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Forging A New Understanding Of Iron In Neurodegenerative Disease.
Funder
National Health and Medical Research Council
Funding Amount
$598,573.00
Summary
Using the versatile model system, C. elegans, this proposal will define how normal functions of the brain become corrupted with age and hijacked by neurodegenerative diseases to cause dementia. Coupling specialised X-ray imaging only available at the Australian Synchrotron with the research excellence of the University of Melbourne, this Fellowship will provide a better understanding of normal ageing and how this relates to the development and progression of neurodegenerative diseases.
Unravelling transthyretin amyloid, bounding ahead using wallabies. Each protein in our body has a unique shape that enables it to function correctly. For unknown reasons, some proteins can change their shape, aggregate with other proteins and stick to the outside of cells of major organs or nerves. This prevents those cells from working properly and results in disease. Transthyretin is a protein that changes shape and aggregates in the heart of most people over the age of 70. The disease is call ....Unravelling transthyretin amyloid, bounding ahead using wallabies. Each protein in our body has a unique shape that enables it to function correctly. For unknown reasons, some proteins can change their shape, aggregate with other proteins and stick to the outside of cells of major organs or nerves. This prevents those cells from working properly and results in disease. Transthyretin is a protein that changes shape and aggregates in the heart of most people over the age of 70. The disease is called Senile Systemic Amyloidosis (SSA). It is not known how or why this happens. There is no cure or therapy. This project will use transthyretins from human and wallaby to explore a possible cause of SSA. If our hypothesis is correct, we will propose preventative actions to reduce the incidence of SSA in the future.Read moreRead less
Identification of novel biomarkers in tears for prostate cancer diagnosis and prognosis. The purpose of this study is to identify novel biomarkers in the tears of patients with CaP. The use of the several techniques will increase the chance of success and enable us to find more diagnostic markers. If successful, the identified proteins may be used to diagnose and determine the stage of cancer. This will help guide clinicians in choosing the best treatment methods for an individual patient. The m ....Identification of novel biomarkers in tears for prostate cancer diagnosis and prognosis. The purpose of this study is to identify novel biomarkers in the tears of patients with CaP. The use of the several techniques will increase the chance of success and enable us to find more diagnostic markers. If successful, the identified proteins may be used to diagnose and determine the stage of cancer. This will help guide clinicians in choosing the best treatment methods for an individual patient. The markers may also be used to monitor the disease progress and the effects of treatment. The results from this study may improve the prognosis of CaP patients.Read moreRead less
Identification of novel biomarkers for diabetic retinopathy in tears. There are around 134,000 people with diabetic retinopathy in Australia. The disease affects patients' physical and mental state and economical and social cost is enormous. This research aims to find new biomarkers for the disease which may lead to better treatment and management. Patient's quality of life may be significantly improved by early diagnosis and treatment and the burden to the community reduced. This project also g ....Identification of novel biomarkers for diabetic retinopathy in tears. There are around 134,000 people with diabetic retinopathy in Australia. The disease affects patients' physical and mental state and economical and social cost is enormous. This research aims to find new biomarkers for the disease which may lead to better treatment and management. Patient's quality of life may be significantly improved by early diagnosis and treatment and the burden to the community reduced. This project also gives industrial partners the opportunity to develop new products to diagnose and monitor the disease.Read moreRead less
The atlas of trace metals in the mouse brain: a new tool for neuroscientists. This project will produce the first atlas of trace metals in the mouse brain: a set of 'maps' of a type of brain often used to study diseases affecting the human brain. This online resource will show neuroscientists unprecedented 3D detail of the distribution in the brain of trace metals, which are implicated in such diseases as Parkinson's and Alzheimer's.
Understanding lens aging: the molecular basis of presbyopia. Ageing has major consequences in the deterioration of vision, notably, the inability to focus on near objects. The understanding gained through this study of age-related lens changes may allow us to prescribe drugs or diets that alter lens properties and thus delay the need for glasses. This would have great benefits not just in decreased inconvenience of users, but also in cost to the middle-aged and elderly. In addition, data will b ....Understanding lens aging: the molecular basis of presbyopia. Ageing has major consequences in the deterioration of vision, notably, the inability to focus on near objects. The understanding gained through this study of age-related lens changes may allow us to prescribe drugs or diets that alter lens properties and thus delay the need for glasses. This would have great benefits not just in decreased inconvenience of users, but also in cost to the middle-aged and elderly. In addition, data will be used to underpin the development of a flexible intraocular lens (IOL). Hard IOLs are routinely inserted into human eyes following cataract surgery. In the future, flexible IOLs based on the properties of young lenses will be used, rather than reading glasses. This new industry could be based in Australia.Read moreRead less
Novel mass spectrometry methods to assess cellular oxidative stress. This project will provide fundamental understanding to the biology of cell stress that may lead to novel approaches for treating age-related diseases. It has the potential to have a significant economic and social impact nationally and internationally and provide Australian scientists with new technologies to study challenging issues in biology.
Understanding The Role And Mechanism Of Interaction Of Small Heat-shock Proteins In Age-related Disease
Funder
National Health and Medical Research Council
Funding Amount
$270,827.00
Summary
Protein precipitation is associated with a diversity of age-related diseases such as cataract and Alzheimer's. Within cells, a group of chaperones called the small heat-shock proteins (sHSPs) function by binding to destabilized proteins, however, common in vivo modifications can disrupt their cellular role leading to co-aggregation in a number of age-related diseases. This study will use state of the art mass spectrometry to examine the mechanism by which sHSPs interact with client proteins.
Proteomic techniques to assess oxidative stress in muscle wasting diseases. Australia will experience a significant increase in the proportion of its population that is over 65 years of age over the next 50 years. There will be an increased demand for health services related to injury from falls unless effective preventive strategies are put in place. Loss of muscle mass contributes to falls, so development of preventative strategies has the potential for considerable benefits. Oxidative stress ....Proteomic techniques to assess oxidative stress in muscle wasting diseases. Australia will experience a significant increase in the proportion of its population that is over 65 years of age over the next 50 years. There will be an increased demand for health services related to injury from falls unless effective preventive strategies are put in place. Loss of muscle mass contributes to falls, so development of preventative strategies has the potential for considerable benefits. Oxidative stress is a key intermediary in muscle wasting. This PhD project examines a possible mechanism by which oxidative stress causes muscle wasting. An appropriately tailored therapy to minimise oxidative stress has the potential to ameliorate loss of muscle mass.
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Discovery Early Career Researcher Award - Grant ID: DE180100859
Funder
Australian Research Council
Funding Amount
$365,058.00
Summary
Phosphatidylserine: a regulator of muscle and mitochondrial biology? This project aims to characterise a novel pathway involved in regulating skeletal muscle mass through effects on mitochondrial function. This project will examine how degradation causes mitochondrial abnormalities leading to severe muscle wasting. This project is expected to advance understanding of how pathways interact, thus identifying novel mechanisms that impact on muscle structure and function. Understanding what makes mu ....Phosphatidylserine: a regulator of muscle and mitochondrial biology? This project aims to characterise a novel pathway involved in regulating skeletal muscle mass through effects on mitochondrial function. This project will examine how degradation causes mitochondrial abnormalities leading to severe muscle wasting. This project is expected to advance understanding of how pathways interact, thus identifying novel mechanisms that impact on muscle structure and function. Understanding what makes muscle vulnerable to atrophy is fundamental to developing strategies to counteract muscle wasting conditions. Methodologies developed will have broad application in the field of life sciences research.Read moreRead less