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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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  • PD Subtypes, 2007
    Longitudinal changes in patterns of motor UPDRS subscore

    Tremor, bradykinesia (slowness of movement), rigidity (stiffness) and walking/balance impairment are the major signs of Parkinson's disease; a middle-age onset with slow progression is archetypal...

  • PD Subtypes, 2007
    Prediction of Death, Dementia, Disability, Depression from the Time Course of UPDRS Motor Status

    Parkinson’s disease is progressive. Early on, its effects are relatively minor, affecting mainly movement and causing shaking of the limbs. Later on, serious events -- early death, dementia...

  • PD Subtypes, 2007
    Defining PD Subtypes Based on Patterns of Long-term Outcome

    The purpose of our study is to identify Parkinson’s disease subtypes based on how individuals are doing approximately seven to eight years after diagnosis. Some patients have few symptoms at this time...

  • Target Validation, 2007
    Functional Inhibition of RasGRF1 in the MPTP-lesioned NHP Model for Treating Levodopa-induced Dyskinesia

    Objective/Rationale: 
    Levodopa-induced dyskinesias are caused by an increased and aberrant response of dopamine receptors to dopamine in the striatum. Among other intracellular pathways, the MAP kinase...

  • Target Validation, 2007
    Validation of metabotropic glutamate-receptor type 5 as a target for the treatment of L-DOPA-induced dyskinesia in a macaque model of Parkinson´s disease

    Objective/Rationale:
    Metabotropic glutamate receptor type 5 (mGluR5) is abundantly expressed in striatal neurons, where it modulates the response to glutamatergic and dopaminergic inputs. Previous...

  • Target Validation, 2007
    Inhibition of c-Abl Tyrosine Kinase as a Novel Therapy to Prevent PD Progression
    Objective/Rationale:              Mutations in the parkin gene cause early-onset autosomal recessive PD. We have discovered that parkin is modified by an oxidative-stress induced signaling kinase, c...
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