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Research Topic : FIBROBLAST
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  • Funded Activity

    Biology And Significance Of The Renal Interstitial Myofibroblast

    Funder
    National Health and Medical Research Council
    Funding Amount
    $142,527.00
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    Funded Activity

    TFN/TNF-LIGAND SUPERFAMILY CYTOKINES & BONE LOSS IN RHEUMATOID ARTHRITIS

    Funder
    National Health and Medical Research Council
    Funding Amount
    $86,108.00
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    Funded Activity

    The Regulation Of Pleiotropic Responses By Bidentate Motifs Embedded In The Fibroblast Growth Factor Receptors

    Funder
    National Health and Medical Research Council
    Funding Amount
    $489,336.00
    Summary
    Cells in our bodies are able to accomplish an impressive array of functions. Diffusible factors (called growth factors) are important in regulating diverse cellular functions. We have identified a new molecular switch inside cells that acts as a master controller of cellular functions. This molecular switch relays information to instruct specific cellular functions. We have shown that these molecular switches are short-circuited in breast cancer promoting cell growth and survival.
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    Funded Activity

    Interactions Between Different Cell Types In The Human Colon

    Funder
    National Health and Medical Research Council
    Funding Amount
    $102,687.00
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    Funded Activity

    The Gastrin-binding Protein: A Common Target For Gastrin And Fibroblast Growth Factor-2 In Colorectal Cancer

    Funder
    National Health and Medical Research Council
    Funding Amount
    $381,791.00
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    Funded Activity

    Therapeutic Targeting Of A New Growth Factor In Mesothelioma

    Funder
    National Health and Medical Research Council
    Funding Amount
    $317,775.00
    Summary
    Malignant mesothelioma is an aggressive and incurable cancer. This study will build on our recent data showing a protein termed FGF-9, not previously linked with mesothelioma, could significantly stimulate mesothelioma growth. This project will examine the biologic activities of FGF-9 and its receptors in mesothelioma, and the therapeutic benefits of antagonizing FGF-9 in mesothelioma in vivo.
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    Funded Activity

    Aberrant Signalling Through Gp130 In The Pathogenesis Of Fibrotic Lung Diseases

    Funder
    National Health and Medical Research Council
    Funding Amount
    $456,500.00
    Summary
    Pulmonary fibrosis is a chronic diffuse interstitial lung disease of unknown cause, characterised pathologically by inflammation and fibrosis of the lung tissue. The prognosis is poor with a 50% mortality at five years after diagnosis and considerable morbidity during those years. Previous investigations have documented the role for inflammation in the development of pulmonary fibrosis and current therapeutic strategies are aimed at suppressing the inflammation. Data generated over the past deca .... Pulmonary fibrosis is a chronic diffuse interstitial lung disease of unknown cause, characterised pathologically by inflammation and fibrosis of the lung tissue. The prognosis is poor with a 50% mortality at five years after diagnosis and considerable morbidity during those years. Previous investigations have documented the role for inflammation in the development of pulmonary fibrosis and current therapeutic strategies are aimed at suppressing the inflammation. Data generated over the past decade also have established the concept that the molecular processes underlying the fibrogenesis component may represent a new opportunity for therapeutic intervention. Attempts to treat fibrosis have for the most part consisted of anti- inflammatory drugs, almost exclusively steroids. The effectiveness of steroids is variable and can be associated with significant side effects. This project will examine the effects of a family of molecules called cytokines that signal through gp130 as critical determinants of disease susceptibility and progression. gp 130 is a shared component in the receptor complexes for IL-6 family cytokines (IL-6, IL-11, LIF, OSM) which are important regulators of both the phenotype and proliferation of fibroblasts in health and in response to injury. Our data raises the possibility of developing pharmacological manipulators of gp130 signalling pathways that would suppress fibrosis but leave normal cellular defense mechanisms necessary for host defense in the lung intact.
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    Funded Activity

    Molecular Dissection Of The Syndromal And Non-syndromal Forms Of Craniosynostosis

    Funder
    National Health and Medical Research Council
    Funding Amount
    $72,047.00
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    Funded Activity

    Identification Of Novel Biomarkers And Risk Factors For Cardiovascular Disease

    Funder
    National Health and Medical Research Council
    Funding Amount
    $425,048.00
    Summary
    Heart disease is the leading cause of death in Australia. In this fellowship, I will investigate different markers in the blood and risk factors that can help to identify people at an increased risk of developing heart disease. The ultimate aim of this project is to identify blood markers or factors that can be used to identify and treat people at the early stages of heart disease, thus reducing the death rate and associated economic burden of the disease.
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    Funded Activity

    Does Enhanced Vitamin D Activity In Bone Heal The Skeleton In Disorders Of FGF23 Excess?

    Funder
    National Health and Medical Research Council
    Funding Amount
    $855,925.00
    Summary
    X-linked hypophosphatemia (XLH) is a genetic disorder which results in phosphate wasting and rickets. This severe disorder has no effective treatment. We have compelling new evidence that the rickets in XLH is not primarily a disorder of low blood phosphate, but rather specific issue of low cellular levels and activity of vitamin D (1,25D) within bone. This proposal is designed to specifically demonstrate this new concept and outline a new paradigm for a new XLH treatment.
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