In vitro synthesis of hemoglobin and hemoglobin chains in the BFUe-derived colonies from persons with α- or β-thalassemia
Author:
Publisher
Wiley
Subject
Hematology
Reference24 articles.
1. Circulating erythropoietic precursors assessed in culture: characterization in normal men and patients with hemoglobinopathies
2. Erythroid Progenitors Circulating in the Blood of Adult Individuals Produce Fetal Hemoglobin in Culture
3. Hemoglobin synthesis in human BFU-E and CFU-E-derived erythroid colonies
4. The Synthesis of Fetal Hemoglobin Types in red Blood Cells and in BFU-E Derived Colonies from Peripheral Blood of Patients with Sickle Cell Anemia, β+- and δβ-Thalassemia, Various forms of Hereditary Persistence of Fetal Hemoglobin, Normal Adults and Newborn
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1. FORTY-FOUR YEARS (1955–1999) DEVOTED TO HEMOGLOBIN RESEARCH: TITUS H. J. HUISMAN (1923–1999);Hemoglobin;2001-01
2. Sickle and Thalassemic Erythroid Progenitor Cells are Different from Normal;Hemoglobin;1992-01
3. Erythropoiesis following bone marrow transplantation from donors heterozygous for β-thalassaemia;British Journal of Haematology;1989-08
4. Application of high-performance liquid chromatographic methodology to the analysis of hemoglobins synthesized in erythroid progenitor cells;Journal of Chromatography B: Biomedical Sciences and Applications;1989-01
5. Adult‘fetal-like’erythropoiesis characterizes recovery from bone marrow transplantation;British Journal of Haematology;1986-07
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