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Research Topic : dna barcoding
Scheme : NHMRC Project Grants
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  • Funded Activity

    Regulation Of The Quality Of DNA Repair By Timing In The Cell Cycle

    Funder
    National Health and Medical Research Council
    Funding Amount
    $468,794.00
    Summary
    During responses to infection or immunisation, antibody-producing _B� cells mutate their antibody genes at extreme rates. Rare mutations which improve the antibodies are selected by competition between B cells favouring those which make the best antibodies: Darwinian evolution on extreme _fast-forward�. We aim to understand this process because it is essential for normal immunity and effective vaccination, and because when it goes wrong, it can cause aggressive human cancers.
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    Funded Activity

    Development Of DNA Targeted Platinum Agents As Potential Anticancer Drugs

    Funder
    National Health and Medical Research Council
    Funding Amount
    $410,250.00
    Summary
    A number of clinically useful anticancer drugs damage DNA. As a result of this damage these drugs kill cancer cells. This project aims to develop new platinum-containing compounds which are specifically targeted to DNA. Through this strategy it is possible that new and more useful anticancer drugs could emerge.
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    Funded Activity

    Relationships Between Processess Responsible For Cell K Illing By Drugs

    Funder
    National Health and Medical Research Council
    Funding Amount
    $129,121.00
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    Funded Activity

    Mosquito Identification By DNA Probes.

    Funder
    National Health and Medical Research Council
    Funding Amount
    $127,085.00
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    Funded Activity

    Genes And DNA In The Polynesians

    Funder
    National Health and Medical Research Council
    Funding Amount
    $118,455.00
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    Funded Activity

    Genetic Changes In A Model Of Virally-induced Human Can Cer

    Funder
    National Health and Medical Research Council
    Funding Amount
    $190,284.00
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    Funded Activity

    Mechanisms Of Macrophage Activation By Immunostimulatory DNA

    Funder
    National Health and Medical Research Council
    Funding Amount
    $230,728.00
    Summary
    This project is based upon the observation that the mammalian immune system can distinguish between its own genetic material (DNA) and the genes of infectious agents such as bacteria. This fact has implications for understanding how the immune system copes with infection, and also for design of new therapies and vaccines. Our central aim is to define exactly how this recognition system works. The cells that respond most vigorously to foreign DNA are large white blood cells called macrophages. We .... This project is based upon the observation that the mammalian immune system can distinguish between its own genetic material (DNA) and the genes of infectious agents such as bacteria. This fact has implications for understanding how the immune system copes with infection, and also for design of new therapies and vaccines. Our central aim is to define exactly how this recognition system works. The cells that respond most vigorously to foreign DNA are large white blood cells called macrophages. We aim to find the macrophage protein which binds to foreign DNA and triggers the activation of the immune system. The type of immune responses initiated by foreign DNA may be useful in treatment of allergies and cancer and for improving vaccinations.
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    Funded Activity

    X Inactivation And X-linked Dominant Disease

    Funder
    National Health and Medical Research Council
    Funding Amount
    $78,477.00
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    Funded Activity

    Cell Division And The Regulation Of Immunoglobulin Switch Recombination At The Molecular Level

    Funder
    National Health and Medical Research Council
    Funding Amount
    $392,545.00
    Summary
    The B lymphocyte is an important cell in the immune response as it generates protective antibody against invading pathogens. The effectiveness of an antibody response partly depends on the type of antibody made (there are eight different types). This attribute alters as the immune response progresses in a poorly understood and highly complex way. However, our recent studies have revealed a simple underlying order that can be dissected using new methods. The key to the underlying simplicity is a .... The B lymphocyte is an important cell in the immune response as it generates protective antibody against invading pathogens. The effectiveness of an antibody response partly depends on the type of antibody made (there are eight different types). This attribute alters as the immune response progresses in a poorly understood and highly complex way. However, our recent studies have revealed a simple underlying order that can be dissected using new methods. The key to the underlying simplicity is a cell division clock used to relate and promote cell changes. Here we intend to apply this new concept and the new methods to dissecting the molecular events associated with linking division to the changing properties of antibody selection. Our aim is to accurately model the process of changing antibody types at both the molecular and whole tissue levels. These studies will give us new insights into how the immune response may be directed to make the most appropriate (effective) response during infection and vaccination.
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    Funded Activity

    Epigenetic Variation In Early Human Development

    Funder
    National Health and Medical Research Council
    Funding Amount
    $519,000.00
    Summary
    One of the interesting questions in human biology is why monozygotic twins, which have an identical genetic make up, can still vary in many complex traits such as height, eye colour and susceptibility to various mental and disease states. It is clear that this variation is not always due simply to environment. We propose in this application to show that, even if the genetic code is identical in monozygotic twins, epigenetic marks such as DNA methylation and histone modifications can vary between .... One of the interesting questions in human biology is why monozygotic twins, which have an identical genetic make up, can still vary in many complex traits such as height, eye colour and susceptibility to various mental and disease states. It is clear that this variation is not always due simply to environment. We propose in this application to show that, even if the genetic code is identical in monozygotic twins, epigenetic marks such as DNA methylation and histone modifications can vary between critical genes giving rise to differences in gene expression patterns. We propose that the variation in the methylation pattern arises after the two embryos have split, at a time when the developing embryo undergoes genome-wide demethylation followed by de novo re-methylation. The importance of this project is NOT what it tells us about twins themselves, but that twins can provide the clue to disease processes which affect everybody in the population. The results of these experiments will determine the extent to which epigenetic changes to the genome that occur early in embryonic development provide an additional source of variation in gene expression that could contribute to phenotypic variation. By using identical twins we eliminate the possibility that epigenetic modifications that we observe are themselves influenced by genotype. Determining these epigenetic differences will provide an insight into the mechanisms underlying complex traits and human disease.
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