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Field of Research : Cell Development, Proliferation and Death
Research Topic : TRANSFECTED CELLS
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Cell Development, Proliferation and Death (25)
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  • Researchers (31)
  • Funded Activities (25)
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  • Funded Activity

    Molecular Regulation Of Human Haematopoietic Stem Cell Development.

    Funder
    National Health and Medical Research Council
    Funding Amount
    $168,425.00
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    Funded Activity

    Promoting Intestinal Stem-cell Mediated Regeneration Following Damage: A Critical Role For Neuregulin 1

    Funder
    National Health and Medical Research Council
    Funding Amount
    $648,447.00
    Summary
    Diseases, infections and pathologies are common clinical problems of the intestine in humans that can lead to loss of intestinal tissue. Individuals with these conditions can experience nutritional problems and severe cases result in death. Promoting regeneration of the damaged tissue is critical to re-establish intestinal function. In this study, we will examine the regenerative potential of a growth factor called Neuregulin1 in the intestine with the aim of facilitating tissue regeneration.
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    Funded Activity

    The Role Of Raptor And Rictor Signalling Pathways In Osteogenesis And Mesenchymal Stem Cell Fate Determination

    Funder
    National Health and Medical Research Council
    Funding Amount
    $562,742.00
    Summary
    Skeletal diseases associated with excessive bone loss and skeletal fragility, such as osteoporosis, affect 2.2 million Australians and cost our health system approximately $7.4 billion per annum. Studies from our laboratory suggest a critical role for the mTOR signalling pathway in bone development. Using transgenic animals and state-of-the-art techniques, we will investigate the role of mTOR in pre- and post-natal skeletal development. Results from these studies may provide novel approaches to .... Skeletal diseases associated with excessive bone loss and skeletal fragility, such as osteoporosis, affect 2.2 million Australians and cost our health system approximately $7.4 billion per annum. Studies from our laboratory suggest a critical role for the mTOR signalling pathway in bone development. Using transgenic animals and state-of-the-art techniques, we will investigate the role of mTOR in pre- and post-natal skeletal development. Results from these studies may provide novel approaches to treat age-related bone loss syndromes.
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    Funded Activity

    De-differentiation Of Committed Cells Into Haematopoietic Stem Cells By The Instructive Role Of The Transcription Factor HOXB4

    Funder
    National Health and Medical Research Council
    Funding Amount
    $683,040.00
    Summary
    Blood stem cells are long-lived and can give rise to every cell type of the blood system and due to these properties they are currently used in the clinics. Despite their importance, our knowledge of the mechanisms the control the multiplication of these rare cells is very scarce. This proposal aims to identify key factors that have the potential to convert mature, easy available blood cells into stem cells. This knowledge has to potential to lead to novel system that allow the expansion of stem .... Blood stem cells are long-lived and can give rise to every cell type of the blood system and due to these properties they are currently used in the clinics. Despite their importance, our knowledge of the mechanisms the control the multiplication of these rare cells is very scarce. This proposal aims to identify key factors that have the potential to convert mature, easy available blood cells into stem cells. This knowledge has to potential to lead to novel system that allow the expansion of stem cells for transplantations in the future.
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    Funded Activity

    Genetic Regulation Of Cellular Repair Responses In A Mouse Model Of Central Nervous System Demyelination

    Funder
    National Health and Medical Research Council
    Funding Amount
    $385,383.00
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    Funded Activity

    Investigating The Formation And Utility Of The Prenatal Platelet Forming System

    Funder
    National Health and Medical Research Council
    Funding Amount
    $793,442.00
    Summary
    A major challenge to regenerative medicine is discovering how to produce useful cell types in the laboratory. Particularly urgent is the need to generate large numbers of platelets, the building blocks of the clotting system, for clinical use. Current laboratory methods are woefully inefficient, thus cannot meet demand. This project aims to discover how platelets are made in nature. With this information we will be able to devise better platelet production strategies in the laboratory.
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    Funded Activity

    A Stem Cell-specific MicroRNA-independent Function Of Drosha

    Funder
    National Health and Medical Research Council
    Funding Amount
    $637,702.00
    Summary
    Stem cells are responsible for producing and replenishing the ~200 specialised cell types in our body. Our goal is to understand the molecular switches that control the function of these cells. We recently discovered that the activity of certain genes within stem cells is controlled by degradation. This degradation is absolutely crucial for safeguarding the function of stem cells. This project will investigate how this novel mechanism is controlled within these cells.
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    Funded Activity

    The Regulation Of Pluripotency And Self-renewal In Embryonic And Germline Stem Cells.

    Funder
    National Health and Medical Research Council
    Funding Amount
    $491,767.00
    Summary
    Regulation of self-renewal and developmental potential in embryonic and germline stem cells. The capacity of some stem cells to self-renew and under specific conditions, give rise to all adult cell types, a property known as pluripotency , is the key to unlocking the potential of cell based therapies. The development of stem cell based therapies promises to revolutionize the treatment of many common human diseases. For instance, in neurodegenerative conditions such as Parkinsons disease, normal .... Regulation of self-renewal and developmental potential in embryonic and germline stem cells. The capacity of some stem cells to self-renew and under specific conditions, give rise to all adult cell types, a property known as pluripotency , is the key to unlocking the potential of cell based therapies. The development of stem cell based therapies promises to revolutionize the treatment of many common human diseases. For instance, in neurodegenerative conditions such as Parkinsons disease, normal embryonic stem cells grown in culture could be used to replace the lost or disabled neurons in the patient. Many other conditions including diabetes, cystic fibrosis, myocardial infarction (heart attack) and stroke could potentially be treated with stem cell based therapies. Understanding the molecular regulators that govern establishment and maintenance in culture of stem cell lines derived from embryos and from germ cells is the primary goal of this study. We will use well-established techniques to genetically manipulate mouse embryonic stem cells and embryos to examine the role of a specific gene, NANOG. Named after the Celtic legend of Tir NaNog (land of the ever young). When NANOG was forced to remain active, embryonic stem cells were able to grow in media deficient in factors usually required for self-renewal and did not lose their pluripotency even when treated with chemical agents that usually induce differentiation. Understanding the full capacity of NANOG to influence stem cell self-renewal and elucidation of the underlying molecular pathways regulated by this gene will provide valuable insights into the establishment and manipulation of stem cell lines from embryonic and adult tissues.
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    Funded Activity

    Understanding The Ancestry Of De Novo Blood Formation In The Early Embryo

    Funder
    National Health and Medical Research Council
    Funding Amount
    $484,666.00
    Summary
    Current laboratory methods rely on a hit-or-miss approach for the production of such cells, making the prospect of producing patient-specific cells an inefficient/financially prohibitive process. This project aims to generate new knowledge into when and how fate of early blood cells in selected in nature. With this information we will be able to devise effective blood progenitor cell production strategies in the laboratory.
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    Funded Activity

    DECIPHERING THE ROLE OF FOXP1 IN MAMMARY STEM CELLS AND DEVELOPMENT

    Funder
    National Health and Medical Research Council
    Funding Amount
    $569,109.00
    Summary
    Breast (mammary) epithelial cells undergo major changes across developmental stages, including puberty, pregnancy and lactation. This project will focus on the role of the molecular regulator, Foxp1, and how it influences normal mammary maturation. This work will inform whether Foxp1 is critical for controlling the activation of dormant stem cells and if this pathway can contribute to breast cancer formation when disrupted.
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    Showing 1-10 of 25 Funded Activites

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