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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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  • Community Fast Track, 2007
    The Protein Engrailed as a Potential Therapeutic Target in Parkinson's Disease

    Promising Outcomes of Original Grant:
    In our original grant, we have confirmed that a protein called Engrailed (which plays an important role both in the developping and in the adult dopaminergic...

  • Community Fast Track, 2007
    CDNF - A Novel Conserved Neurotrophic Factor that Protects Midbrain Dopaminergic Neurons in vivo

    Promising Outcomes of Original Grant:
    Future treatment of Parkinson’s disease aim at therapies which would stop the progress of the disease and restore the function of injured dopamine nerves in the...

  • Target Validation, 2007
    Targeting Urate: A Molecular Correlate of Both Risk and Progression in PD

    Objective/Rationale:
    Urate (a natural antioxidant, caffeine analog and DNA metabolite) is the first molecule linked to both the risk of typical Parkinson’s disease and its rate of progression. Higher...

  • Rapid Response Innovation Awards, 2007
    Potential Utility of Novel CNS-active Experimental Therapeutics for Parkinson's Disease

    Objective/Rationale:
    Evidence suggests that overproduction of inflammatory molecules, called proinflammatory cytokines, from glial cells in the brain can contribute to nerve cell death and accelerate...

  • Rapid Response Innovation Awards, 2007
    Neuroprotective effects of isradipine in a pre-clinical model of Parkinson’s disease

    Objective/Rationale: 
    Recent work by our group has shown that blocking L-type Ca2+ channels protects vulnerable dopaminergic neurons in three animal models Parkinson’s disease (PD). Isradipine, a high...

  • Rapid Response Innovation Awards, 2007
    Genetic characterization of Omi/Htra2 (PARK13) in autosomal dominant and sporadic Parkinson’s disease

    Objective/Rationale: 

    Identification of DNA variations that cause familial/sporadic parkinsonism has provided insight into the biological pathways involved in disease. Thirteen loci (PARK1-13) have...

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