Globin chain synthesis in sickle beta-thalassaemic bone marrow and reticulocytes.

Author:

Ladas S,Chalevelakis G,Lyberatos C,Vaidakis E,Arapakis G

Publisher

BMJ

Subject

Genetics(clinical),Genetics

Reference32 articles.

1. Globin chain synthesis in thalassemia;Bank, A.; Braverman, A.S.; Marks, P.A.;Annals of the New York Academy of Sciences,1969

2. Changes in globin synthesis with erythroid cell maturation in sickle thalassaemia;Bank, A.; Dow, L.W.; Farace, M.G.; O'Donnell, J.V.; Ford, S.; Natta, C.;Blood,1973

3. Excess a-chain synthesis relative to P-chain synthesis in thalassaemia major and minor;Bank, A.; Marks, P.A.;Nature,1966

4. Preferential binding of 3S-globin chains associated with stroma in sickle cell disorders;Bank, A.; Mears, G.; Weiss, R.; O'Donnell, J.V.; Natta, C.;Journal of Clinical Investigation,1974

5. Changing rates of globin chain synthesis during erythroid cell maturation in thalassaemia;Braverman, A.S.; Bank, A.;Journal of Molecular Biology,1969

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