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Recent evolution of a TET-controlled and DPPA3/STELLA-driven pathway of passive demethylation in mammals

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Outgoing claims: the papers this work cites, builds on, or argues with.

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Age‐Dependent Levels of 5‐Methyl‐, 5‐Hydroxymethyl‐, and 5‐Formylcytosine in Human and Mouse Brain Tissues

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Optimized Sleeping Beauty transposons rapidly generate stable transgenic cell lines

inferredcites →https://doi.org/10.1002/gene.20187openalex-snapshot

Generation ofstella-GFP transgenic mice: A novel tool to study germ cell development

inferredcites →https://doi.org/10.1006/dbio.2001.0560openalex-snapshot

DNA Methylation at Promoter Regions Regulates the Timing of Gene Activation in Xenopus laevis Embryos

inferredcites →https://doi.org/10.1007/s10577-015-9493-5openalex-snapshot

Evolutionary impact of transposable elements on genomic diversity and lineage-specific innovation in vertebrates

inferredcites →https://doi.org/10.1016/j.bbrc.2014.09.101openalex-snapshot

Inhibition of maintenance DNA methylation by Stella

inferredcites →https://doi.org/10.1016/j.bpj.2008.09.051openalex-snapshot

Detecting Protein Complexes in Living Cells from Laser Scanning Confocal Image Sequences by the Cross Correlation Raster Image Spectroscopy Method

inferredcites →https://doi.org/10.1016/j.bpj.2016.09.012openalex-snapshot

Arbitrary-Region Raster Image Correlation Spectroscopy

inferredcites →https://doi.org/10.1016/j.bpj.2018.02.035openalex-snapshot

PAM: A Framework for Integrated Analysis of Imaging, Single-Molecule, and Ensemble Fluorescence Data

inferredcites →https://doi.org/10.1016/j.cell.2011.06.020openalex-snapshot

Thymine DNA Glycosylase Is Essential for Active DNA Demethylation by Linked Deamination-Base Excision Repair

inferredcites →https://doi.org/10.1016/j.cell.2012.03.026openalex-snapshot

The Transcriptional and Epigenomic Foundations of Ground State Pluripotency

inferredcites →https://doi.org/10.1016/j.cell.2013.04.002openalex-snapshot

Genome-wide Analysis Reveals TET- and TDG-Dependent 5-Methylcytosine Oxidation Dynamics

inferredcites →https://doi.org/10.1016/j.cell.2014.04.017openalex-snapshot

Programming and Inheritance of Parental DNA Methylomes in Mammals

inferredcites →https://doi.org/10.1016/j.cell.2015.07.011openalex-snapshot

Inhibiting DNA Methylation Causes an Interferon Response in Cancer via dsRNA Including Endogenous Retroviruses

inferredcites →https://doi.org/10.1016/j.cell.2015.07.056openalex-snapshot

DNA-Demethylating Agents Target Colorectal Cancer Cells by Inducing Viral Mimicry by Endogenous Transcripts

inferredcites →https://doi.org/10.1016/j.cell.2017.03.035openalex-snapshot

mTOR Signaling in Growth, Metabolism, and Disease

inferredcites →https://doi.org/10.1016/j.celrep.2016.01.019openalex-snapshot

Post-translational Regulation of Cas9 during G1 Enhances Homology-Directed Repair

inferredcites →https://doi.org/10.1016/j.cub.2003.11.026openalex-snapshot

stella Is a Maternal Effect Gene Required for Normal Early Development in Mice

inferredcites →https://doi.org/10.1016/j.devcel.2015.10.011openalex-snapshot

Lineage-Specific Profiling Delineates the Emergence and Progression of Naive Pluripotency in Mammalian Embryogenesis

inferredcites →https://doi.org/10.1016/j.jmb.2017.10.014openalex-snapshot

Ubiquitome Analysis Reveals PCNA-Associated Factor 15 (PAF15) as a Specific Ubiquitination Target of UHRF1 in Embryonic Stem Cells

inferredcites →https://doi.org/10.1016/j.mod.2004.03.012openalex-snapshot

Stages of normal development in the medaka Oryzias latipes

inferredcites →https://doi.org/10.1016/j.molcel.2014.06.029openalex-snapshot

Dynamic Heterogeneity and DNA Methylation in Embryonic Stem Cells

inferredcites →https://doi.org/10.1016/j.molcel.2016.04.025openalex-snapshot

Impairment of DNA Methylation Maintenance Is the Main Cause of Global Demethylation in Naive Embryonic Stem Cells

inferredcites →https://doi.org/10.1016/j.molcel.2016.10.013openalex-snapshot

Cooperative Action between SALL4A and TET Proteins in Stepwise Oxidation of 5-Methylcytosine

inferredcites →https://doi.org/10.1016/j.molcel.2017.01.023openalex-snapshot

Comparative Analysis of Single-Cell RNA Sequencing Methods

inferredcites →https://doi.org/10.1016/j.molcel.2017.09.037openalex-snapshot

Structure of the Dnmt1 Reader Module Complexed with a Unique Two-Mono-Ubiquitin Mark on Histone H3 Reveals the Basis for DNA Methylation Maintenance

inferredcites →https://doi.org/10.1016/j.stem.2008.07.027openalex-snapshot

Dynamic Equilibrium and Heterogeneity of Mouse Pluripotent Stem Cells with Distinct Functional and Epigenetic States

inferredcites →https://doi.org/10.1016/j.stem.2012.12.012openalex-snapshot

PRDM14 Ensures Naive Pluripotency through Dual Regulation of Signaling and Epigenetic Pathways in Mouse Embryonic Stem Cells

inferredcites →https://doi.org/10.1016/j.stem.2013.06.002openalex-snapshot

Whole-Genome Bisulfite Sequencing of Two Distinct Interconvertible DNA Methylomes of Mouse Embryonic Stem Cells

inferredcites →https://doi.org/10.1016/j.stem.2013.06.004openalex-snapshot

FGF Signaling Inhibition in ESCs Drives Rapid Genome-wide Demethylation to the Epigenetic Ground State of Pluripotency

inferredcites →https://doi.org/10.1016/j.stem.2014.05.008openalex-snapshot

Reprogramming the Methylome: Erasing Memory and Creating Diversity

inferredcites →https://doi.org/10.1016/j.stem.2014.08.003openalex-snapshot

Active and Passive Demethylation of Male and Female Pronuclear DNA in the Mammalian Zygote

inferredcites →https://doi.org/10.1016/j.stem.2014.09.002openalex-snapshot

Tet3 and DNA Replication Mediate Demethylation of Both the Maternal and Paternal Genomes in Mouse Zygotes

inferredcites →https://doi.org/10.1016/j.stemcr.2013.11.010openalex-snapshot

Synergistic Mechanisms of DNA Demethylation during Transition to Ground-State Pluripotency

inferredcites →https://doi.org/10.1016/j.tig.2019.07.007openalex-snapshot

DNA Methylation: Shared and Divergent Features across Eukaryotes

inferredcites →https://doi.org/10.1016/j.virol.2010.12.007openalex-snapshot

Dynamic control of endogenous retroviruses during development

inferredcites →https://doi.org/10.1016/s0167-4781(01)00280-9openalex-snapshot

Constitutive genomic methylation during embryonic development of Xenopus

inferredcites →https://doi.org/10.1016/s1096-4959(02)00144-6openalex-snapshot

Absence of global genomic cytosine methylation pattern erasure during medaka (Oryzias latipes) early embryo development

inferredcites →https://doi.org/10.1017/s0016672306008184openalex-snapshot

Targeted reduction of the DNA methylation level with 5-azacytidine promotes excision of the medaka fish Tol2 transposable element

inferredcites →https://doi.org/10.1021/pr101065jopenalex-snapshot

Andromeda: A Peptide Search Engine Integrated into the MaxQuant Environment

inferredcites →https://doi.org/10.1021/pr201219eopenalex-snapshot

SprayQc: A Real-Time LC–MS/MS Quality Monitoring System To Maximize Uptime Using Off the Shelf Components

inferredcites →https://doi.org/10.1038/2413openalex-snapshot

Transcription of IAP endogenous retroviruses is constrained by cytosine methylation

inferredcites →https://doi.org/10.1038/31927openalex-snapshot

A molecular timescale for vertebrate evolution

inferredcites →https://doi.org/10.1038/83730openalex-snapshot

Loss of genomic methylation causes p53-dependent apoptosis and epigenetic deregulation

inferredcites →https://doi.org/10.1038/cr.2015.72openalex-snapshot

DNA methylation requires a DNMT1 ubiquitin interacting motif (UIM) and histone ubiquitination

inferredcites →https://doi.org/10.1038/embor.2013.67openalex-snapshot

Prdm14 promotes germline fate and naive pluripotency by repressing FGF signalling and DNA methylation

inferredcites →https://doi.org/10.1038/nature06397openalex-snapshot

The SRA protein Np95 mediates epigenetic inheritance by recruiting Dnmt1 to methylated DNA

inferredcites →https://doi.org/10.1038/nature07280openalex-snapshot

The SRA domain of UHRF1 flips 5-methylcytosine out of the DNA helix

inferredcites →https://doi.org/10.1038/nature09303openalex-snapshot

Role of Tet proteins in 5mC to 5hmC conversion, ES-cell self-renewal and inner cell mass specification

inferredcites →https://doi.org/10.1038/nature10443openalex-snapshot

The role of Tet3 DNA dioxygenase in epigenetic reprogramming by oocytes

inferredcites →https://doi.org/10.1038/nature11093openalex-snapshot

PGC7 binds histone H3K9me2 to protect against conversion of 5mC to 5hmC in early embryos

inferredcites →https://doi.org/10.1038/nature12488openalex-snapshot

Uhrf1-dependent H3K23 ubiquitylation couples maintenance DNA methylation and replication

inferredcites →https://doi.org/10.1038/nature13760openalex-snapshot

An evolutionary arms race between KRAB zinc-finger genes ZNF91/93 and SVA/L1 retrotransposons

inferredcites →https://doi.org/10.1038/nature20095openalex-snapshot

TET-mediated DNA demethylation controls gastrulation by regulating Lefty–Nodal signalling

inferredcites →https://doi.org/10.1038/nbt.1511openalex-snapshot

MaxQuant enables high peptide identification rates, individualized p.p.b.-range mass accuracies and proteome-wide protein quantification

inferredcites →https://doi.org/10.1038/ncb1519openalex-snapshot

PGC7/Stella protects against DNA demethylation in early embryogenesis

inferredcites →https://doi.org/10.1038/ncb2798openalex-snapshot

A tripartite transcription factor network regulates primordial germ cell specification in mice

inferredcites →https://doi.org/10.1038/ncb3296openalex-snapshot

De novo DNA methylation drives 5hmC accumulation in mouse zygotes

inferredcites →https://doi.org/10.1038/nchembio.1532openalex-snapshot

Tet oxidizes thymine to 5-hydroxymethyluracil in mouse embryonic stem cell DNA

inferredcites →https://doi.org/10.1038/ncomms11197openalex-snapshot

Hemi-methylated DNA opens a closed conformation of UHRF1 to facilitate its histone recognition

inferredcites →https://doi.org/10.1038/ncomms1240openalex-snapshot

5-Hydroxymethylcytosine in the mammalian zygote is linked with epigenetic reprogramming

inferredcites →https://doi.org/10.1038/ncomms12464openalex-snapshot

Dissecting the precise role of H3K9 methylation in crosstalk with DNA maintenance methylation in mammals

inferredcites →https://doi.org/10.1038/ncomms3660openalex-snapshot

Visualization and targeted disruption of protein interactions in living cells

inferredcites →https://doi.org/10.1038/ncomms7008openalex-snapshot

Dppa3 expression is critical for generation of fully reprogrammed iPS cells and maintenance of Dlk1-Dio3 imprinting

inferredcites →https://doi.org/10.1038/ng.3258openalex-snapshot

Targeted disruption of DNMT1, DNMT3A and DNMT3B in human embryonic stem cells

inferredcites →https://doi.org/10.1038/ng.343openalex-snapshot

Molecular evolution of a novel hyperactive Sleeping Beauty transposase enables robust stable gene transfer in vertebrates

inferredcites →https://doi.org/10.1038/ng.3522openalex-snapshot

Active DNA demethylation at enhancers during the vertebrate phylotypic period

inferredcites →https://doi.org/10.1038/ng.3844openalex-snapshot

Conserved roles of mouse DUX and human DUX4 in activating cleavage-stage genes and MERVL/HERVL retrotransposons

inferredcites →https://doi.org/10.1038/ng.3858openalex-snapshot

DUX-family transcription factors regulate zygotic genome activation in placental mammals

inferredcites →https://doi.org/10.1038/ng.3868openalex-snapshot

Lineage-specific functions of TET1 in the postimplantation mouse embryo

inferredcites →https://doi.org/10.1038/ng.3945openalex-snapshot

LINE-1 activation after fertilization regulates global chromatin accessibility in the early mouse embryo

inferredcites →https://doi.org/10.1038/nmeth.1318openalex-snapshot

Enzymatic assembly of DNA molecules up to several hundred kilobases

inferredcites →https://doi.org/10.1038/nmeth.2019openalex-snapshot

Fiji: an open-source platform for biological-image analysis

inferredcites →https://doi.org/10.1038/nmeth.2089openalex-snapshot

NIH Image to ImageJ: 25 years of image analysis

inferredcites →https://doi.org/10.1038/nmeth.3901openalex-snapshot

The Perseus computational platform for comprehensive analysis of (prote)omics data

inferredcites →https://doi.org/10.1038/nprot.2007.261openalex-snapshot

Protocol for micro-purification, enrichment, pre-fractionation and storage of peptides for proteomics using StageTips

inferredcites →https://doi.org/10.1038/nprot.2013.090openalex-snapshot

Generation of eggs from mouse embryonic stem cells and induced pluripotent stem cells

inferredcites →https://doi.org/10.1038/nprot.2013.143openalex-snapshot

Genome engineering using the CRISPR-Cas9 system

inferredcites →https://doi.org/10.1038/nrg.2017.33openalex-snapshot

TET-mediated active DNA demethylation: mechanism, function and beyond

inferredcites →https://doi.org/10.1038/nrm2950openalex-snapshot

Active DNA demethylation: many roads lead to Rome

inferredcites →https://doi.org/10.1038/nsmb.2000openalex-snapshot

Sequence-specific regulator Prdm14 safeguards mouse ESCs from entering extraembryonic endoderm fates

inferredcites →https://doi.org/10.1038/nsmb.2391openalex-snapshot

Association of UHRF1 with methylated H3K9 directs the maintenance of DNA methylation

inferredcites →https://doi.org/10.1038/nsmb.2510openalex-snapshot

Naive pluripotency is associated with global DNA hypomethylation

inferredcites →https://doi.org/10.1038/s41421-019-0081-2openalex-snapshot

Differential roles of Stella in the modulation of DNA methylation during oocyte and zygotic development

inferredcites →https://doi.org/10.1038/s41467-017-01387-6openalex-snapshot

Cytoplasmic cleavage of DPPA3 is required for intracellular trafficking and cleavage-stage development in mice

inferredcites →https://doi.org/10.1038/s41467-019-10894-7openalex-snapshot

Zebrafish preserve global germline DNA methylation while sex-linked rDNA is amplified and demethylated during feminisation

inferredcites →https://doi.org/10.1038/s41467-019-10895-6openalex-snapshot

Retention of paternal DNA methylome in the developing zebrafish germline

inferredcites →https://doi.org/10.1038/s41586-018-0751-5openalex-snapshot

Stella safeguards the oocyte methylome by preventing de novo methylation mediated by DNMT1

inferredcites →https://doi.org/10.1038/s41588-017-0002-yopenalex-snapshot

TET proteins safeguard bivalent promoters from de novo methylation in human embryonic stem cells

inferredcites →https://doi.org/10.1038/s41588-018-0055-6openalex-snapshot

Embryonic defects induced by maternal obesity in mice derive from Stella insufficiency in oocytes

inferredcites →https://doi.org/10.1038/s41598-017-00136-5openalex-snapshot

Usp7-dependent histone H3 deubiquitylation regulates maintenance of DNA methylation

inferredcites →https://doi.org/10.1038/s41598-018-21750-xopenalex-snapshot

Heterogeneous localisation of membrane proteins in Staphylococcus aureus

inferredcites →https://doi.org/10.1073/pnas.1002720107openalex-snapshot

Conservation and divergence of methylation patterning in plants and animals

inferredcites →https://doi.org/10.1073/pnas.1203701109openalex-snapshot

Recognition of modification status on a histone H3 tail by linked histone reader modules of the epigenetic regulator UHRF1

inferredcites →https://doi.org/10.1073/pnas.1617802113openalex-snapshot

Tet proteins influence the balance between neuroectodermal and mesodermal fate choice by inhibiting Wnt signaling

inferredcites →https://doi.org/10.1074/jbc.m114.605881openalex-snapshot

Phosphorylation of TET Proteins Is Regulated via O-GlcNAcylation by the O-Linked N-Acetylglucosamine Transferase (OGT)

inferredcites →https://doi.org/10.1074/jbc.ra119.008008openalex-snapshot

Stella protein facilitates DNA demethylation by disrupting the chromatin association of the RING finger–type E3 ubiquitin ligase UHRF1

inferredcites →https://doi.org/10.1074/mcp.m113.031591openalex-snapshot

Accurate Proteome-wide Label-free Quantification by Delayed Normalization and Maximal Peptide Ratio Extraction, Termed MaxLFQ

inferredcites →https://doi.org/10.1083/jcb.201504006openalex-snapshot

Live-cell observation of cytosolic HIV-1 assembly onset reveals RNA-interacting Gag oligomers

inferredcites →https://doi.org/10.1083/jcb.201807044openalex-snapshot

Genomic insights into chromatin reprogramming to totipotency in embryos

inferredcites →https://doi.org/10.1093/bioinformatics/btl529openalex-snapshot

Interactive Tree Of Life (iTOL): an online tool for phylogenetic tree display and annotation

inferredcites →https://doi.org/10.1093/bioinformatics/btt350openalex-snapshot

Data-based filtering for replicated high-throughput transcriptome sequencing experiments

inferredcites →https://doi.org/10.1093/bioinformatics/btw313openalex-snapshot

Complex heatmaps reveal patterns and correlations in multidimensional genomic data

inferredcites →https://doi.org/10.1093/emboj/20.18.5187openalex-snapshot

A novel active site‐directed probe specific for deubiquitylating enzymes reveals proteasome association of USP14

inferredcites →https://doi.org/10.1093/gigascience/giy059openalex-snapshot

zUMIs - A fast and flexible pipeline to process RNA sequencing data with UMIs

inferredcites →https://doi.org/10.1093/molbev/msy083openalex-snapshot

Neutral Theory, Transposable Elements, and Eukaryotic Genome Evolution

inferredcites →https://doi.org/10.1093/nar/25.17.3389openalex-snapshot

Gapped BLAST and PSI-BLAST: a new generation of protein database search programs

inferredcites →https://doi.org/10.1093/nar/gki665openalex-snapshot

PCNA acts as a stationary loading platform for transiently interacting Okazaki fragment maturation proteins

inferredcites →https://doi.org/10.1093/nar/gkv550openalex-snapshot

A modular open platform for systematic functional studies under physiological conditions

inferredcites →https://doi.org/10.1093/nar/gkw257openalex-snapshot

deepTools2: a next generation web server for deep-sequencing data analysis

inferredcites →https://doi.org/10.1095/biolreprod.112.105932openalex-snapshot

Effects of Dppa3 on DNA Methylation Dynamics During Primordial Germ Cell Development in Mice1

inferredcites →https://doi.org/10.1101/gad.1.10.1039openalex-snapshot

Differences in DNA methylation during oogenesis and spermatogenesis and their persistence during early embryogenesis in the mouse.

inferredcites →https://doi.org/10.1101/gad.12.14.2108openalex-snapshot

Chromosome methylation patterns during mammalian preimplantation development

inferredcites →https://doi.org/10.1101/gad.220467.113openalex-snapshot

Multivalent histone engagement by the linked tandem Tudor and PHD domains of UHRF1 is required for the epigenetic inheritance of DNA methylation

inferredcites →https://doi.org/10.1101/gad.276568.115openalex-snapshot

Role of TET enzymes in DNA methylation, development, and cancer

inferredcites →https://doi.org/10.1101/gad.327312.119openalex-snapshot

Host–transposon interactions: conflict, cooperation, and cooption

inferredcites →https://doi.org/10.1101/gad.6.12b.2536openalex-snapshot

Properties and localization of DNA methyltransferase in preimplantation mouse embryos: implications for genomic imprinting.

inferredcites →https://doi.org/10.1126/science.1147939openalex-snapshot

UHRF1 Plays a Role in Maintaining DNA Methylation in Mammalian Cells

inferredcites →https://doi.org/10.1126/science.1170116openalex-snapshot

Conversion of 5-Methylcytosine to 5-Hydroxymethylcytosine in Mammalian DNA by MLL Partner TET1

inferredcites →https://doi.org/10.1126/science.1186366openalex-snapshot

Genome-Wide Evolutionary Analysis of Eukaryotic DNA Methylation

inferredcites →https://doi.org/10.1126/science.1210597openalex-snapshot

Tet Proteins Can Convert 5-Methylcytosine to 5-Formylcytosine and 5-Carboxylcytosine

inferredcites →https://doi.org/10.1126/science.1210944openalex-snapshot

Tet-Mediated Formation of 5-Carboxylcytosine and Its Excision by TDG in Mammalian DNA

inferredcites →https://doi.org/10.1128/mcb.01598-07openalex-snapshot

ICBP90, a Novel Methyl K9 H3 Binding Protein Linking Protein Ubiquitination with Heterochromatin Formation

inferredcites →https://doi.org/10.1128/mcb.20.22.8602-8612.2000openalex-snapshot

Chromatin Association of Human Origin Recognition Complex, Cdc6, and Minichromosome Maintenance Proteins during the Cell Cycle: Assembly of Prereplication Complexes in Late Mitosis

inferredcites →https://doi.org/10.1128/mcb.24.6.2526-2535.2004openalex-snapshot

Np95 Is a Histone-Binding Protein Endowed with Ubiquitin Ligase Activity

inferredcites →https://doi.org/10.1146/annurev-cellbio-100814-125514openalex-snapshot

The Developmental Control of Transposable Elements and the Evolution of Higher Species

inferredcites →https://doi.org/10.1186/gb-2008-9-9-r137openalex-snapshot

Model-based Analysis of ChIP-Seq (MACS)

inferredcites →https://doi.org/10.1186/gb-2012-13-10-r87openalex-snapshot

methylKit: a comprehensive R package for the analysis of genome-wide DNA methylation profiles

inferredcites →https://doi.org/10.1186/gb-2012-13-10-r92openalex-snapshot

Gel-free multiplexed reduced representation bisulfite sequencing for large-scale DNA methylation profiling

inferredcites →https://doi.org/10.1186/s12977-015-0173-5openalex-snapshot

Retrotransposons shape species-specific embryonic stem cell gene expression

inferredcites →https://doi.org/10.1186/s13059-014-0545-5openalex-snapshot

Ontogeny of CpG island methylation and specificity of DNMT3 methyltransferases during embryonic development in the mouse

inferredcites →https://doi.org/10.1186/s13059-014-0550-8openalex-snapshot

Moderated estimation of fold change and dispersion for RNA-seq data with DESeq2

inferredcites →https://doi.org/10.1242/dev.099622openalex-snapshot

PRDM14 promotes active DNA demethylation through the Ten-eleven translocation (TET)-mediated base excision repair pathway in embryonic stem cells

inferredcites →https://doi.org/10.1242/dev.113.1.119openalex-snapshot

Methylation levels of maternal and paternal genomes during preimplantation development

inferredcites →https://doi.org/10.1242/dev.142711openalex-snapshot

Tracking the embryonic stem cell transition from ground state pluripotency

inferredcites →https://doi.org/10.1242/dev.147629openalex-snapshot

Loss of DNA methylation in zebrafish embryos activates retrotransposons to trigger antiviral signaling

inferredcites →https://doi.org/10.1242/dev.99.3.371openalex-snapshot

Temporal and regional changes in DNA methylation in the embryonic, extraembryonic and germ cell lineages during mouse embryo development

inferredcites →https://doi.org/10.1371/journal.pbio.2005970openalex-snapshot

CellProfiler 3.0: Next-generation image processing for biology

inferredcites →https://doi.org/10.1371/journal.pgen.1001134openalex-snapshot

Orphan CpG Islands Identify Numerous Conserved Promoters in the Mammalian Genome

inferredcites →https://doi.org/10.1529/biophysj.105.062836openalex-snapshot

Measuring Fast Dynamics in Solutions and Cells with a Laser Scanning Microscope

inferredcites →https://doi.org/10.1529/biophysj.105.064766openalex-snapshot

Pulsed Interleaved Excitation

inferredcites →https://doi.org/10.3390/biom9020061openalex-snapshot

Light-Induced Protein Clustering for Optogenetic Interference and Protein Interaction Analysis in Drosophila S2 Cells

inferredcites →https://doi.org/10.4161/cc.8.11.8580openalex-snapshot

Prediction of novel families of enzymes involved in oxidative and other complex modifications of bases in nucleic acids

inferredcites →https://doi.org/10.4161/epi.19375openalex-snapshot

5-hydroxymethyl-cytosine enrichment of non-committed cells is not a universal feature of vertebrate development

inferredcites →https://doi.org/10.7554/elife.17101openalex-snapshot

Hemi-methylated DNA regulates DNA methylation inheritance through allosteric activation of H3 ubiquitylation by UHRF1

inferredcites →https://doi.org/10.7554/elife.22345openalex-snapshot

Stella modulates transcriptional and endogenous retrovirus programs during maternal-to-zygotic transition

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

inferred← citeshttps://doi.org/10.1016/j.ceb.2019.05.006openalex-snapshot

Transcriptional and epigenetic control of germline competence and specification

inferred← citeshttps://doi.org/10.1038/s41594-020-0445-1openalex-snapshot

Dppa2 and Dppa4 counteract de novo methylation to establish a permissive epigenome for development

inferred← citeshttps://doi.org/10.1038/s41598-021-84708-6openalex-snapshot

Loss-of-function mutations in the histone methyltransferase EZH2 promote chemotherapy resistance in AML

inferred← citeshttps://doi.org/10.1242/dev.183129openalex-snapshot

The roles of TET family proteins in development and stem cells

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