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Scheme : NHMRC Project Grants
Research Topic : axon sprouting
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  • Funded Activity

    Does Plasticity In Adult Cortex Induce Growth Of Connec Tions?

    Funder
    National Health and Medical Research Council
    Funding Amount
    $195,269.00
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    Funded Activity

    Cellular And Molecular Mechanisms Of Axonal Sprouting In The CNS

    Funder
    National Health and Medical Research Council
    Funding Amount
    $363,431.00
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    Funded Activity

    Regulation Of The Effects Of Nerve Injury Or Limb Amput Ation On Brain Pathways

    Funder
    National Health and Medical Research Council
    Funding Amount
    $896,887.00
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    Funded Activity

    Molecular And Cellular Mechanisms Of Axon Growth And Guidance In The Vertebrate Nervous System

    Funder
    National Health and Medical Research Council
    Funding Amount
    $467,545.00
    Summary
    There are millions of nerve cells in the vertebrate brain, each forming very precise and specific connections within neural circuits. During development of the embryo most of these cells are wired together. A Telstra technician will use the different colours of telephone cables to correctly connect them. Likewise, the growing processes of nerve cells in the brain use specific markers or labels as cues to establish the correct wiring. The aim of the present project is to characterize the specific .... There are millions of nerve cells in the vertebrate brain, each forming very precise and specific connections within neural circuits. During development of the embryo most of these cells are wired together. A Telstra technician will use the different colours of telephone cables to correctly connect them. Likewise, the growing processes of nerve cells in the brain use specific markers or labels as cues to establish the correct wiring. The aim of the present project is to characterize the specific role of some of these labels on nerve cells during development. This project will provide new fundamental knowledge about how brain cells are wired together during development of the embryo. This knowledge is essential for establishing strategies to enhance repair of brain cells following ischemic, excitotoxic or mechanical injury.
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    Funded Activity

    Molecular And Cellular Mechanisms Of Axon Guidance In The Vertebrate Nervous System

    Funder
    National Health and Medical Research Council
    Funding Amount
    $399,600.00
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    Funded Activity

    Restoration Of The Nigrostriatal Pathway In The Parkinsonian Brain

    Funder
    National Health and Medical Research Council
    Funding Amount
    $299,431.00
    Summary
    Many obstacles exist for cell transplantation in Parkinson's disease; namely poor restoration of the host brain circuitry due to incorrect graft placement. This results in incomplete motor function and unwanted side effects. Through iterative studies we endeavor to restore this circuitry by placing grafts in the appropriate location and promoting their survival and growth-integrations. This will require: optimizing the donor tissue and exposure of the graft to growth stimulating factors.
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    Funded Activity

    Wnt Signaling In Dopaminergic Neuronal Connectivity

    Funder
    National Health and Medical Research Council
    Funding Amount
    $564,721.00
    Summary
    A major obstacle in repairing the injured or diseased brain is inducing axons (nerve cell processes) to make the appropriate connections. This is especially true following cell replacement therapy (CRT) in Parkinson's disease (PD). We will examine the processes inducing axons in the dopamine pathways to grow. We hypothesize that Wnt signaling plays and important role and that therapeutic introduction of Wnt is required to repair the dopamine pathways following CRT in PD.
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    Funded Activity

    Molecular And Cellular Mechanisms Of Axon Guidance In The Vertebrate Nervous System

    Funder
    National Health and Medical Research Council
    Funding Amount
    $330,735.00
    Summary
    There are, at least, two major obstacles that have to be overcome in the design of therapies to assist the repair of injured brain tissue. First, the nerve cells that are damaged have to be encouraged to regrow - typically this regrowth is inhibited in the brain; and second, this regrowth has to be directed so that the correct connections are re-established. This project will begin to unravel some of the mechanisms that nerve cells use to wire up together during development. This information can .... There are, at least, two major obstacles that have to be overcome in the design of therapies to assist the repair of injured brain tissue. First, the nerve cells that are damaged have to be encouraged to regrow - typically this regrowth is inhibited in the brain; and second, this regrowth has to be directed so that the correct connections are re-established. This project will begin to unravel some of the mechanisms that nerve cells use to wire up together during development. This information can be used to assist in trying to modulate and facilitate directed regrowth following injury.
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    Funded Activity

    Changes In Pelvic Autonomic Neurons After Spinal Nerve Injury

    Funder
    National Health and Medical Research Council
    Funding Amount
    $176,734.00
    Summary
    This project is about the effects of spinal injury on autonomic neurons that control the bladder, lower bowel and reproductive organs. One of the consequences of some types of spinal injury is that there are no signals being sent from the spinal cord to the nerve cells outside the cord, and this leads to poor bladder control, impotence, etc. We are mimicking this problem experimentally by damaging the spinal nerves that carry these signals. We have found that after this type of damage the pelvic .... This project is about the effects of spinal injury on autonomic neurons that control the bladder, lower bowel and reproductive organs. One of the consequences of some types of spinal injury is that there are no signals being sent from the spinal cord to the nerve cells outside the cord, and this leads to poor bladder control, impotence, etc. We are mimicking this problem experimentally by damaging the spinal nerves that carry these signals. We have found that after this type of damage the pelvic autonomic neurons make many new connections between each other, and the types of new connections depend on which spinal nerves have been injured. This leads to the question: are these new connections good or bad? ie are they helpful in trying to get organ control back to normal or will they stop the correct connections from the spinal cord from being made in the future? This project addresses these questions by using sophisticated techniques for staining and visualising individual nerve fibres growing out from the spinal cord. We will track how well these fibres grow back and connect with the pelvic autonomic neurons. In particular, we will see whether they make correct connections, and if these connections are influenced by the new fibres that have grown between the autonomic neurons in the interim period. We will also do physiological tests to see if the new connections have the correct function. The ultimate aim of these studies is not only to understand more about regeneration, but to see what determines whether the correct connections have been made - and ideally, to give us insight into how we can make regeneration work more quickly and accurately. We believe that this work is an important adjunct to other studies on spinal injury, which mostly focuses on regaining voluntary motor control (e.g. walking); however loss of bladder, bowel and reproductive function is another important quality of life issue for spinal injury patients.
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    Funded Activity

    The Role Of Cell Adhesion Molecules In Regulation Of Axon Advance

    Funder
    National Health and Medical Research Council
    Funding Amount
    $426,006.00
    Summary
    All cells contain on their surface a class of molecules, cell adhesion molecules, that enable them to adhere to other cells in tissues. Cell adhesion molecules have long been known to be involved in the guidance of axons to their targets during development. However the molecular mechanisms by which these molecules act are largely unknown. We propose to use the powerful genetic tools available in the fruitfly to dissect the mechanisms by which two cell adhesion molecules promote axon growth.
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    Showing 1-10 of 45 Funded Activites

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