Sickle hemoglobin disturbs normal coupling among erythrocyte O2 content, glycolysis, and antioxidant capacity

Assessment of oxidative stress in patients with sickle cell disease: The glutathione system and the oxidant–antioxidant status

(2011) Anna Gizi et al.   BLOOD CELLS MOLECULES AND DISEASES

Role of oxidative stress in the pathogenesis of sickle cell disease

(2011) Erica N. Chirico et al.   IUBMB LIFE

Pathophysiology of sickle cell disease is mirrored by the red blood cell metabolome

(2010) D. Darghouth et al.   BLOOD

Deoxygenation affects tyrosine phosphoproteome of red cell membrane from patients with sickle cell disease

(2010) Angela Siciliano et al.   BLOOD CELLS MOLECULES AND DISEASES

Hypoxia limits antioxidant capacity in red blood cells by altering glycolytic pathway dominance

(2009) Stephen C. Rogers et al.   FASEB JOURNAL

Role of band 3 in regulating metabolic flux of red blood cells

(2009) I. A. Lewis et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

G6PD deficiency, absence of  -thalassemia, and hemolytic rate at baseline are significant independent risk factors for abnormally high cerebral velocities in patients with sickle cell anemia

(2008) F. Bernaudin et al.   BLOOD

Protein area occupancy at the center of the red blood cell membrane

(2008) A. D. Dupuy et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

Characterization of the deoxyhemoglobin binding site on human erythrocyte band 3: implications for O2 regulation of erythrocyte properties

(2007) H. Chu et al.   BLOOD