3771 - 3780 of 8808 Results
Title
Year
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OPENTitle: CYP1B1-RMDN2 Alzheimer’s disease endophenotype locus identified for cerebral tau PETJournal Name: Nature CommunicationsPublisher: Springer Science and Business Media LLCVol: 15Issue #: 1Start Page:End Page:Publication Date:Open Access(OA) Status: OPENLicense: cc-by, cc-byDOI - Digital Object Identifier: 10.1038/s41467-024-52298-2Best OA location URL: https://doi.org/10.1038/s41467-024-52298-2Citation Count: 4
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OPENTitle: Carlos II of Spain, ‘The Bewitched’: cursed by aspartylglucosaminuria?Journal Name: BMJ Neurology OpenPublisher: BMJVol: 3Issue #: 2Start Page: e000072End Page: e000072Publication Date:Open Access(OA) Status: OPENLicense: cc-by-ncDOI - Digital Object Identifier: 10.1136/bmjno-2020-000072Best OA location URL: https://neurologyopen.bmj.com/content/bmjno/3/2/e000072.full.pdfCitation Count: 1
- Spatial single-cell isotope tracing reveals heterogeneity of de novo fatty acid synthesis in cancer2024OPENTitle: Spatial single-cell isotope tracing reveals heterogeneity of de novo fatty acid synthesis in cancerJournal Name: Nature MetabolismPublisher: Springer Science and Business Media LLCVol: 6Issue #: 9Start Page: 1695End Page: 1711Publication Date:Open Access(OA) Status: OPENLicense: cc-byDOI - Digital Object Identifier: 10.1038/s42255-024-01118-4Best OA location URL: https://doi.org/10.1038/s42255-024-01118-4Citation Count: 17
- Gene-Specific Effects on Brain Volume and Cognition of TMEM106B in Frontotemporal Lobar Degeneration2024RESTRICTEDTitle: Gene-Specific Effects on Brain Volume and Cognition of TMEM106B in Frontotemporal Lobar DegenerationJournal Name: NeurologyPublisher: Ovid Technologies (Wolters Kluwer Health)Vol: 103Issue #: 8Start Page:End Page:Publication Date:Open Access(OA) Status: RESTRICTEDLicense:DOI - Digital Object Identifier: 10.1212/wnl.0000000000209832Best OA location URL: https://escholarship.org/uc/item/7hv590fnCitation Count: 3
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OPENTitle: Inhibition of striatal dopamine release by the L‐type calcium channel inhibitor isradipine co‐varies with risk factors for Parkinson'sJournal Name: European Journal of NeurosciencePublisher: WileyVol: 59Issue #: 6Start Page: 1242End Page: 1259Publication Date:Open Access(OA) Status: OPENLicense: cc-by, cc-by, cc-byDOI - Digital Object Identifier: 10.1111/ejn.16180Best OA location URL: https://onlinelibrary.wiley.com/doi/pdfdirect/10.1111/ejn.16180Citation Count: 5
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OPENTitle: APOE contributes to longitudinal impulse control disorders progression in Parkinson’s diseaseJournal Name: BMC PsychiatryPublisher: Springer Science and Business Media LLCVol: 24Issue #: 1Start Page:End Page:Publication Date:Open Access(OA) Status: OPENLicense: cc-by-nc-ndDOI - Digital Object Identifier: 10.1186/s12888-024-06084-5Best OA location URL: https://link.springer.com/content/pdf/10.1186/s12888-024-06084-5.pdfCitation Count: 0
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OPENTitle: Surface‐Based Morphometry Analysis of the Cerebral Cortex in Patients With Probable Idiopathic Rapid Eye Movement Sleep Behavior DisorderJournal Name: Brain and BehaviorPublisher: WileyVol: 14Issue #: 10Start Page:End Page:Publication Date:Open Access(OA) Status: OPENLicense: cc-byDOI - Digital Object Identifier: 10.1002/brb3.70057Best OA location URL: https://doi.org/10.1002/brb3.70057Citation Count: 1
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OPENTitle: An interpretable deep learning framework identifies proteomic drivers of Alzheimer’s diseaseJournal Name: Frontiers in Cell and Developmental BiologyPublisher: Frontiers Media SAVol: 12Issue #:Start Page:End Page:Publication Date:Open Access(OA) Status: OPENLicense: cc-byDOI - Digital Object Identifier: 10.3389/fcell.2024.1379984Best OA location URL: https://doi.org/10.3389/fcell.2024.1379984Citation Count: 5
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OPENTitle: Identification of Novel Single-Nucleotide Variants With Potential of Mediating Malfunction of MicroRNA in Congenital Heart DiseaseJournal Name: Frontiers in Cardiovascular MedicinePublisher: Frontiers Media SAVol: 8Issue #:Start Page:End Page:Publication Date:Open Access(OA) Status: OPENLicense: cc-byDOI - Digital Object Identifier: 10.3389/fcvm.2021.739598Best OA location URL: https://doi.org/10.3389/fcvm.2021.739598Citation Count: 3
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OPENTitle: Rare variants in the endocytic pathway are associated with Alzheimer’s disease, its related phenotypes, and functional consequencesJournal Name: PLOS GeneticsPublisher: Public Library of Science (PLoS)Vol: 17Issue #: 9Start Page: e1009772End Page: e1009772Publication Date:Open Access(OA) Status: OPENLicense: cc-byDOI - Digital Object Identifier: 10.1371/journal.pgen.1009772Best OA location URL: https://journals.plos.org/plosgenetics/article/file?id=10.1371/journal.pgen.1009772&type=printableCitation Count: 6