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Status : Active
Research Topic : Immunochemistry
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Humoural immunology and immunochemistry (2)
Immunology (2)
Animal immunology (1)
Epigenetics (incl. Genome Methylation and Epigenomics) (1)
Epigenetics (incl. genome methylation and epigenomics) (1)
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  • Active Funded Activity

    Discovery Projects - Grant ID: DP240100714

    Funder
    Australian Research Council
    Funding Amount
    $500,495.00
    Summary
    Development of an immunology toolbox to combat emerging marsupial diseases. Disease is increasingly a driver of wildlife population declines in Australia. However, basic immunology tools for >99% of vertebrate species are scarce, limiting our ability to prevent and respond to emerging and endemic diseases, such as devil facial tumour disease and wobbly possum disease. The overarching goal of this project is to improve wildlife health and fill the marsupial immunology gap by developing a long-ove .... Development of an immunology toolbox to combat emerging marsupial diseases. Disease is increasingly a driver of wildlife population declines in Australia. However, basic immunology tools for >99% of vertebrate species are scarce, limiting our ability to prevent and respond to emerging and endemic diseases, such as devil facial tumour disease and wobbly possum disease. The overarching goal of this project is to improve wildlife health and fill the marsupial immunology gap by developing a long-overdue multispecies marsupial immunology toolbox. The toolbox is needed to accelerate devil facial tumour disease vaccine progress and conservation immunology research. It will expand our knowledge of wobbly possum disease virus that is increasingly reported in Tasmania and the risk posed by the virus to other possum species.
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    Active Funded Activity

    Discovery Projects - Grant ID: DP230102695

    Funder
    Australian Research Council
    Funding Amount
    $533,967.00
    Summary
    Histone H3.3-dependent transcriptional control and B cell differentiation. This project aims to investigate the fundamental way cells assemble transcriptional machinery to turn on genes and retain transcriptional memory. This project expects to generate new knowledge in the areas of both chromatin biology and immunology, using interdisciplinary approaches. Expected outcomes of this project include an enhanced capacity, through institutional and international collaborations, to determine whether .... Histone H3.3-dependent transcriptional control and B cell differentiation. This project aims to investigate the fundamental way cells assemble transcriptional machinery to turn on genes and retain transcriptional memory. This project expects to generate new knowledge in the areas of both chromatin biology and immunology, using interdisciplinary approaches. Expected outcomes of this project include an enhanced capacity, through institutional and international collaborations, to determine whether the rapid transcription and function characteristic of immune memory in response to stimuli is due to histone H3 variant and its associated nuclear bodies. This should provide significant benefits, such as understanding epigenetic mechanisms that underlie transcription initiation and maintenance across many species.
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    Active Funded Activity

    Discovery Projects - Grant ID: DP220102867

    Funder
    Australian Research Council
    Funding Amount
    $609,847.00
    Summary
    Epigenetic regulation of immune memory. Immune memory cells emerge from the dynamic and transient immune response to deliver two critical abilities: to produce rapid recall responses upon reinfection but also to persist for decades. This project aims to define how the polycomb repressive complexes regulate immune cell fate, by utilising cutting-edge cell and chromatin biology techniques coupled with bioinformatic pipelines. Expected outcomes of the proposed research include key insights into epi .... Epigenetic regulation of immune memory. Immune memory cells emerge from the dynamic and transient immune response to deliver two critical abilities: to produce rapid recall responses upon reinfection but also to persist for decades. This project aims to define how the polycomb repressive complexes regulate immune cell fate, by utilising cutting-edge cell and chromatin biology techniques coupled with bioinformatic pipelines. Expected outcomes of the proposed research include key insights into epigenetic programming required for immune cell differentiation and longevity. This should provide significant benefits such as knowledge creation that may lead to development of technology that reprograms cell behaviour, and contribution to Australian research recognition and capacity.
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