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Research Topic : MOUSE MODEL
Australian State/Territory : VIC
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  • Funded Activity

    A Novel Pathway For Drug-seeking

    Funder
    National Health and Medical Research Council
    Funding Amount
    $527,886.00
    Summary
    Substance abuse is a significant social and economic burden upon Australian societies and on societies around the world. Treatment remains problematic due to the multi-layer nature of the disease, difficulties with treatment compliance and less than ideal treatment regimes. The present study aims to improve treatments for alcohol and drug abuse using pre-clinical models to identify and characterize a new brain system implicated in drug-seeking.
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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

    Development Of Therapeutically Useful Human Artificial Chromosomes For Gene Delivery And Optimal Gene Expression

    Funder
    National Health and Medical Research Council
    Funding Amount
    $496,986.00
    Summary
    Gene therapy is an exciting new form of treatment for genetic disorders aimed at providing long-term correction of the problems at source - namely the affected gene. The biggest technical hurdle facing gene therapy is to be able to deliver the therapeutic genes efficiently and safely into patient cells. Many gene therapy protocols are currently being trialled clinically. These protocols, based mostly on the use of attenuated viruses to deliver the genes, carry potential risks to the patients in .... Gene therapy is an exciting new form of treatment for genetic disorders aimed at providing long-term correction of the problems at source - namely the affected gene. The biggest technical hurdle facing gene therapy is to be able to deliver the therapeutic genes efficiently and safely into patient cells. Many gene therapy protocols are currently being trialled clinically. These protocols, based mostly on the use of attenuated viruses to deliver the genes, carry potential risks to the patients in terms of infection, immune response, and germline modification. We have developed the first stage of a new technology for gene delivery that does not require the use of viruses. This technology is based on the generation of human artificial chromosomes, which are smaller versions of the naturally occurring chromosomes that carry all the genes inside our cells. Safety in these artificial chromosomes comes from the use of entirely human materials for their engineering. These artificial chromosomes also have other advantages over the viral approaches, including allowing large genes to be carried, and providing a permanent cure in a single treatment. We have already successfully constructed, published, and patented a number of first-generation human artificial chromosomes. The current project aims to complete the next proof-of-concept milestone towards the further development of this technology. Specifically, we propose to demonstrate the ability of the artificial chromosomes to carry genes and provide sustainable expression of these genes in cells and in animal models. Success in this study will allow the technology to proceed rapidly into commercialisation and clinical trial as a new improved tool for gene delivery and gene therapy.
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    Funded Activity

    Salt, Opiates And Addiction

    Funder
    National Health and Medical Research Council
    Funding Amount
    $565,152.00
    Summary
    Salt (sodium) is an essential electrolyte. Our convincing and complementary findings provide compelling evidence for a link between evolutionarily ancient “instincts” and substance abuse. This proposal is translational, including studies in opiate dependent humans. Our studies will establish how and where in the brain endogenous opioids are implicated in the gratification of salt appetite, how salt appetite is altered in opiate dependency and if salt appetite recovers following opiate withdrawal
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    Funded Activity

    Roles Of The EMT Transcription Factors In Epigenetic Remodelling And Myeloid Cell Transformation.

    Funder
    National Health and Medical Research Council
    Funding Amount
    $809,520.00
    Summary
    This project is based upon our novel discoveries that identified ZEB2 and SNAI1 as novel genes involved in the development of aggressive forms of blood cancer. During the course of this proposal we will find new drug targets and new drug treatment options using existing drugs that will specifically target cancer initiating cells in order to kill aggressive forms of blood cancers that are currently refractory to treatment.
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    Funded Activity

    Identifying The Pathological Mechanism Of PCDH19-Girls Clustering Epilepsy

    Funder
    National Health and Medical Research Council
    Funding Amount
    $523,988.00
    Summary
    Changes in the PCDH19 gene are a relatively common cause of epilepsy. To better understand the basis of this disorder, we have developed unique mouse models that mimic the genetic changes and symptoms of this condition. We will perform careful analysis of brain development in these models to determine the primary cause of this condition. These experiments will create greater understanding of how changes in PCDH19 cause epilepsy in girls and facilitate the development of new treatments.
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    Funded Activity

    The Role Of TNF Superfamily In Skin Disease

    Funder
    National Health and Medical Research Council
    Funding Amount
    $86,484.00
    Summary
    Inflammatory skin disorders, such as psoriasis and dermatitis, are responsible for a large burden of human disease and affect people across alldemographics. Knockout (KO) of TNF signalling members in mice is known to induce skin inflammation. This project proposes to use these genetic mouse models to investigate how and why disruption of particular TNF superfamily members leads to disease and potentially identify new targets for treatment.
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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

    Engineering MYCN Models Of High-grade Serous Ovarian Cancer (HGSC)

    Funder
    National Health and Medical Research Council
    Funding Amount
    $797,478.00
    Summary
    The most lethal type of ovarian cancer, high-grade serous cancer (HGSC), can be divided into four subtypes based on gene patterns. One subtype involves a set of genes/proteins that, in their specific combination, result in activation of a pathway known as MYCN. As most HGSC start in the fallopian tube, we are using fallopian tube material to make new MYCN HGSC models to observe development in the earliest stages. We hope to generate new tests and treatments for this subtype of ovarian cancer.
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    Funded Activity

    Role Of MACROD2 Loss In DNA Repair, Chromosomal Instability And Development Of Colorectal Cancer: Clinical And Therapeutic Implications

    Funder
    National Health and Medical Research Council
    Funding Amount
    $772,871.00
    Summary
    The MACROD2 gene is deleted in one-third of human bowel cancers. We have discovered that MACROD2 deletion causes defective DNA repair and tumour chromosomal instability. Here, we will use novel laboratory models to show that MACROD2 loss actively promotes bowel cancer development. We will test the clinical implication of MACROD2 loss for predicting tumour therapy response and will investigate the potential of exploiting this deficiency for drug targeting.
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    Showing 1-10 of 19 Funded Activites

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