Hb F production in stressed erythropoiesis: observations and kinetic models.
about
Genomic approaches to identifying targets for treating β hemoglobinopathiesSickle cell disease in childrenFuture prospects for treatment of hemoglobinopathies.Control of globin gene expression during development and erythroid differentiationStage-specific functional roles of integrins in murine erythropoiesis.Fetal hemoglobin synthesis in vivo: direct evidence for control at the level of erythroid progenitorsNegative autoregulation by Fas stabilizes adult erythropoiesis and accelerates its stress responseMurine erythroid short-term radioprotection requires a BMP4-dependent, self-renewing population of stress erythroid progenitors.Stress erythropoiesis: new signals and new stress progenitor cells.Pharmacologic induction of fetal hemoglobin synthesis: cellular and molecular mechanisms.In vitro culture of stress erythroid progenitors identifies distinct progenitor populations and analogous human progenitors.Absolute Reticulocyte Count Acts as a Surrogate for Fetal Hemoglobin in Infants and Children with Sickle Cell Anemia.Pharmacological induction of fetal hemoglobin synthesis using histone deacetylase inhibitors.Mechanism of Hb F stimulation by S-stage compounds. In vitro studies with bone marrow cells exposed to 5-azacytidine, Ara-C, or hydroxyurea.Developmental- and differentiation-specific patterns of human gamma- and beta-globin promoter DNA methylation.Neither DNA hypomethylation nor changes in the kinetics of erythroid differentiation explain 5-azacytidine's ability to induce human fetal hemoglobinSerum factors can modulate the developmental clock of gamma- to beta-globin gene switching in somatic cell hybridsChronic psychological stress activates BMP4-dependent extramedullary erythropoiesis.Novel approaches to the treatment of sickle cell disease: the potential of histone deacetylase inhibitors.Hydroxyurea therapy for sickle cell anemia.Exploring the use of expanded erythroid cells for autologous transfusion for anemia of prematurity.A candidate transacting modulator of fetal hemoglobin gene expression in the Arab-Indian haplotype of sickle cell anemia.To respond or not to respond to hydroxyurea in thalassemia: a matter of stress adaptation?Fetal haemoglobin induction in sickle cell disease.Heterogeneity of F cells in β-thalassemia.Comparison of MicroRNAs Mediated in Reactivation of the γ-Globin in β-Thalassemia Patients, Responders and Non-Responders to Hydroxyurea.
P2860
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P2860
Hb F production in stressed erythropoiesis: observations and kinetic models.
description
1985 nî lūn-bûn
@nan
1985年の論文
@ja
1985年学术文章
@wuu
1985年学术文章
@zh-cn
1985年学术文章
@zh-hans
1985年学术文章
@zh-my
1985年学术文章
@zh-sg
1985年學術文章
@yue
1985年學術文章
@zh
1985年學術文章
@zh-hant
name
Hb F production in stressed erythropoiesis: observations and kinetic models.
@en
Hb F production in stressed erythropoiesis: observations and kinetic models.
@nl
type
label
Hb F production in stressed erythropoiesis: observations and kinetic models.
@en
Hb F production in stressed erythropoiesis: observations and kinetic models.
@nl
prefLabel
Hb F production in stressed erythropoiesis: observations and kinetic models.
@en
Hb F production in stressed erythropoiesis: observations and kinetic models.
@nl
P2093
P2860
P1476
Hb F production in stressed erythropoiesis: observations and kinetic models.
@en
P2093
Galanello R
Papayannopoulou T
Stamatoyannopoulos G
P2860
P304
P356
10.1111/J.1749-6632.1985.TB17188.X
P577
1985-01-01T00:00:00Z