Absence of Messenger RNA for Beta Globin Chain in β°-Thalassaemia
- 1 February 1974
- journal article
- Published by Springer Nature in Nature
- Vol. 247 (5440), 379-381
- https://doi.org/10.1038/247379a0
Abstract
No abstract availableThis publication has 9 references indexed in Scilit:
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- Hemoglobin Messenger RNA from Human Bone Marrow ISOLATION AND TRANSLATION IN HOMOZYGOUS AND HETEROZYGOUS β-THALASSEMIAJournal of Clinical Investigation, 1973
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- Quantitative Deficiency of Chain-Specific Globin Messenger Ribonucleic Acids in the Thalassemia SyndromesProceedings of the National Academy of Sciences, 1973
- Distinction between Two Types of Beta-Thalassaemia by Inducibility of the Cell-free Synthesis of Beta-Chains by Nonthalassaemic Soluble FractionNature New Biology, 1972
- Induction of β-Globin Synthesis in the β-Thalassaemia of FerraraNature New Biology, 1972
- Defect in messenger RNA for human hemoglobin synthesis in beta thalassemiaJournal of Clinical Investigation, 1971
- Isolation and translation of hemoglobin messenger RNA from thalassemia, sickle cell anemia, and normal human reticulocytesJournal of Clinical Investigation, 1971
- Three Cases of Homozygous βδ-Thalassaemia (or Microcythaemia) with High Haemoglobin F in a Sicilian FamilyActa Haematologica, 1968