6721 - 6730 of 8785 Results
Title
Year
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OPENTitle: Intracellular delivery of Parkin-RING0-based fragments corrects Parkin-induced mitochondrial dysfunction through interaction with SLP-2Journal Name: Journal of Translational MedicinePublisher: Springer Science and Business Media LLCVol: 22Issue #: 1Start Page:End Page:Publication Date:Open Access(OA) Status: OPENLicense: cc-byDOI - Digital Object Identifier: 10.1186/s12967-024-04850-3Best OA location URL: https://bia.unibz.it/esploro/outputs/journalArticle/Intracellular-delivery-of-Parkin-RING0-based-fragments-corrects/991006696798601241Citation Count: 2
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OPENTitle: Loss of α-Synuclein Does Not Affect Mitochondrial Bioenergetics in Rodent NeuronsJournal Name: eneuroPublisher: Society for NeuroscienceVol: 4Issue #: 2Start Page: ENEURO.0216End Page: 16.2017Publication Date:Open Access(OA) Status: OPENLicense: cc-byDOI - Digital Object Identifier: 10.1523/eneuro.0216-16.2017Best OA location URL: https://escholarship.org/uc/item/87h1c8dbCitation Count: 15
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OPENTitle: Phenotypic Reprogramming of Striatal Neurons into Dopaminergic Neuron-like Cells in the Adult Mouse BrainJournal Name: Stem Cell ReportsPublisher: Elsevier BVVol: 11Issue #: 5Start Page: 1156End Page: 1170Publication Date:Open Access(OA) Status: OPENLicense: cc-by-nc-ndDOI - Digital Object Identifier: 10.1016/j.stemcr.2018.09.004Best OA location URL: http://www.cell.com/article/S2213671118303898/pdfCitation Count: 43
- Smell status in functional movement disorders: New clues for diagnosis and underlying mechanisms2019RESTRICTEDTitle: Smell status in functional movement disorders: New clues for diagnosis and underlying mechanismsJournal Name: Clinical Neurology and NeurosurgeryPublisher: Elsevier BVVol: 177Issue #:Start Page: 68End Page: 72Publication Date:Open Access(OA) Status: RESTRICTEDLicense:DOI - Digital Object Identifier: 10.1016/j.clineuro.2018.12.017Best OA location URL: https://repositorio.udes.edu.co/handle/001/3108Citation Count: 4
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OPENTitle: LRRK2 Kinase Inhibition Rescues Deficits in Lysosome Function Due to Heterozygous GBA1 Expression in Human iPSC-Derived NeuronsJournal Name: Frontiers in NeurosciencePublisher: Frontiers Media SAVol: 14Issue #:Start Page:End Page:Publication Date:Open Access(OA) Status: OPENLicense: cc-byDOI - Digital Object Identifier: 10.3389/fnins.2020.00442Best OA location URL: https://www.frontiersin.org/articles/10.3389/fnins.2020.00442/pdfCitation Count: 44
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OPENTitle: Protein Phosphatase 2A and Its Methylation Modulating Enzymes LCMT-1 and PME-1 Are Dysregulated in Tauopathies of Progressive Supranuclear Palsy and Alzheimer DiseaseJournal Name: Journal of Neuropathology & Experimental NeurologyPublisher: Oxford University Press (OUP)Vol: 77Issue #: 2Start Page: 139End Page: 148Publication Date:Open Access(OA) Status: OPENLicense:DOI - Digital Object Identifier: 10.1093/jnen/nlx110Best OA location URL: https://academic.oup.com/jnen/article-pdf/77/2/139/23373432/nlx110.pdfCitation Count: 47
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OPENTitle: Comparison of two protocols for the generation of iPSC-derived human astrocytesJournal Name: Biological Procedures OnlinePublisher: Springer Science and Business Media LLCVol: 25Issue #: 1Start Page:End Page:Publication Date:Open Access(OA) Status: OPENLicense: cc-byDOI - Digital Object Identifier: 10.1186/s12575-023-00218-xBest OA location URL: https://biologicalproceduresonline.biomedcentral.com/counter/pdf/10.1186/s12575-023-00218-xCitation Count: 6
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RESTRICTEDTitle: Carrying on a Father's LegacyJournal Name: Brain & LifePublisher: Ovid Technologies (Wolters Kluwer Health)Vol: 21Issue #: 4Start Page: 40End Page: 40Publication Date:Open Access(OA) Status: RESTRICTEDLicense:DOI - Digital Object Identifier: 10.1097/01.nnn.0001125860.72537.e7Citation Count: 0
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RESTRICTEDTitle: P1‐021: Diurnal and intersubject variability of cerebrospinal fluid biomarkers, Aβ‐40/42, alpha‐synuclein and DJ‐1 in healthy volunteersJournal Name: Alzheimer's & DementiaPublisher: WileyVol: 8Issue #: 4S_Part_3Start Page:End Page:Publication Date:Open Access(OA) Status: RESTRICTEDLicense:DOI - Digital Object Identifier: 10.1016/j.jalz.2012.05.296Citation Count: 0
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OPENTitle: The ZFHX3 GGC Repeat Expansion Underlying Spinocerebellar Ataxia Type 4 has a Common Ancestral FounderJournal Name: Movement DisordersPublisher: WileyVol: 40Issue #: 2Start Page:End Page:Publication Date:Open Access(OA) Status: OPENLicense: cc-by, cc-by, cc-byDOI - Digital Object Identifier: 10.1002/mds.30077Best OA location URL: https://doi.org/10.1002/mds.30077Citation Count: 1