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Australian State/Territory : VIC
Scheme : Project Grants
Research Topic : nervous system disorders
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  • Funded Activity

    Characterisation Of Eurl, A Novel Gene Implicated In The Etiology Of Abnormal Brain Development And Intellectual Disability

    Funder
    National Health and Medical Research Council
    Funding Amount
    $597,541.00
    Summary
    Intellectual disability affects around one per cent of Australians, and can arise from genetic abnormalities during fetal life, such as through abnormal regulation of gene expression. We have identified a novel gene, known as eurl, which controls brain assembly as well as the ability of neurons to form functional connections within the brain. We will investigate how this novel gene controls brain development, and characterise eurl as a potential therapeutic target for learning and memory.
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    Funded Activity

    Next Generation Cybernetics: Long Term Carbon Fibre Dual Stimulation / Recording Electrode Arrays For Closed Loop Neural Implants

    Funder
    National Health and Medical Research Council
    Funding Amount
    $679,670.00
    Summary
    Electrodes implanted in the brain have enormous potential for treating a range of conditions from epilepsy to control of prosthetics for patients with limb loss. Currently, the electrodes used in such system fail rapidly because they are rejected by the body. We aim to use diamond with ultra-fine carbon fibre electrodes to make arrays that are invisible to the human immune system. Such arrays will function for the lifetime of the patient without needing replacement.
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    Funded Activity

    The Brain As A Therapeutic Target For Heart Failure

    Funder
    National Health and Medical Research Council
    Funding Amount
    $923,432.00
    Summary
    In heart failure there is a large increase in sympathetic nerve activity to the heart that leads to damage to the heart and sudden death. We have shown that lesion of the area postrema, a brain nucleus that senses hormones in the blood, reduces nerve activity to the heart and, importantly, improves cardiac function. We aim to translate these findings into a treatment that can be used clinically, which our findings compellingly indicate should improve cardiac function in heart failure
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    Funded Activity

    Central Neural Regulation Of Brown Fat Function – Glucose Sensing And CNS Pathways

    Funder
    National Health and Medical Research Council
    Funding Amount
    $761,942.00
    Summary
    Our research aims to identify how specific brain cells detect changes in glucose levels and how ageing and diet affect their function. We identified a subset of nerve cells that detect changes in glucose and the “hunger” hormone ghrelin, their ability to do so adapting with age and nutritional status. This project will investigate the potential of these nerve cells as targets for therapeutic and diet- intervention strategies to target obesity, diabetes and promote healthy ageing.
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    Funded Activity

    Targeting The Sympathetic Nervous System To Reduce The Burden Of Fatty Liver Disease

    Funder
    National Health and Medical Research Council
    Funding Amount
    $728,152.00
    Summary
    The metabolic syndrome is characterised by abdominal obesity, high blood pressure and an increased risk of diabetes development. It is clear from our own observations that the sympathetic nervous system (SNS) is important in the generation of obesity-related illness and, through its stimulation of the liver, plays an important role in the development of obesity-related liver disease. We will target the SNS in order to reduce the burden of obesity-related liver disease.
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    Funded Activity

    Defining The Epigenetic Origins Of Maternally Inherited Disease.

    Funder
    National Health and Medical Research Council
    Funding Amount
    $731,162.00
    Summary
    Epigenetic (non genetic) changes to the DNA in sperm and eggs can alter outcomes in children. Despite the potential for drugs and diet to mediate some of these inherited effects, the processes involved are very poorly understood. By determining the mechanisms that regulate epigenetic inheritance, this project will improve our understanding of how epigenetic mechanisms acting in the parent, can mediate inherited disease and life-long health outcomes in our children.
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    Funded Activity

    Pubertal Transitions In Mental Health And Behaviour: The PHASE-A Study Of Social Roleand Lifestyle Transitions

    Funder
    National Health and Medical Research Council
    Funding Amount
    $1,656,785.00
    Summary
    Over the past four decades problems such as depression, anxiety, self-harm and substance abuse have increased in young people. Recent research indicates that puberty is a time when these problems commonly first emerge. This five-year study of 4000 students will examine a question of whether social transitions that are too soon (e.g. early initiation of sex) or problematic (e.g. bullying from peers) may explain the increase in these health problems as children pass through puberty.
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    Funded Activity

    Genetic Etiologies Of Congenital Esotropia

    Funder
    National Health and Medical Research Council
    Funding Amount
    $371,837.00
    Summary
    Strabismus is the pathological misalignment of the eyes associated with loss of binocular vision and is one of the most common human ophthalmological disorders. Patients with comitant strabismus have full eye movements, whereas patients with incomitant strabismus have limited eye movements, which causes the angle of strabismus to vary with gaze direction. This project aims to define genetic contributors to comitant congenital strabismus.
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    Funded Activity

    The Persisting Vascular Effects Of Activation Of The Renin-Angiotensin System

    Funder
    National Health and Medical Research Council
    Funding Amount
    $628,456.00
    Summary
    Heart attacks and strokes are the major cause of death and disability in Australians. Heart disease is widely viewed to be the legacy of our diet and lifestyle, and even that of our parents. We propose to explore in detail the molecular mechanism of how this imprinting comes about and identify new targets to prevent, retard or reverse heart disease.
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    Funded Activity

    The Calcium Channel TRPV4 In Skeletal Development And Arthritis

    Funder
    National Health and Medical Research Council
    Funding Amount
    $683,069.00
    Summary
    We have discovered that mutations in a calcium channel gene, TRPV4, cause an inherited osteoarthritis in the hands and feet. This work suggests that TRPV4 may be important in osteoarthritis and suggests the exciting possibility that modulating TRPV4 activity may provide a new therapeutic approach for arthritis. We will study how and why the mutations disrupt channel function and study mouse models to see if they are more or less susceptible to arthritis.
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    Showing 1-10 of 29 Funded Activites

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