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Scheme : Project Grants
Research Topic : complex assembly
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Quantitative Genetics (incl. Disease and Trait Mapping Genetics) (4)
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  • Funded Activity

    Dynamics And Mechanisms Of Immune Complex-mediated Skin Inflammation

    Funder
    National Health and Medical Research Council
    Funding Amount
    $526,467.00
    Summary
    Type III hypersensitivity underlies a number of common autoimmune diseases, including rheumatoid arthritis and lupus erythematosus. These diseases are caused by the deposition of immune complexes (IC) and the accumulation of neutrophils within small blood vessels. We will use real time imaging to dissect in space and time the recruitment of neutrophils and IC deposition during type III hypersensitivity reactions in order to better understand the pathogenesis of these conditions.
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    Funded Activity

    Methods And Software Tool For Complex Trait Analyses Using Multi-omics Data

    Funder
    National Health and Medical Research Council
    Funding Amount
    $573,999.00
    Summary
    This project aims to develop methods to disentangle the contribution of people’s difference in DNA sequence, DNA methylation, and gene expression to their difference in characteristics (including risks to diseases), and to utilise these information to predict disease risks of different people. This project also aims to develop a versatile and efficient computer software to implement the methods being proposed in this project, as well as all other commonly used methods in the research community.
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    Funded Activity

    Understanding The Role Of The Scaffolding Protein D13 In Poxvirus Assembly And Its Inhibition By Rifampicin

    Funder
    National Health and Medical Research Council
    Funding Amount
    $371,275.00
    Summary
    Smallpox is one the most notorious diseases in human history. Despite its eradication in the 1970s, human cases of animal poxviruses such as monkeypox virus and the potential use of smallpox as a bioterrorism weapon have called for an improved preparedness of Australia against (re)-emerging poxviruses. This project combines structural biology approaches to understand the complex assembly of poxviruses and provide the basis for the development of broad-spectrum antiviral drugs.
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    Funded Activity

    Identification Of Host Restriction Factors That Block Respiratory Virus Infection

    Funder
    National Health and Medical Research Council
    Funding Amount
    $956,898.00
    Summary
    Following inhalation, respiratory viruses can infect and grow in airway epithelial cells. Although immune cells such as macrophages are also susceptible to infection, this is generally abortive and new viruses are not released. This project will identify proteins induced in macrophages that block respiratory viruses and prevent their spread in the airways. We will also define mechanisms by which some virulent strains overcome this block to grow in macrophages.
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    Funded Activity

    Structure And Function Of FcR IgG Interactions

    Funder
    National Health and Medical Research Council
    Funding Amount
    $988,953.00
    Summary
    This research will redefine our understanding of how antibodies normally protect us and can be used to generate new treatments for disease.
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    Funded Activity

    Structure And Function Of Human Fc Receptors

    Funder
    National Health and Medical Research Council
    Funding Amount
    $695,523.00
    Summary
    We have discovered how a rare type of human antibody called IgG4 exerts a major regulatory influence on the body's immune system. We have discovered how IgG4 can "switch" off inflammatory white blood cells which has broad implications for the development of new forms of therapy for switching off allergies and autoimmune diseases and for switching on immunity to infections and cancers.
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    Funded Activity

    Identification Of Protein Altering Variants Influencing Preeclampsia Risk

    Funder
    National Health and Medical Research Council
    Funding Amount
    $572,014.00
    Summary
    Preeclampsia is a common and serious pregnancy disorder for which there is currently no early diagnostic test or cure other than delivery. It is also associated with later life cardiovascular disease. The identification of gene mutations for preeclampsia in this study will provide insight into the cause of this disorder that may lead to new treatments and tests to predict those women at risk.
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    Funded Activity

    Identifying Novel Susceptibility Loci For Osteoporosis Through Whole Genome Sequencing

    Funder
    National Health and Medical Research Council
    Funding Amount
    $623,969.00
    Summary
    Our highly successful genome-wide studies of bone mineral density (a risk factor for osteoporosis) have highlighted 60 loci relevant to the disease. However, a substantial amount of genetic variance remains unexplained. This project will focus on less common variants that have larger effect sizes and are relevant to osteoporosis, but are not well studied by approaches such as high-density SNP arrays and genome-wide association studies.
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    Funded Activity

    Structural Studies On The Immune Effector Perforin: Developing Mechanism-based Inhibitors

    Funder
    National Health and Medical Research Council
    Funding Amount
    $1,116,594.00
    Summary
    Perforin is an essential weapon deployed by the human immune cells in order to destroy virally infected or cancerous cells. Despite this key role, unwanted or excessive perforin function can result in disease and can severely impact on successful treatment of leukaemia through bone marrow transplantation. This application aims to understand the molecular details of perforin function, and to apply this knowledge to develop perforin inhibitors.
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    Funded Activity

    Exome Sequencing By NGS To Identify Rare Variants Affecting Type 2 Diabetes

    Funder
    National Health and Medical Research Council
    Funding Amount
    $570,425.00
    Summary
    Rates of type 2 diabetes are rising dramatically, and current efforts are failing to stem its progression. More information about why the disease develops is urgently needed. We apply the latest technological innovations in DNA analysis to accelerate the discovery of the mechanism behind the development of type 2 diabetes. This knowledge will lead to new ways to control diabetes through development of novel therapies.
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    Showing 1-10 of 21 Funded Activites

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