Literature Review] Genetic architecture of the red blood cell proteome in genetically diverse mice reveals central role of hemoglobin beta cysteine redox status in maintaining circulating glutathione pools Red blood cell metabolism in Rhesus macaques and humans: comparative biology of blood storage Haematologica Erythrocyte and plasma oxidative stress appears to be compensated in patients with sickle cell disease during a period of relative health, despite the presence of known oxidative agents ScienceDirect Storage lesion: History and perspectives Hereditary Hemolytic Anemias Due to Red Blood Cell Enzyme Disorders Oncohema Key L glutamine for sickle cell disease: more than reducing redox Annals of Hematology Springer Nature Link