How brains become lateralised. This project aims to understand how the left and right sides of the brain become specialised for different cognitive functions, a phenomenon called lateralisation. Lateralisation is one of the least understood organisational principles of the brain, yet is crucial to the way we think and behave. Manifested most clearly as handedness, the brain is lateralised for many cognitive tasks such as language, reasoning, memory and emotion. However, the developmental origin ....How brains become lateralised. This project aims to understand how the left and right sides of the brain become specialised for different cognitive functions, a phenomenon called lateralisation. Lateralisation is one of the least understood organisational principles of the brain, yet is crucial to the way we think and behave. Manifested most clearly as handedness, the brain is lateralised for many cognitive tasks such as language, reasoning, memory and emotion. However, the developmental origin and anatomical substrate of most cognitive asymmetries are unknown. This project will use a chick model of brain lateralisation to quantify and localise to specific brain circuits the patterns of differential gene expression that give rise to anatomical and functional asymmetries.Read moreRead less
Discovery Early Career Researcher Award - Grant ID: DE200100164
Funder
Australian Research Council
Funding Amount
$387,551.00
Summary
How do neural circuits coordinate to produce adaptive changes in behaviour? This project aims to discover how neurons alter their function in coordinated ways to produce adaptive changes in behaviour. Behavioural outputs result from the activity of multiple cells in a functional network, but current methods are limited to studying signalling effects on single neurons. To address this, I will develop new methods to visualise every cell in the brain of the living nematode worm to provide a unique ....How do neural circuits coordinate to produce adaptive changes in behaviour? This project aims to discover how neurons alter their function in coordinated ways to produce adaptive changes in behaviour. Behavioural outputs result from the activity of multiple cells in a functional network, but current methods are limited to studying signalling effects on single neurons. To address this, I will develop new methods to visualise every cell in the brain of the living nematode worm to provide a unique systems-level understanding of a model brain. Through collaboration with engineers and psychologists, I will describe molecular switches that trigger reorganisation of entire neural networks. Expected outcomes include new insights on neural circuit plasticity, which will advance discovery in neuroscience and robotics.Read moreRead less
Understanding gender differences in pain: Cellular therapies for animal pain. Understanding gender differences in pain: Cellular therapies for animal pain. This project aims to relieve chronic pain in animals and lay the foundations for future human therapies, using molecular assays, cell technologies and immune/hormonal pain generators. Chronic pain affects females more than males. Establishing the fundamental mechanism in pain, the role of immune signalling and molecular mediators will enable ....Understanding gender differences in pain: Cellular therapies for animal pain. Understanding gender differences in pain: Cellular therapies for animal pain. This project aims to relieve chronic pain in animals and lay the foundations for future human therapies, using molecular assays, cell technologies and immune/hormonal pain generators. Chronic pain affects females more than males. Establishing the fundamental mechanism in pain, the role of immune signalling and molecular mediators will enable true pain-modifying treatments that address pivotal triggers in both genders. This project will then use specially selected stem cells separately targeting arthritic male and female pain and demonstrate novel veterinary chronic pain treatments. Expected outcomes are more effective gender-targeted treatments of pain and the realisation of economic value of molecular assays and cell technologies.Read moreRead less
How do protein quality control mechanisms maintain neuronal ageing? This project aims to interrogate how mechanisms of protein quality control act in the brain - an organ that is particularly vulnerable to a high load of misfolded protein - to maintain normal physiology during ageing. This project expects to make advances in cellular biochemistry and neuroscience, using an innovative proximity labelling approach to identify quality control regulators in neurons that specifically engage with misf ....How do protein quality control mechanisms maintain neuronal ageing? This project aims to interrogate how mechanisms of protein quality control act in the brain - an organ that is particularly vulnerable to a high load of misfolded protein - to maintain normal physiology during ageing. This project expects to make advances in cellular biochemistry and neuroscience, using an innovative proximity labelling approach to identify quality control regulators in neurons that specifically engage with misfolded proteins during ageing, within the nervous system of a living animal. Expected outcomes of this project will generate new knowledge of brain physiology and ageing relevant to all animals. This should provide significant benefits, such as a greater understanding of long-term brain functions including memory.Read moreRead less
Discovery Early Career Researcher Award - Grant ID: DE120102034
Funder
Australian Research Council
Funding Amount
$375,000.00
Summary
How did mammals evolve large brains? A multidisciplinary view from the pouch. This project applies novel data collection techniques to explain how the large brain sizes of today's mammals (including humans) are possible. The focus will be on brain structure, development, and evolution in the mostly Australian marsupials, whose ancestral mode of brain development makes them an ideal group for studies of brain size evolution.