3521 - 3530 of 6515 Results
Title
Year
- Lack of interleukin-13 receptor α1 delays the loss of dopaminergic neurons during chronic stress2017OPENTitle: Lack of interleukin-13 receptor α1 delays the loss of dopaminergic neurons during chronic stressJournal Name: Journal of NeuroinflammationPublisher: Springer Science and Business Media LLCVol: 14Issue #: 1Start Page: 88End Page: 88Publication Date:Open Access(OA) Status: OPENLicense: cc-byDOI - Digital Object Identifier: 10.1186/s12974-017-0862-1Best OA location URL: https://jneuroinflammation.biomedcentral.com/track/pdf/10.1186/s12974-017-0862-1Citation Count: 43
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OPENTitle: Analysis of number needed to treat for droxidopa in patients with symptomatic neurogenic orthostatic hypotensionJournal Name: BMC NeurologyPublisher: Springer Science and Business Media LLCVol: 16Issue #: 1Start Page: 143End Page: 143Publication Date:Open Access(OA) Status: OPENLicense: cc-byDOI - Digital Object Identifier: 10.1186/s12883-016-0665-5Best OA location URL: https://bmcneurol.biomedcentral.com/track/pdf/10.1186/s12883-016-0665-5Citation Count: 4
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OPENTitle: Association of red cell distribution width with all-cause and cardiovascular-specific mortality in African American and white adults: a prospective cohort studyJournal Name: Journal of Translational MedicinePublisher: Springer Science and Business Media LLCVol: 15Issue #: 1Start Page: 208End Page: 208Publication Date:Open Access(OA) Status: OPENLicense: cc-byDOI - Digital Object Identifier: 10.1186/s12967-017-1313-6Best OA location URL: https://translational-medicine.biomedcentral.com/track/pdf/10.1186/s12967-017-1313-6Citation Count: 30
- Parkinson disease-associated mutations in LRRK2 cause centrosomal defects via Rab8a phosphorylation2018OPENTitle: Parkinson disease-associated mutations in LRRK2 cause centrosomal defects via Rab8a phosphorylationJournal Name: Molecular NeurodegenerationPublisher: Springer Science and Business Media LLCVol: 13Issue #: 1Start Page: 3End Page: 3Publication Date:Open Access(OA) Status: OPENLicense: cc-byDOI - Digital Object Identifier: 10.1186/s13024-018-0235-yBest OA location URL: https://molecularneurodegeneration.biomedcentral.com/track/pdf/10.1186/s13024-018-0235-yCitation Count: 109
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OPENTitle: Slower saccadic reading in Parkinson’s diseaseJournal Name: PLOS ONEPublisher: Public Library of Science (PLoS)Vol: 13Issue #: 1Start Page: e0191005End Page: e0191005Publication Date:Open Access(OA) Status: OPENLicense: cc-byDOI - Digital Object Identifier: 10.1371/journal.pone.0191005Best OA location URL: https://journals.plos.org/plosone/article/file?id=10.1371/journal.pone.0191005&type=printableCitation Count: 23
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OPENTitle: Mutant torsinA in the heterozygous DYT1 state compromises HSV propagation in infected neurons and fibroblastsJournal Name: Scientific ReportsPublisher: Springer Science and Business Media LLCVol: 8Issue #: 1Start Page: 2324End Page: 2324Publication Date:Open Access(OA) Status: OPENLicense: cc-byDOI - Digital Object Identifier: 10.1038/s41598-018-19865-2Best OA location URL: https://doi.org/10.1038/s41598-018-19865-2Citation Count: 9
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OPENTitle: TDP-43 pathology disrupts nuclear pore complexes and nucleocytoplasmic transport in ALS/FTDJournal Name: Nature NeurosciencePublisher: Springer Science and Business Media LLCVol: 21Issue #: 2Start Page: 228End Page: 239Publication Date:Open Access(OA) Status: OPENLicense: cc-byDOI - Digital Object Identifier: 10.1038/s41593-017-0047-3Best OA location URL: https://www.nature.com/articles/s41593-017-0047-3.pdfCitation Count: 587
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OPENTitle: Effects of small-molecule amyloid modulators on a Drosophila model of Parkinson’s diseaseJournal Name: PLOS ONEPublisher: Public Library of Science (PLoS)Vol: 12Issue #: 9Start Page: e0184117End Page: e0184117Publication Date:Open Access(OA) Status: OPENLicense: cc-byDOI - Digital Object Identifier: 10.1371/journal.pone.0184117Best OA location URL: https://journals.plos.org/plosone/article/file?id=10.1371/journal.pone.0184117&type=printableCitation Count: 17
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OPENTitle: A proteomic network approach across the ALS ‐ FTD disease spectrum resolves clinical phenotypes and genetic vulnerability in human brainJournal Name: EMBO Molecular MedicinePublisher: Springer Science and Business Media LLCVol: 10Issue #: 1Start Page: 48End Page: 62Publication Date:Open Access(OA) Status: OPENLicense: cc-byDOI - Digital Object Identifier: 10.15252/emmm.201708202Best OA location URL: https://onlinelibrary.wiley.com/doi/pdfdirect/10.15252/emmm.201708202Citation Count: 173
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OPENTitle: Genome-wide pleiotropy analysis of neuropathological traits related to Alzheimer’s diseaseJournal Name: Alzheimer's Research & TherapyPublisher: Springer Science and Business Media LLCVol: 10Issue #: 1Start Page: 22End Page: 22Publication Date:Open Access(OA) Status: OPENLicense: cc-byDOI - Digital Object Identifier: 10.1186/s13195-018-0349-zBest OA location URL: https://doi.org/10.1186/s13195-018-0349-zCitation Count: 38