| Literature DB >> 14194103 |
Abstract
Rates of synthesis of hemoglobin A by erythroid cells from thalassemic subjects are markedly decreased. Formation of hemoglobin F, however, proceeds at similar rates in cells from subjects with thalassemia and other types of hemolytic anemias. A mechanism is suggested regarding the altered patterns of hemoglobin synthesis under conditions of erythropoietic stimulation in subjects with and without thalassemia.Entities:
Keywords: CARBON ISOTOPES; DNA; ERYTHROPOIESIS; HEMOGLOBINS, ABNORMAL; HISTOCYTOCHEMISTRY; ISOLEUCINE; LEUCINE; PROTEIN METABOLISM; RIBOSOMES; RNA; THALASSEMIA
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Year: 1964 PMID: 14194103 DOI: 10.1126/science.144.3618.552
Source DB: PubMed Journal: Science ISSN: 0036-8075 Impact factor: 47.728