The Correlation between Red-Cell Survival and Excess of α-Globin Synthesis in β-Thalassaemia
- 1 January 1969
- journal article
- Published by Wiley in British Journal of Haematology
- Vol. 16 (1) , 25-30
- https://doi.org/10.1111/j.1365-2141.1969.tb00375.x
Abstract
No abstract availableKeywords
This publication has 9 references indexed in Scilit:
- Absence of β-Globin Synthesis and Excess of α-Globin Synthesis in Homozygous β-Thalassaemic Subjects from the Ferrara RegionNature, 1968
- Excess of α‐Globin Synthesis in Homozygous β‐Thalassemia and its Removal from the Red Blood Cell CytoplasmEuropean Journal of Biochemistry, 1968
- Excess α Chain Synthesis Relative to β Chain Synthesis in Thalassaemia Major and MinorNature, 1966
- Abnormal human haemoglobins: Separation and characterization of the α and β chains by chromatography, and the determination of two new variants, Hb chesapeake and Hb J (Bangkok)Journal of Molecular Biology, 1966
- Peptide analysis of the inclusions of erythroid cells in β-thalassemiaBiochimica et Biophysica Acta (BBA) - General Subjects, 1966
- Rapid Qualitative and Quantitative Hemoglobin Fractionation: Cellulose Acetate ElectrophoresisAmerican Journal of Clinical Pathology, 1965
- Globin Synthesis in Thalassaemia: An in vitro StudyNature, 1965
- Normal and Abnormal Human HemoglobinsPublished by Elsevier ,1963
- HEMATOLOGIC AND GENETIC STUDY OF THE TRANSMISSION OF THALASSEMIAArchives of internal medicine (1960), 1944