Most eye diseases have a genetic contribution, whether rare disorders affecting children such as retinoblastoma or congenital cataracts through to common disorders of older people such as myopia, age-related macular degeneration or glaucoma. We will continue our successful research to find genes that cause these diseases and use this to improve patient care and prevent blindness. We will work out how families can use this genetic information to participate in trials to develop new treatments.
Bio-molecular Studies For Improved Diagnosis And Management Of Australian Children With Fish Allergy
Funder
National Health and Medical Research Council
Funding Amount
$496,602.00
Summary
Allergy to fish among children is often life-long and emerging as a significant healthcare issue worldwide, while management of fish allergy is challenging due to the lack of reliable diagnostic assays. This research grant will lead to the development of novel diagnostics for fish allergy in Australia, addressing aspects of the worldwide food allergy epidemic and forms the ideal platform for the study of fish specific allergens, generating novel knowledge for greatly improved patient management.
Neural Mechanisms That Limit The Visual Sensitivity Of Primates
Funder
National Health and Medical Research Council
Funding Amount
$379,400.00
Summary
This project concerns the way nerve cells in the brain enable the detection and perception of objects in the visual world. It is thought that nerve cells early in the visual pathway signal the presence or absence of light in a small part of the visual field, but the nature of the neuronal code carried by these pathways remains poorly understood. The aim of our project is to address this basic question, in experimental studies of the intact primate visual system. We will conduct two sets of exper ....This project concerns the way nerve cells in the brain enable the detection and perception of objects in the visual world. It is thought that nerve cells early in the visual pathway signal the presence or absence of light in a small part of the visual field, but the nature of the neuronal code carried by these pathways remains poorly understood. The aim of our project is to address this basic question, in experimental studies of the intact primate visual system. We will conduct two sets of experiments. Firstly, we will test the hypothesis that nerve cells in the early visual system are sensitive to only a small part of the visual field. We will determine whether the signals of pre-cortical nerve cells are dependant on spatial context. Secondly we wll study the signals of several nerve cells simultaneously using multiple electrodes. We will determine if the signals of many nerve cells are required to detect small visual stimuli like those used in perimetry. These experiments address basic questions, but have application to human vision and visual dysfunction. Good acuity is essential for everyday tasks such as reading, and defects in visual sensitivity are used for early detection of neurological dysfunction in diseases such as glaucoma and macular degeneration. Understanding the properties of neurons which underlie visual perception can thus help us to understand normal visual performance, and how this changes in partial sight. This can help develop better methods for detection and treatments for such disorders.Read moreRead less
ARMC5 And Other Genetic Contributions In Endocrine Neoplasia
Funder
National Health and Medical Research Council
Funding Amount
$124,676.00
Summary
The adrenal glands secrete essential hormones and can enlarge or develop tumours leading to conditions including obesity, high blood pressure, diabetes, brittle bones and infections. We recently found that adrenal enlargement and tumours may be due to changes in the ARMC5 gene. We will perform genetic testing in affected patients across Australia to evaluate the roles of ARMC5 & other genes. Our goal is to better understand how these conditions develop so as to improve diagnosis and treatment.
Age-related Macular Degeneration: A Cause And A Cure
Funder
National Health and Medical Research Council
Funding Amount
$828,300.00
Summary
Age-related macular degeneration (AMD) is a leading cause of vision loss and there is urgent need for an intervention to slow disease progression. AMD is characterised by debris accumulation in the retina and I will investigate if loss of function in cells that should clear this debris is a critical step in the development of AMD. I will trial a novel laser intervention to slow progression of disease and use basic science techniques to investigate the mechanisms of action of the laser.