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Oxygen equilibrium of hemoglobin E.
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Hemoglobin Hope: studies of oxygen equilibrium in heterozygotes, hemoglobin S-Hope disease, and isolated hemoglobin Hope.
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[Erythrocytosis due to a high-affinity hemoglobulin: mutant hemoglobin Saint-Jacques beta 140 (H18) Ala----Thr with a change in the 2,3-diphosphoglycerate binding site].
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Polycythemia produced by hemoglobin Osler (beta-145 (HC2) Tyr yields Asp).
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Oxygen equilibrium of hemoglobin J Cape Town.
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Structural and functional studies on hemoglobin Bethesda (alpha2beta2 145His), a varient associated with compensatory erythrocytosis.
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8
Effect of 2,3-diphosphoglycerate on oxygen affinity of blood in sickle cell anemia.
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9
Hemoglobin Rahere, a human hemoglobin variant with amino acid substitution at the 2,3-diphosphoglycerate binding site. Functional consequences of the alteration and effects of bezafibrate on the oxygen bindings.
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10
Oxygen equilibrium characteristics of abnormal hemoglobins. Hirose (alpha-2-beta-2-37Ser), L Ferrara (alpha-2-47-Gly-beta-2), Broussais (alpha-2-90-Asn-beta-2), and Dhofar (alpha-2-beta-2-58Arg).
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Hemoglobin Henri Mondor [β26(B8) Glu → Val, GAG > GTG], A First Case Report in South-East Asia.
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Oxidized Mutant Human Hemoglobins S and E Induce Oxidative Stress and Bioenergetic Dysfunction in Human Pulmonary Endothelial Cells.
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Structural and functional studies indicating altered redox properties of hemoglobin E: implications for production of bioactive nitric oxide.
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Modern cross-linking strategies for synthesizing acellular hemoglobin-based oxygen carriers.
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Haemoglobin E trait and probable alpha-thalassaemia in a black American family: a family study.
J Med Genet. 1980 Aug;17(4):285-7. doi: 10.1136/jmg.17.4.285.
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Hemoglobin E in Indochinese refugees.
West J Med. 1982 Sep;137(3):186-90.
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Hemoglobin brigham (alpha2Abeta2100 Pro--Leu). Hemoglobin variant associated with familial erythrocytosis.
J Clin Invest. 1973 Aug;52(8):2060-7. doi: 10.1172/JCI107390.
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