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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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  • Rapid Response Innovation Awards, 2010
    Mechanism and Modulation of Alpha-Synuclein Expression

    Promising Outcomes of Original Grant:
    In the initial grant, we tested the hypothesis that GATA-2 is a direct regulator of alpha-synuclein expression in dopaminergic neurons and therefore represents a...

  • Rapid Response Innovation Awards, 2010
    In Vivo Assessment of Alpha-Synuclein Secretion

    Objective/Rationale
    Recent data from our lab (Emmanouilidou et al, 2010) suggest that cell-produced physiologically secreted alpha-synuclein can cause the death of neuronal recipient cells. Although...

  • MJFF Research Grant, 2010
    Regulated rAAV-GDNF to treat Parkinson's disease: Translational research plan

    Objective/Rationale
    We are attempting to perfect gene therapy using glial cell line-derived neurotrophic factor (GDNF) for Parkinson’s disease. One part of developing this gene therapy is...

  • Neurotrophic Factor Therapies for Parkinson's Disease, 2010
    CDNF (Cerebral Dopamine Neurotrophic Factor) for Therapy of Parkinson's Disease

    Objective/Rationale:
    CDNF protein is expressed in human brain, acts differently from known neurotrophic factors and can protect and repair dopamine neurons in two pre-clinical models of Parkinson’s...

  • Rapid Response Innovation Awards, 2010
    Selective Neuroprotective Effects of the S18Y Polymorphic Variant of UCH-L1

    Promising Outcomes of Original Grant:
    We were able to replicate in an in vivo setting in the nigrostriatal system our previous observation in neuronal cell cultures that lack of UCH-L1 did not alter...

  • Rapid Response Innovation Awards, 2010
    Dopamine D1-D3 Receptor Heteromer as a New Target for Parkinson's Disease

    Objective/Rationale:   
    Receptor heteromers must be understood as dimeric or higher order molecular entities that are the result of combinatorial evolution and that are endowed with unique...

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