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
Research Topic : Inositol phosphates
Clear All
Filter by Field of Research
Applied immunology (incl. antibody engineering xenotransplantation and t-cell therapies) (1)
Cardiology (incl. Cardiovascular Diseases) (1)
Medical Biochemistry: Lipids (1)
Medical Microbiology not elsewhere classified (1)
Medical and Health Sciences (1)
Medical biochemistry and metabolomics not elsewhere classified (1)
Oral medicine and pathology (1)
Protein Targeting And Signal Transduction (1)
Structural Biology (incl. Macromolecular Modelling) (1)
Filter by Socio-Economic Objective
Search did not return any results.
Filter by Funding Provider
National Health and Medical Research Council (14)
Filter by Status
Closed (14)
Filter by Scheme
NHMRC Project Grants (10)
Project Grants (3)
NHMRC Research Fellowships (1)
Filter by Country
Australia (1)
Filter by Australian State/Territory
NSW (1)
  • Researchers (0)
  • Funded Activities (14)
  • Organisations (0)
  • Funded Activity

    Targeting Phosphoinositide Metabolism In Leishmania

    Funder
    National Health and Medical Research Council
    Funding Amount
    $990,904.00
    Summary
    There is an urgent need to develop new drugs to treat human leishmaniasis, a disease that causes debilitating and life-threatening diseases in millions of people worldwide. This project will investigate whether it is possible to develop a new generation of drugs that target an important signaling pathway in these parasites that we have shown to be essential for virulence
    More information
    Funded Activity

    Phosphoinositide 4-phosphatases In Health And Disease

    Funder
    National Health and Medical Research Council
    Funding Amount
    $678,560.00
    Summary
    This project aims to understand the structure and function of an important group of signalling enzymes involved in the development of cancers such as melanoma.
    More information
    Funded Activity

    Uncoupled Research Fellowship

    Funder
    National Health and Medical Research Council
    Funding Amount
    $558,000.00
    More information
    Funded Activity

    Regulation Of Cell Signalling Molecules

    Funder
    National Health and Medical Research Council
    Funding Amount
    $152,187.00
    More information
    Funded Activity

    Signals Within Cells Which Permit Hormones To Control L Iver Function

    Funder
    National Health and Medical Research Council
    Funding Amount
    $285,166.00
    More information
    Funded Activity

    Inositol Polyphosphate 1-phosphatase, A Novel Anti-hypertrophic Factor

    Funder
    National Health and Medical Research Council
    Funding Amount
    $399,750.00
    Summary
    Growth of the heart muscle cells occurs after heart attack and in people with high blood pressure or who suffer from diseases such as diabetes. Such growth leads eventually to the development of heart failure, a major cause of death and disability in western societies. We have identified a novel inhibitor of this growth, an enzyme that destroys a signalling intermediate called inositol(1,4)bisphosphate (or IP2). We now need to define how reduction in IP2 reduces growth and whether it provides a .... Growth of the heart muscle cells occurs after heart attack and in people with high blood pressure or who suffer from diseases such as diabetes. Such growth leads eventually to the development of heart failure, a major cause of death and disability in western societies. We have identified a novel inhibitor of this growth, an enzyme that destroys a signalling intermediate called inositol(1,4)bisphosphate (or IP2). We now need to define how reduction in IP2 reduces growth and whether it provides a useful target for therapy.
    Read more Read less
    More information
    Funded Activity

    Ischaemia-induced Sarcolemmal Changes And Their Role In Ins(1,4,5)P3 Generation And Arrhythmogenesis

    Funder
    National Health and Medical Research Council
    Funding Amount
    $468,750.00
    Summary
    Studies in our laboratory at the Baker Heart Research Institute over the last several years have identified a novel mechanism causing the development of arrhythmias, a primary cause of sudden cardiac death in heart failure as well as during an acute heart attack caused by acutely reduced blood flow. The reduced blood flow leads to lowered oxygen and nutrients and thus the beating heart cells have insufficient energy to properly maintain function. Under these stressed conditions, cardiac myocytes .... Studies in our laboratory at the Baker Heart Research Institute over the last several years have identified a novel mechanism causing the development of arrhythmias, a primary cause of sudden cardiac death in heart failure as well as during an acute heart attack caused by acutely reduced blood flow. The reduced blood flow leads to lowered oxygen and nutrients and thus the beating heart cells have insufficient energy to properly maintain function. Under these stressed conditions, cardiac myocytes produce large amounts of a small molecule called IP3, which interferes with the normal electrical balance of the cells. Blocking IP3 generation prevents arrhythmias under these acutely ischaemic conditions. In more recent studies, we have identified many of the enzymes responsible for generation of IP3 in heart cells and have defined the properties of the regions of the cell responsible for this response. We now want to establish exactly how a period of ischaemia alters the localization or functioning of the enzymes that are responsible for this pathological change that leads to fatal arrhythmias.
    Read more Read less
    More information
    Funded Activity

    Signalling Pathways And Fungal Virulence – The Inositol Polyphosphate Kinase Pathway In Cryptococcus Neoformans

    Funder
    National Health and Medical Research Council
    Funding Amount
    $545,189.00
    Summary
    Bloodstream fungal infections kill millions of people per year world-wide and are costly to treat. A potentially fruitful strategy for developing new, urgently-needed drugs to fight these infections, is to target signalling pathways, which in fungi, are essential for establishing infection. This proposal investigates how one such pathway, the inositolpolyphosphate kinase pathway, allows fungi to establish infection and will determine which components are suitable targets for drug development.
    More information
    Funded Activity

    Chatacterization Of The 43 KDa Inositol Polyphosphate 5-phosphatase

    Funder
    National Health and Medical Research Council
    Funding Amount
    $329,722.00
    More information
    Funded Activity

    How Liver Cell Function Is Controlled By Hormones And I Ntracellular Calcium

    Funder
    National Health and Medical Research Council
    Funding Amount
    $375,025.00
    More information

    Showing 1-10 of 14 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