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Research Topic : gene array
Socio-Economic Objective : Nervous System and Disorders
Status : Closed
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Genetics (4)
Gene Expression (incl. Microarray and other genome-wide approaches) (3)
Neurogenetics (3)
Central Nervous System (2)
Epigenetics (incl. Genome Methylation and Epigenomics) (2)
Medical Biochemistry: Amino Acids and Metabolites (2)
Neurosciences (2)
Analytical Biochemistry (1)
Biochemistry and Cell Biology (1)
Cellular Nervous System (1)
Genome Structure and Regulation (1)
Molecular Evolution (1)
Neurocognitive Patterns and Neural Networks (1)
Neurology and Neuromuscular Diseases (1)
Proteomics and Intermolecular Interactions (excl. Medical Proteomics) (1)
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Nervous System and Disorders (7)
Inherited Diseases (incl. Gene Therapy) (4)
Expanding Knowledge in the Biological Sciences (3)
Neurodegenerative Disorders Related to Ageing (2)
Expanding Knowledge in the Medical and Health Sciences (1)
Hearing, Vision, Speech and Their Disorders (1)
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Australian Research Council (7)
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Closed (7)
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Discovery Projects (3)
ARC Future Fellowships (2)
Discovery Early Career Researcher Award (1)
Linkage Infrastructure, Equipment and Facilities (1)
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  • Researchers (37)
  • Funded Activities (7)
  • Organisations (34)
  • Funded Activity

    Discovery Projects - Grant ID: DP120102389

    Funder
    Australian Research Council
    Funding Amount
    $300,000.00
    Summary
    Brain sodium channel: functional role of developmentally regulated alternative splicing. This project will identify the roles of neonatal and adult forms of a sodium channel in the function of neurons in the developing brain. Sodium channels are vital for brain function and this study will improve our understanding of the function of healthy brain as well as of underlying mechanisms of some neurological disorders.
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    Funded Activity

    Discovery Projects - Grant ID: DP120100285

    Funder
    Australian Research Council
    Funding Amount
    $510,000.00
    Summary
    Elucidating the neural pathways and genetic basis of speech. The project will elucidate the biological basis of speech, a unique feature of the human condition. The project will do this by i) discovering genes associated with speech disorder and ii) defining the neural pathways associated with speech production. This study will address critical questions regarding gene, brain and behaviour relationships in speech.
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    Funded Activity

    ARC Future Fellowships - Grant ID: FT100100546

    Funder
    Australian Research Council
    Funding Amount
    $803,217.00
    Summary
    Unraveling the role of N-acetyl-aspartate in normal brain function and disease. The purpose of this project is to define the role of the predominating brain chemical N-acetyl-aspartate for normal nerve cell function and as toxic agent causing neurological illness and severe mental health problems. Findings of this research will enhance the design of novel therapies involving pharmacological and genetic treatment.
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    Funded Activity

    Discovery Projects - Grant ID: DP120100729

    Funder
    Australian Research Council
    Funding Amount
    $500,000.00
    Summary
    The role of RNA editing by the brain-specific enzym ADAR3 in learning and memory. Higher-order cognition sets us apart from other species but how this is achieved is still under debate. The project will test the idea, strongly supported by recent genomic analyses, that subtle changes in the sequences of RNA in response to environmental stimuli underpin this extraordinary ability.
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    Funded Activity

    Discovery Early Career Researcher Award - Grant ID: DE140101033

    Funder
    Australian Research Council
    Funding Amount
    $315,220.00
    Summary
    Genomic Diversity in the Human Brain: the Functional Role of Expandable DNA Repeats. Neuronal cells accumulate genetic changes during development and adult life, and recent evidence suggests that the resulting genomic diversity may underlie neuronal functional diversity. To date only a few types of somatic genetic variation have been characterised in the human brain. Trinucleotide repeats (TNR) are hotspots of genomic instability and TNR expansions at specific loci cause dozens of brain disorder .... Genomic Diversity in the Human Brain: the Functional Role of Expandable DNA Repeats. Neuronal cells accumulate genetic changes during development and adult life, and recent evidence suggests that the resulting genomic diversity may underlie neuronal functional diversity. To date only a few types of somatic genetic variation have been characterised in the human brain. Trinucleotide repeats (TNR) are hotspots of genomic instability and TNR expansions at specific loci cause dozens of brain disorders, suggesting that the human brain is particularly vulnerable to this type of genetic variation. This project aims to investigate, for the first time, TNR somatic instability in the human brain on a genome-wide scale, therefore, addressing the genetic diversity of the brain from a novel and highly relevant angle.
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    Funded Activity

    ARC Future Fellowships - Grant ID: FT120100039

    Funder
    Australian Research Council
    Funding Amount
    $707,628.00
    Summary
    Defining the cellular impacts of protein aggregation in neurodegenerative disease with an aggreomics platform. The brain disease Huntington’s is caused by abnormally shaped proteins that assemble into toxic clusters. This project will design new bioprobes to track how these clusters form and cause damage to cells. This strategy will also provide new opportunities for discovering novel therapeutic targets.
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    Funded Activity

    Linkage Infrastructure, Equipment And Facilities - Grant ID: LE110100068

    Funder
    Australian Research Council
    Funding Amount
    $240,000.00
    Summary
    Mass spectrometry platform for high throughput genotyping, epigenetic analysis and validation of genome wide sequencing studies. This facility will provide a platform for Australian researchers to quantitatively measure genetic information in a rapid, accurate and cost-efficient manner. This technology will enhance Australia's ability to perform basic research into the genetic and epigenetic mechanisms of cellular function.
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    Showing 1-7 of 7 Funded Activites

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