Mechanisms Of Abnormal Expression Of The IGF2 Gene In Disorders Affectin Foetal Growth
Funder
National Health and Medical Research Council
Funding Amount
$420,872.00
Summary
The IGF2 gene is crucial for foetal growth. Only the copy inherited from the father is active, a phenomenon named parental imprinting. In some children with foetal overgrowth or growth retardation, the deregulation of imprinting of the IGF2 gene during the first days of foetal development will influence subsequent growth and will also have major implications in post-natal and adult life. We will investigate the mechanisms resulting in abnormal imprinting of IGF2 early in development.
MECHANISMS OF ABNORMAL EXPRESSION OF THE IGF2 GENE IN DISORDERS AFFECTING FOETAL GROWTH
Funder
National Health and Medical Research Council
Funding Amount
$560,434.00
Summary
The IGF2 gene is crucial for foetal growth. Only the copy inherited from the father is active, a phenomenon named parental imprinting. In some children with foetal overgrowth or growth retardation, the deregulation of imprinting of the IGF2 gene during the first days of foetal development will influence subsequent growth and will also have major implications in post-natal and adult life. We will investigate the mechanisms resulting in abnormal imprinting of the IGF2 early in development.
Adrenal Cushings:natural History And Genetic Analysis Of Inherited Forms, And Prevalence In High Risk Groups.
Funder
National Health and Medical Research Council
Funding Amount
$100,381.00
Summary
This study aims to diagnose early Cushing's in certain high risk groups - before debilitating complications have developed which increase mortality. Early treatment normalises life expectancy and improves quality of life. We aim to discover the genetic cause of inherited Cushing's. This will allow a genetic test to be developed - so gene carriers can be carefully followed for onset of symptoms of Cushing's and those who are not carriers can be reassured.