The Effect Of Genetic Polymorphisms On The Development Of Systemic Lupus Erythematosus
Funder
National Health and Medical Research Council
Funding Amount
$50,741.00
Summary
Systemic lupus erythematosus is a debilitating disease that predominantly affects women of child-bearing age and may involve any organ. Genetics is one of the most well-recognised risk factors, and yet how genetics can cause lupus is unclear. This study involves examining the entire genetic sequence of individual patients to identify the mutations that cause the immune system to be dysregulated leading to disease.
Determinants Of Outcomes In SLE: Impact Of Models Of Care, Socioeconomic Factors And Biologic Variables In A Multiethnic Australian Population
Funder
National Health and Medical Research Council
Funding Amount
$134,124.00
Summary
Lupus is a chronic disease where the immune cells attack multiple systems in the body, which can lead to severe organ damage and even death. It is known that genes, socioeconomics and models of care all individually influence the outcomes in lupus. The exact contribution of each one is poorly understood, because they are studied in isolation. This project will take an integrated approach to investigating the factors that influence outcomes in lupus, looking for potentially addressable effects.
Assessment Of Calcium Signaling In Breast Cancer Cells Associated With Epithelial-mesenchymal Transition
Funder
National Health and Medical Research Council
Funding Amount
$116,762.00
Summary
This research will assess the role of specific proteins that control cell function in a process which is important in the spread of cancer cells throughout the body. The work is aimed at identifying new targets for drugs that may be used to prevent or stop the spread of breast cancer cells to other organs such as the brain and liver.
The Biophysical Basis Of HCN Channels In Human Peripheral Nerve
Funder
National Health and Medical Research Council
Funding Amount
$50,315.00
Summary
Hyperpolarization-activated cyclic nucleotide-gated (HCN) channels play an important role as pacemakers in the cardiac and nervous systems. HCN channel dysfunction is implicated in a number of disorders including neuropathic pain and epilepsy. My aim is to determine the kinetics and voltage dependence of HCN channels in human peripheral nerve in vivo. Understanding these channels is a prerequisite to the development of safe targeted therapies against neuropathic pain.