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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, 2010
    Peroxisome-Proliferator Activated Receptor gamma as a Target for Anti-Dyskinesia Pharmacotherapy

    Objective/Rationale
    We plan to develop new pharmacological approaches to treat levodopa-induced dyskinesia (LID) in a pre-clinical model of Parkinson’s disease (PD). Preliminary data from our...

  • Target Validation, 2010
    Targeting the Unfolded Protein Response (UPR) Transcription Factor XBP-1 to Treat Parkinson's Disease

    Objective/Rationale
    Our general objective is to investigate the role of a specific component of a cellular stress responses linked to organelle damage, the Unfolded Protein Response (UPR), in the...

  • Target Validation, 2010
    Modulation of the Rho Kinase pathway for improvement of regeneration in PD

    Objective/Rationale
    A characteristic feature of Parkinson’s disease is the loss of axons, the long processes of neuronal cells. This loss of axons seems to occur early in the course of the disease...

  • Rapid Response Innovation Awards, 2010
    SNCA Haplotyping in Parkinson's Disease and Multiple System Atrophy

    Objective/Rationale:
    A succinct, lay-oriented statement of the scientific rationale for this project. We have recently shown that genetic variants at the SNCA gene locus, coding for the alpha-synuclein...

  • Rapid Response Innovation Awards, 2010
    Resting State fMRI as a Biomarker for Parkinson's Disease

    Objective/Rationale
    There is an increasingly interest in finding biomarkers that can objectively evaluate the disease progression and the effects of neuroprotective treatment on the course of...

  • Rapid Response Innovation Awards, 2010
    Identification and Validation of the Modifiers of LRRK2-induced Toxicity

    Objective/Rationale
    Mutations in LRRK2 gene have been identified as an unambiguous cause of rare autosomal dominant forms of PD. A number of useful models have been developed to study the...

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