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MJFF Publications

2301 - 2310 of 9034 Results
Title
Year
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  • 2024
  • Summary Details
    OPEN
    Title: Evidence for a role of the rare p.A152T variant in MAPT in increasing the risk for FTD-spectrum and Alzheimer's diseases
    Journal Name: Human Molecular Genetics
    Publisher: Oxford University Press (OUP)
    Publication Date:
    Open Access(OA) Status: OPEN
    License:
    DOI - Digital Object Identifier: 10.1093/hmg/dds161
    Citation Count: 235
  • Summary Details
    OPEN
    Title: Unbiased screen for interactors of leucine-rich repeat kinase 2 supports a common pathway for sporadic and familial Parkinson disease
    Journal Name: Proceedings of the National Academy of Sciences
    Publisher: National Academy of Sciences
    Publication Date:
    Open Access(OA) Status: OPEN
    License:
    DOI - Digital Object Identifier: 10.1073/pnas.1318306111
    Citation Count: 365
  • Summary Details
    OPEN
    Title: Genetics and Pathophysiology of Neurodegeneration with Brain Iron Accumulation (NBIA)
    Journal Name: Current Neuropharmacology
    Publisher: Bentham Science Publishers Ltd.
    Publication Date:
    Open Access(OA) Status: OPEN
    License:
    DOI - Digital Object Identifier: 10.2174/157015913804999469
    Citation Count: 127
  • Summary Details
    OPEN
    Title: Creation of an Open-Access, Mutation-Defined Fibroblast Resource for Neurological Disease Research
    Journal Name: PLoS ONE
    Publisher: Public Library of Science (PLoS)
    Publication Date:
    Open Access(OA) Status: OPEN
    License: cc0, cc0
    DOI - Digital Object Identifier: 10.1371/journal.pone.0043099
    Citation Count: 141
  • Summary Details
    OPEN
    Title: A Tangled Web – Tau and Sporadic Parkinson's Disease
    Journal Name: Frontiers in Psychiatry
    Publisher: Frontiers Media SA
    Publication Date:
    Open Access(OA) Status: OPEN
    License: cc-by, cc-by
    DOI - Digital Object Identifier: 10.3389/fpsyt.2010.00150
    Citation Count: 32
  • Summary Details
    OPEN
    Title: Kinase inhibitors arrest neurodegeneration in cell and C. elegans models of LRRK2 toxicity
    Journal Name: Human Molecular Genetics
    Publisher: Oxford University Press (OUP)
    Publication Date:
    Open Access(OA) Status: OPEN
    License:
    DOI - Digital Object Identifier: 10.1093/hmg/dds431
    Citation Count: 74
  • Summary Details
    OPEN
    Title: Parkinson's disease-linked mutations in VPS35 induce dopaminergic neurodegeneration
    Journal Name: Human Molecular Genetics
    Publisher: Oxford University Press (OUP)
    Publication Date:
    Open Access(OA) Status: OPEN
    License:
    DOI - Digital Object Identifier: 10.1093/hmg/ddu178
    Citation Count: 174
  • Summary Details
    OPEN
    Title: LRRK2 functions as a Wnt signaling scaffold, bridging cytosolic proteins and membrane-localized LRP6
    Journal Name: Human Molecular Genetics
    Publisher: Oxford University Press (OUP)
    Publication Date:
    Open Access(OA) Status: OPEN
    License: other-oa
    DOI - Digital Object Identifier: 10.1093/hmg/dds342
    Citation Count: 103
  • The Role of Stable α-Synuclein Oligomers in the Molecular Events Underlying Amyloid Formation
    2014
    Summary Details
    RESTRICTED
    Title: The Role of Stable α-Synuclein Oligomers in the Molecular Events Underlying Amyloid Formation
    Journal Name: Journal of the American Chemical Society
    Publisher: American Chemical Society (ACS)
    Publication Date:
    Open Access(OA) Status: RESTRICTED
    License:
    DOI - Digital Object Identifier: 10.1021/ja411577t
    Citation Count: 257
  • Summary Details
    OPEN
    Title: Viral overexpression of human alpha-synuclein in mouse substantia nigra dopamine neurons results in hyperdopaminergia but no neurodegeneration
    Journal Name: Experimental Neurology
    Publisher: Elsevier BV
    Publication Date:
    Open Access(OA) Status: OPEN
    License: cc-by
    DOI - Digital Object Identifier: 10.1016/j.expneurol.2024.114959
    Citation Count: 8
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