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Research Topic : ION PERMEATION
Australian State/Territory : VIC
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  • Funded Activity

    Neourobiology Of Human Epilepsy: Genes, Cellular Mechanisms,network And Whole Brain

    Funder
    National Health and Medical Research Council
    Funding Amount
    $17,652,824.00
    Summary
    The team is comprised of neurologists, molecular geneticists, physiologists and brain imaging specialists and leads the world in the discovery of the genetic causes of epilepsy. They will continue to identify genes underlying epilepsy and study how genetic variations result in development of seizures. Advanced brain imaging will be used to understand the effects of genetic variation on brain structure and function. This study may lead to new diagnostic methods and treatments for epilepsy.
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    Funded Activity

    Determining Fundamental Mechanisms Compromised In Kir-linked Disease States

    Funder
    National Health and Medical Research Council
    Funding Amount
    $600,040.00
    Summary
    The human nervous system and organs are reliant on precisely controlled transmission of electrical currents through sodium and potassium channels. Their core functions are compromised when currents fail to switch on and off normally. Faulty potassium channels are implicated in diabetes, epilepsy and heart failure. This project re-examines the mechanisms controlling potassium channels, with a view to scientific and therapeutic discrimination between the different classes present in human cells.
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    Funded Activity

    Modelling TRPV4 Skeletal Disorders Using Human IPSCs

    Funder
    National Health and Medical Research Council
    Funding Amount
    $1,171,187.00
    Summary
    Inherited skeletal disorders are a significant disease burden. Many gene mutations have been defined but we only have limited understanding about how they cause the disease. We will use patient skin cells and new in vitro re-programing technology to induce them to form cartilage cells to produce “disease in a dish” models of human skeletal disorders. These models will allow us to answer questions about how specific mutations cause disease and identify potential therapies
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    Funded Activity

    Epilepsy: Molecular Basis And Mechanisms In The Era Of Functional Genomics

    Funder
    National Health and Medical Research Council
    Funding Amount
    $12,062,533.00
    Summary
    The team comprises of neurologists with a special interest in epilepsy (both adult and child) molecular geneticists, physiologists and brain imaging specialists. The team leads the world in the discovery of the genetic causes of epilepsy and epilepsy associated with intellectual disability. The team will continue to identify the genes underlying epilepsy, and study how genetic variations result in the development of seizures and will continue to develop advanced imaging techniques for these stud .... The team comprises of neurologists with a special interest in epilepsy (both adult and child) molecular geneticists, physiologists and brain imaging specialists. The team leads the world in the discovery of the genetic causes of epilepsy and epilepsy associated with intellectual disability. The team will continue to identify the genes underlying epilepsy, and study how genetic variations result in the development of seizures and will continue to develop advanced imaging techniques for these studies. This will include extensive laboratory studies, including the development of mice with the exact mutations that we find in the human condition. Stateof-the-art imaging techniques with magnetic resonance and positron emission tomography are used in human subjects to further understand the effects of the mutations on the structure and function of the brain. This will allow deep understanding of how seizures develop and may lead to new diagnostic methods and treatments. The laboratory and clinical aspects of the research are tightly integrated in this internationally leading collaborative program.
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    Funded Activity

    Mechanisms Of Protease-driven Visceral Pain

    Funder
    National Health and Medical Research Council
    Funding Amount
    $363,555.00
    Summary
    Chronic inflammation underlies common and debilitating diseases and causes pain by unknown mechanisms. There is an urgent need to gain a deeper understanding of the mechanisms of chronic pain, which will allow the development of improved therapies with fewer side-effects. Our research program investigates the mechanisms of pain that are associated with inflammatory bowel disease and irritable bowel syndrome, with the goal of developing more effective and selective therapies.
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    Funded Activity

    Epilepsy: A Collaborative Research Program From Gemone To Patient

    Funder
    National Health and Medical Research Council
    Funding Amount
    $6,607,142.00
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    Funded Activity

    Discovery And Development Of Better Pain Treatments

    Funder
    National Health and Medical Research Council
    Funding Amount
    $9,613,850.00
    Summary
    Many forms of pain remain poorly treated, leading to significant quality of life and economic losses. This Program grant will discover and characterise new peptides from cone snails and spiders that modulate specific channels in nerves that are critical to the transmission of pain signals to the brain. Using advanced chemical and structural approaches, promising leads will be optimised for potency and stability and evaluated in disease and pathway-specific models of pain to establish their clini .... Many forms of pain remain poorly treated, leading to significant quality of life and economic losses. This Program grant will discover and characterise new peptides from cone snails and spiders that modulate specific channels in nerves that are critical to the transmission of pain signals to the brain. Using advanced chemical and structural approaches, promising leads will be optimised for potency and stability and evaluated in disease and pathway-specific models of pain to establish their clinical potential.
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    Funded Activity

    Mechanisms Underlying Generation Of Febrile Seizures In Mouse Models Of Human Familial Epilepsy

    Funder
    National Health and Medical Research Council
    Funding Amount
    $304,559.00
    Summary
    Febrile Seizures (FS) affect 3% of children aged 0.5 - 6 yrs and have been proposed as an indicator of severe forms of adult generalized epilepsy. Mechanisms underlying FS generation are unknown although studies of Australian families suffering from epilepsy have linked 2 genes to FS. We have generated mice expressing these 2 genes. Aims and Outcomes: to investigate events triggering FS which will provide important insights into why FS occurs in children. (NB: CIA 2 yr career interruption)
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