No matching publications found
Papillomavirus-like particles as vectors for ex vivo gene therapy of the skin.
Molecular therapy. Nucleic acids, 2025
doi:10.1016/j.omtn.2025.102501.
Systematic epigenome editing captures the context-dependent instructive function of chromatin modifications.
Nature genetics, 2024
doi:10.1038/s41588-024-01706-w.
Paternal microbiome perturbations impact offspring fitness.
Nature, 2024
doi:10.1038/s41586-024-07336-w.
Esrrb guides naive pluripotent cells through the formative transcriptional programme.
Nature cell biology, 2023
doi:10.1038/s41556-023-01131-x.
Epigenetic inheritance is gated by naïve pluripotency and Dppa2.
The EMBO journal, 2022
doi:10.15252/embj.2021108677.
Genome-scale CRISPR screening for regulators of cell fate transitions.
Methods in molecular biology (Clifton, N.J.), 2021
doi:10.1007/978-1-0716-0958-3_7.
Epigenetic editing: dissecting chromatin function in context.
BioEssays : news and reviews in molecular, cellular and developmental biology, 2021
doi:10.1002/bies.202000316.
Cell surface mechanics gate embryonic stem cell differentiation.
Cell stem cell, 2020
doi:10.1016/j.stem.2020.10.017.
Dppa2 and Dppa4 counteract de novo methylation to establish a permissive epigenome for development.
Nature structural & molecular biology, 2020
doi:10.1038/s41594-020-0445-1.
A ligand-based system for receptor-specific delivery of proteins.
Scientific reports, 2019
doi:10.1038/s41598-019-55797-1.
Tracing the transitions from pluripotency to germ cell fate with CRISPR screening.
Nature communications, 2018
doi:10.1038/s41467-018-06230-0.
Activation of lineage regulators and transposable elements across a pluripotent Spectrum.
Stem cell reports, 2017
doi:10.1016/j.stemcr.2017.05.014.
STELLA modulates transcriptional and endogenous retrovirus programs during maternal-to-zygotic transition.
eLife, 2017
doi:10.7554/elife.22345.
Stella modulates transcriptional and endogenous retrovirus programs during maternal-to-zygotic transition.
ELIFE, 2017
doi:10.7554/eLife.22345.
Chromatin dynamics and the role of G9a in gene regulation and enhancer silencing during early mouse development.
ELIFE, 2015
doi:10.7554/eLife.09571.
A unique gene regulatory network resets the human germline epigenome for development.
Cell, 2015
doi:10.1016/j.cell.2015.04.053.
Regulatory principles of pluripotency: from the ground state up.
Cell Stem Cell , 2014
doi:10.1016/j.stem.2014.09.015.
Dynamic heterogeneity and DNA methylation in embryonic stem cells.
Molecular cell, 2014
doi:10.1016/j.molcel.2014.06.029.
Synergistic mechanisms of DNA demethylation during transition to ground-state pluripotency.
Stem Cell Reports, 2013
doi:10.1016/j.stemcr.2013.11.010.
Prdm14 promotes germline fate and naive pluripotency by repressing FGF signalling and DNA methylation.
EMBO Reports, 2013
doi:10.1038/embor.2013.67.
Beyond DNA: programming and inheritance of parental methylomes.
Cell, 2013
doi:10.1016/j.cell.2013.04.044.
Germline DNA demethylation dynamics and imprint erasure through 5-hydroxymethylcytosine.
Science, 2013
doi:10.1126/science.1229277.
Promoter DNA methylation couples genome-defence mechanisms to epigenetic reprogramming in the mouse germline.
Development (Cambridge, England), 2012
doi:10.1242/dev.081661.
Parallel mechanisms of epigenetic reprogramming in the germline.
Trends in Genetics, 2012
doi:10.1016/j.tig.2012.01.005.
Non-genotoxic carcinogen exposure induces defined changes in the 5-hydroxymethylome.
Genome Biology, 2012
doi:10.1186/gb-2012-13-10-R93.