Interaction of hemoglobin, nitric oxide and the stress protein haem oxygenase-1 : functional implications in sickle cell disease
Haemoglobin and nitric oxide (NO) strongly induce the stress protein haem oxygenase-1 (HO-1), which degrades haem to carbon monoxide (CO), a signalling and vasoactive molecule, the anti-oxidant biliverdin (BV) and iron. Raised HO-1 levels have been detected in the endothelium and kidneys of animals,...
Main Author: | Bains, Sandip Kaur |
---|---|
Published: |
University College London (University of London)
2008
|
Subjects: | |
Online Access: | http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.500150 |
Similar Items
-
The Role of Complement and Nitric Oxide in the Pathophysiology of Paroxysmal Nocturnal Haemoglobinuria
by: Hill, Anita
Published: (2008) -
The spleen in sickle cell disease in childhood
by: Edmond, A. M.
Published: (1988) -
Proteinuria and the nephrotic syndrome in sickle cell disease
by: Nicholson, G. D.
Published: (1979) -
The relationship between non transferrin bound iron and iron overload in thalassaemia and sickle syndromes
by: Shah, Farrukh Tasnim
Published: (2007) -
Studies on Salt and Water Homeostasis and its Relationship to Urinary Kininogenase (Kallikrein) Excretion in Essential Hypertension and Sickle Cell Haemoglobinopathy
by: Adetujibi, A.
Published: (1976)