5651 - 5660 of 8715 Results
Title
Year
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OPENTitle: Modeling of mitochondrial genetic polymorphisms reveals induction of heteroplasmy by pleiotropic disease locus 10398A>GJournal Name: Scientific ReportsPublisher: Springer Science and Business Media LLCVol: 13Issue #: 1Start Page:End Page:Publication Date:Open Access(OA) Status: OPENLicense: cc-byDOI - Digital Object Identifier: 10.1038/s41598-023-37541-yBest OA location URL: https://www.nature.com/articles/s41598-023-37541-y.pdfCitation Count: 2
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OPENTitle: Machine learning-based prediction of longitudinal cognitive decline in early Parkinson’s disease using multimodal featuresJournal Name: Scientific ReportsPublisher: Springer Science and Business Media LLCVol: 13Issue #: 1Start Page:End Page:Publication Date:Open Access(OA) Status: OPENLicense: cc-byDOI - Digital Object Identifier: 10.1038/s41598-023-37644-6Best OA location URL: https://www.nature.com/articles/s41598-023-37644-6.pdfCitation Count: 28
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OPENTitle: Reference LINE-1 insertion polymorphisms correlate with Parkinson’s disease progression and differential transcript expression in the PPMI cohortJournal Name: Scientific ReportsPublisher: Springer Science and Business Media LLCVol: 13Issue #: 1Start Page:End Page:Publication Date:Open Access(OA) Status: OPENLicense: cc-byDOI - Digital Object Identifier: 10.1038/s41598-023-41052-1Best OA location URL: https://www.nature.com/articles/s41598-023-41052-1.pdfCitation Count: 6
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OPENTitle: Transcriptomic signatures of brain regional vulnerability to Parkinson’s diseaseJournal Name: Communications BiologyPublisher: Springer Science and Business Media LLCVol: 3Issue #: 1Start Page:End Page:Publication Date:Open Access(OA) Status: OPENLicense: cc-byDOI - Digital Object Identifier: 10.1038/s42003-020-0804-9Best OA location URL: https://www.nature.com/articles/s42003-020-0804-9.pdfCitation Count: 72
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OPENTitle: Beyond ATP, new roles of mitochondriaJournal Name: The BiochemistPublisher: Portland Press Ltd.Vol: 44Issue #: 4Start Page: 2End Page: 8Publication Date:Open Access(OA) Status: OPENLicense: cc-by-nc-ndDOI - Digital Object Identifier: 10.1042/bio_2022_119Best OA location URL: https://portlandpress.com/biochemist/article-pdf/44/4/2/937405/bio_2022_119.pdfCitation Count: 65
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OPENTitle: Golgi-IP, a tool for multimodal analysis of Golgi molecular contentJournal Name: Proceedings of the National Academy of SciencesPublisher: Proceedings of the National Academy of SciencesVol: 120Issue #: 20Start Page:End Page:Publication Date:Open Access(OA) Status: OPENLicense: cc-by, cc-byDOI - Digital Object Identifier: 10.1073/pnas.2219953120Best OA location URL: https://doi.org/10.1073/pnas.2219953120Citation Count: 43
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OPENTitle: In vivoreduction of age-dependent neuromelanin accumulation mitigates features of Parkinson’s diseaseJournal Name: BrainPublisher: Oxford University Press (OUP)Vol: 146Issue #: 3Start Page: 1040End Page: 1052Publication Date:Open Access(OA) Status: OPENLicense: cc-by-nc, cc-by-ncDOI - Digital Object Identifier: 10.1093/brain/awac445Best OA location URL: https://academic.oup.com/brain/article-pdf/146/3/1040/49356347/awac445.pdfCitation Count: 24
- Mitochondrial function-associated genes underlie cortical atrophy in prodromal synucleinopathies2023OPENTitle: Mitochondrial function-associated genes underlie cortical atrophy in prodromal synucleinopathiesJournal Name: BrainPublisher: Oxford University Press (OUP)Vol: 146Issue #: 8Start Page: 3301End Page: 3318Publication Date:Open Access(OA) Status: OPENLicense: cc-by-ncDOI - Digital Object Identifier: 10.1093/brain/awad044Best OA location URL: https://academic.oup.com/brain/advance-article-pdf/doi/10.1093/brain/awad044/49329244/awad044.pdfCitation Count: 22
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OPENTitle: The non-specific lethal complex regulates genes and pathways genetically linked to Parkinson’s diseaseJournal Name: BrainPublisher: Oxford University Press (OUP)Vol: 146Issue #: 12Start Page: 4974End Page: 4987Publication Date:Open Access(OA) Status: OPENLicense: cc-by-nc, cc-by-ncDOI - Digital Object Identifier: 10.1093/brain/awad246Best OA location URL: https://academic.oup.com/brain/advance-article-pdf/doi/10.1093/brain/awad246/51010946/awad246.pdfCitation Count: 5
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OPENTitle: MAPT H2 haplotype and risk of Pick's disease in the Pick's disease International Consortium: a genetic association studyJournal Name: The Lancet NeurologyPublisher: Elsevier BVVol: 23Issue #: 5Start Page: 487End Page: 499Publication Date:Open Access(OA) Status: OPENLicense: cc-by, cc-by, cc-byDOI - Digital Object Identifier: 10.1016/s1474-4422(24)00083-8Best OA location URL: https://pub.dzne.de/record/269189Citation Count: 15