Abnormalities of Heme and Pyrrole Metabolism 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.tb54051.x/fullpdf
Reference33 articles.
1. Genetic basis of the thalassemia diseases;INGRAM;Nature (London),1959
2. Ribosomes active in protein synthesis in human reticulocytes: a defect in thalassaemia major;BURKA;Nature (London),1963
3. Haemoglobin synthesis in thalassaemia; in-vitro studies;BANNERMAN;Brit. J. Haemat.,1959
4. Biosynthesis of hemoglobin;RIMINGTON;Brit. Med. Bull.,1959
5. Porphyrin biosynthesis. Phyriaporphyrinogen III, a normal intermediate in the biosynthesis of protoporphyrin 9;BATLLE;Biochim. Biophys. Acta.,1962
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1. Erythrocyte δ-Aminolaevulinic Acid Dehydratase in Homozygous b-Thalassaemia;Scandinavian Journal of Haematology;2009-04-24
2. Inhibition of heme synthesis induces apoptosis in human erythroid progenitor cells;Journal of Cellular Physiology;1995-04
3. 5-Aminolaevulinic acid synthase activity in developing human erythroblasts;British Journal of Haematology;1988-06
4. The Thalassemias: Models for Analysis of Quantitative Gene Control;Advances in Human Genetics;1975
5. FEVER IN THALASSÆMIA;The Lancet;1974-09
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