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Research Topic : NEURODEVELOPMENTAL
Scheme : NHMRC Project Grants
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  • Funded Activity

    1H MRS In Schizophrenia: An In Vivo Study Of Neuronal Integrity In High-risk, First-episode And Chronic Illnes

    Funder
    National Health and Medical Research Council
    Funding Amount
    $305,117.00
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    Funded Activity

    A Two Year Follow-up MRI Study Of Hippocampal Changes I N Schizophrenia

    Funder
    National Health and Medical Research Council
    Funding Amount
    $220,658.00
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    Funded Activity

    Prenatal Alcohol Exposure: A Molecular Mechanism For Memory Deficits Involving The Zinc-binding Protein, Metallothionein

    Funder
    National Health and Medical Research Council
    Funding Amount
    $277,645.00
    Summary
    Damage to the developing brain is the major social and economic consequence of prenatal alcohol exposure but it is unclear the mechanism by which this occurs. This study will assess whether the maternal zinc-binding protein, metallothionein, causes: 1) alcohol-related cognitive deficits, 2) changes in the expression of alcohol-sensitive cognitive genes. We will further assess whether dietary zinc supplementation throughout pregnancy can prevent alcohol-related anomalies in neurodevelopment.
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    Funded Activity

    Examining The Contribution Of The Mirror Neuron System Toward Social Cognitive Impairment In Autism Spectrum Disorders

    Funder
    National Health and Medical Research Council
    Funding Amount
    $149,154.00
    Summary
    Despite a rapidly increasing prevalence, our neurobiological understanding of autism and Asperger's disorder remains limited. Using modern neuroscience techniques, this study investigates whether dysfunction within a specific brain cell, the mirror neuron, underlies social and language impairments in these disorders. This research provides exciting new directions for the understanding, diagnosis, and potential treatment of autism and Asperger's disorder.
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    Funded Activity

    Molecular And Cellular Characterisation Of Schizophrenia Associated Dysfunction In MicroRNA Biogenesis

    Funder
    National Health and Medical Research Council
    Funding Amount
    $496,205.00
    Summary
    We have identified substantial changes in the biogenesis of microRNA in schizophrenia. These small non-coding molecules derived from junk DNA, play a significant role in genetic regulation, with each one capable of silencing hundreds of target genes. This has major implications for schizophrenia, which is known to involve substantial changes in gene activity. The project will identify the molecular basis of this alteration in gene silencing, and its biological implications for schizophrenia.
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    Funded Activity

    Mechanisms Of Glutamate Receptor Maturation In Chicken Brain

    Funder
    National Health and Medical Research Council
    Funding Amount
    $418,980.00
    Summary
    In the brain, many key proteins involved in signalling change during development as part of the fine tuning of the network of connections between nerve cells. Disorders of this fine tuning are thought to result in a number of neurological or psychiatric conditions such as epilepsy and schizophrenia. This project will investigate the maturation of signalling molecules in the brain (receptors for the neurotransmitter glutamate, key enzymes called protein kinases and protein phosphatases that contr .... In the brain, many key proteins involved in signalling change during development as part of the fine tuning of the network of connections between nerve cells. Disorders of this fine tuning are thought to result in a number of neurological or psychiatric conditions such as epilepsy and schizophrenia. This project will investigate the maturation of signalling molecules in the brain (receptors for the neurotransmitter glutamate, key enzymes called protein kinases and protein phosphatases that control the activity of receptors and scaffolding proteins that bind the whole lot into a signalling complex). The project uses chickens as a novel animal model because chicken brain has a slow maturation that occurs well after the initial wiring of the brain is complete. This enables the maturation changes to be clearly identified and experimentally modified. The project combines investigations at the molecular, physiological and behavioural levels. The effects of hormones and drugs on maturation will be investigated. Because brain maturation in humans is also slow an understanding of the way in which this maturation is controlled may provide insights into what causes some neurological-psychiatric disorders in children and adolescents and how to treat or prevent them.
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    Funded Activity

    Cloning And Characterisation Of A Novel Developmental Gene Involved In Myelination.

    Funder
    National Health and Medical Research Council
    Funding Amount
    $150,880.00
    Summary
    This project aims to identify and characterise a novel human gene involved in the formation of different organs and tissues, with an essential role in nervous system development. One of the most interesting facts of life, emerging from the completion of the Human Genome Project, is that it is not the number of genes but rather their regulation that plays the major role in evolution and determines the differences between species. The development of a human being from conception to birth is among .... This project aims to identify and characterise a novel human gene involved in the formation of different organs and tissues, with an essential role in nervous system development. One of the most interesting facts of life, emerging from the completion of the Human Genome Project, is that it is not the number of genes but rather their regulation that plays the major role in evolution and determines the differences between species. The development of a human being from conception to birth is among the most complex processes, where fine regulation of the timing and site of gene expression is crucial. We have recently identified a novel disorder where a mutation in a single gene disrupts the development and function of the eyes, the skull, the nervous, and the endocrine systems. The most disabling manifestations of the disease result from involvement of the peripheral nervous system. This is due to the failure of affected individuals to produce myelin, the insulating material that enwraps nerve fibres and facilitates the rapid conduction of nerve impulses. The mutated gene, which the project aims to identify, is likely to be involved in regulating the expression of multiple other genes essential for the early stages of myelination, as well as for the development of other tissues. The disease gene has been localised to a small interval on the long arm of chromosome 18, which does not contain any known developmental genes, suggesting that the project will provide novel information on the molecular pathways governing normal human development. As a result, the study may have important implications for understanding the general pathogenesis of disorders of the peripheral nervous system, including its common forms which affect thousand of people worldwide.
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    Funded Activity

    Post Synaptic Density Scaffold Proteins In The Growth Cone: Homer And Shank, Crucial For Calcium Signaling.

    Funder
    National Health and Medical Research Council
    Funding Amount
    $237,909.00
    Summary
    Our brain is a complex, yet precise electrical circuit. Understanding how the embryonic brain is wired has direct implications for all aspects of life, from the growing foetus in mother's womb, to learning algebra and for maintaining the active memories of our ageing population. This project aims to provide new insight into understanding how the embryonic brain is wired, crucial information for future pharmacological or gene therapy approaches to mental illness, ageing, and neuronal injury.
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    Funded Activity

    Clinical Genetic Phenotyping Of Autism Spectrum Disorders

    Funder
    National Health and Medical Research Council
    Funding Amount
    $582,114.00
    Summary
    Individuals with autism spectrum disorders (ASD) have difficulty with communication, social interaction and intellectual disability. The cause is generally not known although most cases have a genetic basis involving multiple genes and possibly environmental factors. We will study families of children with ASD and carefully characterize features related to ASD in family members. This will help us to understand how ASD is inherited and serve as the basis for the discovery of autism genes.
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    Funded Activity

    MEASURING AND MODELLING VISUAL CORTICAL PLASTICITY

    Funder
    National Health and Medical Research Council
    Funding Amount
    $612,693.00
    Summary
    We are the product of both our genes and our environment. Scientists have already shown that the physical structure of our brain can be changed by our experiences. But how much can it be changed? Our experiments will address this question for a particular case: how far our visual experiences can affect the structure of the part of our brain that processes visual images. This will help us understand the delicate balance between our genes and our environment in shaping who we are.
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    Showing 1-10 of 29 Funded Activites

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