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Scheme : Postgraduate Scholarships
Research Topic : Tumour Suppressor Gene
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  • Funded Activity

    The Importance Of RUNX3 In Preventing Gastrointestinal Diseases And Tumour Metastasis

    Funder
    National Health and Medical Research Council
    Funding Amount
    $113,322.00
    Summary
    Stomach cancer is the second leading cause of cancer-related deaths. It is estimated that in 2010, more than 1 million people will die of stomach cancer with an increase of 19%. Studies have revealed that RUNX3 has the ability to suppress the growth of stomach cancer. However the role of RUNX3 in preventing metastasis is yet unknown. Therefore, an understanding of the factors that govern metastasis will inform the design of effective therapies to prevent mortality which is high for this disease.
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    Funded Activity

    Identification And Characterisation Of Novel Tumour Suppressor Genes Involved In Breast Cancer

    Funder
    National Health and Medical Research Council
    Funding Amount
    $50,360.00
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    Funded Activity

    Identification Of Genetic Markers To Distinguish Pituitary Tumour Subtypes Using CDNA

    Funder
    National Health and Medical Research Council
    Funding Amount
    $112,592.00
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    Funded Activity

    Early Detection Of Melanoma Metastases Using MicroRNA As Novel Biomarkers

    Funder
    National Health and Medical Research Council
    Funding Amount
    $109,363.00
    Summary
    The use of a minimally invasive blood test to measure the circulating levels of melanoma-specific miRNAs may provide a rapid assessment for clinical management of the disease during dissemination of the tumour. This work has the potential to provide new prognostic markers for melanoma as well as to identify new gene targets for the design of rational therapies to treat this disease.
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    Funded Activity

    Parathyroid Hormone-related Protein (PTHrP), Common Genetic Variants In The PTHrP Gene (PTHLH), And Breast Cancer Risk And Survival

    Funder
    National Health and Medical Research Council
    Funding Amount
    $120,253.00
    Summary
    In a partnership between Peter MacCallum Cancer Centre, St Vincent's Hospital, and The University of Melbourne, we are investigating the role of PTHrP, a peptide integral to the growth and spread of Cancer. Initially thought to facilitate cancer spread, recent studies suggest it may actually be protective. In a new approach, we will analyse new DNA databases and patient data from around the world. We hope to extend our understanding of PTHrP, and perhaps find novel drug and therapeutic targets.
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    Funded Activity

    Mechanisms Of Gender Differences In Genetic Aortopathy

    Funder
    National Health and Medical Research Council
    Funding Amount
    $122,686.00
    Summary
    This project will investigate the molecular mechanisms that underly the gender differences in phenotypic expression in young adults with genetic aortopathy.
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    Funded Activity

    Functional Analysis Of A Novel Mammalian Zinc-finger Centromere Protein

    Funder
    National Health and Medical Research Council
    Funding Amount
    $80,068.00
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    Funded Activity

    Genomic Changes In Lung Malignancy

    Funder
    National Health and Medical Research Council
    Funding Amount
    $89,699.00
    Summary
    Lung cancer is a leading cause of cancer death globally. Symptoms may not develop until disease is advanced, so it is often incurable at diagnosis. Scientific developments have greatly improved our ability to test for the changes in DNA structure and function responsible for this deadly disease and its progression. This study examines whole lung cancer genomes then uses these findings to develop safer methods for detection based on changes in DNA sequence.
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    Funded Activity

    For Every Question, There Is An Answer: Application Of Genomic Sequencing And Functional Genomics For Disease Gene Discovery In Children With Orphan Phenotypes

    Funder
    National Health and Medical Research Council
    Funding Amount
    $99,682.00
    Summary
    My PhD study will look closely at the genes in a family to see what is different and whether this difference is the cause of rare health problems. I will focus on children with highly unique conditions in which intellectual disability/developmental delay is a key feature. My study is important because if I can find the exact cause of rare genetic conditions, then I hope to improve the welfare of patients and families affected by these types of conditions.
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    Funded Activity

    Mechanisms Of T Cell Mediated Injury In Renal Vasculitis

    Funder
    National Health and Medical Research Council
    Funding Amount
    $133,351.00
    Summary
    Anti-MPO glomerulonephritis (GN) is an aggressive disease causing severe and permanent injury to kidneys. This disease is thought to be due to an immune-mediated response to a protein (MPO) in neutrophils (a type of white blood cell). There is some evidence that other immune cells, CD4+ T cells, may be important in this disease. Experiments using models of anti-MPO GN will aim to define the role and mechanisms by which CD4+ T cells cause inflammation in the kidney.
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    Showing 1-10 of 23 Funded Activites

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