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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, 2014
    Role of Kinase Fyn in Levodopa-induced Dyskinesia

    Study Rationale:
    Levodopa frequently induces dyskinesia, an abnormal involuntary movement. In our laboratory we study how and where the prolonged use of levodopa modifies the brain of pre-clinical...

  • Rapid Response Innovation Awards, 2014
    Inhibition of Retinoic Acid Metabolism for the Treatment of Parkinson’s Disease

    Study Rationale:  
    Several lines of evidence point to the therapeutic potential of Retinoic acid (RA), a metabolite of vitamin A, in the treatment of Parkinson’s disease. For example, RA treatment...

  • LRRK2 Challenge, 2014
    Role of LRRK2 in the Regulation of Dopamine Receptor Trafficking

    Study Rationale:
    Mutation of the LRRK2 gene is the greatest known genetic contributor to Parkinson’s disease. However, the molecular mechanisms and pathological pathways by which LRRK2 induces neuronal...

  • Therapeutic Pipeline Program, 2014
    Cell Assays to Measure Peripheral Response to GCase Activators

    Objective/Rationale:             
    Individuals who carry one copy of the gene for Gaucher’s disease are at significantly increased risk of Parkinson’s disease. Lysosomal Therapeutics Inc. (LTI) is...

  • Access to Data and Biospecimens, 2014
    Metabolomic Analysis of Parkinsonian Disorders

    Study Rationale:
    This study is a search for biomarkers of Parkinson’s disease (PD) that would provide early diagnostic clues or a means to monitor disease progression (or both). The analysis involves...

  • Rapid Response Innovation Awards, 2014
    Directed Evolution of Bacteria for Recombinant Expression and Purification of LRRK2

    Study Rationale:                  
    Mutations in the gene that encodes the LRRK2 protein are frequent causes of Parkinson’s disease (PD). An obstacle to understanding how these mutations lead to PD is...

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