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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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  • Therapeutics Development Initiative, 2009
    Optimization of Selective Mu Opioid Receptor Antagonists for the Treatment of Levodopa-Induced Dyskinesias in Parkinson's Disease

    Objective/Rationale: 
    In Parkinson’s disease, L-DOPA-induced dyskinesias (LID) are therapeutically limiting side effects that occur with long-term L-DOPA treatment, and their presence significantly...

  • Rapid Response Innovation Awards, 2009
    Identification of Nurr1 Agonists for the Treatment of Parkinson's Disease

    Objective/Rationale:
    Nurr1 is a nuclear hormone receptor strongly implicated in the growth, maintenance, and survival of dopaminergic neurons, that represents a very promising therapeutic target for...

  • Rapid Response Innovation Awards, 2009
    Isotopic Stabilization of Dietary Polyunsaturated Fatty Acids as a New Treatment Paradigm for Parkinson's Disease: MPTP and Paraquat Pre-clinical Model Feasibility Studies

    Objective/Rationale:
    Oxidative stress plays a major role in the development of Parkinson’s disease (PD). Essential (available from diet only) polyunsaturated fatty acids (PUFAs) are one of the first...

  • Rapid Response Innovation Awards, 2009
    Targeting Glia in PD with Novel Anti-Inflammatory Therapeutics

    Objective/Rationale:
    Loss of dopamine-producing neurons in Parkinson’s disease (PD) is accompanied by inflammation in surrounding support cells, called glial cells. This inflammatory state in glial...

  • MJFF Research Grant, 2009
    Parkinson's Disease, Ashkenazi Jews and LRRK2: a consortium proposal

    Objective/Rationale:
    Mutations in the LRRK2 gene are the most common genetic cause of classic or typical Parkinson’s disease (PD). One mutation, G2019S, is especially frequent in Jewish (about 14%)...

  • MJFF Research Grant, 2009
    Clinicogenetic Studies of LRRK2 G2019S in Tunisia

    Objective/Rationale:
    Parkinson’s disease (PD) is a prevalent, heterogeneous disorder with a complex, multifactorial etiology. In Tunisia, North Africa, the burden of genetically-defined LRRK2 G2019S...

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