Requirements for therapeutic inhibition of sickle haemoglobin gelation
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J. Hofrichter | W. Eaton | H. Sunshine | HELEN R. SUNSHINE | JAMES HOFRICHTER | WILLIAM A. EATON | HELEN R. SUNSHINE | WILLIAM A. EATON
[1] H. Bunn. The interaction of sickle hemoglobin with DPG, CO 2 and with other hemoglobins: formation of asymmetrical hybrids. , 1972, Advances in experimental medicine and biology.
[2] H. Bunn,et al. Asymmetrical hemoglobin hybrids. An approach to the study of subunit interactions. , 1974, Biochemistry.
[3] S. Charache. MEASUREMENT OF HOMEOSTATIC RESPONSES TO ALTERED P 50 IN PATIENTS WITH ABNORMAL HEMOGLOBINS , 1978 .
[4] A. Schechter,et al. Effects of amino acids on gelation kinetics and solubility of sickle hemoglobin. , 1977, Biochemical and biophysical research communications.
[5] M. Behe,et al. Sickle hemoglobin gelation. Reaction order and critical nucleus size. , 1978, Biophysical journal.
[6] J. Hofrichter,et al. SUCCESSES AND FAILURES OF A SIMPLE NUCLEATION THEORY FOR SICKLE CELL HEMOGLOBIN GELATION , 1978 .
[7] J. Hofrichter,et al. Thermodynamics of gelation of sickle cell deoxyhemoglobin. , 1977, Journal of molecular biology.
[8] I. Wells,et al. Ratio of sickle-cell anemia hemoglobin to normal hemoglobin in sicklemics. , 1951, The Journal of biological chemistry.
[9] Harris Jw,et al. The kinetics of the sol-gel transformation of deoxyhemoglobin S by continuous monitoring of viscosity. , 1975 .
[10] J. Hofrichter,et al. Kinetics and mechanism of deoxyhemoglobin S gelation: a new approach to understanding sickle cell disease. , 1974, Proceedings of the National Academy of Sciences of the United States of America.
[11] A. Minton. Non-ideality and the thermodynamics of sickle-cell hemoglobin gelation. , 1977, Journal of molecular biology.
[12] K. Singer,et al. Studies on abnormal hemoglobins. VIII. The gelling phenomenon of sickle cell hemoglobin: its biologic and diagnostic significance. , 1953, Blood.
[13] J. Hofrichter,et al. Comparison of sickle cell hemoglobin gelation kinetics measured by NMR and optical methods. , 1976, Biochemical and biophysical research communications.
[14] M. Goldberg,et al. Participation of hemoglobins A and F in polymerization of sickle hemoglobin. , 1977, The Journal of biological chemistry.
[15] K. Moffat,et al. The rates of polymerization and depolymerization of sickle cell hemoglobin. , 1974, Biochemical and biophysical research communications.
[16] J. Hofrichter,et al. Supersaturation in sickle cell hemoglobin solutions. , 1976, Proceedings of the National Academy of Sciences of the United States of America.
[17] J. Bertles,et al. Hemoglobin Interaction: Modification of Solid Phase Composition in the Sickling Phenomenon , 1970, Science.
[18] J. B. Clegg,et al. The thalassaemia syndromes , 1965 .
[19] R M Hochmuth,et al. Sickling times of individual erythrocytes at zero Po2. , 1975, The Journal of clinical investigation.
[20] R. Nagel,et al. Ligand-induced conformational dependence of hemoglobin in sickling interactios. , 1971, Journal of molecular biology.
[21] J. Steinhardt,et al. A temperature-dependent latent-period in the aggregation of sickle-cell deoxyhemoglobin. , 1974, Biochemical and biophysical research communications.
[22] G. Brewer. Hemoglobin and Red Cell Structure and Function , 1972, Advances in Experimental Medicine and Biology.
[23] Constance M. Park. ISOELECTRIC FOCUSING AND THE STUDY OF INTERACTING PROTEIN SYSTEMS: LIGAND BINDING, PHOSPHATE BINDING, AND SUBUNIT EXCHANGE IN HEMOGLOBIN , 1973, Annals of the New York Academy of Sciences.
[24] E. Beutler. The red cell indices in the diagnosis of iron-deficiency anemia. , 1959, Annals of internal medicine.
[25] William A. Eaton,et al. Editorial: Delay time of gelation: a possible determinant of clinical severity in sickle cell disease , 1976 .