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Australian State/Territory : QLD
Field of Research : Genetics
Research Topic : Protein interactions
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Genetics (7)
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  • Researchers (19)
  • Funded Activities (7)
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  • Funded Activity

    Discovery Early Career Researcher Award - Grant ID: DE120102954

    Funder
    Australian Research Council
    Funding Amount
    $375,000.00
    Summary
    Identifying and understanding the genetic regulators of cardiac development. The project aims to discover new genes involved in cardiac development so we can understand how to build a heart. Armed with this information, we can devise strategies for the repair of congenital and acquired heart disease.
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    Funded Activity

    ARC Future Fellowships - Grant ID: FT110100496

    Funder
    Australian Research Council
    Funding Amount
    $673,528.00
    Summary
    Genetic dissection of cardiac morphogenesis. The human heart is critical for survival and yet, despite its importance, we still lack a basic understanding of how it forms. This project aims to discover new genes involved in cardiac development so we can understand how to build a heart. Armed with this information, this research will assist in devising strategies for the repair of congenital and acquired heart disease.
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    Funded Activity

    ARC Centres Of Excellence - Grant ID: CE0348239

    Funder
    Australian Research Council
    Funding Amount
    $15,878,900.00
    Summary
    ARC Centre of Excellence in Biotechnology and Development. The Centre will create a multidisciplinary research team focusing on the molecular mechanisms that drive the specification and differentiation of male germ cells. This research will improve our fundamental understanding of how complex regulatory networks control the expression of a complex phenotype, the spermatozoon. It will also create a platform of knowledge from which we can stimulate the growth of the Australian Biotechnology indust .... ARC Centre of Excellence in Biotechnology and Development. The Centre will create a multidisciplinary research team focusing on the molecular mechanisms that drive the specification and differentiation of male germ cells. This research will improve our fundamental understanding of how complex regulatory networks control the expression of a complex phenotype, the spermatozoon. It will also create a platform of knowledge from which we can stimulate the growth of the Australian Biotechnology industry, the protection of the Australian Environment and the well-being of the Australian people. Key issues for this Centre include testicular cancer, male infertility, contraception, pest animal control, environmental impacts on human health and gene pharming.
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    Funded Activity

    Discovery Projects - Grant ID: DP0985025

    Funder
    Australian Research Council
    Funding Amount
    $360,000.00
    Summary
    The MYB gene as a model for global transcriptional regulation: stopping, starting and looping. This project will study how transcriptional elongation controls the MYB gene, a key regulator of normal and cancerous growth and regulation. There are three major benefits that are likely to flow from the proposed research It will strengthen research in new and important areas of transcriptional regulation, by building research capacity in Australia in the area of gene expression, particularly with res .... The MYB gene as a model for global transcriptional regulation: stopping, starting and looping. This project will study how transcriptional elongation controls the MYB gene, a key regulator of normal and cancerous growth and regulation. There are three major benefits that are likely to flow from the proposed research It will strengthen research in new and important areas of transcriptional regulation, by building research capacity in Australia in the area of gene expression, particularly with respect to transcriptional elongation and long-range regulation. It will highlight a new approach to the therapeutic targeting of MYB in cancer: data generated from this research may enable us to target MYB expression in a range of cancers including breast cancer by inhibiting transcriptional elongation. And it will provide training in advanced molecular biology to postdoctoral scientists and students.
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    Funded Activity

    Discovery Projects - Grant ID: DP140100485

    Funder
    Australian Research Council
    Funding Amount
    $405,000.00
    Summary
    Deciphering the cellular functions of caveolae that govern lymphatic vascular development. Lymphatic vessels play crucial roles in tissue fluid homeostasis, immunity, and fatty acid transport. Despite our recent understanding of genetic pathways that modulate lymphatic cell fate specification, how cellular changes mediate morphogenesis of the lymphatic tree remains to be elucidated. This study will combine cell biology and developmental genetics approaches using mouse and zebrafish transgenic li .... Deciphering the cellular functions of caveolae that govern lymphatic vascular development. Lymphatic vessels play crucial roles in tissue fluid homeostasis, immunity, and fatty acid transport. Despite our recent understanding of genetic pathways that modulate lymphatic cell fate specification, how cellular changes mediate morphogenesis of the lymphatic tree remains to be elucidated. This study will combine cell biology and developmental genetics approaches using mouse and zebrafish transgenic lines that label lymphatic endothelial cells to investigate the role of caveolae proteins in the construction of the lymphatic vascular network. This project aims to improve our fundamental understanding of the processes that govern vascular system assembly and will broaden basic knowledge of organ morphogenesis.
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    Funded Activity

    Discovery Projects - Grant ID: DP0346724

    Funder
    Australian Research Council
    Funding Amount
    $225,000.00
    Summary
    Co-ordinated Action of ATM and DNA-PK in DNA damage recognition. The aim of this project is to investigate the mechanism of repair of double straind breaks in DNA sustained after radiation damage. Specifically we will focus on two proteins ATM (mutated in the genetic disorder ataxia-telangiectasia) and DNA-PK mutated in scid mice. There two proteins recognize double straind breaks in DNA and signal this damage to the DNA repair machinery of the cell and to cell cycle checkpoints. The emphasis .... Co-ordinated Action of ATM and DNA-PK in DNA damage recognition. The aim of this project is to investigate the mechanism of repair of double straind breaks in DNA sustained after radiation damage. Specifically we will focus on two proteins ATM (mutated in the genetic disorder ataxia-telangiectasia) and DNA-PK mutated in scid mice. There two proteins recognize double straind breaks in DNA and signal this damage to the DNA repair machinery of the cell and to cell cycle checkpoints. The emphasis here will be in the relationship between the two proteins in co-ordinating the repair of breaks in DNA. This information will be important in understanding mechanisms for maintaining the integrity of the genome.
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    Funded Activity

    Discovery Projects - Grant ID: DP0558901

    Funder
    Australian Research Council
    Funding Amount
    $370,000.00
    Summary
    The making of a sea shell: function and evolution of genes encoding calcareous architectures of phenomenal strength, purity and beauty. The mollusc shell is composed of microscopic layers of tabular calcium carbonate crystals and thin sheets of proteins with precise nanoscale architectures. This configuration produces a high-performance composite material that exceeds the present capabilities of human engineering. This integrated study will elucidate the molecular mechanisms controlling the fab .... The making of a sea shell: function and evolution of genes encoding calcareous architectures of phenomenal strength, purity and beauty. The mollusc shell is composed of microscopic layers of tabular calcium carbonate crystals and thin sheets of proteins with precise nanoscale architectures. This configuration produces a high-performance composite material that exceeds the present capabilities of human engineering. This integrated study will elucidate the molecular mechanisms controlling the fabrication of these architectures. This knowledge will contribute significantly to the development of materials for advanced electronics and energy transducers, human bone therapeutics and marine?based products such as pearls and cements, through the identification of genes underlying biofabrication networks and the development of in vitro bioproduction systems.
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