
AbstractMouse blastocyst stage embryo stained for histone H3 lysine‐27 trimethylation (red) and DNA (blue). H3K27me3 marks the inactive X chromosome. The study by Chiba et al. in this issue suggests that de novo DNA methyltransferases are dispensable for setting the imprint on the maternally‐derived X chromsome in growing oocytes. See Chiba et al. in this issue.
Male, X Chromosome, Lysine, Gene Expression Regulation, Developmental, DNA Methylation, DNA Methyltransferase 3A, Trophoblasts, Histones, Genomic Imprinting, Mice, Blastocyst, Oocytes, Animals, Female, DNA (Cytosine-5-)-Methyltransferases, Transgenes, Alleles
Male, X Chromosome, Lysine, Gene Expression Regulation, Developmental, DNA Methylation, DNA Methyltransferase 3A, Trophoblasts, Histones, Genomic Imprinting, Mice, Blastocyst, Oocytes, Animals, Female, DNA (Cytosine-5-)-Methyltransferases, Transgenes, Alleles
| selected citations These citations are derived from selected sources. This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically). | 37 | |
| popularity This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network. | Top 10% | |
| influence This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically). | Top 10% | |
| impulse This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network. | Top 10% |
