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Research Topic : tissue microarray
Scheme : ARC Future Fellowships
Australian State/Territory : NSW
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Gene Expression (incl. Microarray and other genome-wide approaches) (6)
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  • Active Funded Activity

    ARC Future Fellowships - Grant ID: FT170100359

    Funder
    Australian Research Council
    Funding Amount
    $921,067.00
    Summary
    How does the noncoding genome regulate gene expression in the human brain? The non-coding genome is recognized as a major player in orchestrating gene expression in higher eukaryotes. This project aims to identify regions of the human genome that are important for gene expression during neuronal differentiation and depolarisation (i.e. neural enhancers), and to investigate their evolutionary properties. The roles of non-coding DNA in regulating the dynamic gene expression patterns underlying com .... How does the noncoding genome regulate gene expression in the human brain? The non-coding genome is recognized as a major player in orchestrating gene expression in higher eukaryotes. This project aims to identify regions of the human genome that are important for gene expression during neuronal differentiation and depolarisation (i.e. neural enhancers), and to investigate their evolutionary properties. The roles of non-coding DNA in regulating the dynamic gene expression patterns underlying complex human brain functions remains to be elucidated. By combining transcriptome quantification and bioinformatics methods, this project will close an important knowledge gap in our understanding of transcriptional regulation underlying human brain function. This will provide benefits such as the potential to influence public health policy including in cognitive functions and aging.
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    Active Funded Activity

    ARC Future Fellowships - Grant ID: FT210100355

    Funder
    Australian Research Council
    Funding Amount
    $925,739.00
    Summary
    Dissecting cell cycle regulation using programmable gene editing technology. This program aims to harness the unprecedented power of CRISPR-Cas13 gene-editing technology to develop high-throughput tools to explore the role of RNA regulation in cell cycle control. This project expects to generate new knowledge about cell division and RNA biology by utilizing this new technology and applying interdisciplinary approaches. Expected outcomes of this proposal include new research tools capable of broa .... Dissecting cell cycle regulation using programmable gene editing technology. This program aims to harness the unprecedented power of CRISPR-Cas13 gene-editing technology to develop high-throughput tools to explore the role of RNA regulation in cell cycle control. This project expects to generate new knowledge about cell division and RNA biology by utilizing this new technology and applying interdisciplinary approaches. Expected outcomes of this proposal include new research tools capable of broadly addressing biological questions across multiple disciplines (e.g. from health to food production). This project intends to provide significant benefits, such as enhanced biological knowledge, multidisciplinary training opportunities and will build Australia’s capability in this rapidly expanding field.
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    Funded Activity

    ARC Future Fellowships - Grant ID: FT110100836

    Funder
    Australian Research Council
    Funding Amount
    $673,728.00
    Summary
    Dissecting endocardial signals required for cardiac muscle regeneration in zebrafish. Unlike humans, zebrafish have an extraordinary ability to regenerate their damaged hearts. This project will study the endocardium, a thin layer of cells lining the inner heart, to find important genes for regeneration. Results from this study may provide insights into proper repair of human hearts after injury.
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    Funded Activity

    ARC Future Fellowships - Grant ID: FT110100254

    Funder
    Australian Research Council
    Funding Amount
    $816,756.00
    Summary
    RNA-based analysis for prediction of islet death in diabetes. Death of insulin-producing cells is a common feature in diabetes. Presently, a blood glucose test remains the only blunt instrument to diagnose diabetes. The RNA-based analysis for prediction of islet death in diabetes (RAPID) study links with eight clinical trials to test this newly developed non-invasive assay for predicting diabetes. Early diagnosis will help to reduce diabetic complications in later life.
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    Funded Activity

    ARC Future Fellowships - Grant ID: FT130100096

    Funder
    Australian Research Council
    Funding Amount
    $705,585.00
    Summary
    Exploring novel coding genomic features through integrative proteogenomics. Knowledge of the full extent to which the human genome is made into proteins is of fundamental importance in the study of health and disease. New technological advances are now enabling functional studies of genomes with increasing detail. This project aims to develop and apply cutting edge bioinformatics methods to perform an integrative and comprehensive exploration of the extent to which the genes of a human cell line .... Exploring novel coding genomic features through integrative proteogenomics. Knowledge of the full extent to which the human genome is made into proteins is of fundamental importance in the study of health and disease. New technological advances are now enabling functional studies of genomes with increasing detail. This project aims to develop and apply cutting edge bioinformatics methods to perform an integrative and comprehensive exploration of the extent to which the genes of a human cell line are made into proteins. The project will improve our understanding of the human genome and deliver cutting edge methodology applicable for genome annotation in all living organisms.
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    Funded Activity

    ARC Future Fellowships - Grant ID: FT120100704

    Funder
    Australian Research Council
    Funding Amount
    $680,658.00
    Summary
    The role of toxin biosynthesis for marine dinoflagellates - an evolutionary ecological approach. Dinoflagellates are a group of microalgae that include coral symbionts and phytoplankton. Many species produce potent toxins that can be a problem in the aquaculture industry. This project will use novel genetic methods to investigate the evolution and ecology of toxin production in a variety of marine dinoflagellates.
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    Showing 1-6 of 6 Funded Activites

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