Related references
Note: Only part of the references are listed.Heme oxygenase-1 deficiency alters erythroblastic island formation, steady-state erythropoiesis and red blood cell lifespan in mice
Stuart T. Fraser et al.
HAEMATOLOGICA (2015)
Validation of WHO classification-based Prognostic Scoring System (WPSS) for myelodysplastic syndromes and comparison with the revised International Prognostic Scoring System (IPSS-R). A study of the International Working Group for Prognosis in Myelodysplasia (IWG-PM)
M. G. Della Porta et al.
LEUKEMIA (2015)
Comparison of three prognostic scoring systems in a series of 146 cases of chronic myelomonocytic leukemia (CMML): MD Anderson prognostic score (MDAPS), CMML-specific prognostic scoring system (CPSS) and Mayo prognostic model. A detailed review of prognostic factors in CMML
Xavier Calvo et al.
LEUKEMIA RESEARCH (2015)
Developmental Control of Polycomb Subunit Composition by GATA Factors Mediates a Switch to Non-Canonical Functions
Jian Xu et al.
MOLECULAR CELL (2015)
A Systems Approach Identifies Essential FOXO3 Functions at Key Steps of Terminal Erythropoiesis
Raymond Liang et al.
PLOS GENETICS (2015)
Heme oxygenase-1 deficiency alters erythroblastic island formation, steady-state erythropoiesis and red blood cell lifespan in mice
Stuart T. Fraser et al.
HAEMATOLOGICA (2015)
CITED2-mediated human hematopoietic stem cell maintenance is critical for acute myeloid leukemia
P. M. Korthuis et al.
LEUKEMIA (2015)
Loss of Asxl1 leads to myelodysplastic syndrome-like disease in mice
Jiapeng Wang et al.
BLOOD (2014)
Global transcriptome analyses of human and murine terminal erythroid differentiation
Xiuli An et al.
BLOOD (2014)
Developmental transcriptome analysis of human erythropoiesis
Lihong Shi et al.
HUMAN MOLECULAR GENETICS (2014)
Chronic myelomonocytic leukemia: 2013 update on diagnosis, risk stratification, and management
Sameer A. Parikh et al.
AMERICAN JOURNAL OF HEMATOLOGY (2013)
Isolation and functional characterization of human erythroblasts at distinct stages: implications for understanding of normal and disordered erythropoiesis in vivo
Jingping Hu et al.
BLOOD (2013)
Quantitative analysis of murine terminal erythroid differentiation in vivo: novel method to study normal and disordered erythropoiesis
Jing Liu et al.
BLOOD (2013)
Deletion of Asxl1 results in myelodysplasia and severe developmental defects in vivo
Omar Abdel-Wahab et al.
JOURNAL OF EXPERIMENTAL MEDICINE (2013)
Mayo prognostic model for WHO-defined chronic myelomonocytic leukemia: ASXL1 and spliceosome component mutations and outcomes
M. M. Patnaik et al.
LEUKEMIA (2013)
ASXL1 Mutations Promote Myeloid Transformation through Loss of PRC2-Mediated Gene Repression
Omar Abdel-Wahab et al.
CANCER CELL (2012)
Mutation analysis of ASXL1, CBL, DNMT3A, IDH1, IDH2, JAK2, MPL, NF1, SF3B1, SUZ12, and TET2 in myeloproliferative neoplasms
Mandy Brecqueville et al.
GENES CHROMOSOMES & CANCER (2012)
Mutations in ASXL1 are associated with poor prognosis across the spectrum of malignant myeloid diseases
Veronique Gelsi-Boyer et al.
JOURNAL OF HEMATOLOGY & ONCOLOGY (2012)
Single-lineage transcriptome analysis reveals key regulatory pathways in primitive erythroid progenitors in the mouse embryo
Joan Isern et al.
BLOOD (2011)
From stem cell to red cell: regulation of erythropoiesis at multiple levels by multiple proteins, RNAs, and chromatin modifications
Shilpa M. Hattangadi et al.
BLOOD (2011)
Epigenetics and mutations in chronic myeloproliferative neoplasms
Alessandro M. Vannucchi et al.
HAEMATOLOGICA-THE HEMATOLOGY JOURNAL (2011)
Impact of the degree of anemia on the outcome of patients with myelodysplastic syndrome and its integration into the WHO classification-based Prognostic Scoring System (WPSS)
Luca Malcovati et al.
HAEMATOLOGICA-THE HEMATOLOGY JOURNAL (2011)
Disruption of the ASXL1 gene is frequent in primary, post-essential thrombocytosis and post-polycythemia vera myelofibrosis, but not essential thrombocytosis or polycythemia vera: analysis of molecular genetics and clinical phenotypes
Brady L. Stein et al.
HAEMATOLOGICA-THE HEMATOLOGY JOURNAL (2011)
Nuclear Receptors TR2 and TR4 Recruit Multiple Epigenetic Transcriptional Corepressors That Associate Specifically with the Embryonic β-Type Globin Promoters in Differentiated Adult Erythroid Cells
Shuaiying Cui et al.
MOLECULAR AND CELLULAR BIOLOGY (2011)
Clinical Effect of Point Mutations in Myelodysplastic Syndromes
Rafael Bejar et al.
NEW ENGLAND JOURNAL OF MEDICINE (2011)
Identification and Analysis of Mouse Erythroid Progenitors using the CD71/TER119 Flow-cytometric Assay
Miroslav Koulnis et al.
JOVE-JOURNAL OF VISUALIZED EXPERIMENTS (2011)
ASXL1 mutation is associated with poor prognosis and acute transformation in chronic myelomonocytic leukaemia
Veronique Gelsi-Boyer et al.
BRITISH JOURNAL OF HAEMATOLOGY (2010)
Frequent mutation of the polycomb-associated gene ASXL1 in the myelodysplastic syndromes and in acute myeloid leukemia
J. Boultwood et al.
LEUKEMIA (2010)
Histone H2A deubiquitinase activity of the Polycomb repressive complex PR-DUB
Johanna C. Scheuermann et al.
NATURE (2010)
Resolving the distinct stages in erythroid differentiation based on dynamic changes in membrane protein expression during erythropoiesis
Ke Chen et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2009)
International MDS risk analysis workshop (IMRAW)/IPSS reanalyzed: Impact of cytopenias on clinical outcomes in myelodysplastic syndromes
Jelena M. Kao et al.
AMERICAN JOURNAL OF HEMATOLOGY (2008)
Additional sex comb-like 1 (ASXL1), in cooperation with SRC-1, acts as a ligand-dependent coactivator for retinoic acid receptor
Yang-Sook Cho et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2006)
Ex vivo generation of fully mature human red blood cells from hematopoietic stem cells
MC Giarratana et al.
NATURE BIOTECHNOLOGY (2005)
An intrinsic but cell-nonautonomous defect in GATA-1-overexpressing mouse erythroid cells
D Whyatt et al.
NATURE (2000)