The role of alpha-haemoglobin stabilising protein in haemoglobin production and as a therapeutic for thalassaemia. [ 2009 - 2011 ]

Research Grant

Researchers: Dr David Gell (Principal investigator) ,  Dr Mitchell Weiss ,  Professor Mitchell Guss

Brief description Thalassaemias are the most common hereditary diseases effecting the production of red blood cells. The underlying cause of disease is a failure to produce normal quantities of haemoglobin (Hb; the essential oxygen-carrying molecule in blood), resulting in severe anaemia. We have discovered a new protein with an important role in Hb production. We will elucidate the function of this protein in red blood cells and investigate novel treatments for thalssaemia disease.

Funding Amount $AUD 320,936.34

Funding Scheme NHMRC Project Grants

Notes Standard Project Grant