Skip to main content

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 (2347${count})

  • Research Grant, 2018
    Inflammatory Phenotypes in Differentiated Human LRRK2 and GBA Mutation IPS Cell Lines

    Promising Outcomes of Original Grant:
    With previous funding from MJFF, we determined how the activity of LRRK2 genetic mutations contributed to inflammation in Parkinson's. We found that inflammation...

  • Research Grant, 2018
    Assess p935 LRRK2 and Total LRRK2 Levels Using an MSD Assay in Whole Blood

    Study Rationale:
    Some variants in the LRRK2 gene have been linked to increased risk of Parkinson's disease. This has made LRRK2 a promising target for Parkinson's drug development. To increase our...

  • Research Grant, 2018
    Autologous Long-Term Cell Restorative Therapy for Parkinson's Disease

    Study Rationale:
    Cell replacement using induced pluripotent stem cells (iPSCs) is a potential restorative therapy for Parkinson's disease. Replacing brain cells that produce dopamine, a chemical...

  • Research Grant, 2018
    Clinicopathological Correlates in LRRK2-Related Parkinson's Disease

    Promising Outcomes of Original Grant:
    With previous funding from MJFF, we established the largest collection of clinically characterized autopsies from Parkinson's patients with a LRRK2 mutation, from...

  • Research Grant, 2018
    Alpha-synuclein/Tau Imaging Consortium

    Study Rationale:
    Abnormal forms of alpha-synuclein and tau proteins are hallmarks of Parkinson's disease and frontotemporal dementia (FTD), respectively, and believed to be early disease indicators...

  • Research Grant, 2018
    Exploring the Mechanisms of Neuropathology in D620N VPS35 Knockin Mice

    Study Rationale:
    Recent findings indicate that mutations in the VPS35 gene cause a type of familial Parkinson's disease. Normally VPS35 is involved in the trafficking of protein cargo, but we don't...

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.