The genome-wide impact of trisomy 21 on DNA methylation and its implications for hematopoiesis
出版年份 2021 全文链接
标题
The genome-wide impact of trisomy 21 on DNA methylation and its implications for hematopoiesis
作者
关键词
-
出版物
Nature Communications
Volume 12, Issue 1, Pages -
出版商
Springer Science and Business Media LLC
发表日期
2021-02-05
DOI
10.1038/s41467-021-21064-z
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注意:仅列出部分参考文献,下载原文获取全部文献信息。- Cell type specific novel lncRNAs and circRNAs in the BLUEPRINT haematopoietic transcriptomes atlas.
- (2020) Luigi Grassi et al. HAEMATOLOGICA
- Increased neonatal level of arginase 2 in cases of childhood acute lymphoblastic leukemia implicates immunosuppression in etiology
- (2019) Amalie B. Nielsen et al. HAEMATOLOGICA
- Whole genome bisulfite sequencing of Down syndrome brain reveals regional DNA hypermethylation and novel disorder insights
- (2019) Benjamin I. Laufer et al. Epigenetics
- Inherited genetic susceptibility of acute lymphoblastic leukemia in Down syndrome
- (2019) Austin L. Brown et al. BLOOD
- Mechanisms of Progression of Myeloid Preleukemia to Transformed Myeloid Leukemia in Children with Down Syndrome
- (2019) Maurice Labuhn et al. CANCER CELL
- Elevated Nucleated Red Blood Cells in Neonates with Down Syndrome and Pulmonary Hypertension
- (2019) Itamar Nitzan et al. JOURNAL OF PEDIATRICS
- Discovery of a CD10-negative B-progenitor in human fetal life identifies unique ontogeny-related developmental programs
- (2019) Sorcha O’Byrne et al. BLOOD
- Integrated genetic and epigenetic analysis revealed heterogeneity of acute lymphoblastic leukemia in Down syndrome
- (2019) Yasuo Kubota et al. CANCER SCIENCE
- A compendium of promoter-centered long-range chromatin interactions in the human genome
- (2019) Inkyung Jung et al. NATURE GENETICS
- Systematic evaluation and validation of reference and library selection methods for deconvolution of cord blood DNA methylation data
- (2019) Kristina Gervin et al. Clinical Epigenetics
- Epigenome-wide meta-analysis of blood DNA methylation and its association with subcortical volumes: findings from the ENIGMA Epigenetics Working Group
- (2019) Tianye Jia et al. MOLECULAR PSYCHIATRY
- Regulation of RUNX1 dosage is crucial for efficient blood formation from hemogenic endothelium
- (2018) Michael Lie-A-Ling et al. DEVELOPMENT
- Widespread domain-like perturbations of DNA methylation in whole blood of Down syndrome neonates
- (2018) Peter Henneman et al. PLoS One
- Transcription factor Runx1 is pro-neurogenic in adult hippocampal precursor cells
- (2018) Hirokazu Fukui et al. PLoS One
- Single-cell transcriptomics reveals a new dynamical function of transcription factors during embryonic hematopoiesis
- (2018) Isabelle Bergiers et al. eLife
- methylGSA: a Bioconductor package and Shiny app for DNA methylation data length bias adjustment in gene set testing
- (2018) Xu Ren et al. BIOINFORMATICS
- The NHGRI-EBI GWAS Catalog of published genome-wide association studies, targeted arrays and summary statistics 2019
- (2018) Annalisa Buniello et al. NUCLEIC ACIDS RESEARCH
- Genome-wide methylation data mirror ancestry information
- (2017) Elior Rahmani et al. Epigenetics & Chromatin
- Complex heatmaps reveal patterns and correlations in multidimensional genomic data
- (2016) Zuguang Gu et al. BIOINFORMATICS
- DNA methylation of cord blood cell types: Applications for mixed cell birth studies
- (2016) Kelly M. Bakulski et al. Epigenetics
- Low risk of solid tumors in persons with Down syndrome
- (2016) Henrik Hasle et al. GENETICS IN MEDICINE
- Global hypermethylation in fetal cortex of Down syndrome due to DNMT3L overexpression
- (2016) Jie Lu et al. HUMAN MOLECULAR GENETICS
- Senp1 drives hypoxia-induced polycythemia via GATA1 and Bcl-xL in subjects with Monge’s disease
- (2016) Priti Azad et al. JOURNAL OF EXPERIMENTAL MEDICINE
- Sparse PCA corrects for cell type heterogeneity in epigenome-wide association studies
- (2016) Elior Rahmani et al. NATURE METHODS
- Down syndrome and the complexity of genome dosage imbalance
- (2016) Stylianos E. Antonarakis NATURE REVIEWS GENETICS
- Transient Abnormal Myelopoiesis and AML in Down Syndrome: an Update
- (2016) Neha Bhatnagar et al. Current Hematologic Malignancy Reports
- Identification of a DNA methylation signature in blood cells from persons with Down Syndrome
- (2016) Maria Giulia Bacalini et al. Aging-US
- DNA-Methylation Patterns in Trisomy 21 Using Cells from Monozygotic Twins
- (2015) M. Reza Sailani et al. PLoS One
- Stem and progenitor cell dysfunction in human trisomies
- (2014) B. Liu et al. EMBO REPORTS
- Divergent functions of hematopoietic transcription factors in lineage priming and differentiation during erythro-megakaryopoiesis
- (2014) Maxim Pimkin et al. GENOME RESEARCH
- Domains of genome-wide gene expression dysregulation in Down’s syndrome
- (2014) Audrey Letourneau et al. NATURE
- Triplication of a 21q22 region contributes to B cell transformation through HMGN1 overexpression and loss of histone H3 Lys27 trimethylation
- (2014) Andrew A Lane et al. NATURE GENETICS
- Full-length RNA-seq from single cells using Smart-seq2
- (2014) Simone Picelli et al. Nature Protocols
- Prdm8 Regulates the Morphological Transition at Multipolar Phase during Neocortical Development
- (2014) Mayuko Inoue et al. PLoS One
- DNA methylation of Runx1 regulatory regions correlates with transition from primitive to definitive hematopoietic potential in vitro and in vivo
- (2013) B. R. Webber et al. BLOOD
- GATA1-mutant clones are frequent and often unsuspected in babies with Down syndrome: identification of a population at risk of leukemia
- (2013) I. Roberts et al. BLOOD
- Enrichment of FLI1 and RUNX1 mutations in families with excessive bleeding and platelet dense granule secretion defects
- (2013) J. Stockley et al. BLOOD
- Super-Enhancers in the Control of Cell Identity and Disease
- (2013) Denes Hnisz et al. CELL
- Low-level processing of Illumina Infinium DNA Methylation BeadArrays
- (2013) Timothy J. Triche et al. NUCLEIC ACIDS RESEARCH
- Comb-p: software for combining, analyzing, grouping and correcting spatially correlated P-values
- (2012) B. S. Pedersen et al. BIOINFORMATICS
- STAR: ultrafast universal RNA-seq aligner
- (2012) Alexander Dobin et al. BIOINFORMATICS
- Transcription as a source of genome instability
- (2012) Nayun Kim et al. NATURE REVIEWS GENETICS
- Perturbation of fetal liver hematopoietic stem and progenitor cell development by trisomy 21
- (2012) A. Roy et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- The Essential Role of Centrosomal NDE1 in Human Cerebral Cortex Neurogenesis
- (2011) Mehmet Bakircioglu et al. AMERICAN JOURNAL OF HUMAN GENETICS
- Infections and immunodeficiency in Down syndrome
- (2011) G. Ram et al. CLINICAL AND EXPERIMENTAL IMMUNOLOGY
- Updated national birth prevalence estimates for selected birth defects in the United States, 2004-2006
- (2010) Samantha E. Parker et al. BIRTH DEFECTS RESEARCH PART A-CLINICAL AND MOLECULAR TERATOLOGY
- Nonredundant roles for Runx1 alternative promoters reflect their activity at discrete stages of developmental hematopoiesis
- (2010) T. Bee et al. BLOOD
- The NIH Roadmap Epigenomics Mapping Consortium
- (2010) Bradley E Bernstein et al. NATURE BIOTECHNOLOGY
- New Intrauterine Growth Curves Based on United States Data
- (2010) I. E. Olsen et al. PEDIATRICS
- Altered DNA Methylation in Leukocytes with Trisomy 21
- (2010) Kristi Kerkel et al. PLoS Genetics
- VarScan: variant detection in massively parallel sequencing of individual and pooled samples
- (2009) Daniel C. Koboldt et al. BIOINFORMATICS
- The differential activities of Runx1 promoters define milestones during embryonic hematopoiesis
- (2009) P. Sroczynska et al. BLOOD
- Differentiation-Dependent Interactions between RUNX-1 and FLI-1 during Megakaryocyte Development
- (2009) H. Huang et al. MOLECULAR AND CELLULAR BIOLOGY
- Runx1 is required for the endothelial to haematopoietic cell transition but not thereafter
- (2009) Michael J. Chen et al. NATURE
- Abnormalities in the myeloid progenitor compartment in Down syndrome fetal liver precede acquisition of GATA1 mutations
- (2008) O. Tunstall-Pedoe et al. BLOOD
- Treatment and prognostic impact of transient leukemia in neonates with Down syndrome
- (2008) J.-H. Klusmann et al. BLOOD
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