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Research Topic : gene array
Australian State/Territory : VIC
Scheme : Project Grants
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  • Funded Activity

    Integrating Immunity And Genetics In Follicular Lymphoma To Establish A Prognostic Score Fit For The Modern Era

    Funder
    National Health and Medical Research Council
    Funding Amount
    $1,377,174.00
    Summary
    Follicular lymphoma (FL) is divided into early and advanced stages. Early stage FL is frequently cured, but there is no way to identify who will be cured and who won't. By contrast advanced stage FL is incurable. Our unique access to well-annotated clinical trial and population based cohorts allows us to perform a detailed biological comparison of early and advanced FL, to gain a deeper understanding of the impediments to eradicating the disease, and to predict outcome to conventional therapy.
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    Funded Activity

    Biomaterials For The Direct Reprograming Of Reactive Astrocytes Into Functional Neurons

    Funder
    National Health and Medical Research Council
    Funding Amount
    $630,500.00
    Summary
    We will employ peptide inspired hydrogel nanoscaffolds that can be injected into a brain lesion as a single injection to provide chemical and physical support for the surrounding cells. We will utilize various modifications to these materials to reprogram inflammatory cells into neurons, whilst also promoting the survival, maintenance and growth of existing neurons to encourage repair.
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    Funded Activity

    High Penetrance Deleterious Mutations In Blinding Glaucoma

    Funder
    National Health and Medical Research Council
    Funding Amount
    $1,345,055.00
    Summary
    This project aims to identify the genes most commonly mutated in individuals with advanced glaucoma. Identification of such genes will lead to improved understanding of glaucoma pathogenesis, a better ability to predict risk, and the identification of drug targets for novel therapies.
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    Funded Activity

    Activin Control Of The Male Germline For Reproductive Health

    Funder
    National Health and Medical Research Council
    Funding Amount
    $915,786.00
    Summary
    The growth factor activin provides key signals in embryonic and infant testes to coordinate development of male germline cells into sperm. This project tests how activin controls genetic stability when the human testis is vulnerable to forming germline cells that become tumours in young men. We will study how activin acts to allow sperm stem cells to multiply and develop in sufficient numbers for adult fertility.
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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

    Elucidating The Cellular Processes That Are Critical For P53 Mediated Tumour Suppression

    Funder
    National Health and Medical Research Council
    Funding Amount
    $1,016,108.00
    Summary
    p53 is a tumour suppressor gene that is mutated in ~50% of human cancers. Mutations in p53 cause development of cancer and render malignant cells resistant to chemotherapy. We have identified genes regulated by p53 that appear critical for its tumour suppressive function. In this project, we will use innovative novel genetic tools to discover the cellular and biochemical functions of these genes. The ultimate goal of our studies is to identify novel targets for anti-cancer therapy.
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    Funded Activity

    Investigating The Anti-tumour Efficacy And On Target Toxicity Of Gene-modified T Cell Therapy In Vivo

    Funder
    National Health and Medical Research Council
    Funding Amount
    $337,614.00
    Summary
    White blood cells from cancer patients can be modified in the laboratory to react against tumours. Although these cells can induce cancer regression when given back to the patient, these cells can often cause associated pathology. In this study we propose to fully investigate the limits of this type of therapy for mediating anti-tumour responses and potential toxicity in mouse models that closely recapitulate the human setting. These studies will lead to a more effective therapy for patients.
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    Funded Activity

    Understanding The Role Of The Essential Regulator WalKR In Staphylococcus Aureus

    Funder
    National Health and Medical Research Council
    Funding Amount
    $555,239.00
    Summary
    Staphylococcus aureus is one of the most common human bacterial pathogens. This project aims to characterise an important global control system in S. aureus, and determine if chemical inhibitors of this control system could be used to treat S. aureus disease in the future.
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    Funded Activity

    Identification Of Factors Critical For Maintenance Of The Epidermal Barrier

    Funder
    National Health and Medical Research Council
    Funding Amount
    $616,950.00
    Summary
    The human skin plays a crucial role in the body’s defence against our hostile environment. The outer most layer of the skin, the epidermis is the key structural component of the skin barrier and is essential for its integrity. We have identified a family of genes that are pivotal for epidermal barrier formation, maintenance and repair. This project examines the mechanisms that underpin the function of this family, and has broad ramifications in a host of dermatological conditions.
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    Funded Activity

    Understanding The Neurobiology Of Autism Spectrum Disorder

    Funder
    National Health and Medical Research Council
    Funding Amount
    $1,630,739.00
    Summary
    Autism Spectrum Disorder (ASD) is a condition that causes difficulties with social interactions and communication, and unusual or intense behaviours. In most cases, the cause is unknown; however, there is evidence that the cause is likely genetic. We are using a new method to discover genes for ASD in families by looking at how features of ASD are inherited. Discovering genes for ASD will aid the development of new therapies and help parents of children with ASD with family planning.
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