about
Ineffective erythropoiesis and thalassemiasIneffective erythropoiesis in β -thalassemiaLoss of alpha-hemoglobin-stabilizing protein impairs erythropoiesis and exacerbates beta-thalassemiaHemozoin (malarial pigment) directly promotes apoptosis of erythroid precursors.A mechanism of ineffective erythropoiesis in β-thalassemia/Hb E diseaseIron Loading and Overloading due to Ineffective Erythropoiesis.Growth differentiation factor 15 in erythroid health and disease.Hematopoietic stem cell transplantation in thalassemia and sickle cell disease. Unicenter experience in a multi-ethnic populationA synthetic model of human beta-thalassemia erythropoiesis using CD34+ cells from healthy adult donors.Genetic insights into the clinical diversity of beta thalassaemia.Haemoglobinopathies and resistance to malaria.Apoptotic mechanisms in the control of erythropoiesis.Ineffective erythropoiesis in beta-thalassemia is characterized by increased iron absorption mediated by down-regulation of hepcidin and up-regulation of ferroportin.α-Globin as a molecular target in the treatment of β-thalassemiaHeme-regulated eIF2α kinase activated Atf4 signaling pathway in oxidative stress and erythropoiesis.HbE/β-Thalassemia and Oxidative Stress: The Key to Pathophysiological Mechanisms and Novel Therapeutics.Postnatal and non-invasive prenatal detection of β-thalassemia mutations based on Taqman genotyping assays.Production of beta-globin and adult hemoglobin following G418 treatment of erythroid precursor cells from homozygous beta(0)39 thalassemia patients.Seroprevalence of Hepatitis C, Hepatitis B, Cytomegalovirus, and Human Immunodeficiency Viruses in Multitransfused Thalassemic Children in Upper Egypt.Molecular therapies in beta-thalassaemia.The thalassaemia syndromes.Decreased differentiation of erythroid cells exacerbates ineffective erythropoiesis in beta-thalassemiaChaperoning erythropoiesis.Fetal Hemoglobin Inducers from the Natural World: A Novel Approach for Identification of Drugs for the Treatment of {beta}-Thalassemia and Sickle-Cell Anemia.Regulation of iron absorption in hemoglobinopathies.The impact of hematopoietic stem cell transplantation on the management of thalassemia.Natural Remedies for the Treatment of Beta-Thalassemia and Sickle Cell Anemia-Current Status and Perspectives in Fetal Hemoglobin Reactivation.Expression of CD55 on red blood cells of β-thalassemia patients.beta-Thalassemia: HiJAKing Ineffective Erythropoiesis and Iron OverloadGeneration and Characterization of a Transgenic Mouse Carrying a Functional Human β -Globin Gene with the IVSI-6 Thalassemia Mutation.Differential gene expression analysis in early and late erythroid progenitor cells in β-thalassaemia.Study of serum haptoglobin level and its relation to erythropoietic activity in Beta thalassemia childrenIn Vitro Hb Production in B-thalassemia Patients Is Not a Predictor of Clinical Responsiveness to HydroxyureaErythropoietin-driven signaling ameliorates the survival defect of DMT1-mutant erythroid progenitors and erythroblastsMutation near the binding interfaces at α-hemoglobin stabilizing protein is highly pathogenic.A combined approach for β-thalassemia based on gene therapy-mediated adult hemoglobin (HbA) production and fetal hemoglobin (HbF) induction.Unravelling pathways downstream Sox6 induction in K562 erythroid cells by proteomic analysis.Circulating platelet and erythrocyte microparticles in young children and adolescents with sickle cell disease: Relation to cardiovascular complications.Acute haemolytic crisis in a Thai patient with homozygous haemoglobin Constant Spring (Hb CS/CS): a case report.Normalized levels of red blood cells expressing phosphatidylserine, their microparticles, and activated platelets in young patients with β-thalassemia following bone marrow transplantation.
P2860
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P2860
description
2002 nî lūn-bûn
@nan
2002 թուականի Մարտին հրատարակուած գիտական յօդուած
@hyw
2002 թվականի մարտին հրատարակված գիտական հոդված
@hy
2002年の論文
@ja
2002年論文
@yue
2002年論文
@zh-hant
2002年論文
@zh-hk
2002年論文
@zh-mo
2002年論文
@zh-tw
2002年论文
@wuu
name
Pathophysiology of thalassemia.
@ast
Pathophysiology of thalassemia.
@en
Pathophysiology of thalassemia.
@nl
type
label
Pathophysiology of thalassemia.
@ast
Pathophysiology of thalassemia.
@en
Pathophysiology of thalassemia.
@nl
prefLabel
Pathophysiology of thalassemia.
@ast
Pathophysiology of thalassemia.
@en
Pathophysiology of thalassemia.
@nl
P1476
Pathophysiology of thalassemia.
@en
P2093
Stanley L Schrier
P304
P356
10.1097/00062752-200203000-00007
P577
2002-03-01T00:00:00Z