ARDC Research Link Australia Research Link Australia   BETA Research
Link
Australia
  • ARDC Newsletter Subscribe
  • Contact Us
  • Home
  • About
  • Feedback
  • Explore Collaborations
  • Researcher
  • Funded Activity
  • Organisation
  • Researcher
  • Funded Activity
  • Organisation
  • Researcher
  • Funded Activity
  • Organisation

Need help searching? View our Search Guide.

Advanced Search

Current Selection
Field of Research : Cell Development, Proliferation and Death
Research Topic : tissue factor
Clear All
Filter by Field of Research
Cell Development, Proliferation and Death (16)
Regenerative Medicine (incl. Stem Cells and Tissue Engineering) (3)
Medical Biotechnology (2)
Biomaterials (1)
Biomedical Engineering (1)
Biomedical Engineering not elsewhere classified (1)
Cellular Interactions (incl. Adhesion, Matrix, Cell Wall) (1)
Filter by Socio-Economic Objective
Expanding Knowledge in the Biological Sciences (3)
Expanding Knowledge in the Medical and Health Sciences (2)
Expanding Knowledge in Engineering (1)
Expanding Knowledge in Technology (1)
Health Related to Ageing (1)
Filter by Funding Provider
National Health and Medical Research Council (13)
Australian Research Council (3)
Filter by Status
Closed (15)
Active (1)
Filter by Scheme
NHMRC Project Grants (7)
Project Grants (5)
ARC Future Fellowships (1)
Discovery Early Career Researcher Award (1)
Linkage Infrastructure, Equipment and Facilities (1)
Program Grants (1)
Filter by Country
Australia (5)
Filter by Australian State/Territory
VIC (3)
QLD (2)
ACT (1)
NSW (1)
  • Researchers (29)
  • Funded Activities (16)
  • Organisations (30)
  • Funded Activity

    Dissecting The Embryonic Blood-endothelial Regulatory Code And Investigating Its Role In Leukaemia

    Funder
    National Health and Medical Research Council
    Funding Amount
    $646,389.00
    Summary
    Cancer initiating cells acquire stem cell characteristics and multiply within a supportive environment that helps maintain and propagate malignant cells. Identifying the normal hierarchy of gene control within blood stem cells and designing therapies that target cancer cells is the ultimate goal of this body of work.
    More information
    Funded Activity

    De-differentiation Of Committed Cells Into Haematopoietic Stem Cells By The Instructive Role Of The Transcription Factor HOXB4

    Funder
    National Health and Medical Research Council
    Funding Amount
    $683,040.00
    Summary
    Blood stem cells are long-lived and can give rise to every cell type of the blood system and due to these properties they are currently used in the clinics. Despite their importance, our knowledge of the mechanisms the control the multiplication of these rare cells is very scarce. This proposal aims to identify key factors that have the potential to convert mature, easy available blood cells into stem cells. This knowledge has to potential to lead to novel system that allow the expansion of stem .... Blood stem cells are long-lived and can give rise to every cell type of the blood system and due to these properties they are currently used in the clinics. Despite their importance, our knowledge of the mechanisms the control the multiplication of these rare cells is very scarce. This proposal aims to identify key factors that have the potential to convert mature, easy available blood cells into stem cells. This knowledge has to potential to lead to novel system that allow the expansion of stem cells for transplantations in the future.
    Read more Read less
    More information
    Funded Activity

    Revealing How Transcription Factors Search The DNA To Control Preimplantation Development In Mammals

    Funder
    National Health and Medical Research Council
    Funding Amount
    $605,251.00
    Summary
    The development of mammalian embryos relies on proteins that bind to DNA to activate different genes. While several proteins regulating genes during embryonic development have been identified, it remains unknown how these proteins find their specific DNA targets. We will apply new non-invasive methods to analyse the movement of DNA–binding proteins in intact mouse embryos undergoing normal development, and will determine the molecular mechanisms that control DNA–protein interactions.
    More information
    Funded Activity

    Regulation Of TNF Expression In Inflammation And Cancer

    Funder
    National Health and Medical Research Council
    Funding Amount
    $728,447.00
    Summary
    By studying a spontaneous mutation in mice, we have found an error in the TNF gene (a major factor in many inflammatory diseases) that causes severe arthritis, heart valve disease and gut inflammation. We have also identified new regulators of TNF expression, which might be useful therapeutic targets to limit inflammation. We intend to study the role of these regulators in controlling the expression of TNF, and the link between chronic inflammation and the development of cancer.
    More information
    Funded Activity

    Developmental Therapeutics For The Treatment Of Gastrointestinal Cancers

    Funder
    National Health and Medical Research Council
    Funding Amount
    $5,392,649.00
    More information
    Funded Activity

    The Role Of MOZ In The Development Of The Hematopoietic System, Spleen And Thymus

    Funder
    National Health and Medical Research Council
    Funding Amount
    $324,375.00
    Summary
    Current treatment of leukaemia in adults is unsatisfactory with the majority of patients dying. In the past most treatments for cancer have been empirical, that is a particular drug has been found to be effective by trial and error rather than a process of rational design. In order to improve the rate at which effective treatments for leukaemia are found it is necessary to understand how hematopoiesis is regulated and what the critical points are where things can go wrong, leading to cancer. Som .... Current treatment of leukaemia in adults is unsatisfactory with the majority of patients dying. In the past most treatments for cancer have been empirical, that is a particular drug has been found to be effective by trial and error rather than a process of rational design. In order to improve the rate at which effective treatments for leukaemia are found it is necessary to understand how hematopoiesis is regulated and what the critical points are where things can go wrong, leading to cancer. Some genes are commonly found to be mutated in leukaemia. Clearly these genes are involved in some key aspect of regulation of hematopoiesis. We are studying one of these genes, MOZ, which is mutated in acute myeloid leukaemia. The purpose of this grant is to determine what the normal function of this gene is. One of the most promising new treatments for leukaemia is directly targeting the regulation of gene expression inside the cell. MOZ is one of the proteins, which regulates gene expression in hematopoiesis and controls the differentiation of different types of blood cells. One of the possible effects of these new types of anticancer drugs is to accentuate the normal function of MOZ. However, at the moment we don't know what the normal function of MOZ is so it is impossible to test this prediction. If we know which pathways controlling blood formation MOZ is acting in it may be possible, in the future, to use this information to improve on the current anti cancer drugs in a more directed way than has been possible in the past.
    Read more Read less
    More information
    Funded Activity

    Defining The Role Of VEGF And Vascular Formation In Craniofacial Development

    Funder
    National Health and Medical Research Council
    Funding Amount
    $636,417.00
    Summary
    Aberrant neural crest cell development gives rise to common congenital malformations such as cleft lip and/or palate and cardiac outflow tract defects that effect over 1% of all births. As the aetiology of these disorders are largely unknown it is critical to understand the cell and molecular mechanisms coordinating NCC development such that alternative therapies may be devised to target the underlying pathological defects and to provide definitive diagnostic / prognostic tools.
    More information
    Funded Activity

    The Role Of Necroptosis In Inflammatory Skin Diseases

    Funder
    National Health and Medical Research Council
    Funding Amount
    $548,690.00
    Summary
    Diseases associated with exaggerated inflammation account for a large toll of human disease. We have recently described how mice with a mutation in the Sharpin gene, that causes the chronic proliferative dermatitis phenotype (cpdm), can be rescued by crossing these mice to TNF (Tumor Necrosis Factor) knock-out mice. Our findings suggest that TNF induced cell death, rather than TNF induced cytokine production, may be at the root of many inflammatory diseases and we aim to test this hypothesis in .... Diseases associated with exaggerated inflammation account for a large toll of human disease. We have recently described how mice with a mutation in the Sharpin gene, that causes the chronic proliferative dermatitis phenotype (cpdm), can be rescued by crossing these mice to TNF (Tumor Necrosis Factor) knock-out mice. Our findings suggest that TNF induced cell death, rather than TNF induced cytokine production, may be at the root of many inflammatory diseases and we aim to test this hypothesis in this proposal.
    Read more Read less
    More information
    Funded Activity

    The Role Of Scribble In Prostate Cancer

    Funder
    National Health and Medical Research Council
    Funding Amount
    $601,803.00
    Summary
    Every cell in our body has an intrinsic orientation that is controlled by a universal set of genes known as polarity genes. Loss of this orientation is a common and early feature of cancer. We have identified the gene Scribble as a gene that controls cell orientation and is essential to prevent the development of prostate cancer. We propose experiments to discover how Scribble controls prostate cancer and whether it can be used to better predict outcome for prostate cancer patients.
    More information
    Funded Activity

    Role Of Primary Cilia And PCP Proteins In Lens Development: Implications For Lens Regeneration After Cataract Surgery

    Funder
    National Health and Medical Research Council
    Funding Amount
    $413,742.00
    Summary
    Cataract extraction is the most common surgical procedure conducted in our hospitals today. Unfortunately, a complication of surgery is the development of a secondary cataract. This is caused by residual lens epithelial cells undergoing a wound healing response that leads to severe scarring and loss of vision. This project will identify the factors that are needed to maintain lens epithelial cells in a normal state so that they can act as stem cells that can be induced to regenerate a new lens t .... Cataract extraction is the most common surgical procedure conducted in our hospitals today. Unfortunately, a complication of surgery is the development of a secondary cataract. This is caused by residual lens epithelial cells undergoing a wound healing response that leads to severe scarring and loss of vision. This project will identify the factors that are needed to maintain lens epithelial cells in a normal state so that they can act as stem cells that can be induced to regenerate a new lens that can transmit and focus light as normal.
    Read more Read less
    More information

    Showing 1-10 of 16 Funded Activites

    • 1
    • 2
    Advanced Search

    Advanced search on the Researcher index.

    Advanced search on the Funded Activity index.

    Advanced search on the Organisation index.

    National Collaborative Research Infrastructure Strategy

    The Australian Research Data Commons is enabled by NCRIS.

    ARDC CONNECT NEWSLETTER

    Subscribe to the ARDC Connect Newsletter to keep up-to-date with the latest digital research news, events, resources, career opportunities and more.

    Subscribe

    Quick Links

    • Home
    • About Research Link Australia
    • Product Roadmap
    • Documentation
    • Disclaimer
    • Contact ARDC

    We acknowledge and celebrate the First Australians on whose traditional lands we live and work, and we pay our respects to Elders past, present and emerging.

    Copyright © ARDC. ACN 633 798 857 Terms and Conditions Privacy Policy Accessibility Statement
    Top
    Quick Feedback