标题
Is ZFP57 binding to H19/IGF2:IG-DMR affected in Silver-Russell syndrome?
作者
关键词
Genomic imprinting, Silver-Russell syndrome, DNA methylation, ZFP57, <em class=EmphasisTypeItalic >H19/IGF2</em>:IG-DMR deletions, Beckwith-Wiedemann syndrome
出版物
Clinical Epigenetics
Volume 10, Issue 1, Pages -
出版商
Springer Nature
发表日期
2018-02-21
DOI
10.1186/s13148-018-0454-7
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。- Recommendations for a nomenclature system for reporting methylation aberrations in imprinted domains
- (2018) David Monk et al. Epigenetics
- KRAB zinc-finger proteins contribute to the evolution of gene regulatory networks
- (2017) Michaël Imbeault et al. NATURE
- Recent Advances in Imprinting Disorders
- (2016) L. Soellner et al. CLINICAL GENETICS
- 11p15 ICR1 Partial Deletions Associated withIGF2/H19DMR Hypomethylation and Silver-Russell Syndrome
- (2016) Walid Abi Habib et al. HUMAN MUTATION
- ZFP57 maintains the parent-of-origin-specific expression of the imprinted genes and differentially affects non-imprinted targets in mouse embryonic stem cells
- (2016) Vincenzo Riso et al. NUCLEIC ACIDS RESEARCH
- HumanizedH19/Igf2locus reveals diverged imprinting mechanism between mouse and human and reflects Silver–Russell syndrome phenotypes
- (2016) Stella K. Hur et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- Germline-derived DNA methylation and early embryo epigenetic reprogramming: The selected survival of imprints
- (2015) David Monk INTERNATIONAL JOURNAL OF BIOCHEMISTRY & CELL BIOLOGY
- ZFP57 recognizes multiple and closely spaced sequence motif variants to maintain repressive epigenetic marks in mouse embryonic stem cells
- (2015) Zahra Anvar et al. NUCLEIC ACIDS RESEARCH
- Mutations in NLRP5 are associated with reproductive wastage and multilocus imprinting disorders in humans
- (2015) Louise E. Docherty et al. Nature Communications
- Extensive investigation of the IGF2/H19 imprinting control region reveals novel OCT4/SOX2 binding site defects associated with specific methylation patterns in Beckwith-Wiedemann syndrome
- (2014) Walid Abi Habib et al. HUMAN MOLECULAR GENETICS
- Epigenetics and imprinting in human disease
- (2014) Jennifer M. Kalish et al. INTERNATIONAL JOURNAL OF DEVELOPMENTAL BIOLOGY
- A novelde novopoint mutation of the OCT-binding site in theIGF2/H19-imprinting control region in a Beckwith-Wiedemann syndrome patient
- (2013) K. Higashimoto et al. CLINICAL GENETICS
- Transient Neonatal Diabetes, ZFP57, and Hypomethylation of Multiple Imprinted Loci: A detailed follow-up
- (2012) S. E. Boonen et al. DIABETES CARE
- The molecular function and clinical phenotype of partial deletions of the IGF2/H19 imprinting control region depends on the spatial arrangement of the remaining CTCF-binding sites
- (2012) Jasmin Beygo et al. HUMAN MOLECULAR GENETICS
- New insights into establishment and maintenance of DNA methylation imprints in mammals
- (2012) G. Kelsey et al. PHILOSOPHICAL TRANSACTIONS OF THE ROYAL SOCIETY B-BIOLOGICAL SCIENCES
- Beckwith–Wiedemann syndrome caused by maternally inherited mutation of an OCT-binding motif in the IGF2/H19-imprinting control region, ICR1
- (2011) Rebecca L Poole et al. EUROPEAN JOURNAL OF HUMAN GENETICS
- A novel microdeletion in the IGF2/H19 imprinting centre region defines a recurrent mutation mechanism in familial Beckwith–Wiedemann syndrome
- (2011) Agostina De Crescenzo et al. European Journal of Medical 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
- Deletions and rearrangements of the H19/IGF2 enhancer region in patients with Silver-Russell syndrome and growth retardation
- (2011) K. Gronskov et al. JOURNAL OF MEDICAL GENETICS
- In Embryonic Stem Cells, ZFP57/KAP1 Recognize a Methylated Hexanucleotide to Affect Chromatin and DNA Methylation of Imprinting Control Regions
- (2011) Simon Quenneville et al. MOLECULAR CELL
- Screening for genomic variants in ZFP57 in Silver-Russell syndrome patients with 11p15 epimutations
- (2009) Sabrina Spengler et al. European Journal of Medical Genetics
- Analysis of the IGF2/H19 imprinting control region uncovers new genetic defects, including mutations of OCT-binding sequences, in patients with 11p15 fetal growth disorders
- (2009) Julie Demars et al. HUMAN MOLECULAR GENETICS
- A Maternal-Zygotic Effect Gene, Zfp57, Maintains Both Maternal and Paternal Imprints
- (2008) Xiajun Li et al. DEVELOPMENTAL CELL
- Hypomethylation of multiple imprinted loci in individuals with transient neonatal diabetes is associated with mutations in ZFP57
- (2008) Deborah J G Mackay et al. NATURE GENETICS
- Constitutional 11p15 abnormalities, including heritable imprinting center mutations, cause nonsyndromic Wilms tumor
- (2008) Richard H Scott et al. NATURE GENETICS
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