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Research Topic : comparative genetics
Scheme : Project Grants
Australian State/Territory : NSW
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  • Funded Activity

    An International Whole Genome Study To Definitively Map Heritable Risk In Sarcomas

    Funder
    National Health and Medical Research Council
    Funding Amount
    $836,550.00
    Summary
    We want to understand why some people get sarcomas, and others do not. This is likely due to genetic causes, because these cancers affect the young. We now have the tools to address this question, and have created the largest and best characterised study of sarcoma families in the world upon which to apply these tools. This project will create an enduring foundation for research into the genetic basis of sarcomas for the next 20 years.
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    Funded Activity

    Circulating Tumour DNA To Monitor Treatment Response And Resistance In Chronic Lymphocytic Leukaemia

    Funder
    National Health and Medical Research Council
    Funding Amount
    $876,950.00
    Summary
    Many cancers shed small amounts of DNA (ctDNA) into the patient’s bloodstream and recent advances in genomic technologies now allow levels of ctDNA to be accurately measured in the blood. Changes in ctDNA levels have potential to be used as specific markers of disease progression and/or response to cancer therapy. This project will evaluate if ctDNA can be used to monitor treatment responses and individualise treatment decisions in patients with chronic lymphocytic leukaemia.
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    Funded Activity

    The Older Australian Twins Study (OATS) Of Healthy Brain Ageing And Age-related Neurocognitive Disorders

    Funder
    National Health and Medical Research Council
    Funding Amount
    $940,960.00
    Summary
    Ageing is associated with cognitive decline and dementia. It is still not completely understood what relative contributions genes and environment play in these. This project is an extension of the Older Australian Twins Study to examine genetic and environmental factors associated with late life brain changes and dementia, and will establish an internationally significant cohort for novel discovery.
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    Funded Activity

    A CTCF Code For The 3D Cancer Genome Architecture

    Funder
    National Health and Medical Research Council
    Funding Amount
    $905,697.00
    Summary
    CTCF is a unique architectural protein that regulates the three-dimensional (3D) folding of the genome to switch our genes on, or off. This is important, as it affects how DNA is arranged inside the cells, which is turn assures correct gene expression patterns. Here, we will define the role of CTCF in organizing the 3D genome architecture and identify genetic and epigenetic states that control its function.
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    Funded Activity

    Horizontal And Vertical Transmission Mechanisms Of Staphylococcus Aureus Multiresistance Plasmids

    Funder
    National Health and Medical Research Council
    Funding Amount
    $408,993.00
    Summary
    Strains of Golden Staph bacteria resistant to many antibiotics are a major cause of serious hospital-acquired, and increasingly community-acquired, infections. The bacteria have mechanisms that cause efficient transmission of resistance genes to their offspring as well as to other strains. This project aims to elucidate key features of these mechanisms so that treatments can be devised that disrupt the maintenance and transfer of resistance, so as to prolong the effectiveness of antibiotics.
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    Funded Activity

    The Final Common Channel: Measurement Of Nerve Excitability In Epilepsy.

    Funder
    National Health and Medical Research Council
    Funding Amount
    $301,376.00
    Summary
    Epilepsy may be due to either one single genetic mutation or a combination of several gene-environment interactions, affecting how ion channels function. It is not possible to directly interrogate channels in the living human brain but, because similar channels are found in peripheral nerve, much may be learned about aberrant channel function from peripheral nerve. This project aims to measure peripheral nerve excitability in epilepsy patients, using it as a marker of the final common pathway of .... Epilepsy may be due to either one single genetic mutation or a combination of several gene-environment interactions, affecting how ion channels function. It is not possible to directly interrogate channels in the living human brain but, because similar channels are found in peripheral nerve, much may be learned about aberrant channel function from peripheral nerve. This project aims to measure peripheral nerve excitability in epilepsy patients, using it as a marker of the final common pathway of channel dysfunction.
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