Sickle cell anemia has been considered the first molecular disease. A single genetic point mutation, affecting the structure of hemoglobin, leads to deformations in blood cells which can cause cardiovascular crisis. Sickle cell hemoglobin (HbS) polymerizes and forms long rigid fibers, which deform the cell. Free heme has been shown to significantly enhance HbS nucleation, leading to polymerization. In this study, we investigated different density layer fractions of erythrocytes and the concentration of free heme present in the erythrocyte cytosol. Through centrifugation of erythrocytes in Percoll, we were able to form a density gradient of erythrocytes. Using enzyme-linked chemiluminescence, we quantified the concentration of free heme in e...
Introduction: The sickle cell disease is a genetic disease of the red blood cell. It results in the ...
AbstractSickle cell anemia is a debilitating genetic disease that affects hundreds of thousands of b...
International audiencePolymerization of the sickle hemoglobin (HbS) is a key determinant of sickle c...
AbstractIn search of novel control parameters for the polymerization of sickle cell hemoglobin (HbS)...
Sickle cell hemoglobin (HbS) polymerization is considered to be the primary pathogenic event in the ...
Recent work has enabled us to quantitate the four variables (2,3-DPG concentration, pHi, non-S hemog...
Recent work has enabled us to quantitate the four variables (2,3-DPG concentration, phi, non-S hemog...
We analyzed the effects of protein and water nonideality and of erythrocyte heterogeneity on the pol...
AbstractPathology in sickle cell disease begins with nucleation-dependent polymerization of deoxyhem...
International audienceIntravascular hemolysis describes the relocalization of heme and hemoglobin (H...
The primary pathogenic event of sickle cell anemia is the polymerization of the mutant hemoglobin (H...
The critical importance of red cell hydration in sickle cell dis-ease derives from the huge effects ...
Precision scale models of sickle cell hemoglobin molecules indicate that the genetic substitution of...
AbstractTo understand the physical basis of the wide variety of shapes of deoxygenated red cells fro...
Severe hemolysis or myolysis occurring during pathological states, such as sickle cell disease, isch...
Introduction: The sickle cell disease is a genetic disease of the red blood cell. It results in the ...
AbstractSickle cell anemia is a debilitating genetic disease that affects hundreds of thousands of b...
International audiencePolymerization of the sickle hemoglobin (HbS) is a key determinant of sickle c...
AbstractIn search of novel control parameters for the polymerization of sickle cell hemoglobin (HbS)...
Sickle cell hemoglobin (HbS) polymerization is considered to be the primary pathogenic event in the ...
Recent work has enabled us to quantitate the four variables (2,3-DPG concentration, pHi, non-S hemog...
Recent work has enabled us to quantitate the four variables (2,3-DPG concentration, phi, non-S hemog...
We analyzed the effects of protein and water nonideality and of erythrocyte heterogeneity on the pol...
AbstractPathology in sickle cell disease begins with nucleation-dependent polymerization of deoxyhem...
International audienceIntravascular hemolysis describes the relocalization of heme and hemoglobin (H...
The primary pathogenic event of sickle cell anemia is the polymerization of the mutant hemoglobin (H...
The critical importance of red cell hydration in sickle cell dis-ease derives from the huge effects ...
Precision scale models of sickle cell hemoglobin molecules indicate that the genetic substitution of...
AbstractTo understand the physical basis of the wide variety of shapes of deoxygenated red cells fro...
Severe hemolysis or myolysis occurring during pathological states, such as sickle cell disease, isch...
Introduction: The sickle cell disease is a genetic disease of the red blood cell. It results in the ...
AbstractSickle cell anemia is a debilitating genetic disease that affects hundreds of thousands of b...
International audiencePolymerization of the sickle hemoglobin (HbS) is a key determinant of sickle c...