Sickle and Thalassemic Erythroid Progenitor Cells are Different from Normal-Reference-Cited by-同舟云学术

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Sickle and Thalassemic Erythroid Progenitor Cells are Different from Normal

Published:1992-01 Issue:6 Volume:16 Page:447-467
ISSN:0363-0269
Container-title:Hemoglobin
language:en
Short-container-title:Hemoglobin

Author:

Alter Blanche P,He Liya,Acosta Robert,Knobloch Mary Ellen,Thomson JoAnn C,Giardina Patricia,Weinberg Rona S

Publisher

Informa UK Limited

Subject

Biochemistry (medical),Clinical Biochemistry,Genetics (clinical),Hematology

Link

http://www.tandfonline.com/doi/pdf/10.3109/03630269208993114

Reference37 articles.

1. Circulating erythropoietic precursors assessed in culture: characterization in normal men and patients with hemoglobinopathies

2. Augmentation of fetal hemoglobin (HbF) synthesis in culture by human erythropoietic precursors in the marrow and peripheral blood: studies in sickle cell anemia and nonhemoglobinopathic adults

3. Effects of dexamethasone on fetal hemoglobin synthesis in peripheral blood erythroid burst-forming units

Cited by 10 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Haematopoietic stem cell health in sickle cell disease and its implications for stem cell therapies and secondary haematological disorders;Blood Reviews;2024-01

2. Early circulating erythroid progenitor cells and expression of erythropoietin receptors in sickle cell disease;European Journal of Haematology;2009-04-24

3. Human CD34+ and CD34+CD38− hematopoietic progenitors in sickle cell disease differ phenotypically and functionally from normal and suggest distinct subpopulations that generate F cells;Experimental Hematology;2004-05

4. The predictive value of clonogenic stem cell assays for the diagnosis of polycythaemia vera;British Journal of Haematology;2002-05-19

5. Ineffective erythropoiesis in β-thalassemia major is due to apoptosis at the polychromatophilic normoblast stage;Experimental Hematology;2000-12

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