1051 - 1060 of 6230 Results
Title
Year
- Mitochondrial damage triggers the concerted degradation of negative regulators of neuronal autophagy2025OPENTitle: Mitochondrial damage triggers the concerted degradation of negative regulators of neuronal autophagyJournal Name: Nature CommunicationsPublisher: Springer Science and Business Media LLCVol: 16Issue #: 1Start Page:End Page:Publication Date:Open Access(OA) Status: OPENLicense: cc-byDOI - Digital Object Identifier: 10.1038/s41467-025-62379-5Best OA location URL: https://www.nature.com/articles/s41467-025-62379-5.pdfCitation Count: 0
- Genetic Diversity and Expanded Phenotypes in Dystonia: Insights From Large‐Scale Exome Sequencing2025OPENTitle: Genetic Diversity and Expanded Phenotypes in Dystonia: Insights From Large‐Scale Exome SequencingJournal Name: Annals of Clinical and Translational NeurologyPublisher: WileyVol: 12Issue #: 8Start Page: 1648End Page: 1659Publication Date:Open Access(OA) Status: OPENLicense: cc-byDOI - Digital Object Identifier: 10.1002/acn3.70100Best OA location URL: https://onlinelibrary.wiley.com/doi/pdfdirect/10.1002/acn3.70100Citation Count: 0
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OPENTitle: Criminal Behavior in Frontotemporal Dementia: A Multimodal MRI StudyJournal Name: Human Brain MappingPublisher: WileyVol: 46Issue #: 11Start Page:End Page:Publication Date:Open Access(OA) Status: OPENLicense: cc-by-nc-ndDOI - Digital Object Identifier: 10.1002/hbm.70308Best OA location URL: https://onlinelibrary.wiley.com/doi/pdf/10.1002/hbm.70308Citation Count: 0
- Levodopa Responsive Dystonia Parkinsonism, Intellectual Disability, and Optic Atrophy Due to a Heterozygous Missense Variant in AFG3L22022OPENTitle: Levodopa Responsive Dystonia Parkinsonism, Intellectual Disability, and Optic Atrophy Due to a Heterozygous Missense Variant in AFG3L2Journal Name: Movement Disorders Clinical PracticePublisher: WileyVol: 9Issue #: S2Start Page:End Page:Publication Date:Open Access(OA) Status: OPENLicense: cc-by-nc-ndDOI - Digital Object Identifier: 10.1002/mdc3.13538Best OA location URL: https://onlinelibrary.wiley.com/doi/pdfdirect/10.1002/mdc3.13538Citation Count: 3
- Loss of the lysosomal lipid flippase ATP10B leads to progressive dopaminergic neurodegeneration and parkinsonian motor deficits2025OPENTitle: Loss of the lysosomal lipid flippase ATP10B leads to progressive dopaminergic neurodegeneration and parkinsonian motor deficitsJournal Name: Acta NeuropathologicaPublisher: Springer Science and Business Media LLCVol: 150Issue #: 1Start Page:End Page:Publication Date:Open Access(OA) Status: OPENLicense:DOI - Digital Object Identifier: 10.1007/s00401-025-02908-0Best OA location URL: https://link.springer.com/content/pdf/10.1007/s00401-025-02908-0.pdfCitation Count: 0
- Reply to: “Overlapping Ranges in Levels Indicate That Hexosylsphingosine Is Not a Clinically Relevant Biomarker for GBA1‐Associated Parkinson's Disease”2022OPENTitle: Reply to: “Overlapping Ranges in Levels Indicate That Hexosylsphingosine Is Not a Clinically Relevant Biomarker for GBA1‐Associated Parkinson's Disease”Journal Name: Movement DisordersPublisher: WileyVol: 37Issue #: 8Start Page: 1781End Page: 1782Publication Date:Open Access(OA) Status: OPENLicense:DOI - Digital Object Identifier: 10.1002/mds.29131Best OA location URL: https://www.ncbi.nlm.nih.gov/pmc/articles/9756875Citation Count: 0
- No Evidence That Glucosylsphingosine Is a Biomarker for Parkinson's Disease: Statistical Differences Do Not Necessarily Indicate Biological Significance2022OPENTitle: No Evidence That Glucosylsphingosine Is a Biomarker for Parkinson's Disease: Statistical Differences Do Not Necessarily Indicate Biological SignificanceJournal Name: Movement DisordersPublisher: WileyVol: 37Issue #: 3Start Page: 653End Page: 653Publication Date:Open Access(OA) Status: OPENLicense:DOI - Digital Object Identifier: 10.1002/mds.28935Best OA location URL: https://www.ncbi.nlm.nih.gov/pmc/articles/8940713Citation Count: 5
- The Roc domain of LRRK2 as a hub for protein-protein interactions: a focus on PAK6 and its impact on RAB phosphorylation2022OPENTitle: The Roc domain of LRRK2 as a hub for protein-protein interactions: a focus on PAK6 and its impact on RAB phosphorylationJournal Name: Brain ResearchPublisher: Elsevier BVVol: 1778Issue #:Start Page: 147781End Page: 147781Publication Date:Open Access(OA) Status: OPENLicense:DOI - Digital Object Identifier: 10.1016/j.brainres.2022.147781Best OA location URL: https://ars.els-cdn.com/content/image/1-s2.0-S0006899322000051-ga1_lrg.jpgCitation Count: 21
- Tackling a disease on a global scale, the Global Parkinson’s Genetics Program, GP2: A new generation of opportunities2025OPENTitle: Tackling a disease on a global scale, the Global Parkinson’s Genetics Program, GP2: A new generation of opportunitiesJournal Name: The American Journal of Human GeneticsPublisher: Elsevier BVVol:Issue #:Start Page:End Page:Publication Date:Open Access(OA) Status: OPENLicense:DOI - Digital Object Identifier: 10.1016/j.ajhg.2025.07.014Best OA location URL: https://www.cell.com/ajhg/pdf/S0002-9297(25)00284-8.pdfCitation Count: 0
- Abstract 1201 Bridge-like lipid transfer protein 3A (BLTP3A) is associated with membranes of the late endocytic pathway and is an effector of CASM2025OPENTitle: Abstract 1201 Bridge-like lipid transfer protein 3A (BLTP3A) is associated with membranes of the late endocytic pathway and is an effector of CASMJournal Name: Journal of Biological ChemistryPublisher: Elsevier BVVol: 301Issue #: 5Start Page: 109390End Page: 109390Publication Date:Open Access(OA) Status: OPENLicense:DOI - Digital Object Identifier: 10.1016/j.jbc.2025.109390Best OA location URL: https://www.jbc.org/action/showPdf?pii=S0021925825012396Citation Count: 0