861 - 870 of 6230 Results
Title
Year
- LRRK2 functions as a Wnt signaling scaffold, bridging cytosolic proteins and membrane-localized LRP62012OPENTitle: LRRK2 functions as a Wnt signaling scaffold, bridging cytosolic proteins and membrane-localized LRP6Journal Name: Human Molecular GeneticsPublisher: Oxford University Press (OUP)Vol: 21Issue #: 22Start Page: 4966End Page: 4979Publication Date:Open Access(OA) Status: OPENLicense:DOI - Digital Object Identifier: 10.1093/hmg/dds342Best OA location URL: https://academic.oup.com/hmg/article-pdf/21/22/4966/17257652/dds342.pdfCitation Count: 99
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OPENTitle: Evidence for a role of the rare p.A152T variant in MAPT in increasing the risk for FTD-spectrum and Alzheimer's diseasesJournal Name: Human Molecular GeneticsPublisher: Oxford University Press (OUP)Vol: 21Issue #: 15Start Page: 3500End Page: 3512Publication Date:Open Access(OA) Status: OPENLicense:DOI - Digital Object Identifier: 10.1093/hmg/dds161Best OA location URL: https://www.ncbi.nlm.nih.gov/pmc/articles/3392107Citation Count: 223
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OPENTitle: LRRK2 secretion in exosomes is regulated by 14-3-3Journal Name: Human Molecular GeneticsPublisher: Oxford University Press (OUP)Vol: 22Issue #: 24Start Page: 4988End Page: 5000Publication Date:Open Access(OA) Status: OPENLicense:DOI - Digital Object Identifier: 10.1093/hmg/ddt346Best OA location URL: https://academic.oup.com/hmg/article-pdf/22/24/4988/14140078/ddt346.pdfCitation Count: 161
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OPENTitle: In vitro-differentiated neural cell cultures progress towards donor-identical brain tissueJournal Name: Human Molecular GeneticsPublisher: Oxford University Press (OUP)Vol: 22Issue #: 17Start Page: 3534End Page: 3546Publication Date:Open Access(OA) Status: OPENLicense:DOI - Digital Object Identifier: 10.1093/hmg/ddt208Citation Count: 23
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OPENTitle: Functional interaction of Parkinson's disease-associated LRRK2 with members of the dynamin GTPase superfamilyJournal Name: Human Molecular GeneticsPublisher: Oxford University Press (OUP)Vol: 23Issue #: 8Start Page: 2055End Page: 2077Publication Date:Open Access(OA) Status: OPENLicense: cc-byDOI - Digital Object Identifier: 10.1093/hmg/ddt600Best OA location URL: https://academic.oup.com/hmg/article-pdf/23/8/2055/14143078/ddt600.pdfCitation Count: 124
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OPENTitle: Membrane recruitment of endogenous LRRK2 precedes its potent regulation of autophagyJournal Name: Human Molecular GeneticsPublisher: Oxford University Press (OUP)Vol: 23Issue #: 16Start Page: 4201End Page: 4214Publication Date:Open Access(OA) Status: OPENLicense:DOI - Digital Object Identifier: 10.1093/hmg/ddu138Best OA location URL: https://academic.oup.com/hmg/article-pdf/23/16/4201/1737006/ddu138.pdfCitation Count: 220
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OPENTitle: Parkinson's disease-linked mutations in VPS35 induce dopaminergic neurodegenerationJournal Name: Human Molecular GeneticsPublisher: Oxford University Press (OUP)Vol: 23Issue #: 17Start Page: 4621End Page: 4638Publication Date:Open Access(OA) Status: OPENLicense:DOI - Digital Object Identifier: 10.1093/hmg/ddu178Best OA location URL: https://academic.oup.com/hmg/article-pdf/23/17/4621/2215861/ddu178.pdfCitation Count: 148
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OPENTitle: Genome-wide mapping of IBD segments in an Ashkenazi PD cohort identifies associated haplotypesJournal Name: Human Molecular GeneticsPublisher: Oxford University Press (OUP)Vol: 23Issue #: 17Start Page: 4693End Page: 4702Publication Date:Open Access(OA) Status: OPENLicense:DOI - Digital Object Identifier: 10.1093/hmg/ddu158Best OA location URL: https://academic.oup.com/hmg/article-pdf/23/17/4693/2193406/ddu158.pdfCitation Count: 61
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OPENTitle: Additional rare variant analysis in Parkinson’s disease cases with and without known pathogenic mutations: evidence for oligogenic inheritanceJournal Name: Human Molecular GeneticsPublisher: Oxford University Press (OUP)Vol:Issue #:Start Page: ddw348End Page: ddw348Publication Date:Open Access(OA) Status: OPENLicense: cc-byDOI - Digital Object Identifier: 10.1093/hmg/ddw348Best OA location URL: https://academic.oup.com/hmg/article-pdf/25/24/5483/10408585/ddw348.pdfCitation Count: 50
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OPENTitle: LRRK2(I2020T) functional genetic interactors that modify eye degeneration and dopaminergic cell loss in DrosophilaJournal Name: Human Molecular GeneticsPublisher: Oxford University Press (OUP)Vol: 26Issue #: 7Start Page: 1247End Page: 1257Publication Date:Open Access(OA) Status: OPENLicense:DOI - Digital Object Identifier: 10.1093/hmg/ddx030Best OA location URL: https://academic.oup.com/hmg/article-pdf/26/7/1247/25421311/ddx030.pdfCitation Count: 21