Enzymatic Defects of Heme Synthesis In Thalassemia*
Author:
Publisher
Wiley
Subject
History and Philosophy of Science,General Biochemistry, Genetics and Molecular Biology,General Neuroscience
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1749-6632.1965.tb54055.x/fullpdf
Reference9 articles.
1. Ribosomes active in protein synthesis in human reticulocytes: a defect in thalassemia major;BURKA;Nature,1963
2. Globin synthesis in reticulocytes;KARPATKIN;J. Lab. Clin. Med.,,1963
3. Haemoglobin synthesis in thalassaemia; in vitro studies;BANNERMAN;Brit. J. Haemat.,1959
4. Hemoglobin metabolism in thalassemia: in vivo studies;GRINSTEIN;Am. J. Med.,,1960
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1. Erythrocyte δ-Aminolaevulinic Acid Dehydratase in Homozygous b-Thalassaemia;Scandinavian Journal of Haematology;2009-04-24
2. The Relationship between Haem and Globin Synthesis by Erythroid Precursors in Refractory Normoblastic Anaemia;Scandinavian Journal of Haematology;2009-04-24
3. Erythrocyte Catalase Activity in Thalassaemia;Scandinavian Journal of Haematology;2009-04-24
4. Inhibition of heme synthesis induces apoptosis in human erythroid progenitor cells;Journal of Cellular Physiology;1995-04
5. Studies on porphyrin biosynthesis in lead-intoxicated rabbits;Clinica Chimica Acta;1976-06
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