References
- Giardina B, Messana I, Scatena R, Castagnola M. The multiple functions of hemoglobin. Crit Rev Biochem Mol Biol. 1995; 30: 165–196
- Ranney H, Briehl R, Jacobs A. Oxygen equilibrium of HbA, and of hemoglobin reconstituted from hemoglobins αA and H. J Biol Chem. 1965; 240: 2442
- Brunori M, Noble R, Antonini E, Wyman J. The reactions of the isolated a and B chains of human hemoglobin with oxygen and carbon monoxide. J Biol Chem. 1966; 241: 5238
- Tyuma I, Benesch RE, Benesch R. The preparation and properties of the isolated α and β subunits of HbA. Biochemistry 1966; 5: 2957
- Mc Donald M, Noble R. The effect of pH on the rates of ligand replacement reactions of human adult and fetal hemoglobins and their subunits. J Biol Chem. 1972; 247: 4282
- Rollema H, de Bruin S, van Os G. The Bohr effect of isolated α and β chains of human hemoglobin. FEBS Lett. 1976; 61: 148
- Bonaventura J, Bonaventura C, Amiconi G, Tentori L, Brunori M, Antonini E. Allosteric interactions in non a-chains isolated from normal human hemoglobin, fetal hemoglobin and Hb Abruzzo (β143 (H21) His→Arg). J Biol Chem. 1966; 250: 6278
- Benesh RE, Ranney H, Benesch R, Smith G. The chemistry of the Bohr effect. II. Some properties of hemoglobin H. J Biol Chem. 1961; 236: 2926
- Kattamis C, Tzotzos S, Kanavakis E, Synodinos J, Metaxotou A. Correlation of clinical phenotype to genotype in HbH disease. Lancet 1988; 1: 442–444
- Traeger-Synodinos J, Kanavakis E, Tzetis M, Kattamis A, Kattamis C. Characterization of nondeletion α-thalassemia mutations in the Greek population. Am J Hematol. 1993; 44: 162–167
- Rodkey F, Hill T, Pitts L, Robertson R. Spectrophotometric measurement of carboxy-Hb and methemoglobin in blood. Clin Chem. 1979; 25: 1388–1393
- Kutlar F, Kutlar A, Huisman T. Separation of normal and abnormal hemoglobin chains by reversed phase HPLC. J Chromatogr. 1986; 357: 147–153
- Powers D, Martin J, Wood S. A comparative study of the oxygen equilibria of blood from 40 genera of Amazonian fish. Comp Biochem Physiol. 1979; 62: 67–85
- Hallam J, Holland R, Dawson T. The blood of carnivorous marsupials: low hemoglobin oxygen affinity. Physiol Zool. 1995; 68: 342–354
- Festa R, Asakura T. The use of an oxygen dissociation curve analyzer in transfusion therapy. Transfusion. 1979; 19: 107–113
- Ericson A, de Verdier C. A modified method for the determination of 2,3-DPG in erythrocytes. Scand J Clin Lab Invest. 1972; 29: 85–90
- Bunn H, Forget B. Hemoglobin: Molecular, Genetic and Clinical Aspects. Saunders, Philadelphia 1986; 93
- Tan G, Dustan R, Lee S. Evaluation of high performance liquid chromatography for routine estimation of hemoglobins A2 and F. J Clin Pathol. 1993; 46: 852–856
- Alvarez-Sala F, Villegas A, Galero F, Espinos D. Red cell 2,3-DPG in thalassemia. Haematologica. 1983; 68: 312–319
- Baudin V, Pagnier J, Kister J, Poyart C. Functional consequences of mutations at the allosteric interface in hetero- and homo- hemoglobin tetramers. Protein Sci. 1993; 2: 1320–1330
- Haidas S, Zannos-Mariolea L, Matsaniotis N. Red cell 2,3-DPG levels in children with hereditary haemolytic anaemias. Br J Haematol. 1975; 31: 521–530
- Siggaard-Andersen O, Siggaard-Andersen M. The oxygen status algorithm: a computer program for calculating and displaying pH and blood gas data. Scand J Clin Lab Invest. 1990; 50(suppl 203)29–45
- Morgan T, Endre Z, Kanwski D, Jones M. Siggaard-Andersen algorithm P5(i parameters: perturbation by abnormal hemoglobin-oxygen affinity and acid-base disturbances. J Lab Clin Med. 1995; 126: 365–372
- Galacteros F, Loukopoulos D, Fessas P, Poyart C. Hemoglobin Köln occurring in association with a β° thalassemia: hematologic and functional consequences. Blood 1989; 74: 496–500
- Beguin Y, Clemons G, Pootrakul P, Fillet G. Quantitative assessment of erythropoiesis and functional classification of anemia based on measurements of serum transferrin receptor and erythropoietin. Blood 1993; 81: 1067–1076