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Research Topic : EXCITOTOXICITY
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  • Funded Activity

    Research Fellowship - Grant ID:401229

    Funder
    National Health and Medical Research Council
    Funding Amount
    $735,471.00
    More information
    Funded Activity

    Repeated Hypoxia During Early Development: Neuromodulator And Neuropathologic Response In Piglets

    Funder
    National Health and Medical Research Council
    Funding Amount
    $145,107.00
    More information
    Funded Activity

    Roles And Regulations Of Glutamate Transporters In Neurodegenerative Disease

    Funder
    National Health and Medical Research Council
    Funding Amount
    $20,484.00
    More information
    Funded Activity

    Research Fellowship - Grant ID:454304

    Funder
    National Health and Medical Research Council
    Funding Amount
    $765,882.00
    Summary
    I am a neuroscientist employing strategies of biochemistry, pathology, pharmacology and developmental biology to examine the mechanisms of neuronal injury contributing to degenerative conditions. My major long-term interest has been excitotoxicity and rec
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    Funded Activity

    Targeting The Synaptic Actin Cytoskeleton In Alzheimer's Disease

    Funder
    National Health and Medical Research Council
    Funding Amount
    $840,741.00
    Summary
    Dementias have become one of the fastest growing sources of major disease burdens in developed countries with about one in fifteen Australians older than 65 being affected. We will study how pathological stimuli disrupt nerve cell connections in the brain by impacting on the cellular architecture at these connections. Findings from our study will provide profound new insights in how nerve cells communicate with each other and how this communication is breaking down in disease.
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    Funded Activity

    The Role Of Tau In Stroke

    Funder
    National Health and Medical Research Council
    Funding Amount
    $143,676.00
    Summary
    The majority of stroke results from focal brain infarction, followed by substantial secondary excitotoxic damage in the surrounding areas. Tau has been shown to contribute to excitotoxicity and neurodegeneration in mouse models of Alzheimer’s disease (AD). Preliminary data show that tau reduction also protects against excitotoxic damage after experimental stroke. We aim to dissect the molecular mechanisms of stroke using a tau-deficient mouse model.
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    Funded Activity

    Modulating Cellular Copper Levels To Prevent The Effects Of Excitotoxicity In Neurodegenerative Diseases

    Funder
    National Health and Medical Research Council
    Funding Amount
    $434,652.00
    Summary
    Exitotoxicity has been implicated in many neurological disorders incluing Alzheimer's and Huntington's disesaes. This toxicity can be inhibited by modulated intracellular copper levels. Here we will ascertain the therapeutic potential of strategies designed to increase cellular copper levels.
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    Funded Activity

    The Molecular Mechanism Of Ion-coupled Transport In The Brain

    Funder
    National Health and Medical Research Council
    Funding Amount
    $441,407.00
    Summary
    Cells in the brain communicate through chemical signals called neurotransmitters. Neurotransmitter transporters reside in the membranes of cells and are responsible for regulating levels of these chemicals in the brain. They play an important role in the normal function of the human brain but their dysfunction is responsible for many diseases including Alzheimer's disease and motor neuron disease. It is crucial to understand how these proteins work in both normal and disease states.
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    Funded Activity

    Interaction Of Amyloid-beta And Tau Pathology In Alzheimer's Disease

    Funder
    National Health and Medical Research Council
    Funding Amount
    $122,592.00
    Summary
    Currently, over 200,000 Australians are affected by Alzheimer's disease (AD) and related forms of dementia, causing a huge socio-economic damage. To overcome the lack of effective treatments, we need to understand the underlying causes and translate them into therapy. Using state-of-the-art cell culture and genetic mouse models, I will reveal fundamental processes in AD and related dementias, and develop tailored treatments to battle these devastating disorders.
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    Funded Activity

    To Determine The Role And Mechanism Of Action Of Tissue-type Plasminogen Activator In The Central Nervous System

    Funder
    National Health and Medical Research Council
    Funding Amount
    $504,097.00
    Summary
    Tissue-type plasminogen activator (t-PA) is used clinically to remove blood clots. Recently, a role for t-PA in the brain was discovered where under pathological conditions it can promote ischaemic and excitotoxic brain injury. This project will examine the mechanisms by which t-PA promotes injury to brain cells. It is anticipated that results obtained could be used to devise a means to reduce t-PA toxicity in the brain that would be of therapeutic benefit for patients with ischaemic stroke.
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    Showing 1-10 of 28 Funded Activites

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