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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, 2011
    Defining PARKIN Substrates Through Systematic Quantitative Proteomics

    Objective/Rationale:
    The PARK2 (Parkin) gene is frequently mutated in Parkinson’s disease. Several lines of evidence indicate that Parkin functions to catalyze the conjugation of the small protein...

  • MJFF Research Grant, 2011
    Modulation of Striatal Colinergic Neuronal Activity in LID

    Objective/Rationale:
    The role of striatal cholinergic interneurons (ChIs) in Parkinson’s disease and side effects of treatment like levodopa-induced dyskinesia (LID) have been poorly studied. We have...

  • Rapid Response Innovation Awards, 2011
    Intestinal Microbiota, Permeability and Alpha-synclein Aggregation in Parkinson's Disease

    Objective/Rationale:
    Changes in the intestinal system may occur early in the development of Parkinson’s disease. The intestinal system is important to (1) maintain normal “healthy” bacteria; and (2)...

  • Rapid Response Innovation Awards, 2011
    Alpha-Synuclein Knockdown: Therapeutic or Toxic?

    Objective/Rationale:
    The protein alpha-synuclein (a-syn) has been conclusively linked to Parkinson’s disease. The prevailing theory today states that a-syn is a causative agent in the development of...

  • Improving Levodopa Delivery, 2011
    Dry Powder-Based Delivery of Intrapulmonary Levodopa as a Treatment for Motor Fluctuations in Parkinson's Disease

    Objective/Rationale:
    Oral levodopa pharmacokinetics are subject to excessive within- and between-subject variability, reflecting challenges inherent to gastrointestinal delivery. Aerosol delivery of...

  • LRRK2, 2011
    LRRK2 Physiology in Parkinson's Disease

    Objective/Rationale:
    Mutations in the LRRK2 gene are a common cause of genetic Parkinson’s disease. LRRK2 is highly expressed in circulating and tissue immune cells. We have recently identified that...

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