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Spin Label Studies of the Hemoglobin–Membrane Interaction During Sickle Hemoglobin Polymerization
(Springer Wien, 2010-05)
An enhanced hemoglobin–membrane association has been previously documented in sickle cell anemia. However, it is not known how this interaction is modified during the hemoglobin S polymerization process. In this work, we ...
EPR study of the Hemoglobin rotational correlation time and microviscosity during the polymerization of Hemoglobin S
(Springer Wien, 2006-12)
The microviscosity and the protein rotational correlation time are analyzed in samples of hemoglobin A and hemoglobin S with the intracellular concentration at 36ºC and during spontaneous deoxygenation. With this purpose, ...
Effect of thiol reagents on functional properties and heme oxidation in the hemoglobin of Geochelone carbonaria
(Academic Press AustMarrickvilleAustralia, 1996)
Recent Insights on the Medicinal Chemistry of Sickle Cell Disease
(Bentham Science Publ Ltd, 2011-05-01)
Sickle Cell Disease (SCD) is one of the most prevalent hematological diseases in the world. SCD is a genetic disease characterized by punctual mutation that basis on the exchange of glutamic acid to valine in a beta chain ...
Recent Insights on the Medicinal Chemistry of Sickle Cell Disease
(Bentham Science Publ Ltd, 2011-05-01)
Sickle Cell Disease (SCD) is one of the most prevalent hematological diseases in the world. SCD is a genetic disease characterized by punctual mutation that basis on the exchange of glutamic acid to valine in a beta chain ...
Recent Insights on the Medicinal Chemistry of Sickle Cell Disease
(Bentham Science Publ Ltd, 2014)
Reticulocyte parameters and hemoglobin F production in sickle cell disease patients undergoing hydroxyurea therapy
(Wiley-lissNew YorkEUA, 2003)
Hemoglobin-sulfhydryls from tortoise (Geochelone carbonaria) can reduce oxidative damage induced by organic hydroperoxide in erythrocyte membrane
(Pergamon-elsevier Science LtdOxfordInglaterra, 2000)
A complexa fisiopatologia dos episódios vasooclusivos na anemia falciforme
(2002-12-01)
Hemolytic anemia and vasoocclusion are the cardinal clinical features of sickle cell anemia. Vasoocclusion is a complex process involving not only the polymerization of deoxygenated sickle hemoglobin tetramers, but also ...
A complexa fisiopatologia dos episódios vasooclusivos na anemia falciforme
(2002-12-01)
Hemolytic anemia and vasoocclusion are the cardinal clinical features of sickle cell anemia. Vasoocclusion is a complex process involving not only the polymerization of deoxygenated sickle hemoglobin tetramers, but also ...