Changing rates of globin chain synthesis during erythroid cell maturation in thalassemia
Author:
Publisher
Elsevier BV
Subject
Molecular Biology,Structural Biology
Reference18 articles.
1. Hemoglobin synthesis in β-thalassemia: the properties of the free α-chains
2. Absolute Rates of Globin Chain Synthesis in Thalassemia
3. Protein synthesis in a cell free human reticulocyte system: ribosome function in thalassemia.
4. Excess α Chain Synthesis Relative to β Chain Synthesis in Thalassaemia Major and Minor
5. An Improved Method for the Characterization of Human Haemoglobin Mutants: Identification of α2β295GLU, Haemoglobin N (Baltimore)
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1. Pathophysiology of the Anaemia in Thalassaemia;Novartis Foundation Symposia;2008-05-30
2. GΓ andAΓ globin chain synthesis in bone marrow and peripheral blood of β-thalassaemia homozygotes;British Journal of Haematology;1982-10
3. Bone marrow and peripheral blood globin chain biosynthesis in iron deficiency;Blut;1982-03
4. The Imbalance of Chain Synthesis in Hemoglobin F;Hemoglobin;1981-01
5. Haemoglobin Synthesis in Bone Marrow of Patients with β° and β+-Thalassaemia;Acta Haematologica;1981
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