Decreased β Globin mRNA Activity in Bone Marrow Cells in Homozygous and Heterozygous β Thalassaemia
- 1 August 1973
- journal article
- Published by Springer Nature in Nature New Biology
- Vol. 244 (139) , 280-281
- https://doi.org/10.1038/newbio244280a0
Abstract
No abstract availableKeywords
This publication has 10 references indexed in Scilit:
- Haemoglobin Synthesis during Erythroid Maturation in β-ThalassaemiaNature New Biology, 1972
- Induction of β-Globin Synthesis in the β-Thalassaemia of FerraraNature New Biology, 1972
- Increased Efficiency of Exogenous Messenger RNA Translation in a Krebs Ascites Cell LysateProceedings of the National Academy of Sciences, 1972
- Isolation and translation of hemoglobin messenger RNA from thalassemia, sickle cell anemia, and normal human reticulocytesJournal of Clinical Investigation, 1971
- The synthesis of mouse hemoglobin chains in a rabbit reticulocyte cell-free system programmed with mouse reticulocyte 9S RNABiochemical and Biophysical Research Communications, 1969
- Changing rates of globin chain synthesis during erythroid cell maturation in thalassemiaJournal of Molecular Biology, 1969
- 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
- Protein synthesis in a cell free human reticulocyte system: ribosome function in thalassemia.Journal of Clinical Investigation, 1966
- Purification of viral RNA by means of bentoniteVirology, 1961