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Research Topic : TRANSPORTER
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  • Funded Activity

    Roles And Regulations Of Glutamate Transporters In Neurodegenerative Disease

    Funder
    National Health and Medical Research Council
    Funding Amount
    $20,484.00
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    Funded Activity

    Immunocytochemical Analysis Of Amino Acid Transporters In Developing Brains

    Funder
    National Health and Medical Research Council
    Funding Amount
    $457,850.00
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    Funded Activity

    Drug Binding Sites On Glycine Transporters

    Funder
    National Health and Medical Research Council
    Funding Amount
    $498,465.00
    Summary
    Glycine Transporters regulate the concentration of glycine in the spinal cord and brain. It has been suggested that elevating glycine levels in these regions may be useful in treating pain and schizophrenia. This project will provide the basis for the development of new glycine transport inhibitors that may be used to treat these conditions.
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    Funded Activity

    Molecular Biological Studies Of Insulin-stimulated Gluc Ose Transport

    Funder
    National Health and Medical Research Council
    Funding Amount
    $265,915.00
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    Funded Activity

    Ultracentrifuge For Molecular Biological Studies

    Funder
    National Health and Medical Research Council
    Funding Amount
    $25,775.00
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    Funded Activity

    How Does Insulin Stimulate Glucose Transport In Muscle And Fat Cells?

    Funder
    National Health and Medical Research Council
    Funding Amount
    $154,189.00
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    Funded Activity

    Investigations Into The Crystal Structure And Function Of A Bacterial Glutamate Transporter.

    Funder
    National Health and Medical Research Council
    Funding Amount
    $310,157.00
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    Funded Activity

    Transfer Of Glutamine Between Astrocytes And Neurons

    Funder
    National Health and Medical Research Council
    Funding Amount
    $255,500.00
    Summary
    Brain tissue is comprised of only a few different cell types. These are classified as neurons, glial cells, and cells of mesodermal origin. Glial cells are the most abundant cell type in the brain and include cells known as astrocytes. There is increasing evidence that astrocytes are actively involved in the maintenance and regulation of neuronal function. This study focuses on the mechanisms by which astrocytes supply neurons with precursors for the formation of signalling molecules (neurotrans .... Brain tissue is comprised of only a few different cell types. These are classified as neurons, glial cells, and cells of mesodermal origin. Glial cells are the most abundant cell type in the brain and include cells known as astrocytes. There is increasing evidence that astrocytes are actively involved in the maintenance and regulation of neuronal function. This study focuses on the mechanisms by which astrocytes supply neurons with precursors for the formation of signalling molecules (neurotransmitters) released from neurons in the transmission of nerve impulses. It will establish how these processes are controlled and also try to develop inhibitors that interfere with this process . The project tries to elucidate whether astrocytes actively regulate neuronal functions by regulating precursor supply. The work will make a significant contribution to our understanding of how astrocytes regulate neuronal activity, a process that may be critical in conditions such as stroke and epilepsy. A better understanding of the physiology of astrocytes might lead to improved treatments for these disturbances of brain function.
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    Funded Activity

    Glucose, Glucose Transporters And Blastocyst Formation In The Mouse

    Funder
    National Health and Medical Research Council
    Funding Amount
    $281,650.00
    Summary
    Embryo-based biotechnologies have the potential to improve human reproductive health, notably in treating infertility by In vitro fertilisation (IVF). They are also central to the future use of embryonic stem cells for human tissue replacement. This project investigates the molecular mechanisms controlling one of the earliest differentiations in the growth of the embryo. Using the mouse as an experimental model it will investigate the importance of several factors in the changes which set up the .... Embryo-based biotechnologies have the potential to improve human reproductive health, notably in treating infertility by In vitro fertilisation (IVF). They are also central to the future use of embryonic stem cells for human tissue replacement. This project investigates the molecular mechanisms controlling one of the earliest differentiations in the growth of the embryo. Using the mouse as an experimental model it will investigate the importance of several factors in the changes which set up the placenta and fetus as seperate tissues in the very early embryo. A key focus is the supply of glucose to the newly fertilised embryo and how important this glucose supply is for the survival of the embryo. Moreover there is great interest in the possibility that metabolic events in utero can contribute to the development of diseases in later life, notably, coronary heart diease, stroke, high blood pressure and non-insulin dependent diabetes. The results from these studies will contribute to our understanding of why some couples are infertile, lead to improved management of infertility by diet and invitro fertilisation procedures. It will also be of benefit in dietary advice to women with diabetes mellitus, seeking to have children. The adenoviral strategy for gene delivery into early mouse embryos may in the long term also find wide clinical application in the treatment of genetic defects at the very earliest stages in development and as such is of enormous potential benefit in the management of both animal and human reproduction.
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    Funded Activity

    Noradrenaline Transporter Dysfunction In Neural Circulatory Disorders: Clinical, Molecular And Therapeutic Implications

    Funder
    National Health and Medical Research Council
    Funding Amount
    $510,870.00
    Summary
    We will investigate the clinical relevance of noradrenaline transporter (NET) dysfunction and its molecular and genetic regulation in (1) essential hypertension, (2) postural tachycardia syndrome where the heart rate increases abnormally when the patient assumes an upright position and (3) syncope where subjects experience recurrent blackouts. In a therapeutic approach, we will explore whether NET inhibition can reduce the number of episodes and alleviate the symptoms associated with syncope.
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