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Hemoglobin
international journal for hemoglobin research
Volume 16, 1992 - Issue 6
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Original Article

Sickle and Thalassemic Erythroid Progenitor Cells are Different from Normal

Blanche P Alter The Polly Annenberg Levee Hematology Center Departments of Medicine, Pediatrics Mount Sinai School of Medicine, New York, New York, 10029; Division of Pediatric Hematology-Oncology, University of Texas Medical Branch, Galveston, Texas, 77555
,
Liya He The Polly Annenberg Levee Hematology Center Departments of Medicine, Pediatrics Mount Sinai School of Medicine, New York, New York, 10029
,
Robert Acosta The Polly Annenberg Levee Hematology Center Departments of Medicine, Pediatrics Mount Sinai School of Medicine, New York, New York, 10029
,
Mary Ellen Knobloch The Polly Annenberg Levee Hematology Center Departments of Medicine, Pediatrics Mount Sinai School of Medicine, New York, New York, 10029
,
JoAnn C Thomson The Polly Annenberg Levee Hematology Center Departments of Medicine, Pediatrics Mount Sinai School of Medicine, New York, New York, 10029
,
Patricia Giardina Department of Pediatrics, New York Hospital-Cornell Medical Center, New York, New York, 10021
&
Rona S Weinberg The Polly Annenberg Levee Hematology Center Departments of Medicine, Pediatrics Mount Sinai School of Medicine, New York, New York, 10029
 show all
Pages 447-467 | Received 22 Apr 1992, Accepted 16 Sep 1992, Published online: 07 Jul 2009

Citations (10)

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Read on this site (1)

R. S. Weinberg, R. Acosta, M. E. Knobloch, M. Garber & B. P. Alter. (1995) Low Oxygen Enhances Sickle and Normal Erythropoiesis and Fetal Hemoglobin Synthesis in Vitro. Hemoglobin 19:5, pages 263-275.
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Articles from other publishers (9)

Vishaka Gorur, Kamil R. Kranc, Miguel Ganuza & Paul Telfer. (2023) Haematopoietic stem cell health in sickle cell disease and its implications for stem cell therapies and secondary haematological disorders. Blood Reviews, pages 101137.
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Lori Luck, Licheng Zeng, Alan L Hiti, Kenneth I Weinberg & Punam Malik. (2004) 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 32:5, pages 483-493.
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Caroline Zwicky, Lorenz Theiler, Karin Zbären, Elisabeth Ischi & Anoreas Tobler. (2002) The predictive value of clonogenic stem cell assays for the diagnosis of polycythaemia vera. British Journal of Haematology 117:3, pages 598-604.
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Liesl A Mathias, Timothy C Fisher, Licheng Zeng, Herbert J Meiselman, Kenneth I Weinberg, Alan L Hiti & Punam Malik. (2000) Ineffective erythropoiesis in β-thalassemia major is due to apoptosis at the polychromatophilic normoblast stage. Experimental Hematology 28:12, pages 1343-1353.
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Marie-José BlouinMonique E. De PaepeMarie Trudel. (1999) Altered Hematopoiesis in Murine Sickle Cell Disease. Blood 94:4, pages 1451-1459.
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Marie-José BlouinMonique E. De PaepeMarie Trudel. (1999) Altered Hematopoiesis in Murine Sickle Cell Disease. Blood 94:4, pages 1451-1459.
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R.C.R. Perlingeiro, F.F. Costa, S.T.O. Saad, V.R. Arruda & M.L.S. Queiroz. (1999) Spontaneous erythroid colony formation in Brazilian patients with sickle cell disease. American Journal of Hematology 61:1, pages 40-45.
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R. C. R. Perlingeiro, F. F. Costa, S. T. O. Saad & M. L. S. Queiroz. (2009) Early circulating erythroid progenitor cells and expression of erythropoietin receptors in sickle cell disease. European Journal of Haematology 60:4, pages 226-232.
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Jiann-Shiuh Chen, Kai-Hsin Lin, Shan-Tair Wang, Chao-Jung Tsao & Tsu-Fuh Yeh. (1998) Blunted Serum Erythropoietin Response to Anemia in Patients Polytransfused for β-Thalassemia Major. Journal of Pediatric Hematology/Oncology 20:2, pages 140-144.
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