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Research Topic : APOPTOSIS
Field of Research : Animal Physiology—Cell
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Animal Physiology—Cell (5)
Cell Development (Incl. Cell Division And Apoptosis) (5)
Biochemistry and Cell Biology (4)
Cellular Interactions (Incl. Adhesion, Matrix, Cell Wall) (1)
Meiosis And Recombination (1)
Oncology And Carcinogenesis (1)
Paediatrics and Reproductive Medicine (1)
Reproduction (1)
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Reproductive system and disorders (2)
Beef cattle (1)
Cancer and related disorders (1)
Dairy cattle (1)
Digestive system and disorders (1)
Endocrine organs and diseases (incl. diabetes) (1)
Minimally processed milk (1)
Organs, diseases and abnormal conditions not elsewhere classified (1)
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Prevention—biologicals (e.g. vaccines) (1)
Treatments (e.g. chemicals, antibiotics) (1)
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Australian Research Council (5)
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  • Researchers (9)
  • Funded Activities (5)
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  • Funded Activity

    Discovery Projects - Grant ID: DP0773661

    Funder
    Australian Research Council
    Funding Amount
    $263,000.00
    Summary
    The role of the transcription factor Runx2 during mammary gland development and lactation. This proposal will further our understanding of mammary gland development and lactation and the mechanisms controlling mammary cell fate decisions such as differentiation. Regulation of cell fate lies at the core of most aspects of cell biology from normal development to dysfunction such as cancer. The knowledge gleamed from this project also has the potential to make economic gains for Australia by increa .... The role of the transcription factor Runx2 during mammary gland development and lactation. This proposal will further our understanding of mammary gland development and lactation and the mechanisms controlling mammary cell fate decisions such as differentiation. Regulation of cell fate lies at the core of most aspects of cell biology from normal development to dysfunction such as cancer. The knowledge gleamed from this project also has the potential to make economic gains for Australia by increasing the profitability and ensuring the sustainability of both the dairy and meat industries. Better understanding of the mechanisms controlling mammary epithelial cell differentiation should enable augmentation of lactation such as increasing milk protein content, using marker assisted selection (of targets such as Runx2) in cattle.
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    Funded Activity

    Discovery Projects - Grant ID: DP0986217

    Funder
    Australian Research Council
    Funding Amount
    $325,000.00
    Summary
    Elucidation of the signalling pathways during fertilization in mammals. This grant sets out to understand how the union of the sperm and egg at fertilization generates a viable embryo: this is a fundamental event in biology. We aim to understand the basic signalling pathways from the sperm which allow the egg to become an embryo and are known to influence embryo quality. They are therefore important in our understanding of what constitutes a healthy early start to life. Australia also has econom .... Elucidation of the signalling pathways during fertilization in mammals. This grant sets out to understand how the union of the sperm and egg at fertilization generates a viable embryo: this is a fundamental event in biology. We aim to understand the basic signalling pathways from the sperm which allow the egg to become an embryo and are known to influence embryo quality. They are therefore important in our understanding of what constitutes a healthy early start to life. Australia also has economic interests in understanding the reproductive process in aiding breeding programs for commercially important livestock and endangered species and contraception programs for pest populations.
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    Funded Activity

    ARC Future Fellowships - Grant ID: FT0992234

    Funder
    Australian Research Council
    Funding Amount
    $686,400.00
    Summary
    Role of Histone deacetylase 3 (HDAC3) in intestinal epithelial cell homeostasis and tumorigenesis. Colon cancer is the most common cancer that affects men and women in Australia. Annually, in Victoria alone, more than 3400 people are diagnosed with colon cancer. Colon cancer arises through the accumulation of mutations in key genes over time. Identification of cancer causing genes provides the basis for the design of new cancer therapies. We recently identified a gene called Histone deacetylase .... Role of Histone deacetylase 3 (HDAC3) in intestinal epithelial cell homeostasis and tumorigenesis. Colon cancer is the most common cancer that affects men and women in Australia. Annually, in Victoria alone, more than 3400 people are diagnosed with colon cancer. Colon cancer arises through the accumulation of mutations in key genes over time. Identification of cancer causing genes provides the basis for the design of new cancer therapies. We recently identified a gene called Histone deacetylase 3 (HDAC3) as potentially involved in promoting colon cancer. The current proposal will now extend and validate this finding in mice. Importantly, drugs which inhibit HDAC3 have recently been developed for the treatment of cutaneous T-cell lymphoma. Defining the role HDAC3 plays in colon cancer will justify testing these drugs in colon cancer patients.
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    Funded Activity

    Discovery Projects - Grant ID: DP0211497

    Funder
    Australian Research Council
    Funding Amount
    $276,000.00
    Summary
    Mechanistic basis of a reproductive lesion in transforming growth factor beta-1 (TGFb1) null mutant mice. Null mutation in the gene encoding the cytokine transforming growth factor beta-1 (TGFb1) causes infertility in male and female mice. In recent experiments we have found that TGFb1 deficiency is associated with impaired ovarian and testicular steroidogenesis, arrested development of pre-implantation embryos and disrupted mammary gland morphogenesis. The aims of the current project are to un .... Mechanistic basis of a reproductive lesion in transforming growth factor beta-1 (TGFb1) null mutant mice. Null mutation in the gene encoding the cytokine transforming growth factor beta-1 (TGFb1) causes infertility in male and female mice. In recent experiments we have found that TGFb1 deficiency is associated with impaired ovarian and testicular steroidogenesis, arrested development of pre-implantation embryos and disrupted mammary gland morphogenesis. The aims of the current project are to unravel the mechanistic basis of the reproductive lesion in TGFb1 null mutant mice and to determine the effect of exogenous systemic delivery of TGFb1 in alleviating this lesion. It is expected that the project will provide new insight into key roles for TGFb1 in governing male and female fertility, and shed light on the prospects for exogenous supplementation of TGFb1 for improving reproductive performance in wild-type animals. This knowledge has potentially important applications in the livestock breeding industry, in devising novel contraceptive vaccine strategies, in the human pharmaceutical industry, and in devising novel contraceptive vaccine strategies.
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    Funded Activity

    Discovery Projects - Grant ID: DP0987059

    Funder
    Australian Research Council
    Funding Amount
    $307,000.00
    Summary
    Keeping stem cells on track: maintaining organ and tissue homeostasis. The novel findings from this study are of fundamental importance of understanding how stem cells maintain their characteristic features as they renew themselves over a lifetime. This work will inform the National Research Priority of ''Promoting and maintaining good health''' because stem cell renewal is required during tissue turnover and these results will show how cells communicate with each other to achieve this. This wo .... Keeping stem cells on track: maintaining organ and tissue homeostasis. The novel findings from this study are of fundamental importance of understanding how stem cells maintain their characteristic features as they renew themselves over a lifetime. This work will inform the National Research Priority of ''Promoting and maintaining good health''' because stem cell renewal is required during tissue turnover and these results will show how cells communicate with each other to achieve this. This work is based on a unique combination of expertise in stem cell and reproductive biology and showcases Australian science.
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