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-Reference-Cited by-同舟云学术

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

Published:2004-05 Issue:5 Volume:32 Page:483-493
ISSN:0301-472X
Container-title:Experimental Hematology
language:en
Short-container-title:Experimental Hematology

Author:

Luck Lori,Zeng Licheng,Hiti Alan L,Weinberg Kenneth I,Malik Punam

Publisher

Elsevier BV

Subject

Cancer Research,Cell Biology,Genetics,Hematology,Molecular Biology

Reference37 articles.

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3. 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;Kidoguchi;Blood,1978

4. Stimulation of fetal hemoglobin synthesis in bone marrow cultures from adult individuals;Papayannopoulou;Proc Natl Acad Sci USA,1976

5. Hemoglobin F synthesis in vitro: evidence for control at the level of primitive erythroid stem cells;Papayannopoulou;Proc Natl Acad Sci USA,1977

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