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Research Topic : HEME BIOSYNTHESIS
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  • Funded Activities (31)
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  • Funded Activity

    Control Of Heme Synthesis

    Funder
    National Health and Medical Research Council
    Funding Amount
    $320,693.00
    More information
    Funded Activity

    5-Aminolevulinate Synthase: Regulation During Erythropoiesis And Role In X-linked Sideroblastic Anemia

    Funder
    National Health and Medical Research Council
    Funding Amount
    $374,484.00
    More information
    Funded Activity

    Control Of Heme Biosynthesis And Its Relation To Diseas Es

    Funder
    National Health and Medical Research Council
    Funding Amount
    $233,058.00
    More information
    Funded Activity

    Role Of Placental Heme-oxygenase Pathway In Regulating Preterm Neonatal Cardiovascular Function

    Funder
    National Health and Medical Research Council
    Funding Amount
    $176,719.00
    Summary
    Babies born prematurely are more likely to experience problems as a result of being born early with males doing worse than females. The mechanisms causing this difference are unknown. The control of blood flow in the placenta and fetus is essential for normal growth and development. This project will investigate the influence of duration of pregnancy, gender, and exposure to antenatal steroids on pathways that control blood flow in the placenta and the newborn in babies born after prematurely.
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    Funded Activity

    Control Of Heme Synthesis And Its Relation To Diseases

    Funder
    National Health and Medical Research Council
    Funding Amount
    $189,942.00
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    Funded Activity

    Fatty Acid Biosynthesis In The Malaria Chloroplast As A Drug Target

    Funder
    National Health and Medical Research Council
    Funding Amount
    $131,035.00
    Summary
    Malarial parasites contain a chloroplast similar to that of plants. We recently found genetic evidence suggesting the malaria chloroplast makes fats in the same way as plant chloroplasts. Additionally, we have found that drugs and herbicides that block plant chloroplast fat production stop growth of malaria cultures. Parasitologists had assumed that malaria was unable to make fats and would scavenge them from its human host so we have probably discovered a new metabolic pathway in these parasite .... Malarial parasites contain a chloroplast similar to that of plants. We recently found genetic evidence suggesting the malaria chloroplast makes fats in the same way as plant chloroplasts. Additionally, we have found that drugs and herbicides that block plant chloroplast fat production stop growth of malaria cultures. Parasitologists had assumed that malaria was unable to make fats and would scavenge them from its human host so we have probably discovered a new metabolic pathway in these parasites. We now propose to prove that the drugs work by blocking essential, chloroplast-based fat production in parasites. This could lead to novel treatment of malaria and related parasites.
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    Funded Activity

    Bridging The Gap Between Cartilage Biology And Osteoarthritis Risk Prediction

    Funder
    National Health and Medical Research Council
    Funding Amount
    $512,256.00
    Summary
    Osteoarthritis is a painful and debilitating cartilage disease affecting just under 1 in 10 Australians and costs the Australian economy roughly $12 billion per year. This project will develop computational models of cartilage with the ability to incorporate genetic and environmental risk factors into a predictive model of cartilage disease.
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    Funded Activity

    Analysis Of Bacterial Surface Filaments Important In Infection And Immunity

    Funder
    National Health and Medical Research Council
    Funding Amount
    $161,371.00
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    Funded Activity

    Coenzyme A Synthesis In The Human Malaria Parasite, Plasmodium Falciparum

    Funder
    National Health and Medical Research Council
    Funding Amount
    $428,250.00
    Summary
    Malaria is responsible for hundreds of millions of cases and an estimated 1.5-2.7 million deaths each year. The disease is caused by a microscopic parasite which is becoming increasingly resistant to antimalarial drugs. There is a very real possibility that there will soon be parts of the world in which malaria is an untreatable disease, and there is an urgent need to identify new drug targets. This work focuses on a particular biochemical pathway in the human malaria parasite, Plasmodium falcip .... Malaria is responsible for hundreds of millions of cases and an estimated 1.5-2.7 million deaths each year. The disease is caused by a microscopic parasite which is becoming increasingly resistant to antimalarial drugs. There is a very real possibility that there will soon be parts of the world in which malaria is an untreatable disease, and there is an urgent need to identify new drug targets. This work focuses on a particular biochemical pathway in the human malaria parasite, Plasmodium falciparum. The pathway mediates the conversion of the nutrient, vitamin B5, into a molecule called Coenzyme A. It plays an essential role in the intraerythrocytic parasite and our preliminary data indicate that components of this pathway hold significant potential as antimalarial drug targets. In this project we will use a range of biochemical and molecular biology approaches to characterise in detail the components of this pathway in the parasite and to explore the possibility that compounds that inhibit this pathway may be of value as much-needed new antimalarial agents.
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    Funded Activity

    Targeting Immunopathology In Chronic Diseases

    Funder
    National Health and Medical Research Council
    Funding Amount
    $431,000.00
    Summary
    I have discovered particular factors produced by our white blood cells have the ability to shut down or boost protein production in the gut, pancreas and lung. My vision is to harness these to devise new strategies for treatments for infectious and non-infectious diseases (inflammatory bowel disease, diabetes) that have a high burden on our healthcare system.
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