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Research Topic : NEUROSCIENCE
Scheme : NHMRC Project Grants
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  • Funded Activity

    A Novel View Of Zona Incerta: A Key Thalamic Relay To The Neocortex?

    Funder
    National Health and Medical Research Council
    Funding Amount
    $126,638.00
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    Funded Activity

    Corticotectal Interactions In The Mammalian Visual System

    Funder
    National Health and Medical Research Council
    Funding Amount
    $176,399.00
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    Funded Activity

    Sialyltransferase In The Bipolar And Schizophrenic Brain: Examining The Role Of A Novel Generalised Susceptibility Gene

    Funder
    National Health and Medical Research Council
    Funding Amount
    $512,627.00
    Summary
    Bipolar disorder and schizophrenia are two major psychiatric conditions affecting over 800,000 Australians. We have identified a new gene which contributes to increased risk to developing both bipolar disorder and schizophrenia. We will investigate the function of this gene in normal brain development, and how this function is disrupted in individuals with bipolar disorder and schizophrenia. Understanding the biological cause will help us define better treatments for these severe mental illnesse .... Bipolar disorder and schizophrenia are two major psychiatric conditions affecting over 800,000 Australians. We have identified a new gene which contributes to increased risk to developing both bipolar disorder and schizophrenia. We will investigate the function of this gene in normal brain development, and how this function is disrupted in individuals with bipolar disorder and schizophrenia. Understanding the biological cause will help us define better treatments for these severe mental illnesses.
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    Funded Activity

    Comorbid Affective Disturbance In A Model Of Absence Epilepsy - Shared Causation Linked To Morphological Abnormality?

    Funder
    National Health and Medical Research Council
    Funding Amount
    $502,650.00
    Summary
    People with epilepsy commonly suffer from severe mood disorders, such as depression and anxiety. These disturbances are underdiagnosed and undertreated, and are often more debilitating than the epilepsy. This project will investigate whether treatment of psychiatric disturbance with antidepressants also results in reduced seizure incidence in an animal model of epilepsy. Results generated from the study will provide clinicians strong rationale for aggressive treatment of such mood complaints.
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    Funded Activity

    Organization Of The Human Brainstem: Identification Of Its Regions

    Funder
    National Health and Medical Research Council
    Funding Amount
    $87,568.00
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    Funded Activity

    The Third International Stroke Trial (IST-3)

    Funder
    National Health and Medical Research Council
    Funding Amount
    $218,656.00
    Summary
    Thrombolysis is a method of dissolving the blood clot that is the cause of the majority of strokes in Australia. The first major trial to demonstrate benefit for this treatment was published some 11 years ago but treatment has not been widely implemented across Australia because of the difficulties in giving treatment within the very tight time window for which treatment is currently approved (patients must get to hospital, be scanned and start treatment within 3 hours of the onset of the stroke .... Thrombolysis is a method of dissolving the blood clot that is the cause of the majority of strokes in Australia. The first major trial to demonstrate benefit for this treatment was published some 11 years ago but treatment has not been widely implemented across Australia because of the difficulties in giving treatment within the very tight time window for which treatment is currently approved (patients must get to hospital, be scanned and start treatment within 3 hours of the onset of the stroke). Other factors which have limited implementation of treatment in Australia are continued debate over the trial data for this treatment as only one of the 5 major trials was positive. In addition, virtually no patients aged over 80 years old were included in the previous trials, and as this age group represents about a third of all stroke in Australia, new data in this age group is required. As a result of the difficulty in giving a treatment within such a tight time window and the ongoing debate about the trial data, few Australians are currently treated and thus the public health impact is negligible. In to change clinical practice, we need reliable data from a large convincing further trial of thrombolysis with the more realistic time window of 6 hours. The Third International Stroke Trial (IST-3) is a large international collaborative effort to determine whether thrombolysis treatment offered to a wider range of patients up to 6 hours from stroke onset results in an increase in long-term independent survival. Data from such a trial is most likely to change clinical practice and lead to an important public health benefit.
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    Funded Activity

    Development Of A Scorpion Toxin For Tumour Imaging

    Funder
    National Health and Medical Research Council
    Funding Amount
    $529,577.00
    Summary
    The aim of this project is to develop a tool for visualising tumours during surgery. Surgical removal of tumours remains the foundation of cancer treatment, but the ability to distinguish the margin between cancerous and healthy cells is imprecise. We will explore the potential of a scorpion toxin that selectively targets cancer cells, as a tumour imaging agent. This project has the potential to dramatically enhance patient survival as a result of improving treatments for cancer.
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    Funded Activity

    Patterns Of Connections Between The Thalamus And Other Parts Of The Brain

    Funder
    National Health and Medical Research Council
    Funding Amount
    $118,344.00
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    Funded Activity

    Molecular Mechanisms Involved In The Control Of Neurotr Ansmitter Release

    Funder
    National Health and Medical Research Council
    Funding Amount
    $185,853.00
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    Funded Activity

    Molecular Cell Biology Of HNP22: Role In Alcohol Dependence

    Funder
    National Health and Medical Research Council
    Funding Amount
    $346,320.00
    Summary
    We used a differential screening procedure to detect changes in gene expression in the human alcoholic brain and described a novel gene, which we named hNP22, with increased expression in the superior frontal cortex of the alcoholic cases. This is the first report of a novel alcohol-responsive gene isolated from the human brain. We now propose to further explore the hNP22 gene, its product and its regulation in human brain tissue, and in a variety of experimental systems. We will determine how p .... We used a differential screening procedure to detect changes in gene expression in the human alcoholic brain and described a novel gene, which we named hNP22, with increased expression in the superior frontal cortex of the alcoholic cases. This is the first report of a novel alcohol-responsive gene isolated from the human brain. We now propose to further explore the hNP22 gene, its product and its regulation in human brain tissue, and in a variety of experimental systems. We will determine how protein expression correlates with the level of alcohol consumption. We will use animal and cell culture models to determine the response of the gene to various stimuli. We will express the recombinant protein to determine its function. It is likely that the gene product may be a component in an important signal pathway within neuronal cells and thus may represent a novel target for therapeutic intervention.
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    Showing 1-10 of 60 Funded Activites

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