Chemical Inhibition of Histone Deacetylases 1 and 2 Induces Fetal Hemoglobin through Activation of GATA2
Published 2016 View Full Article
- Home
- Publications
- Publication Search
- Publication Details
Title
Chemical Inhibition of Histone Deacetylases 1 and 2 Induces Fetal Hemoglobin through Activation of GATA2
Authors
Keywords
Cell differentiation, Gene expression, Globins, Histones, Histone acetylation, Flow cytometry, Messenger RNA, Chromatin
Journal
PLoS One
Volume 11, Issue 4, Pages e0153767
Publisher
Public Library of Science (PLoS)
Online
2016-04-14
DOI
10.1371/journal.pone.0153767
References
Ask authors/readers for more resources
Related references
Note: Only part of the references are listed.- Inhibition of G9a methyltransferase stimulates fetal hemoglobin production by facilitating LCR/ -globin looping
- (2015) I. Krivega et al. BLOOD
- EHMT1 and EHMT2 inhibition induces fetal hemoglobin expression
- (2015) A. Renneville et al. BLOOD
- Mutational Cooperativity Linked to Combinatorial Epigenetic Gain of Function in Acute Myeloid Leukemia
- (2015) Alan H. Shih et al. CANCER CELL
- RN-1, a potent and selective lysine-specific demethylase 1 inhibitor, increases γ-globin expression, F reticulocytes, and F cells in a sickle cell disease mouse model
- (2015) Angela Rivers et al. EXPERIMENTAL HEMATOLOGY
- HDAC inhibitors still need a home run, despite recent approval
- (2015) Malini Guha NATURE REVIEWS DRUG DISCOVERY
- Abstract 4784: Selective bioluminogenic HDAC activity assays for profiling HDAC inhibitors
- (2015) Kevin R. Kupcho et al. CANCER RESEARCH
- Modulation of gamma globin genes expression by histone deacetylase inhibitors: anin vitrostudy
- (2014) Luisa Ronzoni et al. BRITISH JOURNAL OF HAEMATOLOGY
- Sin3a-associated Hdac1 and Hdac2 are essential for hematopoietic stem cell homeostasis and contribute differentially to hematopoiesis
- (2014) M. R. Heideman et al. HAEMATOLOGICA
- Mechanism governing a stem cell-generating cis-regulatory element
- (2014) R. Sanalkumar et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- Isolation and functional characterization of human erythroblasts at distinct stages: implications for understanding of normal and disordered erythropoiesis in vivo
- (2013) J. Hu et al. BLOOD
- Three fingers on the switch
- (2013) Michael R. Tallack et al. CURRENT OPINION IN HEMATOLOGY
- Histone Deacetylase (HDAC) Inhibitor Kinetic Rate Constants Correlate with Cellular Histone Acetylation but Not Transcription and Cell Viability
- (2013) Benjamin E. L. Lauffer et al. JOURNAL OF BIOLOGICAL CHEMISTRY
- Lysine-specific demethylase 1 is a therapeutic target for fetal hemoglobin induction
- (2013) Lihong Shi et al. NATURE MEDICINE
- Corepressor-dependent silencing of fetal hemoglobin expression by BCL11A
- (2013) J. Xu et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- Distinct Ldb1/NLI complexes orchestrate -globin repression and reactivation through ETO2 in human adult erythroid cells
- (2011) C. M. Kiefer et al. BLOOD
- Fetal hemoglobin levels and morbidity in untransfused patients with -thalassemia intermedia
- (2011) K. M. Musallam et al. BLOOD
- Mapping and analysis of chromatin state dynamics in nine human cell types
- (2011) Jason Ernst et al. NATURE
- Heritable GATA2 mutations associated with familial myelodysplastic syndrome and acute myeloid leukemia
- (2011) Christopher N Hahn et al. NATURE GENETICS
- A Functional Element Necessary for Fetal Hemoglobin Silencing
- (2011) Vijay G. Sankaran et al. NEW ENGLAND JOURNAL OF MEDICINE
- FOG1 requires NuRD to promote hematopoiesis and maintain lineage fidelity within the megakaryocytic-erythroid compartment
- (2010) G. D. Gregory et al. BLOOD
- Update on fetal hemoglobin gene regulation in hemoglobinopathies
- (2010) Daniel E Bauer et al. CURRENT OPINION IN PEDIATRICS
- Transcriptional silencing of -globin by BCL11A involves long-range interactions and cooperation with SOX6
- (2010) J. Xu et al. GENES & DEVELOPMENT
- GATA Switches as Developmental Drivers
- (2010) Emery H. Bresnick et al. JOURNAL OF BIOLOGICAL CHEMISTRY
- Discovery and characterization of chromatin states for systematic annotation of the human genome
- (2010) Jason Ernst et al. NATURE BIOTECHNOLOGY
- Chemical phylogenetics of histone deacetylases
- (2010) James E Bradner et al. Nature Chemical Biology
- KLF1 regulates BCL11A expression and γ- to β-globin gene switching
- (2010) Dewang Zhou et al. NATURE GENETICS
- Chemical genetic strategy identifies histone deacetylase 1 (HDAC1) and HDAC2 as therapeutic targets in sickle cell disease
- (2010) James E. Bradner et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- Cytokine-mediated increases in fetal hemoglobin are associated with globin gene histone modification and transcription factor reprogramming
- (2009) O. Sripichai et al. BLOOD
- NuRD mediates activating and repressive functions of GATA-1 and FOG-1 during blood development
- (2009) Annarita Miccio et al. EMBO JOURNAL
- Histone modifications at human enhancers reflect global cell-type-specific gene expression
- (2009) Nathaniel D. Heintzman et al. NATURE
- PRMT5-mediated methylation of histone H4R3 recruits DNMT3A, coupling histone and DNA methylation in gene silencing
- (2009) Quan Zhao et al. NATURE STRUCTURAL & MOLECULAR BIOLOGY
- Human Fetal Hemoglobin Expression Is Regulated by the Developmental Stage-Specific RepressorBCL11A
- (2008) Vijay G. Sankaran et al. SCIENCE
- Model-based Analysis of ChIP-Seq (MACS)
- (2008) Yong Zhang et al. GENOME BIOLOGY
- Optimization of biaryl Selective HDAC1&2 Inhibitors (SHI-1:2)
- (2007) David J. Witter et al. BIOORGANIC & MEDICINAL CHEMISTRY LETTERS
- Exploration of the internal cavity of histone deacetylase (HDAC) with selective HDAC1/HDAC2 inhibitors (SHI-1:2)
- (2007) Joey L. Methot et al. BIOORGANIC & MEDICINAL CHEMISTRY LETTERS
Find Funding. Review Successful Grants.
Explore over 25,000 new funding opportunities and over 6,000,000 successful grants.
ExplorePublish scientific posters with Peeref
Peeref publishes scientific posters from all research disciplines. Our Diamond Open Access policy means free access to content and no publication fees for authors.
Learn More