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SMCHD1 maintains heterochromatin, genome compartments and epigenome landscape in human myoblasts.
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3D genome, on repeat: Higher-order folding principles of the heterochromatinized repetitive genome.
Cell. 2022 Jul 21;185(15):2690-2707. doi: 10.1016/j.cell.2022.06.052.
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Hijacking of transcriptional condensates by endogenous retroviruses.
Nat Genet. 2022 Aug;54(8):1238-1247. doi: 10.1038/s41588-022-01132-w. Epub 2022 Jul 21.
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Dynamic reprogramming of H3K9me3 at hominoid-specific retrotransposons during human preimplantation development.
Cell Stem Cell. 2022 Jul 7;29(7):1031-1050.e12. doi: 10.1016/j.stem.2022.06.006.
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Establishment of H3K9-methylated heterochromatin and its functions in tissue differentiation and maintenance.
Nat Rev Mol Cell Biol. 2022 Sep;23(9):623-640. doi: 10.1038/s41580-022-00483-w. Epub 2022 May 13.
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H1.0 C Terminal Domain Is Integral for Altering Transcription Factor Binding within Nucleosomes.
Biochemistry. 2022 Apr 19;61(8):625-638. doi: 10.1021/acs.biochem.2c00001. Epub 2022 Apr 4.
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Chromatin modifier HUSH co-operates with RNA decay factor NEXT to restrict transposable element expression.
Mol Cell. 2022 May 5;82(9):1691-1707.e8. doi: 10.1016/j.molcel.2022.03.004. Epub 2022 Mar 28.
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Rolling back human pluripotent stem cells to an eight-cell embryo-like stage.
Nature. 2022 May;605(7909):315-324. doi: 10.1038/s41586-022-04625-0. Epub 2022 Mar 21.
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Pioneer factors as master regulators of the epigenome and cell fate.
Nat Rev Mol Cell Biol. 2022 Jul;23(7):449-464. doi: 10.1038/s41580-022-00464-z. Epub 2022 Mar 9.
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SETDB1/NSD-dependent H3K9me3/H3K36me3 dual heterochromatin maintains gene expression profiles by bookmarking poised enhancers.
Mol Cell. 2022 Feb 17;82(4):816-832.e12. doi: 10.1016/j.molcel.2021.12.037. Epub 2022 Jan 25.

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