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Research Topic : ENDOTHELIAL CELLS
Field of Research : Cell Development, Proliferation and Death
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Cell Development, Proliferation and Death (27)
Regenerative Medicine (incl. Stem Cells and Tissue Engineering) (3)
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  • Researchers (31)
  • Funded Activities (27)
  • Organisations (42)
  • Funded Activity

    Defining The Molecular Events That Initiate The Genesis Of Lymphatic Vessels.

    Funder
    National Health and Medical Research Council
    Funding Amount
    $555,325.00
    Summary
    Lymphatic vessels are a vital component of the cardiovascular system. Abnormalities in the growth and development of lymphatic vessels are associated with human disorders including lymphoedema, cancer and inflammatory diseases. The focus of this application is to determine the molecular events that initiate the construction of lymphatic vessels, with the aim of identifying targets to which novel therapeutics for the treatment of lymphatic vascular diseases could be generated.
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    Funded Activity

    Defining The Role Of VEGF And Vascular Formation In Craniofacial Development

    Funder
    National Health and Medical Research Council
    Funding Amount
    $636,417.00
    Summary
    Aberrant neural crest cell development gives rise to common congenital malformations such as cleft lip and/or palate and cardiac outflow tract defects that effect over 1% of all births. As the aetiology of these disorders are largely unknown it is critical to understand the cell and molecular mechanisms coordinating NCC development such that alternative therapies may be devised to target the underlying pathological defects and to provide definitive diagnostic / prognostic tools.
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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

    Expansion Of TGF-beta-Smad Signaling Network And Intrinsic Epithelial-mesenchymal-endothelial Transition

    Funder
    National Health and Medical Research Council
    Funding Amount
    $557,297.00
    Summary
    The majority of tumor death occurs due to tumor metastasis. Both tumor growth and tumor spread require angiogenesis, which is thought to be driven by tumor but originated from host endothelial cells. Could tumor cells behave and function like endothelial cells? This application aims to detect the transition of adult epithelial cells to endothelial cells through a transient mesenchymal state. Our studies should reveal both the molecular and cellular causes of vasculogenic mimicry, thus establishi .... The majority of tumor death occurs due to tumor metastasis. Both tumor growth and tumor spread require angiogenesis, which is thought to be driven by tumor but originated from host endothelial cells. Could tumor cells behave and function like endothelial cells? This application aims to detect the transition of adult epithelial cells to endothelial cells through a transient mesenchymal state. Our studies should reveal both the molecular and cellular causes of vasculogenic mimicry, thus establishing a new paradigm in understanding tumor growth and metastasis. Such novel molecular understanding will open up new anti-tumor therapeutic opportunities.
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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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    Showing 1-10 of 27 Funded Activites

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