Stella safeguards the oocyte methylome by preventing de novo methylation mediated by DNMT1
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Title
Stella safeguards the oocyte methylome by preventing de novo methylation mediated by DNMT1
Authors
Keywords
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Journal
NATURE
Volume 564, Issue 7734, Pages 136-140
Publisher
Springer Nature
Online
2018-11-27
DOI
10.1038/s41586-018-0751-5
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Related references
Note: Only part of the references are listed.- Embryonic defects induced by maternal obesity in mice derive from Stella insufficiency in oocytes
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- (2014) Soichiro Funaki et al. BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS
- Tet3 and DNA Replication Mediate Demethylation of Both the Maternal and Paternal Genomes in Mouse Zygotes
- (2014) Li Shen et al. Cell Stem Cell
- Ascorbic Acid Enhances Tet-Mediated 5-Methylcytosine Oxidation and Promotes DNA Demethylation in Mammals
- (2013) Ruichuan Yin et al. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
- Mouse Oocyte Methylomes at Base Resolution Reveal Genome-Wide Accumulation of Non-CpG Methylation and Role of DNA Methyltransferases
- (2013) Kenjiro Shirane et al. PLoS Genetics
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- Contribution of Intragenic DNA Methylation in Mouse Gametic DNA Methylomes to Establish Oocyte-Specific Heritable Marks
- (2012) Hisato Kobayashi et al. PLoS Genetics
- Gel-free multiplexed reduced representation bisulfite sequencing for large-scale DNA methylation profiling
- (2012) Patrick Boyle et al. GENOME BIOLOGY
- Bismark: a flexible aligner and methylation caller for Bisulfite-Seq applications
- (2011) Felix Krueger et al. BIOINFORMATICS
- The role of Tet3 DNA dioxygenase in epigenetic reprogramming by oocytes
- (2011) Tian-Peng Gu et al. NATURE
- Dynamic CpG island methylation landscape in oocytes and preimplantation embryos
- (2011) Sébastien A Smallwood et al. NATURE GENETICS
- Preparation of reduced representation bisulfite sequencing libraries for genome-scale DNA methylation profiling
- (2011) Hongcang Gu et al. Nature Protocols
- Orphan CpG Islands Identify Numerous Conserved Promoters in the Mammalian Genome
- (2010) Robert S. Illingworth et al. PLoS Genetics
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