相关参考文献
注意：仅列出部分参考文献，下载原文获取全部文献信息。Successful matched sibling donor marrow transplantation following reduced intensity conditioning in children with hemoglobinopathies
Allison A. King et al.
AMERICAN JOURNAL OF HEMATOLOGY (2015)
The Interplay Between Peroxiredoxin-2 and Nuclear Factor-Erythroid 2 Is Important in Limiting Oxidative Mediated Dysfunction in β-Thalassemic Erythropoiesis
Alessandro Matte et al.
ANTIOXIDANTS & REDOX SIGNALING (2015)
Knockdown of transcription factor forkhead box O3 (FOXO3) suppresses erythroid differentiation in human cells and zebrafish
Hai Wang et al.
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS (2015)
Emerging EPO and EPO receptor regulators and signal transducers
David Kuhrt et al.
BLOOD (2015)
Erythroferrone contributes to hepcidin suppression and iron overload in a mouse model of β-thalassemia
Leon Kautz et al.
BLOOD (2015)
Genotype-phenotype correlation and report of novel mutations in β-globin gene in thalassemia patients
Rachana Nagar et al.
BLOOD CELLS MOLECULES AND DISEASES (2015)
Differences in the erythropoiesis-hepcidin-iron store axis between hemoglobin H disease and β-thalassemia intermedia
Raffaella Origa et al.
HAEMATOLOGICA (2015)
Efficacy of Rapamycin as Inducer of Hb F in Primary Erythroid Cultures from Sickle Cell Disease and beta-Thalassemia Patients
Alice Pecoraro et al.
HEMOGLOBIN (2015)
Regulation of Iron Metabolism by Hepcidin under Conditions of Inflammation
Paul J. Schmidt
JOURNAL OF BIOLOGICAL CHEMISTRY (2015)
miRNA-embedded shRNAs for Lineage-specific BCL11A Knockdown and Hemoglobin F Induction
Swaroopa Guda et al.
MOLECULAR THERAPY (2015)
Breakthrough to genome editing
Marcia McNutt
SCIENCE (2015)
Coupling of Ribostasis and Proteostasis: Hsp70 Proteins in mRNA Metabolism
Robert W. Walters et al.
TRENDS IN BIOCHEMICAL SCIENCES (2015)
Hepcidin and Host Defense against Infectious Diseases
Kathryn Michels et al.
PLOS PATHOGENS (2015)
Differences in the erythropoiesis-hepcidin-iron store axis between hemoglobin H disease and β-thalassemia intermedia
Raffaella Origa et al.
HAEMATOLOGICA (2015)
Hepcidin and the Global Burden of Iron Deficiency
Tomas Ganz
CLINICAL CHEMISTRY (2015)
When to consider transfusion therapy for patients with non-transfusion-dependent thalassaemia
A. T. Taher et al.
VOX SANGUINIS (2015)
FOXO3-mTOR metabolic cooperation in the regulation of erythroid cell maturation and homeostasis
Xin Zhang et al.
AMERICAN JOURNAL OF HEMATOLOGY (2014)
A phase 1 study of ACE-536, a regulator of erythroid differentiation, in healthy volunteers
Kenneth M. Attie et al.
AMERICAN JOURNAL OF HEMATOLOGY (2014)
Modified activin receptor IIB ligand trap mitigates ineffective erythropoiesis and disease complications in murine β-thalassemia
Rajasekhar N. V. S. Suragani et al.
BLOOD (2014)
Induction of fetal hemoglobin through enhanced translation efficiency of γ-globin mRNA
Cynthia K. Hahn et al.
BLOOD (2014)
Global transcriptome analyses of human and murine terminal erythroid differentiation
Xiuli An et al.
BLOOD (2014)
Translational control by heme-regulated eIF2a kinase during erythropoiesis
Jane-Jane Chen
CURRENT OPINION IN HEMATOLOGY (2014)
Resveratrol accelerates erythroid maturation by activation of FoxO3 and ameliorates anemia in beta-thalassemic mice
Sara Santos Franco et al.
HAEMATOLOGICA (2014)
Hematopoietic stem cell transplantation in thalassemia major and sickle cell disease: indications and management recommendations from an international expert panel
Emanuele Angelucci et al.
HAEMATOLOGICA (2014)
Modulation of Hepcidin as Therapy for Primary and Secondary Iron Overload Disorders Preclinical Models and Approaches
Paul J. Schmidt et al.
HEMATOLOGY-ONCOLOGY CLINICS OF NORTH AMERICA (2014)
Identification of erythroferrone as an erythroid regulator of iron metabolism
Leon Kautz et al.
NATURE GENETICS (2014)
An activin receptor IIA ligand trap corrects ineffective erythropoiesis in β-thalassemia
Michael Dussiot et al.
NATURE MEDICINE (2014)
Guidelines for Diagnosis and Management of Beta-Thalassemia Intermedia
Mehran Karimi et al.
PEDIATRIC HEMATOLOGY AND ONCOLOGY (2014)
An RNAi therapeutic targeting Tmprss6 decreases iron overload in Hfe-/- mice and ameliorates anemia and iron overload in murine β-thalassemia intermedia
Paul J. Schmidt et al.
BLOOD (2013)
The gut in iron homeostasis: role of HIF-2 under normal and pathological conditions
Maria Mastrogiannaki et al.
BLOOD (2013)
Erythropoiesis and globin switching in compound Klf1::Bcl11a mutant mice
Fatemehsadat Esteghamat et al.
BLOOD (2013)
A randomized phase I/II trial of HQK-1001, an oral fetal globin gene inducer, in β-thalassaemia intermedia and HbE/β-thalassaemia
Suthat Fucharoen et al.
BRITISH JOURNAL OF HAEMATOLOGY (2013)
The eIF2α kinases: their structures and functions
Neysan Donnelly et al.
CELLULAR AND MOLECULAR LIFE SCIENCES (2013)
A Focus on Heme Oxygenase-1 (HO-1) Inhibitors
V. Pittala et al.
CURRENT MEDICINAL CHEMISTRY (2013)
Therapeutic superiority and safety of combined hydroxyurea with recombinant human erythropoietin over hydroxyurea in young β-thalassemia intermedia patients
Mohsen S. Elalfy et al.
EUROPEAN JOURNAL OF HAEMATOLOGY (2013)
Non-transfusion-dependent thalassemias
Khaled M. Musallam et al.
HAEMATOLOGICA (2013)
Transcription Activator-like Effector Nuclease (TALEN)-mediated Gene Correction in Integration-free β-Thalassemia Induced Pluripotent Stem Cells
Ning Ma et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2013)
Reducing TMPRSS6 ameliorates hemochromatosis and β-thalassemia in mice
Shuling Guo et al.
JOURNAL OF CLINICAL INVESTIGATION (2013)
MicroRNA-486-3p Regulates γ-Globin Expression in Human Erythroid Cells by Directly Modulating BCL11A
Valentina Lulli et al.
PLOS ONE (2013)
Hepcidin and iron homeostasis
Tomas Ganz et al.
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR CELL RESEARCH (2012)
Heme-regulated eIF2α kinase activated Atf4 signaling pathway in oxidative stress and erythropoiesis
Rajasekhar N. V. S. Suragani et al.
BLOOD (2012)
Deletion of TMPRSS6 attenuates the phenotype in a mouse model of β-thalassemia
Antonella Nai et al.
BLOOD (2012)
HLA-matched sibling stem cell transplantation in children with β-thalassemia with anti-thymocyte globulin as part of the preparative regimen: the Greek experience
E. Goussetis et al.
BONE MARROW TRANSPLANTATION (2012)
Structural studies of the TGF-βs and their receptors - insights into evolution of the TGF-β superfamily
Andrew P. Hinck
FEBS LETTERS (2012)
Hematopoietic Stem Cell Transplantation in Thalassemia and Sickle Cell Anemia
Guido Lucarelli et al.
COLD SPRING HARBOR PERSPECTIVES IN MEDICINE (2012)
Induction of Fetal Hemoglobin In Vivo Mediated by a Synthetic γ-Globin Zinc Finger Activator
Flavia C. Costa et al.
ANEMIA (2012)
Therapeutic levels of fetal hemoglobin in erythroid progeny of β-thalassemic CD34+ cells after lentiviral vector-mediated gene transfer
Andrew Wilber et al.
BLOOD (2011)
Oxidative stress modulates heme synthesis and induces peroxiredoxin-2 as a novel cytoprotective response in β-thalassemic erythropoiesis
Lucia De Franceschi et al.
HAEMATOLOGICA-THE HEMATOLOGY JOURNAL (2011)
Administration of high doses of recombinant human erythropoietin to patients with β-thalassemia intermedia: a preliminary trial
K. Bourantas et al.
EUROPEAN JOURNAL OF HAEMATOLOGY (2010)
KLF1 Directly Coordinates Almost All Aspects of Terminal Erythroid Differentiation
Michael R. Tallack et al.
IUBMB LIFE (2010)
Characterization of the Ligand Binding Functionality of the Extracellular Domain of Activin Receptor Type IIB
Dianne Sako et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2010)
Transferrin therapy ameliorates disease in β-thalassemic mice
Huihui Li et al.
NATURE MEDICINE (2010)
Identification of TWSG1 as a second novel erythroid regulator of hepcidin expression in murine and human cells
Toshihiko Tanno et al.
BLOOD (2009)
Hypoxia, hypoxia-inducible factors (HIF), HIF hydroxylases and oxygen sensing
James D. Webb et al.
CELLULAR AND MOLECULAR LIFE SCIENCES (2009)
Single-Dose, Randomized, Double-Blind, Placebo-Controlled Study of ACE-011 (ActRIIA-IgG1) in Postmenopausal Women
Jon Ruckle et al.
JOURNAL OF BONE AND MINERAL RESEARCH (2009)
Decreased differentiation of erythroid cells exacerbates ineffective erythropoiesis in β-thalassemia
Ilaria V. Libani et al.
BLOOD (2008)
Thalidomide therapy in a patient with thalassemia major
Lilia Beatriz Aguilar-Lopez et al.
BLOOD CELLS MOLECULES AND DISEASES (2008)
A soluble activin type IIA receptor induces bone formation and improves skeletal integrity
R. Scott Pearsall et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2008)
Decreased transfusion needs associated with hydroxyurea therapy in Algerian patients with thalassemia major or intermedia
Mohamed Bradai et al.
TRANSFUSION (2007)
High levels of GDF15 in thalassemia suppress expression of the iron regulatory protein hepcidin
Toshihiko Tanno et al.
NATURE MEDICINE (2007)
Foxo3 is required for the regulation of oxidative stress in erythropoiesis
Dragan Marinkovic et al.
JOURNAL OF CLINICAL INVESTIGATION (2007)
Ineffective erythropoiesis in β-thalassemia is characterized by increased iron absorption mediated by down-regulation of hepcidin and up-regulation of ferroportin
Sara Gardenghi et al.
BLOOD (2007)
Hsp70 regulates erythropoiesis by preventing caspase-3-mediated cleavage of GATA-1
Jean-Antoine Ribeil et al.
NATURE (2007)
Ineffective erythropoiesis in mutant mice with deficient pyruvate kinase activity
S Aizawa et al.
EXPERIMENTAL HEMATOLOGY (2005)
Medical progress:: β-thalassemia
D Rund et al.
NEW ENGLAND JOURNAL OF MEDICINE (2005)
Heme-regulated eIF2α kinase modifies the phenotypic severity of murine models of erythropoietic protoporphyria and β-thalassemia
AP Han et al.
JOURNAL OF CLINICAL INVESTIGATION (2005)
Regulation of human erythropoiesis by activin A, BMP2, and BMP4, members of the TGFβ family
W Maguer-Satta et al.
EXPERIMENTAL CELL RESEARCH (2003)
Activin type IIA and IIB receptors mediate Gdf11 signaling in axial vertebral patterning
SP Oh et al.
GENES & DEVELOPMENT (2002)
分享论文
