The role of CTCF in the organization of the centromeric 11p15 imprinted domain interactome
出版年份 2021 全文链接
标题
The role of CTCF in the organization of the centromeric 11p15 imprinted domain interactome
作者
关键词
-
出版物
NUCLEIC ACIDS RESEARCH
Volume 49, Issue 11, Pages 6315-6330
出版商
Oxford University Press (OUP)
发表日期
2021-05-20
DOI
10.1093/nar/gkab475
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。- Why and How Imprinted Genes Drive Fetal Programming
- (2020) Bernard J. Crespi Frontiers in Endocrinology
- Diagnosis and Management of Beckwith-Wiedemann Syndrome
- (2020) Kathleen H. Wang et al. Frontiers in Pediatrics
- Differential 3D chromatin organization and gene activity in genomic imprinting
- (2020) Daan Noordermeer et al. CURRENT OPINION IN GENETICS & DEVELOPMENT
- Improved molecular detection of mosaicism in Beckwith-Wiedemann Syndrome
- (2020) Samuel W Baker et al. JOURNAL OF MEDICAL GENETICS
- Profound alterations of the chromatin architecture at chromosome 11p15.5 in cells from Beckwith-Wiedemann and Silver-Russell syndromes patients
- (2020) Davide Rovina et al. Scientific Reports
- Frequency of KCNQ1 variants causing loss of methylation of Imprinting Centre 2 in Beckwith-Wiedemann syndrome
- (2020) Carla Eßinger et al. Clinical Epigenetics
- Expanded encyclopaedias of DNA elements in the human and mouse genomes
- (2020) Jill E. Moore et al. NATURE
- Chromosome territories and the global regulation of the genome
- (2019) Andrew J. Fritz et al. GENES CHROMOSOMES & CANCER
- Transcription alterations of KCNQ1 associated with imprinted methylation defects in the Beckwith–Wiedemann locus
- (2019) Federica Maria Valente et al. GENETICS IN MEDICINE
- Disruption of KCNQ1 prevents methylation of the ICR2 and supports the hypothesis that its transcription is necessary for imprint establishment
- (2019) Jasmin Beygo et al. EUROPEAN JOURNAL OF HUMAN GENETICS
- The role of 3D genome organization in development and cell differentiation
- (2019) Hui Zheng et al. NATURE REVIEWS MOLECULAR CELL BIOLOGY
- Characterization of the Beckwith‐Wiedemann spectrum: Diagnosis and management
- (2019) Kelly A. Duffy et al. AMERICAN JOURNAL OF MEDICAL GENETICS PART C-SEMINARS IN MEDICAL GENETICS
- Expert consensus document: Clinical and molecular diagnosis, screening and management of Beckwith–Wiedemann syndrome: an international consensus statement
- (2018) Frédéric Brioude et al. Nature Reviews Endocrinology
- Chromosomal rearrangements in the 11p15 imprinted region: 17 new 11p15.5 duplications with associated phenotypes and putative functional consequences
- (2017) Solveig Heide et al. JOURNAL OF MEDICAL GENETICS
- A maternal deletion upstream of the imprint control region 2 in 11p15 causes loss of methylation and familial Beckwith–Wiedemann syndrome
- (2016) Jasmin Beygo et al. EUROPEAN JOURNAL OF HUMAN GENETICS
- Epigenetic Characterization of CDKN1C in Placenta Samples from Non-syndromic Intrauterine Growth Restriction
- (2016) Miriam López-Abad et al. Frontiers in Genetics
- Multiplexed analysis of chromosome conformation at vastly improved sensitivity
- (2015) James O J Davies et al. NATURE METHODS
- circlize implements and enhances circular visualization in R
- (2014) Zuguang Gu et al. BIOINFORMATICS
- Sushi.R: flexible, quantitative and integrative genomic visualizations for publication-quality multi-panel figures
- (2014) D. H. Phanstiel et al. BIOINFORMATICS
- bwtool: a tool for bigWig files
- (2014) Andy Pohl et al. BIOINFORMATICS
- The Role of CCCTC-Binding Factor (CTCF) in Genomic Imprinting, Development, and Reproduction1
- (2014) Maurício M. Franco et al. BIOLOGY OF REPRODUCTION
- Genomic imprinting in development, growth, behavior and stem cells
- (2014) Robert N. Plasschaert et al. DEVELOPMENT
- Epigenetics and imprinting in human disease
- (2014) Jennifer M. Kalish et al. INTERNATIONAL JOURNAL OF DEVELOPMENTAL BIOLOGY
- Long noncoding RNA-mediated intrachromosomal interactions promote imprinting at theKcnq1locus
- (2014) He Zhang et al. JOURNAL OF CELL BIOLOGY
- Genetic variants within the second intron of theKCNQ1gene affect CTCF binding and confer a risk of Beckwith–Wiedemann syndrome upon maternal transmission
- (2014) Julie Demars et al. JOURNAL OF MEDICAL GENETICS
- Enhancers compete with a long non-coding RNA for regulation of the Kcnq1 domain
- (2014) Bryant M. Schultz et al. NUCLEIC ACIDS RESEARCH
- fourSig: a method for determining chromosomal interactions in 4C-Seq data
- (2014) Rex L. Williams et al. NUCLEIC ACIDS RESEARCH
- Mild Beckwith-Wiedemann and severe long-QT syndrome due to deletion of the imprinting center 2 on chromosome 11p
- (2013) Fiorella Gurrieri et al. EUROPEAN JOURNAL OF HUMAN GENETICS
- Looking for CDKN1C enhancers
- (2013) Flavia Cerrato et al. EUROPEAN JOURNAL OF HUMAN GENETICS
- Genome-wide and parental allele-specific analysis of CTCF and cohesin DNA binding in mouse brain reveals a tissue-specific binding pattern and an association with imprinted differentially methylated regions
- (2013) A. R. Prickett et al. GENOME RESEARCH
- High frequency of copy number variations (CNVs) in the chromosome 11p15 region in patients with Beckwith–Wiedemann syndrome
- (2013) Berivan Baskin et al. HUMAN GENETICS
- Analysis of the Human Tissue-specific Expression by Genome-wide Integration of Transcriptomics and Antibody-based Proteomics
- (2013) Linn Fagerberg et al. MOLECULAR & CELLULAR PROTEOMICS
- Beckwith-Wiedemann syndrome and long QT syndrome due to familial-balanced translocation t(11;17)(p15.5;q21.3) involving theKCNQ1gene
- (2012) S Kaltenbach et al. CLINICAL GENETICS
- The Kcnq1ot1 Long Non-Coding RNA Affects Chromatin Conformation and Expression of Kcnq1, but Does Not Regulate Its Imprinting in the Developing Heart
- (2012) Lisa Korostowski et al. PLoS Genetics
- Chromatin signatures of active enhancers
- (2012) salvatore spicuglia et al. Nucleus
- FLASH: fast length adjustment of short reads to improve genome assemblies
- (2011) T. Magoc et al. BIOINFORMATICS
- Estrogen-mediated epigenetic repression of the imprinted gene cyclin-dependent kinase inhibitor 1C in breast cancer cells
- (2011) Benjamin A.T. Rodriguez et al. CARCINOGENESIS
- Genomic imprinting: recognition and marking of imprinted loci
- (2011) Lara K Abramowitz et al. CURRENT OPINION IN GENETICS & DEVELOPMENT
- Depletion of Kcnq1ot1 non-coding RNA does not affect imprinting maintenance in stem cells
- (2011) M. C. Golding et al. DEVELOPMENT
- The KCNQ1OT1 imprinting control region and non-coding RNA: new properties derived from the study of Beckwith–Wiedemann syndrome and Silver–Russell syndrome cases
- (2011) Nicoletta Chiesa et al. HUMAN MOLECULAR GENETICS
- New insights into the pathogenesis of beckwith-wiedemann and silver-russell syndromes: Contribution of small copy number variations to 11p15 imprinting defects
- (2011) Julie Demars et al. HUMAN MUTATION
- Nonallelic Transcriptional Roles of CTCF and Cohesins at Imprinted Loci
- (2011) S. Lin et al. MOLECULAR AND CELLULAR BIOLOGY
- An 11p15 Imprinting Centre Region 2 Deletion in a Family with Beckwith Wiedemann Syndrome Provides Insights into Imprinting Control at CDKN1C
- (2011) Elizabeth Algar et al. PLoS One
- Enhancer-driven chromatin interactions during development promote escape from silencing by a long non-coding RNA
- (2011) Lisa Korostowski et al. Epigenetics & Chromatin
- BEDTools: a flexible suite of utilities for comparing genomic features
- (2010) Aaron R. Quinlan et al. BIOINFORMATICS
- Kcnq1ot1 noncoding RNA mediates transcriptional gene silencing by interacting with Dnmt1
- (2010) F. Mohammad et al. DEVELOPMENT
- The long noncoding RNA Kcnq1ot1 organises a lineage-specific nuclear domain for epigenetic gene silencing
- (2009) L. Redrup et al. DEVELOPMENT
- A case of Beckwith-Wiedemann syndrome caused by a cryptic 11p15 deletion encompassing the centromeric imprinted domain of the BWS locus
- (2009) M. Zollino et al. JOURNAL OF MEDICAL GENETICS
- Comprehensive Mapping of Long-Range Interactions Reveals Folding Principles of the Human Genome
- (2009) E. Lieberman-Aiden et al. SCIENCE
- Kcnq1ot1/Lit1 Noncoding RNA Mediates Transcriptional Silencing by Targeting to the Perinucleolar Region
- (2008) F. Mohammad et al. MOLECULAR AND CELLULAR BIOLOGY
- Kcnq1ot1 Antisense Noncoding RNA Mediates Lineage-Specific Transcriptional Silencing through Chromatin-Level Regulation
- (2008) Radha Raman Pandey et al. MOLECULAR CELL
Discover Peeref hubs
Discuss science. Find collaborators. Network.
Join a conversationAsk a Question. Answer a Question.
Quickly pose questions to the entire community. Debate answers and get clarity on the most important issues facing researchers.
Get Started