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Defending the genome from the enemy within: mechanisms of retrotransposon suppression in the mouse germline

Cellular and molecular life sciences : CMLS, 2014-05, Vol.71 (9), p.1581-1605

2014

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Enzymatic approaches and bisulfite sequencing cannot distinguish between 5-methylcytosine and 5-hydroxymethylcytosine in DNA

BioTechniques, 2010-04, Vol.48 (4), p.317-319

2010

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Redistribution of H3K27me3 upon DNA hypomethylation results in de-repression of Polycomb target genes

Genome Biology, 2013-03, Vol.14 (3), p.R25-R25

2013

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xDnmt1 regulates transcriptional silencing in pre-MBT Xenopus embryos independently of its catalytic function

Development (Cambridge), 2008-04, Vol.135 (7), p.1295-1302

2008

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The CXXC-TET bridge - mind the methylation gap

Cell research, 2013-08, Vol.23 (8), p.973-974

2013

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Kaiso is a genome-wide repressor of transcription that is essential for amphibian development

Development (Cambridge), 2004-12, Vol.131 (24), p.6185-6194

2004

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The interaction of xKaiso with xTcf3: a revised model for integration of epigenetic and Wnt signalling pathways

Development (Cambridge), 2009-03, Vol.136 (5), p.723-727

2009

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MBD4 and MLH1 are required for apoptotic induction in xDNMT1-depleted embryos

Development (Cambridge), 2009-07, Vol.136 (13), p.2277-2286

2009

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The non-methylated DNA-binding function of Kaiso is not required in early Xenopus laevis development

Development (Cambridge), 2009-03, Vol.136 (5), p.729-738

2009

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Senescent cells harbour features of the cancer epigenome

Nature cell biology, 2013-12, Vol.15 (12), p.1495-1506

2013

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Rapid reprogramming of epigenetic and transcriptional profiles in mammalian culture systems

Genome Biology, 2015-02, Vol.16 (1), p.11-11, Article 11

2015

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Gene expression differences between the microsatellite instability (MIN) and chromosomal instability (CIN) phenotypes in colorectal cancer revealed by high-density cDNA array hybridization

Oncogene, 2002-05, Vol.21 (20), p.3253-3257

2002

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Promoter DNA methylation couples genome-defence mechanisms to epigenetic reprogramming in the mouse germline

Development (Cambridge), 2012-10, Vol.139 (19), p.3623-3632

2012

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Expression of a large LINE-1-driven antisense RNA is linked to epigenetic silencing of the metastasis suppressor gene TFPI-2 in cancer

Nucleic acids research, 2013-08, Vol.41 (14), p.6857-6869

2013

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Activation of transcription factor circuity in 2i-induced ground state pluripotency is independent of repressive global epigenetic landscapes

Nucleic acids research, 2020-08, Vol.48 (14), p.7748-7766

2020

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Lsh regulates LTR retrotransposon repression independently of Dnmt3b function

Genome biology, 2013-12, Vol.14 (12), p.R146-R146

2013

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Comparative analysis of affinity-based 5-hydroxymethylation enrichment techniques

Nucleic acids research, 2013-12, Vol.41 (22), p.e206-e206

2013

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Apoptosis and DNA methylation

Cancers, 2011-04, Vol.3 (2), p.1798-1820

2011

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Lsh Is Essential for Maintaining Global DNA Methylation Levels in Amphibia and Fish and Interacts Directly with Dnmt1

BioMed research international, 2015-01, Vol.2015 (2015), p.1-12

2015

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Comparative analysis of affinity-based 5-hydroxymethylation enrichment techniques

Nucleic acids research, 2014-04, Vol.42 (6), p.4142-4142

2014

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Epigenetic silencing in embryogenesis

Experimental cell research, 2005-10, Vol.309 (2), p.241-249

2005

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SMCHD1 mutations associated with a rare muscular dystrophy can also cause isolated arhinia and Bosma arhinia microphthalmia syndrome

Nature genetics, 2017-02, Vol.49 (2), p.238-248

2017

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Corrigendum: SMCHD1 mutations associated with a rare muscular dystrophy can also cause isolated arhinia and Bosma arhinia microphthalmia syndrome

Nature genetics, 2017-06, Vol.49 (6), p.969-969

2017

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Correction: Corrigendum: SMCHD1 mutations associated with a rare muscular dystrophy can also cause isolated arhinia and Bosma arhinia microphthalmia syndrome

Nature genetics, 2017-05, Vol.49 (6), p.969-969

2017

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Gene expression differences between the microsatellite instability (MIN) and chromosomal instability (CIN) phenotypes in colorectal cancer revealed by high-density cDNA array hybridization

Oncogene, 2002-05, Vol.21 (20), p.3253-3257

2002

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Defending the genome from the enemy within: mechanisms of retrotransposon suppression in the mouse germline

Enzymatic approaches and bisulfite sequencing cannot distinguish between 5-methylcytosine and 5-hydroxymethylcytosine in DNA

Redistribution of H3K27me3 upon DNA hypomethylation results in de-repression of Polycomb target genes

xDnmt1 regulates transcriptional silencing in pre-MBT Xenopus embryos independently of its catalytic function

The CXXC-TET bridge - mind the methylation gap

Kaiso is a genome-wide repressor of transcription that is essential for amphibian development

The interaction of xKaiso with xTcf3: a revised model for integration of epigenetic and Wnt signalling pathways

MBD4 and MLH1 are required for apoptotic induction in xDNMT1-depleted embryos

The non-methylated DNA-binding function of Kaiso is not required in early Xenopus laevis development

Senescent cells harbour features of the cancer epigenome

Rapid reprogramming of epigenetic and transcriptional profiles in mammalian culture systems

Gene expression differences between the microsatellite instability (MIN) and chromosomal instability (CIN) phenotypes in colorectal cancer revealed by high-density cDNA array hybridization

Promoter DNA methylation couples genome-defence mechanisms to epigenetic reprogramming in the mouse germline

Expression of a large LINE-1-driven antisense RNA is linked to epigenetic silencing of the metastasis suppressor gene TFPI-2 in cancer

Activation of transcription factor circuity in 2i-induced ground state pluripotency is independent of repressive global epigenetic landscapes

Lsh regulates LTR retrotransposon repression independently of Dnmt3b function

Comparative analysis of affinity-based 5-hydroxymethylation enrichment techniques

Apoptosis and DNA methylation

Lsh Is Essential for Maintaining Global DNA Methylation Levels in Amphibia and Fish and Interacts Directly with Dnmt1

Comparative analysis of affinity-based 5-hydroxymethylation enrichment techniques

Epigenetic silencing in embryogenesis

SMCHD1 mutations associated with a rare muscular dystrophy can also cause isolated arhinia and Bosma arhinia microphthalmia syndrome

Corrigendum: SMCHD1 mutations associated with a rare muscular dystrophy can also cause isolated arhinia and Bosma arhinia microphthalmia syndrome

Correction: Corrigendum: SMCHD1 mutations associated with a rare muscular dystrophy can also cause isolated arhinia and Bosma arhinia microphthalmia syndrome

Gene expression differences between the microsatellite instability (MIN) and chromosomal instability (CIN) phenotypes in colorectal cancer revealed by high-density cDNA array hybridization

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