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2026 ARDC Annual Survey is now open!

The Australian Research Data Commons (ARDC) invites you to participate in a short survey about your interaction with the ARDC and use of our national research infrastructure and services. The survey will take approximately 5 minutes and is anonymous. It’s open to anyone who uses our digital research infrastructure services including Reasearch Link Australia.

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Research Topic : SEPN1-related myopathy
Australian State/Territory : VIC
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  • Funded Activity

    Discovery Projects - Grant ID: DP0770668

    Funder
    Australian Research Council
    Funding Amount
    $630,000.00
    Summary
    Identifying mitogenic signalling proteins with phosphatidyl inositol lipids. Health care of an ageing population is a national priority of the community. In order to understand the factors that control cell growth and death in cancer cells signalling proteins can be identified and studied and compared with model systems from quiescent cells. Using phospholipids attached to 'fishing lines' we can search for, identify and study the function of all the downstream signalling proteins in activated c .... Identifying mitogenic signalling proteins with phosphatidyl inositol lipids. Health care of an ageing population is a national priority of the community. In order to understand the factors that control cell growth and death in cancer cells signalling proteins can be identified and studied and compared with model systems from quiescent cells. Using phospholipids attached to 'fishing lines' we can search for, identify and study the function of all the downstream signalling proteins in activated cancer cells. This will provide the basic information for drug discovery processes to target specific molecules that inhibit and control the function of the signalling proteins implicated in the growth of cancer cells.
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    Funded Activity

    Discovery Projects - Grant ID: DP1094497

    Funder
    Australian Research Council
    Funding Amount
    $540,000.00
    Summary
    Synthesis of phosphatidylinositol and inositol polyphosphate derivatives to probe key signalling proteins associated with cell growth and cancer. Health care of an ageing population is a national priority of the community. In order to understand the factors that control cell growth and death in cancer cells signalling proteins can be identified and studied and compared with model systems from quiescent cells. Using phospholipids and inositol polyphosphates attached to 'fishing lines' we can sea .... Synthesis of phosphatidylinositol and inositol polyphosphate derivatives to probe key signalling proteins associated with cell growth and cancer. Health care of an ageing population is a national priority of the community. In order to understand the factors that control cell growth and death in cancer cells signalling proteins can be identified and studied and compared with model systems from quiescent cells. Using phospholipids and inositol polyphosphates attached to 'fishing lines' we can search for, identify and study the function of many of the downstream signalling proteins in activated cancer cells. This will provide the basic information for discovery processes to target specific molecules that inhibit and control the function of the signalling proteins implicated in the growth of cancer cells.
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    Funded Activity

    Discovery Projects - Grant ID: DP0344565

    Funder
    Australian Research Council
    Funding Amount
    $668,000.00
    Summary
    Novel Inorganic Nanostructures Fabricated using Polymeric Supports and Templates for Environmental and Catalytic Applications. The flexibility and versatility of nanotemplating processes will be exploited to fabricate novel porous inorganic structures with controllable properties. These include tailorable surface area, pore size and structure, particle size and composition. The influence of such properties will be studied in various applications, including the photocatalytic decomposition of pol .... Novel Inorganic Nanostructures Fabricated using Polymeric Supports and Templates for Environmental and Catalytic Applications. The flexibility and versatility of nanotemplating processes will be exploited to fabricate novel porous inorganic structures with controllable properties. These include tailorable surface area, pore size and structure, particle size and composition. The influence of such properties will be studied in various applications, including the photocatalytic decomposition of pollutants, where the ability to control the morphological structure of the inorganic materials introduced by the templating technique will lead to enhanced efficiencies. These nanostructures will also be considered for use in solar cells, an alternative energy source that is currently receiving copious attention worldwide.
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    Funded Activity

    Discovery Projects - Grant ID: DP0664601

    Funder
    Australian Research Council
    Funding Amount
    $330,000.00
    Summary
    Membrane interactions and neurotoxicity of Amyloid Abeta peptides from Alzheimer's disease. A consequence of the increase in human life span is that age-related neurodegenerative diseases such as Alzheimer's disease (AD) are more prevalent. Currently there are limited therapeutic treatments and no cure for AD. The key protein causing AD is Abeta and characterization of the toxic species of this peptide is critical towards identifying potential therapeutic targets. This proposal aims to study mut .... Membrane interactions and neurotoxicity of Amyloid Abeta peptides from Alzheimer's disease. A consequence of the increase in human life span is that age-related neurodegenerative diseases such as Alzheimer's disease (AD) are more prevalent. Currently there are limited therapeutic treatments and no cure for AD. The key protein causing AD is Abeta and characterization of the toxic species of this peptide is critical towards identifying potential therapeutic targets. This proposal aims to study mutant peptides made synthetically and to identify a membrane-binding site. By establishing which lipid is critically involved in membrane binding of Abeta and mediating subsequent cell death, drugs may be developed to prevent the binding of Abeta to membranes resulting in neuronal survival and prevention of memory loss in AD patients.
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    Showing 1-4 of 4 Funded Activites

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