1721 - 1730 of 6230 Results
Title
Year
-
OPENTitle: Genetic variability in the regulation of gene expression in ten regions of the human brainJournal Name: Nature NeurosciencePublisher: Springer Science and Business Media LLCVol: 17Issue #: 10Start Page: 1418End Page: 1428Publication Date:Open Access(OA) Status: OPENLicense:DOI - Digital Object Identifier: 10.1038/nn.3801Best OA location URL: http://doi.org/10.1038/nn.3801Citation Count: 656
- Therapeutic deep brain stimulation reduces cortical phase-amplitude coupling in Parkinson's disease2015OPENTitle: Therapeutic deep brain stimulation reduces cortical phase-amplitude coupling in Parkinson's diseaseJournal Name: Nature NeurosciencePublisher: Springer Science and Business Media LLCVol: 18Issue #: 5Start Page: 779End Page: 786Publication Date:Open Access(OA) Status: OPENLicense:DOI - Digital Object Identifier: 10.1038/nn.3997Best OA location URL: https://www.ncbi.nlm.nih.gov/pmc/articles/4414895Citation Count: 581
-
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: 527
-
OPENTitle: Subthalamic nucleus stimulation reverses mediofrontal influence over decision thresholdJournal Name: Nature NeurosciencePublisher: Springer Science and Business Media LLCVol: 14Issue #: 11Start Page: 1462End Page: 1467Publication Date:Open Access(OA) Status: OPENLicense:DOI - Digital Object Identifier: 10.1038/nn.2925Citation Count: 658
- Enhancers active in dopamine neurons are a primary link between genetic variation and neuropsychiatric disease2018OPENTitle: Enhancers active in dopamine neurons are a primary link between genetic variation and neuropsychiatric diseaseJournal Name: Nature NeurosciencePublisher: Springer Science and Business Media LLCVol: 21Issue #: 10Start Page: 1482End Page: 1492Publication Date:Open Access(OA) Status: OPENLicense:DOI - Digital Object Identifier: 10.1038/s41593-018-0223-0Best OA location URL: https://www.ncbi.nlm.nih.gov/pmc/articles/6334654Citation Count: 95
- Critical Role of Truncated α‐Synuclein and Aggregates in Parkinson's Disease and Incidental Lewy Body Disease2012OPENTitle: Critical Role of Truncated α‐Synuclein and Aggregates in Parkinson's Disease and Incidental Lewy Body DiseaseJournal Name: Brain PathologyPublisher: WileyVol: 22Issue #: 6Start Page: 811End Page: 825Publication Date:Open Access(OA) Status: OPENLicense:DOI - Digital Object Identifier: 10.1111/j.1750-3639.2012.00597.xBest OA location URL: https://www.ncbi.nlm.nih.gov/pmc/articles/5505643Citation Count: 61
- Binding to serine 65‐phosphorylated ubiquitin primes Parkin for optimal PINK 1‐dependent phosphorylation and activation2015OPENTitle: Binding to serine 65‐phosphorylated ubiquitin primes Parkin for optimal PINK 1‐dependent phosphorylation and activationJournal Name: EMBO reportsPublisher: Springer Science and Business Media LLCVol: 16Issue #: 8Start Page: 939End Page: 954Publication Date:Open Access(OA) Status: OPENLicense: cc-byDOI - Digital Object Identifier: 10.15252/embr.201540352Best OA location URL: https://onlinelibrary.wiley.com/doi/pdfdirect/10.15252/embr.201540352Citation Count: 227
-
OPENTitle: Kinase inhibitors arrest neurodegeneration in cell and C. elegans models of LRRK2 toxicityJournal Name: Human Molecular GeneticsPublisher: Oxford University Press (OUP)Vol: 22Issue #: 2Start Page: 328End Page: 344Publication Date:Open Access(OA) Status: OPENLicense:DOI - Digital Object Identifier: 10.1093/hmg/dds431Best OA location URL: https://academic.oup.com/hmg/article-pdf/22/2/328/1857445/dds431.pdfCitation Count: 76
-
OPENTitle: DNAJC13 mutations in Parkinson diseaseJournal Name: Human Molecular GeneticsPublisher: Oxford University Press (OUP)Vol: 23Issue #: 7Start Page: 1794End Page: 1801Publication Date:Open Access(OA) Status: OPENLicense:DOI - Digital Object Identifier: 10.1093/hmg/ddt570Best OA location URL: http://doi.org/10.1093/hmg/ddt570Citation Count: 300
- Genetic analysis implicates APOE, SNCA and suggests lysosomal dysfunction in the etiology of dementia with Lewy bodies2014OPENTitle: Genetic analysis implicates APOE, SNCA and suggests lysosomal dysfunction in the etiology of dementia with Lewy bodiesJournal Name: Human Molecular GeneticsPublisher: Oxford University Press (OUP)Vol: 23Issue #: 23Start Page: 6139End Page: 6146Publication Date:Open Access(OA) Status: OPENLicense:DOI - Digital Object Identifier: 10.1093/hmg/ddu334Best OA location URL: http://doi.org/10.1093/hmg/ddu334Citation Count: 215