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MJFF Publications

5981 - 5990 of 9037 Results
Title
Year
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  • Summary Details
    OPEN
    Title: Role of Elongation and Secondary Pathways in S6 Amyloid Fibril Growth
    Journal Name: Biophysical Journal
    Publisher: Elsevier BV
    Publication Date:
    Open Access(OA) Status: OPEN
    License:
    DOI - Digital Object Identifier: 10.1016/j.bpj.2012.03.047
    Citation Count: 35
  • 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: 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: 75
  • 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: The ZFHX3 GGC Repeat Expansion Underlying Spinocerebellar Ataxia Type 4 has a Common Ancestral Founder
    Journal Name: Movement Disorders
    Publisher: Wiley
    Publication Date:
    Open Access(OA) Status: OPEN
    License: cc-by, cc-by
    DOI - Digital Object Identifier: 10.1002/mds.30077
    Citation Count: 5
  • Summary Details
    OPEN
    Title: Clinical and neuroradiological spectrum of biallelic variants in NOTCH3
    Journal Name: eBioMedicine
    Publisher: Elsevier BV
    Publication Date:
    Open Access(OA) Status: OPEN
    License: cc-by
    DOI - Digital Object Identifier: 10.1016/j.ebiom.2024.105297
    Citation Count: 12
  • Summary Details
    OPEN
    Title: ELFN1 deficiency: The mechanistic basis and phenotypic spectrum of a neurodevelopmental disorder with epilepsy
    Journal Name: Genetics in Medicine
    Publisher: Elsevier BV
    Publication Date:
    Open Access(OA) Status: OPEN
    License: cc-by, cc-by
    DOI - Digital Object Identifier: 10.1016/j.gim.2025.101506
    Citation Count: 2
  • Summary Details
    OPEN
    Title: Genotype–phenotype correlation in PRKN-associated Parkinson’s disease
    Journal Name: npj Parkinson's Disease
    Publisher: Springer Science and Business Media LLC
    Publication Date:
    Open Access(OA) Status: OPEN
    License: cc-by
    DOI - Digital Object Identifier: 10.1038/s41531-024-00677-3
    Citation Count: 58
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