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  • Funded Activity

    Antiphospholipid Syndrome Related Thrombosis: Understanding The Disease Pathogenic Mechanisms Is The Key To Better Diagnosis And Treatment

    Funder
    National Health and Medical Research Council
    Funding Amount
    $607,497.00
    Summary
    Patients with the Antiphospholipid Syndrome develop thrombosis at a young age. It requires long-term treatment with blood thinning medications, which have risks of severe bleeding. Methods are needed to decide which patients require long term treatment, avoiding unnecessary treatment in low risk patients. Such methods do not currently exist. In this study we explore how useful two novel assays developed by us are in identifying which of these patients are at high risk of thrombosis.
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    Funded Activity

    The Role Of Redox-related Post-translational Changes Of Complement Factor H (CFH) In Age-related Macular Degeneration

    Funder
    National Health and Medical Research Council
    Funding Amount
    $652,019.00
    Summary
    Patients with AMD experience loss of central vision and this disorder is the leading cause of blindness in those aged over 50 years in Australia. There are currently no effective treatments for dry AMD. We have identified a protein that undergoes a modification in the blood and the eyes of humans with AMD that has given us new insights into how AMD develops. Specific therapies targeting this modified protein may offer a new treatment for this important cause of blindness.
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    Funded Activity

    Therapeutically Targeting The Major Genetic Risk Factor Of Alzheimer’s Disease

    Funder
    National Health and Medical Research Council
    Funding Amount
    $530,069.00
    Summary
    The second greatest risk factor for Alzheimer’s disease (after age) is genetic variation in a protein called APOE, however it is unknown why APOE increases the risk of disease. We have new clinical and laboratory evidence that APOE incresase risk of Alzheimer’s disease by manipulating iron pathways in the brain. We plan to examine these pathways and apply a new theraputic we have developed that targets these pathways in animal models of Alzheimer’s disease.
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    Funded Activity

    S100 Proteins: Novel Oxidant Scavengers In Allergic Inflammation

    Funder
    National Health and Medical Research Council
    Funding Amount
    $505,814.00
    Summary
    Allergic inflammation includes conditions such as dermatitis and asthma. Asthma, affects one in 10 adults and one in 6 Australians, costing ~$720 million/annum. We will characterize new mediators of oxidant defence which have suppressive effects on key pathogenic processes. The novel oxidative changes in S100 proteins may lead to new diagnostic reagents and new strategies for therapy. Results will open new frontiers in asthma biology and will apply to other chronic inflammatory diseases.
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    Funded Activity

    Characterisation Of Anti-HBs Responses In Patients Undergoing Functional Hepatitis B Cure: Implication For Future Therapies

    Funder
    National Health and Medical Research Council
    Funding Amount
    $723,649.00
    Summary
    The hepatitis B virus causes liver cirrhosis and liver cancer. There is no cure for hepatitis B. However, a small number of patients can naturally rid themselves of the virus. We have identified 14 of these individuals and discovered that they have a unique immune response that is responsible for these “natural” cures. We plan to characterise this immune response and turn it into a therapeutic vaccine which can be used to cure patients who are still chronically infected.
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    Funded Activity

    An Essential Role For Skeletal Muscle FoxO1 In Protecting Against Obesity-induced Insulin Resistance

    Funder
    National Health and Medical Research Council
    Funding Amount
    $593,888.00
    Summary
    Skeletal muscle is the largest organ in the human body and accounts for approximately 80% of glucose disposal after a meal. We have identified a transcription factor, namely FoxO1, that appears protect against obesity-induced insulin resistance by promoting energy consumption. This project will examine whether skeletal muscle specific activation of FoxO1 is a possible therapeutic target for the treatment of obesity-induced insulin resistance.
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    Funded Activity

    Novel Interplay Of Oestrogen And Growth Hormone In Regulating Lipid Metabolism

    Funder
    National Health and Medical Research Council
    Funding Amount
    $673,045.00
    Summary
    These studies provide insights into the mechanisms and role of oestrogen in regulating whole body and liver fat metabolism. Oestrogen-related medications that modify the action or tissue availability of oestrogen are widely used therapeutics and can predispose to obesity and fat accumulation in the liver. Whether the effect is direct or through interplay with other metabolic hormones is unknown. This proposal examines their metabolic consequences and impact on obesity and liver health.
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    Funded Activity

    Towards A Functional Cure For HBV: Exploiting Lessons From HBV-HIV Co-infection

    Funder
    National Health and Medical Research Council
    Funding Amount
    $913,551.00
    Summary
    Hepatitis B virus (HBV) infection can be treated, but therapy is usually lifelong and has side effects, so a cure for HBV is very important. We work closely with colleagues in Asia where both HBV and HIV are common so this provides a unique opportunity to study HBV. We will investigate how an effective immune response against the 2 main HBV proteins is developed. If we can understand how the immune response works against HBV, this could be used to develop new therapies to develop a cure for HBV
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    Funded Activity

    Hepatitis B Virus Covalently Closed Circular DNA

    Funder
    National Health and Medical Research Council
    Funding Amount
    $302,981.00
    Summary
    Worldwide >360 million people have chronic hepatitis B virus (HBV) infection that imparts a 25% lifetime risk of death due to serious liver disease. Current therapies for chronic HBV reduce levels of virus replication but fail to target the stable, nuclear episome, covalently closed circular DNA (cccDNA). The current study will determine what is required to eliminate cccDNA and how current therapies for chronic HBV infection should be modified to achieve this aim.
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    Funded Activity

    Control Of Anabolic And Catabolic Pathways By AMPK

    Funder
    National Health and Medical Research Council
    Funding Amount
    $946,402.00
    Summary
    This project focuses on the role of the metabolic stress-sensing enzyme AMP-activated protein kinase (AMPK) in the control of glucose and fat metabolism. AMPK has been linked to the regulation of exercise capacity, longevity and the control of insulin sensitivity. This is important for our understanding of the metabolic dimensions of our Nations most important health problems including, type-2 diabetes, cardiovascular disease, obesity, neurodegeneration as well as other age onset diseases.
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    Showing 1-10 of 65 Funded Activites

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