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Research Topic : epithelial defect
Australian State/Territory : VIC
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  • Funded Activity

    The Role Of The Mammalian Grainyhead-like Gene Family In Neural Tube Closure

    Funder
    National Health and Medical Research Council
    Funding Amount
    $569,541.00
    Summary
    Failure of the skin to close over the brain and spinal cord during human development results in the devastating congenital birth defects anencephaly and spina bifida, known collectively as the neural tube defects. These are the second most common congenital birth defects affecting 1:1000 pregnancies. Anencephaly is not compatible with life and affected babies die at birth. In contrast children with spina bifida survive, but suffer from limb paralysis, bowel and bladder dysfunction, learning diff .... Failure of the skin to close over the brain and spinal cord during human development results in the devastating congenital birth defects anencephaly and spina bifida, known collectively as the neural tube defects. These are the second most common congenital birth defects affecting 1:1000 pregnancies. Anencephaly is not compatible with life and affected babies die at birth. In contrast children with spina bifida survive, but suffer from limb paralysis, bowel and bladder dysfunction, learning difficulties and psycho-social disturbances. Our laboratories have identified a family of genes essential for the colsure of the neural tube in mammals. The aim of this proposal is to understand the mechanisms of action with a view to developing new therapeutics that mey be used preventatively in these conditions. We also hope that these studies may facilitate the development of a genetic test to screen couples at risk.
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    Funded Activity

    Identifying The Critical Pathways Which Regulate Vertebrate Craniofacial Development

    Funder
    National Health and Medical Research Council
    Funding Amount
    $552,131.00
    Summary
    Understanding the genes which underlie human birth defects is of immense clinical importance. Our laboratory is a world-leader investigating a gene responsible for facial skeleton development, Grhl2. With our wide range of models, we will discover how Grhl2 works to ensure the face and skull develop properly during birth.
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    Funded Activity

    Sonic Hedgehog Signalling In Barrett S Oesophagus

    Funder
    National Health and Medical Research Council
    Funding Amount
    $570,876.00
    Summary
    Barrett's oesophagus (BO) is a condition that arises in some patients with chronic reflux (heartburn) and increases the risk of developing cancer of the oesophagus. However, the exact mechanisms involved in its development are unknown. This project aims to investigate how a protein called sonic hedgehog might be involved using novel cell culturing techniques that allow us to model the growth of oesophageal tissue in the laboratory. This could lead to development of new therapies for treating BO.
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    Funded Activity

    The Mechanisms Of Epithelial Cell Survival That Govern Thymus Function

    Funder
    National Health and Medical Research Council
    Funding Amount
    $620,967.00
    Summary
    The thymus is an organ dedicated to the production of crucial immune cells, called T lymphocytes. Cancer treatments, such as radiation or chemotherapy, destroy thymic function and impair immune recovery in patients. We aim to uncover molecular processes that govern the life and death decisions of cells in the thymus. Our goal is to then use this information to develop treatments to protect this critical organ from damage and improve immune recovery following radiation or chemotherapy.
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    Funded Activity

    Genetic Programs Orchestrated By AP-1 Transcription Factors In Colorectal Cancer Progression

    Funder
    National Health and Medical Research Council
    Funding Amount
    $599,941.00
    Summary
    Colorectal cancer (CRC) is the third most common cancer worldwide. About half of all patients diagnosed with the disease die as a result of its spread in the body. This project will investigate the role that a specific DNA-binding protein plays in orchestrating gene expression programs required for CRCs to spread. The research will provide new insights into underlying mechanisms of CRC progression as well as identify new therapeutic targets for aggressive forms of the disease.
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    Funded Activity

    Mechanistic Basis Of AP-1-regulated Gene Expression During Colorectal Cancer Progression

    Funder
    National Health and Medical Research Council
    Funding Amount
    $597,802.00
    Summary
    The spread of colorectal cancers in the body poses a major clinical problem for which current treatment options are inadequate. This project aims to unravel how a specific DNA-binding protein regulates the expression of genes involved in the spread of these cancers. The research is expected to provide a better mechanistic understanding of how disease progression occurs and to identify novel strategies to treat aggressive tumours.
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    Funded Activity

    Immune Modulatory Effects Of Vaginal Microbiota Metabolites And HIV Susceptibility

    Funder
    National Health and Medical Research Council
    Funding Amount
    $795,110.00
    Summary
    This study will advance knowledge on how acid molecules produced by beneficial and harmful bacteria are able to promote or impede HIV infection of the female genital mucosa through their effects on the barrier and immune function of cells that line the vagina and cervix. The results of this study are anticipated to augment the efficacy of topical HIV prevention strategies and lead to the development of safe vaginal hygiene products that help protect against other sexually transmitted infections.
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    Funded Activity

    Functions Of FZD7 In The Intestine And Colorectal Cancer

    Funder
    National Health and Medical Research Council
    Funding Amount
    $644,761.00
    Summary
    Wnt proteins are a family of signaling molecules that are critical for the function of normal and cancerous epithelial cells in the gut. However, the cell surface receptor that transmits Wnt signals is not known. Our research strongly implicates one Wnt receptor (FZD7). Here we test this using innovative mouse and cell line models. We wish to understand how Wnt-driven processes are activated. This knowledge will lead to novel avenues to block aberrant activation of Wnt signalling in cancer cells
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    Showing 1-8 of 8 Funded Activites

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