In five patients with sickle β-thalassemia there was balanced α- and β-globin synthesis in the bone marrow and decreased total β-chain synthesis relative to that of α-chain in the peripheral blood. These findings are similar to those in patients with simple β-thalassemia trait. Despite a range of hemoglobin concentrations from 6.8 to 12.5 g/100 ml in the patients with sickle thalassemia, there was no evidence of a significant excess of α-chains in the red cells of the bone marrow which could contribute to the hemolysis and anemia.
Frances M. Gill, Elias Schwartz
Title and authors | Publication | Year |
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Bone marrow and peripheral blood globin chain synthesis in sickle cell beta zero thalassaemia
FF Costa, MA Zago |
Journal of medical genetics | 1986 |
β Globin messenger RNA content of bone marrow erythroblasts in heterozygous β-thalassemia
EJ Benz, J Pritchard, D Hillman, J Glass, BG Forget |
American Journal of Hematology | 1984 |
Sickle cell β-thalassaemia compared with sickle cell anaemia in Algeria
M Belhani, L Morle, J Godet, D Bachir, T Henni, F Zerhouni, A Bensenouci, P Colonna |
Scandinavian Journal of Haematology | 1984 |
The interaction of α thalassaemia with heterozygous β thalassaemia
E Kanavakis, JS Wainscoat, WG Wood, DJ Weatherall, A Cao, M Furbetta, R Galanello, D Georgiou, T Sophocleous |
British Journal of Haematology | 1982 |
Globin Synthesis in Bone Marrow Cells of Patients with Sickle Cell Anemia and β O -Thalassemia: Contamination of the β-Chain with Non-Globin Proteins
G Cividalli, H Kerem, EA Rachmilewitz |
Hemoglobin | 1979 |
Globin chain synthesis in sickle beta-thalassaemic bone marrow and reticulocytes
S Ladas, G Chalevelakis, C Lyberatos, E Vaidakis, G Arapakis |
Journal of medical genetics | 1979 |
Proteolytic activity in erythrocyte precursors
SM Hanash, DL Rucknagel |
Proceedings of the National Academy of Sciences | 1978 |
The Interaction of B 0 -Thalassemia with Hemoglorin D Punjab: A Study of Globin Chain Synthesis in an Indian Family
SK Pallas, J Atwater, DG Norris |
Hemoglobin | 1977 |
Heterozygous Beta Thalassaemia of Unusual Severity
S Friedman, S Özsoylu, R Luddy, E Schwartz |
British Journal of Haematology | 1976 |
Variations in Globin Chain Synthesis in Hereditary Persistence of Fetal Haemoglobin
S Friedman, E Schwartz, E Ahern, V Ahern |
British Journal of Haematology | 1976 |
Globin Synthesis in Normal Human Bone Marrow
G Chalevelakis, JB Clegg, DJ Weatherall |
British Journal of Haematology | 1976 |
Hereditary persistence of foetal haemoglobin with β-chain synthesis in cis position (Gγ-β+-HPFH) in a negro family
S Friedman, E Schwartz |
Nature | 1976 |
Sickle β-thalassemia: Identical twins differing in severity implicate nongenetic factors influencing course
SK Joishy, PF Griner, PT Rowley |
American Journal of Hematology | 1976 |
Clinical, hematologic and biosynthetic studies in sickle cell-β°-thalassemia: A comparison with sickle cell anemia
MH Steinberg, BJ Dreiling |
American Journal of Hematology | 1976 |
Sickle cell-β0 thalassemia variant with high hemoglobin F and mild clinical course
JR Shaeffer, JL Moake |
The American Journal of Medicine | 1976 |
Globin synthesis in fractionated Normoblasts of beta-thalassemia heterozygotes
WG Wood, G Stamatoyannopoulos |
Journal of Clinical Investigation | 1975 |
Imbalanced globin chain synthesis in heterozygous beta-thalassemic bone marrow
G Chalevelakis, JB Clegg, DJ Weatherall |
Proceedings of the National Academy of Sciences | 1975 |
Cell Cycle and Cell Differentiation
J Reinert, H Holtzer |
1975 | |
Globin Synthesis in the Jamaican Negro with Beta-Thalassaemia
S Friedman, E Schwartz, V Ahern, E Ahern |
British Journal of Haematology | 1974 |
VARIATION IN ?/? SYNTHESIS RATIOS IN THALASSEMIA AND HEMOGLOBINOPATHIES
RF Rieder |
Annals of the New York Academy of Sciences | 1974 |
THALASSEMIA IN BLACK AMERICANS
S Charache, CL Conley, TD Doeblin, M Bartalos |
Annals of the New York Academy of Sciences | 1974 |
A NEW FORM OF ?-THALASSEMIA TRAIT
G Stamatoyannopoulos, T Papayannopoulou, R Woodson, D Heywood, S Kurachi |
Annals of the New York Academy of Sciences | 1974 |
Inclusion-Body β-Thalassemia Trait: A Form of β Thalassemia Producing Clinical Manifestations in Simple Heterozygotes
G Stamatoyannopoulos, R Woodson, T Papayannopoulou, D Heywood, S Kurachi |
New England Journal of Medicine | 1974 |
Free α-Globin Pool in Human Bone Marrow
FM Gill, E Schwartz |
Journal of Clinical Investigation | 1973 |