Heterozygous Beta Thalassemia: Balanced Globin Synthesis in Bone Marrow Cells
Author:
Affiliation:
1. Cardeza Foundation for Hematologic Research and Department of Pediatrics, Jefferson Medical College, Philadelphia, Pennsylvania 19107
Publisher
American Association for the Advancement of Science (AAAS)
Subject
Multidisciplinary
Reference19 articles.
1. BANK, A, PROTEIN SYNTHESIS IN A CELL FREE HUMAN RETICULOCYTE SYSTEM - RIBOSOME FUNCTION IN THALASSEMIA, JOURNAL OF CLINICAL INVESTIGATION 45: 330 (1966).
2. BANK, A, HEMOGLOBIN SYNTHESIS IN BETA-THALASSEMIA - PROPERTIES OF FREE ALPHA-CHAINS, JOURNAL OF CLINICAL INVESTIGATION 47: 860 (1968).
3. BANK, A, EXCESS ALPHA CHAIN SYNTHESIS RELATIVE TO BETA CHAIN SYNTHESIS IN THALASSAEMIA MAJOR AND MINOR, NATURE 212: 1198 (1966).
4. BARGELLESI, A, EXCESS OF ALPHA-GLOBIN SYNTHESIS IN HOMOZYGOUS BETA-THALASSEMIA AND ITS REMOVAL FROM RED BLOOD CELL CYTOPLASM, EUROPEAN JOURNAL OF BIOCHEMISTRY 3: 364 (1968).
5. BOYER, S, MODULATION OF PROTEIN SYNTHESIS IN MAN - AN IN VITRO STUDY OF HEMOGLOBIN SYNTHESIS BY HETEROZYGOTES, COLD SPRING HARBOR SYMPOSIA ON QUANTITATIVE BIOLOGY 29: 333 (1964).
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4. Bone marrow and peripheral blood globin chain synthesis in sickle cell beta zero thalassaemia.;Journal of Medical Genetics;1986-06-01
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