5871 - 5880 of 6295 Results
Title
Year
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OPENTitle: Mitochondrial therapies for Parkinson's diseaseJournal Name: Movement DisordersPublisher: WileyVol: 25Issue #: S1Start Page:End Page:Publication Date:Open Access(OA) Status: OPENLicense:DOI - Digital Object Identifier: 10.1002/mds.22781Best OA location URL: https://www.ncbi.nlm.nih.gov/pmc/articles/5797696Citation Count: 58
- Quantitative detection of α-Synuclein and Tau oligomers and other aggregates by digital single particle counting2022OPENTitle: Quantitative detection of α-Synuclein and Tau oligomers and other aggregates by digital single particle countingJournal Name: npj Parkinson's DiseasePublisher: Springer Science and Business Media LLCVol: 8Issue #: 1Start Page:End Page:Publication Date:Open Access(OA) Status: OPENLicense: cc-byDOI - Digital Object Identifier: 10.1038/s41531-022-00330-xBest OA location URL: https://www.nature.com/articles/s41531-022-00330-x.pdfCitation Count: 31
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OPENTitle: Glucagon‐like Peptides (GLP‐1) Perspectives in Synucleinopathies TreatmentJournal Name: Movement Disorders Clinical PracticePublisher: WileyVol: 5Issue #: 3Start Page: 255End Page: 258Publication Date:Open Access(OA) Status: OPENLicense:DOI - Digital Object Identifier: 10.1002/mdc3.12611Best OA location URL: https://onlinelibrary.wiley.com/doi/pdfdirect/10.1002/mdc3.12611Citation Count: 7
- Generation of two human induced pluripotent stem cell lines from fibroblasts of unrelated Parkinson’s patients carrying the G2019S mutation in the LRRK2 gene (LCSBi005, LCSBi006)2021OPENTitle: Generation of two human induced pluripotent stem cell lines from fibroblasts of unrelated Parkinson’s patients carrying the G2019S mutation in the LRRK2 gene (LCSBi005, LCSBi006)Journal Name: Stem Cell ResearchPublisher: Elsevier BVVol: 57Issue #:Start Page: 102569End Page: 102569Publication Date:Open Access(OA) Status: OPENLicense: cc-by-nc-ndDOI - Digital Object Identifier: 10.1016/j.scr.2021.102569Best OA location URL: https://doi.org/10.1016/j.scr.2021.102569Citation Count: 2
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OPENTitle: LRRK2 inhibition prevents endolysosomal deficits seen in human Parkinson's diseaseJournal Name: Neurobiology of DiseasePublisher: Elsevier BVVol: 134Issue #:Start Page: 104626End Page: 104626Publication Date:Open Access(OA) Status: OPENLicense: cc-by-nc-ndDOI - Digital Object Identifier: 10.1016/j.nbd.2019.104626Best OA location URL: https://doi.org/10.1016/j.nbd.2019.104626Citation Count: 88
- Multiple system atrophy-associated oligodendroglial protein p25α stimulates formation of novel α-synuclein strain with enhanced neurodegenerative potential2021OPENTitle: Multiple system atrophy-associated oligodendroglial protein p25α stimulates formation of novel α-synuclein strain with enhanced neurodegenerative potentialJournal Name: Acta NeuropathologicaPublisher: Springer Science and Business Media LLCVol: 142Issue #: 1Start Page: 87End Page: 115Publication Date:Open Access(OA) Status: OPENLicense: cc-byDOI - Digital Object Identifier: 10.1007/s00401-021-02316-0Best OA location URL: https://link.springer.com/content/pdf/10.1007/s00401-021-02316-0.pdfCitation Count: 71
- MAPT allele and haplotype frequencies in Nigerian Africans: Population distribution and association with Parkinson's disease risk and age at onset2023OPENTitle: MAPT allele and haplotype frequencies in Nigerian Africans: Population distribution and association with Parkinson's disease risk and age at onsetJournal Name: Parkinsonism & Related DisordersPublisher: Elsevier BVVol: 113Issue #:Start Page: 105517End Page: 105517Publication Date:Open Access(OA) Status: OPENLicense:DOI - Digital Object Identifier: 10.1016/j.parkreldis.2023.105517Best OA location URL: https://discovery.ucl.ac.uk/10177992/3/Hardy_MAPT%20allele%20and%20haplotype%20frequencies%20in%20Nigerian%20Africans_AAM.pdfCitation Count: 3
- Alternating Magnetic Field-Promoted Nanoparticle Mixing: The On-Chip Immunocapture of Serum Neuronal Exosomes for Parkinson’s Disease Diagnostics2023OPENTitle: Alternating Magnetic Field-Promoted Nanoparticle Mixing: The On-Chip Immunocapture of Serum Neuronal Exosomes for Parkinson’s Disease DiagnosticsJournal Name: Analytical ChemistryPublisher: American Chemical Society (ACS)Vol: 95Issue #: 20Start Page: 7906End Page: 7913Publication Date:Open Access(OA) Status: OPENLicense: cc-byDOI - Digital Object Identifier: 10.1021/acs.analchem.3c00357Best OA location URL: https://pubs.acs.org/doi/pdf/10.1021/acs.analchem.3c00357Citation Count: 27
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OPENTitle: LRRK2 G2019S mutations are associated with an increased cancer risk in Parkinson diseaseJournal Name: Movement DisordersPublisher: WileyVol: 25Issue #: 15Start Page: 2536End Page: 2541Publication Date:Open Access(OA) Status: OPENLicense:DOI - Digital Object Identifier: 10.1002/mds.23314Best OA location URL: https://www.ncbi.nlm.nih.gov/pmc/articles/2978749Citation Count: 65
- Thermodynamic characterization of amyloid polymorphism by microfluidic transient incomplete separation2024OPENTitle: Thermodynamic characterization of amyloid polymorphism by microfluidic transient incomplete separationJournal Name: Chemical SciencePublisher: Royal Society of Chemistry (RSC)Vol: 15Issue #: 7Start Page: 2528End Page: 2544Publication Date:Open Access(OA) Status: OPENLicense: cc-by-ncDOI - Digital Object Identifier: 10.1039/d3sc05371gBest OA location URL: https://pubs.rsc.org/en/content/articlepdf/2024/sc/d3sc05371gCitation Count: 13