Converging disease genes in ICF syndrome:ZBTB24controls expression ofCDCA7in mammals
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Title
Converging disease genes in ICF syndrome:ZBTB24controls expression ofCDCA7in mammals
Authors
Keywords
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Journal
HUMAN MOLECULAR GENETICS
Volume 25, Issue 18, Pages 4041-4051
Publisher
Oxford University Press (OUP)
Online
2016-07-28
DOI
10.1093/hmg/ddw243
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- (2014) S. Anders et al. BIOINFORMATICS
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- (2014) Weishi Yu et al. GENOME RESEARCH
- Selective demethylation and altered gene expression are associated with ICF syndrome in human-induced pluripotent stem cells and mesenchymal stem cells
- (2014) Kevin Huang et al. HUMAN MOLECULAR GENETICS
- Identification of Cdca7 as a novel Notch transcriptional target involved in hematopoietic stem cell emergence
- (2014) Jordi Guiu et al. JOURNAL OF EXPERIMENTAL MEDICINE
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- (2013) Corry MR Weemaes et al. EUROPEAN JOURNAL OF HUMAN GENETICS
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- The Transcriptional and Epigenomic Foundations of Ground State Pluripotency
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- (2012) Holger Heyn et al. Epigenetics
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- (2012) Sung-Uk Lee et al. IMMUNOLOGICAL REVIEWS
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- (2011) James T Robinson et al. NATURE BIOTECHNOLOGY
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- (2009) J. M. Ruijter et al. NUCLEIC ACIDS RESEARCH
- The ground state of embryonic stem cell self-renewal
- (2008) Qi-Long Ying et al. NATURE
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