ventricular cerebrospinal fluid cell-free-mtDNA in neurodegenerative diseaseJournal Name: Scientific ReportsPublisher: Springer Science and Business Media LLCVol: 10Issue #: 1Start Page: 15253End Page: 15253Publication Date:Open Access(OA) Status: OPENLicense: cc-by, cc-byDOI - Digital Object Identifier: 10.1038/s41598-020-72190-5Best OA location URL: https://www.nature.com/articles/s41598-020-72190-5.pdfCitation Count: 24
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OPENTitle: Neuroprotective and neurodegenerative effects of the chronic expression of tumor necrosis factor α in the nigrostriatal dopaminergic circuit of adult miceJournal Name: Experimental NeurologyPublisher: Elsevier BVVol: 227Issue #: 2Start Page: 237End Page: 251Publication Date:Open Access(OA) Status: OPENLicense:DOI - Digital Object Identifier: 10.1016/j.expneurol.2010.11.010Best OA location URL: https://pure.rug.nl/ws/files/2521820/2011ExpNeurolChertoff.pdfCitation Count: 68
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OPENTitle: Mitophagy bridges glucose metabolism, inflammation and neuroprotection in astrocytesJournal Name: AutophagyPublisher: Informa UK LimitedVol:Issue #:Start Page: 1End Page: 3Publication Date:Open Access(OA) Status: OPENLicense: cc-byDOI - Digital Object Identifier: 10.1080/15548627.2026.2623987Best OA location URL: https://doi.org/10.1080/15548627.2026.2623987Citation Count: 0
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OPENTitle: Resting state activity and connectivity of the nucleus basalis of Meynert and globus pallidus in Lewy body dementia and Parkinson's disease dementiaJournal Name: NeuroImagePublisher: Elsevier BVVol: 221Issue #:Start Page: 117184End Page: 117184Publication Date:Open Access(OA) Status: OPENLicense: cc-by, cc-byDOI - Digital Object Identifier: 10.1016/j.neuroimage.2020.117184Best OA location URL: https://doi.org/10.1016/j.neuroimage.2020.117184Citation Count: 23
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OPENTitle: Fibrillation and molecular characteristics are coherent with clinical and pathological features of 4-repeat tauopathy caused by MAPT variant G273RJournal Name: Neurobiology of DiseasePublisher: Elsevier BVVol: 146Issue #:Start Page: 105079End Page: 105079Publication Date:Open Access(OA) Status: OPENLicense: cc-by, cc-byDOI - Digital Object Identifier: 10.1016/j.nbd.2020.105079Best OA location URL: https://doi.org/10.1016/j.nbd.2020.105079Citation Count: 8
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OPENTitle: ARSA variants in α-synucleinopathiesJournal Name: BrainPublisher: Oxford University Press (OUP)Vol: 142Issue #: 12Start Page: e70End Page: e70Publication Date:Open Access(OA) Status: OPENLicense:DOI - Digital Object Identifier: 10.1093/brain/awz340Best OA location URL: https://academic.oup.com/brain/article-pdf/142/12/e70/31499429/awz340.pdfCitation Count: 20
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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: 25End Page: 25Publication 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: 20
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OPENTitle: CURTAIN—A unique web-based tool for exploration and sharing of MS-based proteomics dataJournal Name: Proceedings of the National Academy of SciencesPublisher: Proceedings of the National Academy of SciencesVol: 121Issue #: 7Start Page: e2312676121End Page: e2312676121Publication Date:Open Access(OA) Status: OPENLicense: cc-by, cc-by, cc-by, cc-byDOI - Digital Object Identifier: 10.1073/pnas.2312676121Best OA location URL: https://www.pnas.org/doi/pdf/10.1073/pnas.2312676121Citation Count: 22
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OPENTitle: Novel VARS1 variants define new clinical and molecular subtypes of a rare neurodevelopmental syndromeJournal Name: Biochimica et Biophysica Acta (BBA) - Molecular Basis of DiseasePublisher: Elsevier BVVol: 1872Issue #: 4Start Page: 168184End Page: 168184Publication Date:Open Access(OA) Status: OPENLicense: cc-byDOI - Digital Object Identifier: 10.1016/j.bbadis.2026.168184Best OA location URL: https://doi.org/10.1016/j.bbadis.2026.168184Citation Count: 0
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OPENTitle: MDGA2 homozygous loss-of-function variants cause developmental and epileptic encephalopathyJournal Name: The American Journal of Human GeneticsPublisher: Elsevier BVVol: 113Issue #: 2Start Page: 380End Page: 391Publication Date:Open Access(OA) Status: OPENLicense: cc-byDOI - Digital Object Identifier: 10.1016/j.ajhg.2025.12.015Best OA location URL: https://doi.org/10.1016/j.ajhg.2025.12.015Citation Count: 0
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OPENTitle: Detecting and monitoring the symptoms of Parkinson's disease using smartphones: A pilot studyJournal Name: Parkinsonism & Related DisordersPublisher: Elsevier BVVol: 21Issue #: 6Start Page: 650End Page: 653Publication Date:Open Access(OA) Status: OPENLicense:DOI - Digital Object Identifier: 10.1016/j.parkreldis.2015.02.026Citation Count: 376
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OPENTitle: Short hydrogen bonds enhance nonaromatic protein-related fluorescenceJournal Name: Proceedings of the National Academy of SciencesPublisher: Proceedings of the National Academy of SciencesVol: 118Issue #: 21Start Page:End Page:Publication Date:Open Access(OA) Status: OPENLicense: cc-by, cc-byDOI - Digital Object Identifier: 10.1073/pnas.2020389118Best OA location URL: https://doi.org/10.1073/pnas.2020389118Citation Count: 51
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OPENTitle: Distinct spatiotemporal atrophy patterns in corticobasal syndrome are associated with different underlying pathologiesJournal Name: Brain CommunicationsPublisher: Oxford University Press (OUP)Vol: 7Issue #: 2Start Page: fcaf066End Page: fcaf066Publication Date:Open Access(OA) Status: OPENLicense: cc-by, cc-byDOI - Digital Object Identifier: 10.1093/braincomms/fcaf066Best OA location URL: https://doi.org/10.1093/braincomms/fcaf066Citation Count: 1
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OPENTitle: Microelectrode Arrays for Simultaneous Electrophysiology and Advanced Optical MicroscopyJournal Name: Advanced SciencePublisher: WileyVol: 8Issue #: 13Start Page: 2004434End Page: 2004434Publication Date:Open Access(OA) Status: OPENLicense: cc-by, cc-byDOI - Digital Object Identifier: 10.1002/advs.202004434Best OA location URL: https://onlinelibrary.wiley.com/doi/pdfdirect/10.1002/advs.202004434Citation Count: 68
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OPENTitle: Impact ofGBA1variants on long-term clinical progression and mortality in incident Parkinson’s diseaseJournal Name: Journal of Neurology, Neurosurgery & PsychiatryPublisher: BMJVol: 91Issue #: 7Start Page: 695End Page: 702Publication Date:Open Access(OA) Status: OPENLicense: cc-by, cc-byDOI - Digital Object Identifier: 10.1136/jnnp-2020-322857Best OA location URL: https://jnnp.bmj.com/content/jnnp/91/7/695.full.pdfCitation Count: 91
- Imaging mass cytometry reveals generalised deficiency in OXPHOS complexes in Parkinson’s disease2021OPENTitle: Imaging mass cytometry reveals generalised deficiency in OXPHOS complexes in Parkinson’s diseaseJournal Name: npj Parkinson's DiseasePublisher: Springer Science and Business Media LLCVol: 7Issue #: 1Start Page: 39End Page: 39Publication Date:Open Access(OA) Status: OPENLicense: cc-by, cc-byDOI - Digital Object Identifier: 10.1038/s41531-021-00182-xBest OA location URL: https://www.nature.com/articles/s41531-021-00182-x.pdfCitation Count: 30
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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: 108
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OPENTitle: Pathogenic Huntingtin Repeat Expansions in Patients with Frontotemporal Dementia and Amyotrophic Lateral SclerosisJournal Name: NeuronPublisher: Elsevier BVVol: 109Issue #: 3Start Page: 448End Page: 460.e4Publication Date:Open Access(OA) Status: OPENLicense:DOI - Digital Object Identifier: 10.1016/j.neuron.2020.11.005Best OA location URL: https://hdl.handle.net/2292/65532Citation Count: 82
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OPENTitle: Dysregulated Wnt and NFAT signaling in a Parkinson’s disease LRRK2 G2019S knock-in modelJournal Name: Scientific ReportsPublisher: Springer Science and Business Media LLCVol: 14Issue #: 1Start Page: 12393End Page: 12393Publication Date:Open Access(OA) Status: OPENLicense: cc-by, cc-by, cc-byDOI - Digital Object Identifier: 10.1038/s41598-024-63130-8Best OA location URL: https://www.nature.com/articles/s41598-024-63130-8.pdfCitation Count: 15
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OPENTitle: Autosomal recessive VWA1-related disorder: comprehensive analysis of phenotypic variability and genetic mutationsJournal Name: Brain CommunicationsPublisher: Oxford University Press (OUP)Vol: 6Issue #: 6Start Page: fcae377End Page: fcae377Publication Date:Open Access(OA) Status: OPENLicense: cc-by, cc-by, cc-byDOI - Digital Object Identifier: 10.1093/braincomms/fcae377Best OA location URL: https://doi.org/10.1093/braincomms/fcae377Citation Count: 6
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OPENTitle: Parkinson’s disease neurons exhibit alterations in mitochondrial quality control proteinsJournal Name: npj Parkinson's DiseasePublisher: Springer Science and Business Media LLCVol: 9Issue #: 1Start Page: 120End Page: 120Publication Date:Open Access(OA) Status: OPENLicense: cc-by, cc-byDOI - Digital Object Identifier: 10.1038/s41531-023-00564-3Best OA location URL: https://www.nature.com/articles/s41531-023-00564-3.pdfCitation Count: 43
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OPENTitle: Alzheimer's Disease Sequencing Project release 4 whole genome sequencing datasetJournal Name: Alzheimer's & DementiaPublisher: WileyVol: 21Issue #: 5Start Page: e70237End Page: e70237Publication Date:Open Access(OA) Status: OPENLicense: cc-by-nc, cc-by-ncDOI - Digital Object Identifier: 10.1002/alz.70237Best OA location URL: https://onlinelibrary.wiley.com/doi/pdfdirect/10.1002/alz.70237Citation Count: 14
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OPENTitle: ELFN1 deficiency: The mechanistic basis and phenotypic spectrum of a neurodevelopmental disorder with epilepsyJournal Name: Genetics in MedicinePublisher: Elsevier BVVol: 27Issue #: 9Start Page: 101506End Page: 101506Publication Date:Open Access(OA) Status: OPENLicense: cc-by, cc-byDOI - Digital Object Identifier: 10.1016/j.gim.2025.101506Best OA location URL: https://doi.org/10.1016/j.gim.2025.101506Citation Count: 2
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OPENTitle: Optical Structural Analysis of Individual α‐Synuclein OligomersJournal Name: Angewandte ChemiePublisher: WileyVol: 130Issue #: 18Start Page: 4980End Page: 4984Publication Date:Open Access(OA) Status: OPENLicense: cc-by, cc-byDOI - Digital Object Identifier: 10.1002/ange.201710779Best OA location URL: https://doi.org/10.1002/ange.201710779Citation Count: 0