Individual variation in the production and survival of F cells in sickle-cell disease.
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HIF prolyl hydroxylase inhibition results in endogenous erythropoietin induction, erythrocytosis, and modest fetal hemoglobin expression in rhesus macaquesGenome-wide association study identifies genetic variants influencing F-cell levels in sickle-cell patients.5-Azacytidine acts directly on both erythroid precursors and progenitors to increase production of fetal hemoglobin.Fetal hemoglobin in sickle cell anemia: genetic studies of the Arab-Indian haplotypeAlpha thalassemia changes erythrocyte heterogeneity in sickle cell disease.Developing treatment for sickle cell disease.Recombinant erythroid Kruppel-like factor fused to GATA1 up-regulates delta- and gamma-globin expression in erythroid cellsFactors affecting prepubertal growth in homozygous sickle cell diseaseRole of epistatic (modifier) genes in the modulation of the phenotypic diversity of sickle cell anemia.Sickle cell haemoglobinopathies in England.Heterogeneity of sickle-cell anemia based on a profile of hematological variables.Absolute Reticulocyte Count Acts as a Surrogate for Fetal Hemoglobin in Infants and Children with Sickle Cell Anemia.Ion transport pathology in the mechanism of sickle cell dehydration.Genetic variants at HbF-modifier loci moderate anemia and leukocytosis in sickle cell disease in TanzaniaSynthesis of hemoglobin F in adult simian erythroid progenitor-derived colonies.Lack of influence of fetal hemoglobin levels or erythrocyte indices on the severity of sickle cell anemiaCellular mechanisms for increased fetal hemoglobin production in culture. Evidence for continuous commitment to fetal hemoglobin production during burst formation.Production of erythrocytes that contain fetal hemoglobin in anemia. Transient in vivo changesTreatment of sickle cell anemia with 5-azacytidine results in increased fetal hemoglobin production and is associated with nonrandom hypomethylation of DNA around the gamma-delta-beta-globin gene complex.Recombination and balanced chromosome polymorphism suggested by DNA sequences 5' to the human delta-globin gene.Time-dependent changes in the density and hemoglobin F content of biotin-labeled sickle cells.Reawakening fetal hemoglobin: prospects for new therapies for the β-globin disorders.Hematological and clinical features of sickle cell diseases: a review.The laboratory evaluation of microcytic red blood cells.Developmental genetics of the human haemoglobins.Massive splenic infarction in children with sickle cell anemia and the role of splenectomy.Evidence for a direct reticulocyte origin of dense red cells in sickle cell anemia.Determination of the hemoglobin F program in human progenitor-derived erythroid cellsThe effect of fetal hemoglobin on the survival characteristics of sickle cells.Flow cytometric method for simultaneous assay of foetal haemoglobin containing red cells, reticulocytes and foetal haemoglobin containing reticulocytes.
P2860
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P2860
Individual variation in the production and survival of F cells in sickle-cell disease.
description
1978 nî lūn-bûn
@nan
1978年の論文
@ja
1978年論文
@yue
1978年論文
@zh-hant
1978年論文
@zh-hk
1978年論文
@zh-mo
1978年論文
@zh-tw
1978年论文
@wuu
1978年论文
@zh
1978年论文
@zh-cn
name
Individual variation in the production and survival of F cells in sickle-cell disease.
@en
Individual variation in the production and survival of F cells in sickle-cell disease.
@nl
type
label
Individual variation in the production and survival of F cells in sickle-cell disease.
@en
Individual variation in the production and survival of F cells in sickle-cell disease.
@nl
prefLabel
Individual variation in the production and survival of F cells in sickle-cell disease.
@en
Individual variation in the production and survival of F cells in sickle-cell disease.
@nl
P2093
P1476
Individual variation in the production and survival of F cells in sickle-cell disease.
@en
P2093
Charache S
Heintzelman K
P304
P356
10.1056/NEJM197812282992603
P407
P577
1978-12-01T00:00:00Z