Neural Circuits For Active Vision In The Primate Cerebral Cortex
Funder
National Health and Medical Research Council
Funding Amount
$632,938.00
Summary
This project will try to understand how we use visual information to identify objects by their shape and motion, in natural situations in which the eyes are moving all the time. This will be accomplished by recording the electrical activity of brain cells while a trained animal is performing different types of tasks, such as tracking a moving object or exploring a scene with its eyes.
Neuronal Linking Of Attention, Perception And Action
Funder
National Health and Medical Research Council
Funding Amount
$586,469.00
Summary
We are able to perceive and interact with the environment around us primarily because a filter of attention selects just the objects or features of relevance in the world and helps to make appropriate motor responses. This project will study how attentional networks of the brain operate to link our perception and action. An understanding of this process is fundamental to revealing the underlying pathology in many neurological conditions where attention is impaired.
Neural Circuits For Residual Vision After Damage To Striate Cortex
Funder
National Health and Medical Research Council
Funding Amount
$662,220.00
Summary
Brain cells have the ability to rearrange their connections to create alternate pathways, which compensate for loss of function following brain damage. To understand why some people become blind after damage to the visual cortex, and some don't, we will determine how neural connections change following lesions in different stages of life. The project will provide important information that may allow future development of treatments for blindness due to stroke or traumatic brain injury.
Neuronal Activity And Functional Magnetic Resonance Imaging (fMRI)
Funder
National Health and Medical Research Council
Funding Amount
$367,561.00
Summary
How does brain activity relate to perception and behaviour? How does functional magnetic resonance imaging (fMRI) of the brain, which measures changes in blood oxygen, relate to the activity of single cells? I will address these questions, comparing electrical measurements of single cells and functional images, and advance our understanding of the brain in health and disease.
Visuomotor Integration In The Medial Parietal Cortical Areas
Funder
National Health and Medical Research Council
Funding Amount
$665,163.00
Summary
This project will find out how the electrical activity of brain cells is used to direct the arms to a specific position in the space around a person's body. By understanding the code used by brain cells to perform this control of the arms, we will be able to "read" the brain activity directly, and use it to allow control of artificial arms by people who have been paralysed or had amputations.
Developmental Plasticity In The Nonhuman Primate Visual Cortex
Funder
National Health and Medical Research Council
Funding Amount
$464,417.00
Summary
A phenomenon that has puzzled many for a number of years is why damage to the visual brain during infancy has far less of an impact on visual capacity than the same lesion suffered later in life. This project hopes to uncover this mystery and see how brain 'wiring' is altered to compensate.
Promoting Recovery After Neurotrauma: Basic Science, Clinical Trials And Community Engagement
Funder
National Health and Medical Research Council
Funding Amount
$356,269.00
Summary
To promote recovery after neurotrauma by controlling the spread of damage and by maximising function in surviving circuits. The work involves animal models & nanotechnology as well as clinical rehabilitation trials in humans with spinal cord injury.
Molecular And Cellular Changes Following A Cortical Injury: What Role Do They Play In Regeneration?
Funder
National Health and Medical Research Council
Funding Amount
$499,625.00
Summary
Damage to the visual areas of the brain is common after, for example stroke, neurotrauma or hypoxia. The injury often manifests in the form of a scar caused by a specific type of brain cell (astrocyte). This scar acts as a barrier to the cells which transmit information (neurones), preventing re-establishment of connectivity, thus functional recovery. We will see if we can reduce this scar and enhance re-connectivity after injury by blocking some of the molecules that brain cells express.
The Role Of Netrin-DCC In The Development Of The Corpus Callosum
Funder
National Health and Medical Research Council
Funding Amount
$512,065.00
Summary
During embryonic development neurons send out axons that connect to other target neurons within the brain. The proper connectivity of these axons is vital to brain function. The largest axon tract in the brain is called the corpus callosum and connects neurons in the left and right cerebral hemispheres. When the corpus callosum does not form, significant cognitive, motor and sensory deficits occur in patients. This condition, known as agenesis of the corpus callosum (ACC), is associated with ove ....During embryonic development neurons send out axons that connect to other target neurons within the brain. The proper connectivity of these axons is vital to brain function. The largest axon tract in the brain is called the corpus callosum and connects neurons in the left and right cerebral hemispheres. When the corpus callosum does not form, significant cognitive, motor and sensory deficits occur in patients. This condition, known as agenesis of the corpus callosum (ACC), is associated with over 50 different human congenital syndromes. Thus understanding how the genes and molecules involved in the formation of the corpus callosum function in normal development can provide the basis for our understanding of what goes wrong in ACC. In this proposal we will investigate the role of the axon guidance molecule Netrin1, and its receptor DCC, in development of the corpus callosum in both a mouse model and in humans with malformations of the corpus callosum. Although Netrin1-DCC signalling has traditionally been associated with mechanisms of axon guidance, we hypothesize that these molecules may play a different role, specifically in cellular adhesion and ultimately in the fusion of the two cerebral hemispheres, in a manner that allows the corpus callosum to form. A second role for Netrin1-DCC signalling may be in the guidance of these axons once the midline has fused correctly and we investigate this in Aim 2 of the proposal. Finally, we are collaborating with a paediatric neurologist at UCSF, who has identified several mutations in the DCC gene in patients with ACC. In Aim 3 we test whether these mutations disrupt the function of DCC in callosal axon pathfinding. Understanding how these genes function during development of the brain and how their function may be altered in ACC is crucial to providing a proper diagnosis and prognosis for these patients. Ultimately, understanding more about how these genes function could also lead to prevention of these disorders.Read moreRead less