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Scheme : Career Development Fellowships
Research Topic : complex genetics
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  • Funded Activity

    Dissecting Genetic Variation For Human Complex Diseases And Traits

    Funder
    National Health and Medical Research Council
    Funding Amount
    $135,821.00
    Summary
    Understanding the pattern of inheritance for human common diseases such as cancers, obesity, diabetes and mental illness, is of key importance for disease diagnosis, treatment and prevention. In this project, we will develop statistical methods and software tools to analyse DNA and clinical data to better understand the genetic basis of human common diseases and to predict a person�s risk of developing disease.
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    Funded Activity

    The Role Of Non-classical MHC Class I Molecules In Adaptive Immunity

    Funder
    National Health and Medical Research Council
    Funding Amount
    $443,834.00
    Summary
    Specialised proteins called MHC class Ia molecules (MHC-Ia) stimulate killer T cells to lyse virus infected cells. In contrast, the function of the closely related MHC-Ib is uncertain. Recent findings have demonstrated that MHC-Ib can also be recognised by T cells and this interaction is important in the control of viral infections. However, despite the similarity to MHC-Ia, it is unclear how this interaction occurs. This project aims to investigate how killer T cells recognise MHC-Ib molecules.
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    Funded Activity

    Assembly Of Mitochondrial Respiratory Chain Complexes And Their Defects Associated With Disease.

    Funder
    National Health and Medical Research Council
    Funding Amount
    $413,431.00
    Summary
    Mitochondrial “respiratory chain complexes are multi-subunit assemblies that function to produce most of our cellular energy. Defects in the assembly of these complexes can result in mitochondrial disease, including infant death. The assembly of the respiratory complexes is a complicated procedure and the mechanisms involved in disease remain elusive. This work will aid in our understanding of how these protein complexes are built and how defects in their assembly can cause disease.
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    Funded Activity

    Asthma Genetics: Dissecting The Missing Heritability And Biology

    Funder
    National Health and Medical Research Council
    Funding Amount
    $451,716.00
    Summary
    The goal of this application is to apply state-of-the-art technologies to (1) identify genes that increase the risk of developing asthma and (2) help translate this information into knowledge that can be used to improve disease management. I will achieve this by analysing data generated by the Australian Asthma Genetics Consortium and international collaborators.
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    Funded Activity

    The Structure And Composition Of The T-Cell Receptor-CD3 Complex

    Funder
    National Health and Medical Research Council
    Funding Amount
    $419,180.00
    Summary
    My research will use cutting edge imaging techniques to provide a fundamental advance in our understanding of how foreign viruses and pathogens trigger the immune system. Gaining a greater understanding of these central events will facilitate the design of novel therapies to treat immune associated disorders such as transplant rejection, autoimmune disease and some cancers.
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    Funded Activity

    Linkage And Linkage Disequilibrium Mapping In Mice And Humans

    Funder
    National Health and Medical Research Council
    Funding Amount
    $417,790.00
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    Funded Activity

    Molecular Etiology Of Type 2 Diabetes

    Funder
    National Health and Medical Research Council
    Funding Amount
    $296,857.00
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    Funded Activity

    Prenatal Genetic Testing For Birth Defects

    Funder
    National Health and Medical Research Council
    Funding Amount
    $380,000.00
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    Funded Activity

    Massive Parallel Sequencing In The Genetics Of Epilepsy

    Funder
    National Health and Medical Research Council
    Funding Amount
    $451,716.00
    Summary
    Epilepsy is a serious disorder which affects approximately 2% of the population at some stage in their life and around 30% of patients do not gain adequate control of their seizures with medications presently available. Approximately 70% of epilepsy in inherited and so far the majority of the genetic causes are yet to be discovered. My group aims to identify new epilepsy genes. This leads to improved diagnosis, treatment and counseling for patients and increased understanding of the biological m .... Epilepsy is a serious disorder which affects approximately 2% of the population at some stage in their life and around 30% of patients do not gain adequate control of their seizures with medications presently available. Approximately 70% of epilepsy in inherited and so far the majority of the genetic causes are yet to be discovered. My group aims to identify new epilepsy genes. This leads to improved diagnosis, treatment and counseling for patients and increased understanding of the biological mechanisms underlying seizures.
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    Funded Activity

    Integrating Statistical Imputation Of HLA And KIR Alleles Into Studies Of Disease In Diverse Human Populations

    Funder
    National Health and Medical Research Council
    Funding Amount
    $415,218.00
    Summary
    Immune system genes are strongly implicated in many infectious and autoimmune diseases, as well as cancer. Some of these genes have many possible types due to natural selection in response to pathogens. This variability makes typing these genes very expensive. Developing accurate and inexpensive methods to type these genes is vital in understanding the role they play in susceptibility and progression of disease and will be important for the development of better diagnostic tests and treatments.
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    Showing 1-10 of 41 Funded Activites

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