Sickle cell: a metastable disease
Author:
- Robin BriehlRBRobin Briehl
- 1 December 1978
- journal article
- Published by Springer Nature in Nature
- Vol. 276 (5689) , 666-667
Abstract
No abstract availableThis publication has 25 references indexed in Scilit:
- Gelation of sickle cell hemoglobin IV. Phase transitions in hemoglobin S gels: Separate measures of aggregation and solution-gel equilibriumJournal of Molecular Biology, 1978
- Kinetics of hemoglobin S gelation followed by continuously sensitive low-shear viscosityJournal of Molecular Biology, 1977
- Analysis of non-ideal behavior in concentrated hemoglobin solutionsJournal of Molecular Biology, 1977
- Kinetics of the polymerization of hemoglobin S: Studies below normal erythrocyte hemoglobin concentrationBiochemical and Biophysical Research Communications, 1976
- Comparison of sickle cell hemoglobin gelation kinetics measured by NMR and optical methodsBiochemical and Biophysical Research Communications, 1976
- Formation of needle-like aggregates in stirred solutions of hemoglobin SBiochemical and Biophysical Research Communications, 1976
- Calorimetric and optical characterization of sickle cell hemoglobin gelationJournal of Molecular Biology, 1975
- The rates of polymerization and depolymerization of sickle cell hemoglobinBiochemical and Biophysical Research Communications, 1974
- A thermodynamic model for gelation of sickle-cell hemoglobinJournal of Molecular Biology, 1974
- Effects of pH, 2,3-diphosphoglycerate and salts on gelation of sickle cell deoxyhemoglobinJournal of Molecular Biology, 1973