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| Stuart HT, Stirparo GG, Lohoff T, et al. (2019) Distinct Molecular Trajectories Converge to Induce Naive Pluripotency. Cell Stem Cell |
| Pękowska A, Klaus B, Xiang W, et al. (2018) Gain of CTCF-Anchored Chromatin Loops Marks the Exit from Naive Pluripotency. Cell Systems |
| Bornelöv S, Reynolds N, Xenophontos M, et al. (2018) The Nucleosome Remodeling and Deacetylation Complex Modulates Chromatin Structure at Sites of Active Transcription to Fine-Tune Gene Expression. Molecular Cell. 71: 56-72.e4 |
| Guo G, von Meyenn F, Rostovskaya M, et al. (2017) Epigenetic resetting of human pluripotency. Development (Cambridge, England). 144: 2748-2763 |
| Bulstrode H, Johnstone E, Marques-Torrejon MA, et al. (2017) Elevated FOXG1 and SOX2 in glioblastoma enforces neural stem cell identity through transcriptional control of cell cycle and epigenetic regulators. Genes & Development |
| Miller A, Ralser M, Kloet SL, et al. (2016) Sall4 controls differentiation of pluripotent cells independently of the Nucleosome Remodelling and Deacetylation (NuRD) complex. Development (Cambridge, England) |
| Guo G, von Meyenn F, Santos F, et al. (2016) Naive Pluripotent Stem Cells Derived Directly from Isolated Cells of the Human Inner Cell Mass. Stem Cell Reports |
| Foti R, Gnan S, Cornacchia D, et al. (2015) Nuclear Architecture Organized by Rif1 Underpins the Replication-Timing Program. Molecular Cell |
| Carén H, Stricker SH, Bulstrode H, et al. (2015) Glioblastoma Stem Cells Respond to Differentiation Cues but Fail to Undergo Commitment and Terminal Cell-Cycle Arrest. Stem Cell Reports |
| Chen L, Kostadima M, Martens JH, et al. (2014) Transcriptional diversity during lineage commitment of human blood progenitors. Science (New York, N.Y.). 345: 1251033 |