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Funded Studies

The Foundation supports research across basic, translational and clinical science to speed breakthroughs that can lead to the creation of new treatments and a better quality of life for people with Parkinson's disease.

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Previously funded studies appear chronologically, with the most recent appearing first.

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  • Target Validation, 2012
    VPS35 as a Novel Target for Parkinson's Disease

    Objective/Rationale:

    Mutations in the VPS35 gene were recently identified as a cause of autosomal dominant familial Parkinson's disease (PD). How mutations in VPS35 precipitate the demise of...

  • Critical Challenges in PD: Postural Instability and Gait Dis, 2012
    Targeted Cognitive Training Program for Freezing of Gait

    Promising Outcomes of Original Grant:
    In our original study we investigated the processes underlying the freezing phenomenon in PD. In this work we found symptoms of freezing of gait (FOG) could be...

  • Therapeutics Development Initiative, 2011
    Next Generation Parkinson's Disease Treatment through Steering Brain Stimulation (NEXT)

    Objective/Rationale:
    Deep Brain Stimulation (DBS) can provide a radical improvement in the quality of life of Parkinson’s patients. However, it is a complex procedure with a large incidence of...

  • Therapeutics Development Initiative, 2011
    Characterization of NPT001-mediated Alpha-Synuclein Disaggregation and Clearance

    Objective/Rationale:
    Abnormal accumulation of alpha-synuclein in the brain is associated with toxicity and disease progression in Parkinson’s and other neurodegenerative diseases. NPT001 has been...

  • LRRK2, 2011
    fMRI of First Degree Relatives of LRRK2 Positive Parkinson's Disease Patients

    Objective/Rationale:
    First, to study the effect of the presence of the LRRK2 G2019S mutation on brain activation patterns in PD patients who recently converted into a diseased state by comparing...

  • LRRK2, 2011
    Increased Sensitivity to the Loss of Nigrostriatal Dopamine Following Progressive MPTP Treatment in LRRK2 Mutant Small Models

    Objective/Rationale:
    It is known that a mutation of specific gene, called LRRK2, increases the risks of developing Parkinson’s disease in humans. The specific objective of this proposal is to...

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