Skip to main content

Animations

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.

Search or browse funded studies

Previously funded studies appear chronologically, with the most recent appearing first.

Filters
From
To
  • ${value}

Filter Results (2458${count})

  • Research Grant, 2013
    Search for Specific Retinal Biomarkers of Parkinson’s Disease

    Objective/Rationale:       
    Although not usually thought of as part of Parkinson’s disease (PD), relatively subtle changes in vision and retinal structure have been reported among PD patients by...

  • Rapid Response Innovation Awards, 2013
    Epigenetics of Parkinson’s Disease in Japanese Males in the Kuakini Honolulu Heart Program

    Objective/Rationale:
    The goals of the project are to identify a unique set of DNA modifications (methylation) in brain sections of those with and without Parkinson’s disease (PD), exposed to...

  • Research Grant, 2013
    Near Infrared Chronic Intracranial Illumination for Neuroprotection in Parkinson's Disease

    Objective/Rationale:             
    The treatment of Parkinson’s Disease (PD) is based on medication and on surgical procedures. These therapies alleviate symptoms but do not change the evolution of the...

  • Rapid Response Innovation Awards, 2013
    Glycosylation as an Inhibitor of Alpha-synuclein Aggregation

    Objective/Rationale:             
    During the development of Parkinson’s disease the protein alpha-synuclein forms toxic clumps, or aggregates, that have been demonstrated to directly contribute to the...

  • Rapid Response Innovation Awards, 2013
    Investigation of the Contribution of Copy Number Alterations in Parkinson’s Disease Genes to Pathogenesis

    Objective/Rationale:             
    In most cases, the cause of Parkinson’s disease (PD) is unknown. Testing blood for DNA mutations is usually negative, but there is increasing evidence that DNA can...

  • LRRK2 Challenge, 2013
    Functional Analysis of LRRK2 Phosphorylation in Human Dopaminergic Neurodegeneration

    Objective/Rationale:
    Although mutations in LRRK2 are the most common genetic cause of Parkinson’s disease (PD) known, the molecular mechanism is unclear. LRRK2 protein is phosphorylated (addition of a...

Two female doctors talking in the lab.

Apply for a Grant

Our funding programs support basic, translational and clinical research from academia and industry.

See Funding Opportunities
We use cookies to ensure that you get the best experience. By continuing to use this website, you indicate that you have read our Terms of Service and Privacy Policy.