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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, 2008
    A Novel Cell Model for LRRK2 Parkinson's Disease

    Objective/Rationale:
    The aim of this project is to create a model of Parkinson’s disease using skin cells from  patients who have an inherited form of Parkinson’s disease. Using newly developed stem...

  • Rapid Response Innovation Awards, 2008
    Identification of binding proteins for alpha-synuclein oligomers in brain and cells

    Mutations in the PARK-1 and PARK-4 genes leads to alpha-synuclein aggregation with pathology eventually resembling that of sporadic PD. One question is whether the insoluble form of alpha-synuclein is...

  • Target Validation, 2007
    Validation of Sirtuin 2 Deacetylase as a Therapeutic Target in Parkinson’s disease

    Objective/Rationale:
    A major known risk factor in Parkinson’s disease is the misfolding, aggregation and abnormal accumulation of the protein alpha-synuclein. The goal of the proposed work is to...

  • Rapid Response Innovation Awards, 2007
    Understanding the Role of Glucocerebrosidase in Parkinson's Disease Pathogenesis: Toward a New Genetic Model of Sporadic PD

    Gaucher’s disease is a glycosphingolipid-storage disease in which homozygous mutations are found in the lysosomal enzyme glucocerebrosidase (GBA) gene. PD and Gaucher’s disease share many clinical and...

  • Rapid Response Innovation Awards, 2007
    Target Identification of the Mitochondrial Parkinson's Disease PTEN-Induced Kinase 1

    Mutations in PINK1 can cause Parkinson’s disease in certain familial PD cases. The exact cellular function of PINK1 and the impact of disease-relevant mutations remain unknown. PINK1 is known to...

  • Rapid Response Innovation Awards, 2007
    Development of SHG to Discover Drugs to Selectively Block AlphaS toxicity

    Abnormal aggregation of normal or genetically mutated alpha-synuclein protein has been proposed as one possible mechanism for PD. Drugs that can target this abnormal change in the structure of the...

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