Excess of α‐Globin Synthesis in Homozygous β‐Thalassemia and its Removal from the Red Blood Cell Cytoplasm
- 1 January 1968
- journal article
- research article
- Published by Wiley in European Journal of Biochemistry
- Vol. 3 (3) , 364-368
- https://doi.org/10.1111/j.1432-1033.1968.tb19538.x
Abstract
No abstract availableThis publication has 15 references indexed in Scilit:
- Excess α Chain Synthesis Relative to β Chain Synthesis in Thalassaemia Major and MinorNature, 1966
- Polyribosomes and control of protein synthesis: Effects of sodium fluoride and temperature in reticulocytesJournal of Molecular Biology, 1966
- PREPARATIONS OF HUMAN CHROMOSOMESThe Lancet, 1966
- Globin Synthesis in Thalassaemia: An in vitro StudyNature, 1965
- An Improved Method for the Characterization of Human Haemoglobin Mutants: Identification of α2β295GLU, Haemoglobin N (Baltimore)Nature, 1965
- Amino Acids: Incorporation into α- and β-Chains of Hemoglobin by Normal and Thalassemic ReticulocytesScience, 1964
- Protein synthesis in erythroid cellsJournal of Molecular Biology, 1964
- The preparation and properties of haemoglobin αA, a haemoglobin consisting of αA-polypeptide chainsJournal of Molecular Biology, 1962
- Studies on the structure of hemoglobin I. Physicochemical properties of human globinBiochimica et Biophysica Acta, 1958
- Observations on the Chromatographic Heterogeneity of Normal Adult and Fetal Human Hemoglobin: A Study of the Effects of Crystallization and Chromatography on the Heterogeneity and Isoleucine ContentJournal of the American Chemical Society, 1958