Insight into GATA1 transcriptional activity through interrogation ofciselements disrupted in human erythroid disorders
出版年份 2016 全文链接
标题
Insight into GATA1 transcriptional activity through interrogation ofciselements disrupted in human erythroid disorders
作者
关键词
-
出版物
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
Volume 113, Issue 16, Pages 4434-4439
出版商
Proceedings of the National Academy of Sciences
发表日期
2016-04-05
DOI
10.1073/pnas.1521754113
参考文献
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。- Two Novel Missense Mutations and a 5bp Deletion in the Erythroid-Specific Promoter of thePKLRGene in Two Unrelated Patients With Pyruvate Kinase Deficient Transfusion-Dependent Chronic Nonspherocytic Hemolytic Anemia
- (2016) Leo Kager et al. PEDIATRIC BLOOD & CANCER
- KLF1 stabilizes GATA-1 and TAL1 occupancy in the human β-globin locus
- (2015) Yujin Kang et al. Biochimica et Biophysica Acta-Gene Regulatory Mechanisms
- Mutations in the Gardos channel (KCNN4) are associated with hereditary xerocytosis
- (2015) E. Glogowska et al. BLOOD
- Genetic Variation Determines PPARγ Function and Anti-diabetic Drug Response In Vivo
- (2015) Raymond E. Soccio et al. CELL
- X-linked macrocytic dyserythropoietic anemia in females with an ALAS2 mutation
- (2015) Vijay G. Sankaran et al. JOURNAL OF CLINICAL INVESTIGATION
- Predicting the sequence specificities of DNA- and RNA-binding proteins by deep learning
- (2015) Babak Alipanahi et al. NATURE BIOTECHNOLOGY
- A method to predict the impact of regulatory variants from DNA sequence
- (2015) Dongwon Lee et al. NATURE GENETICS
- Anemia: progress in molecular mechanisms and therapies
- (2015) Vijay G Sankaran et al. NATURE MEDICINE
- FTO Obesity Variant Circuitry and Adipocyte Browning in Humans
- (2015) Melina Claussnitzer et al. NEW ENGLAND JOURNAL OF MEDICINE
- Occupancy by key transcription factors is a more accurate predictor of enhancer activity than histone modifications or chromatin accessibility
- (2015) Nergiz Dogan et al. Epigenetics & Chromatin
- Editing the genome to introduce a beneficial naturally occurring mutation associated with increased fetal globin
- (2015) Beeke Wienert et al. Nature Communications
- Global transcriptome analyses of human and murine terminal erythroid differentiation
- (2014) X. An et al. BLOOD
- Performance comparison of four exome capture systems for deep sequencing
- (2014) Chandra Sekhar Chilamakuri et al. BMC GENOMICS
- Role of LDB1 in the transition from chromatin looping to transcription activation
- (2014) I. Krivega et al. GENES & DEVELOPMENT
- Dynamic shifts in occupancy by TAL1 are guided by GATA factors and drive large-scale reprogramming of gene expression during hematopoiesis
- (2014) Weisheng Wu et al. GENOME RESEARCH
- HBS1L-MYB intergenic variants modulate fetal hemoglobin via long-range MYB enhancers
- (2014) Ralph Stadhouders et al. JOURNAL OF CLINICAL INVESTIGATION
- Principles of regulatory information conservation between mouse and human
- (2014) Yong Cheng et al. NATURE
- Guidelines for investigating causality of sequence variants in human disease
- (2014) D. G. MacArthur et al. NATURE
- Genetic and epigenetic fine mapping of causal autoimmune disease variants
- (2014) Kyle Kai-How Farh et al. NATURE
- Analysis of chromatin-state plasticity identifies cell-type-specific regulators of H3K27me3 patterns
- (2014) L. Pinello et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- Altered Chromatin Occupancy of Master Regulators Underlies Evolutionary Divergence in the Transcriptional Landscape of Erythroid Differentiation
- (2014) Jacob C. Ulirsch et al. PLoS Genetics
- Multi-species, multi-transcription factor binding highlights conserved control of tissue-specific biological pathways
- (2014) Benoit Ballester et al. eLife
- X-linked sideroblastic anemia due to ALAS2 intron 1 enhancer element GATA-binding site mutations
- (2013) Dean R. Campagna et al. AMERICAN JOURNAL OF HEMATOLOGY
- Applications of high-throughput DNA sequencing to benign hematology
- (2013) V. G. Sankaran et al. BLOOD
- Ldb1-nucleated transcription complexes function as primary mediators of global erythroid gene activation
- (2013) L. Li et al. BLOOD
- Analysis of disease-causing GATA1 mutations in murine gene complementation systems
- (2013) A. E. Campbell et al. BLOOD
- A survey of tools for variant analysis of next-generation genome sequencing data
- (2013) S. Pabinger et al. BRIEFINGS IN BIOINFORMATICS
- Homozygous mutations in a predicted endonuclease are a novel cause of congenital dyserythropoietic anemia type I
- (2013) C. Babbs et al. HAEMATOLOGICA
- Identification of a novel erythroid-specific enhancer for the ALAS2 gene and its loss-of-function mutation which is associated with congenital sideroblastic anemia
- (2013) K. Kaneko et al. HAEMATOLOGICA
- Identification of Biologically Relevant Enhancers in Human Erythroid Cells
- (2013) Mack Y. Su et al. JOURNAL OF BIOLOGICAL CHEMISTRY
- Clinical Whole-Exome Sequencing for the Diagnosis of Mendelian Disorders
- (2013) Yaping Yang et al. NEW ENGLAND JOURNAL OF MEDICINE
- Ldb1 complexes: the new master regulators of erythroid gene transcription
- (2013) Paul E. Love et al. TRENDS IN GENETICS
- Mutations in the mechanotransduction protein PIEZO1 are associated with hereditary xerocytosis
- (2012) R. Zarychanski et al. BLOOD
- Combinatorial Assembly of Developmental Stage-Specific Enhancers Controls Gene Expression Programs during Human Erythropoiesis
- (2012) Jian Xu et al. DEVELOPMENTAL CELL
- Cyclin D3 coordinates the cell cycle during differentiation to regulate erythrocyte size and number
- (2012) V. G. Sankaran et al. GENES & DEVELOPMENT
- Exome sequencing identifies GATA1 mutations resulting in Diamond-Blackfan anemia
- (2012) Vijay G. Sankaran et al. JOURNAL OF CLINICAL INVESTIGATION
- Interpreting noncoding genetic variation in complex traits and human disease
- (2012) Lucas D Ward et al. NATURE BIOTECHNOLOGY
- Genome-wide ChIP-Seq reveals a dramatic shift in the binding of the transcription factor erythroid Kruppel-like factor during erythrocyte differentiation
- (2011) A. M. Pilon et al. BLOOD
- Regulation of nucleosome landscape and transcription factor targeting at tissue-specific enhancers by BRG1
- (2011) G. Hu et al. GENOME RESEARCH
- Dynamics of the epigenetic landscape during erythroid differentiation after GATA1 restoration
- (2011) W. Wu et al. GENOME RESEARCH
- Transcription factor binding predictions using TRAP for the analysis of ChIP-seq data and regulatory SNPs
- (2011) Morgane Thomas-Chollier et al. Nature Protocols
- Exome sequencing as a tool for Mendelian disease gene discovery
- (2011) Michael J. Bamshad et al. NATURE REVIEWS GENETICS
- Combinatorial Transcriptional Control In Blood Stem/Progenitor Cells: Genome-wide Analysis of Ten Major Transcriptional Regulators
- (2010) Nicola K. Wilson et al. Cell Stem Cell
- Genome-wide identification of TAL1's functional targets: Insights into its mechanisms of action in primary erythroid cells
- (2010) M. T. Kassouf et al. GENOME RESEARCH
- Genes, mutations, and human inherited disease at the dawn of the age of personalized genomics
- (2010) David N. Cooper et al. HUMAN MUTATION
- Mutation of a barrier insulator in the human ankyrin-1 gene is associated with hereditary spherocytosis
- (2010) Patrick G. Gallagher et al. JOURNAL OF CLINICAL INVESTIGATION
- Amelioration of Sardinian 0 thalassemia by genetic modifiers
- (2009) R. Galanello et al. BLOOD
- Erythroid GATA1 function revealed by genome-wide analysis of transcription factor occupancy, histone modifications, and mRNA expression
- (2009) Y. Cheng et al. GENOME RESEARCH
- Discovering Hematopoietic Mechanisms through Genome-wide Analysis of GATA Factor Chromatin Occupancy
- (2009) Tohru Fujiwara et al. MOLECULAR CELL
- A case of congenital red cell pyruvate kinase deficiency associated with hereditary stomatocytosis
- (2008) Anna Paola Marcello et al. BLOOD CELLS MOLECULES AND DISEASES
- Mutations in TMPRSS6 cause iron-refractory iron deficiency anemia (IRIDA)
- (2008) Karin E Finberg et al. NATURE GENETICS
Publish 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 MoreBecome a Peeref-certified reviewer
The Peeref Institute provides free reviewer training that teaches the core competencies of the academic peer review process.
Get Started