On the public citation graph

N6-methyladenosine modification destabilizes developmental regulators in embryonic stem cells

https://doi.org/10.1038/ncb2902
0 signed · 1330 inferred · view as graph

Inferred edges come from two machine sources: sweeps of open repository metadata (mostly SSRN and Zenodo), and a bulk OpenAlex citation snapshot. Every row below is labelled with the one it came from. Neither is a complete citation index — absence here is not evidence of absence.

Is this your work? Sign in with ORCID and put your name on the claims that are yours.
Claim with ORCID
Reference health. See whether every reference in this work resolves to a known work and none has been retracted — and get a dated CiteStamped badge you can embed.
See reference health

What this work says

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

inferredcites →https://doi.org/10.1007/0-387-29362-0openalex-snapshot
Bioinformatics and Computational Biology Solutions Using R and Bioconductor
inferredcites →https://doi.org/10.1007/0-387-29362-0_23openalex-snapshot
limma: Linear Models for Microarray Data
inferredcites →https://doi.org/10.1007/s00239-002-2339-8openalex-snapshot
Structure Prediction and Phylogenetic Analysis of a Functionally Diverse Family of Proteins Homologous to the MT-A70 Subunit of the Human mRNA:m6A Methyltransferase
inferredcites →https://doi.org/10.1016/j.cell.2012.05.003openalex-snapshot
Comprehensive Analysis of mRNA Methylation Reveals Enrichment in 3′ UTRs and near Stop Codons
inferredcites →https://doi.org/10.1016/j.molcel.2010.12.011openalex-snapshot
Genome-wide Identification of Polycomb-Associated RNAs by RIP-seq
inferredcites →https://doi.org/10.1016/j.molcel.2011.06.007openalex-snapshot
Integrative Regulatory Mapping Indicates that the RNA-Binding Protein HuR Couples Pre-mRNA Processing and mRNA Stability
inferredcites →https://doi.org/10.1016/j.molcel.2011.06.008openalex-snapshot
Transcriptome-wide Analysis of Regulatory Interactions of the RNA-Binding Protein HuR
inferredcites →https://doi.org/10.1016/j.molcel.2012.10.015openalex-snapshot
ALKBH5 Is a Mammalian RNA Demethylase that Impacts RNA Metabolism and Mouse Fertility
inferredcites →https://doi.org/10.1016/j.stem.2010.02.014openalex-snapshot
An Oct4-Centered Protein Interaction Network in Embryonic Stem Cells
inferredcites →https://doi.org/10.1016/j.tig.2012.11.003openalex-snapshot
Reversible RNA adenosine methylation in biological regulation
inferredcites →https://doi.org/10.1038/embor.2011.11openalex-snapshot
Reprogramming of mouse and human somatic cells by high‐performance engineered factors
inferredcites →https://doi.org/10.1038/nature11112openalex-snapshot
Topology of the human and mouse m6A RNA methylomes revealed by m6A-seq
inferredcites →https://doi.org/10.1038/nbt.1754openalex-snapshot
Integrative genomics viewer
inferredcites →https://doi.org/10.1038/nchembio.687openalex-snapshot
N6-Methyladenosine in nuclear RNA is a major substrate of the obesity-associated FTO
inferredcites →https://doi.org/10.1038/nmeth.1608openalex-snapshot
A quantitative analysis of CLIP methods for identifying binding sites of RNA-binding proteins
inferredcites →https://doi.org/10.1038/nprot.2008.211openalex-snapshot
Systematic and integrative analysis of large gene lists using DAVID bioinformatics resources
inferredcites →https://doi.org/10.1038/nprot.2009.97openalex-snapshot
Mapping identifiers for the integration of genomic datasets with the R/Bioconductor package biomaRt
inferredcites →https://doi.org/10.1038/nsmb.1991openalex-snapshot
Genome-wide identification of Ago2 binding sites from mouse embryonic stem cells with and without mature microRNAs
inferredcites →https://doi.org/10.1073/pnas.0506580102openalex-snapshot
Gene set enrichment analysis: A knowledge-based approach for interpreting genome-wide expression profiles
inferredcites →https://doi.org/10.1074/mcp.m110.000976openalex-snapshot
Uncovering the Human Methyltransferasome
inferredcites →https://doi.org/10.1093/bioinformatics/btp120openalex-snapshot
TopHat: discovering splice junctions with RNA-Seq
inferredcites →https://doi.org/10.1093/bioinformatics/btp352openalex-snapshot
The Sequence Alignment/Map format and SAMtools
inferredcites →https://doi.org/10.1093/bioinformatics/btq033openalex-snapshot
BEDTools: a flexible suite of utilities for comparing genomic features
inferredcites →https://doi.org/10.1093/nar/18.19.5735openalex-snapshot
Sequence specificity of the human mRNA N6-adenosine methylasein vitro
inferredcites →https://doi.org/10.1093/nar/gkf573openalex-snapshot
Induction of sporulation in Saccharomyces cerevisiae leads to the formation of N6-methyladenosine in mRNA: a potential mechanism for the activity of the IME4 gene
inferredcites →https://doi.org/10.1093/nar/gks148openalex-snapshot
HuR protein attenuates miRNA-mediated repression by promoting miRISC dissociation from the target RNA
inferredcites →https://doi.org/10.1105/tpc.108.058883openalex-snapshot
MTA Is an Arabidopsis Messenger RNA Adenosine Methylase and Interacts with a Homolog of a Sex-Specific Splicing Factor
inferredcites →https://doi.org/10.1126/science.1163045openalex-snapshot
Polycomb Proteins Targeted by a Short Repeat RNA to the Mouse X Chromosome
inferredcites →https://doi.org/10.1158/0008-5472.can-07-2544openalex-snapshot
Hypermethylation of let-7a-3 in Epithelial Ovarian Cancer Is Associated with Low Insulin-like Growth Factor-II Expression and Favorable Prognosis
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-2009-10-3-r25openalex-snapshot
Ultrafast and memory-efficient alignment of short DNA sequences to the human genome
inferredcites →https://doi.org/10.1371/journal.pgen.1000242openalex-snapshot
Genomewide Analysis of PRC1 and PRC2 Occupancy Identifies Two Classes of Bivalent Domains
inferredcites →https://doi.org/10.1371/journal.pgen.1002242openalex-snapshot
Conserved Regulation of p53 Network Dosage by MicroRNA–125b Occurs through Evolving miRNA–Target Gene Pairs
inferredcites →https://doi.org/10.1371/journal.pgen.1002732openalex-snapshot
RNA Methylation by the MIS Complex Regulates a Cell Fate Decision in Yeast
inferredcites →https://doi.org/10.14806/ej.17.1.200openalex-snapshot
Cutadapt removes adapter sequences from high-throughput sequencing reads
inferredcites →https://doi.org/10.2174/138920312801619394openalex-snapshot
Functional Interplay between RNA-Binding Protein HuR and microRNAs
inferredcites →https://doi.org/10.3389/fpls.2012.00001openalex-snapshot
Protein Phylogenetic Analysis of Ca2+/cation Antiporters and Insights into their Evolution in Plants
inferredcites →https://doi.org/10.3389/fpls.2012.00048openalex-snapshot
Adenosine Methylation in Arabidopsis mRNA is Associated with the 3′ End and Reduced Levels Cause Developmental Defects

What points at this work

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

inferred← citeshttps://doi.org/10.2139/ssrn.3940258openalex-extracted
METTL14 Regulates Autophagy and Osteogenic Differentiation of BMSCs Targeting Beclin-1 via an M 6 A-IGF2BPs-Dependent Mechanism
inferred← citeshttps://doi.org/10.1002/1873-3468.13107openalex-snapshot
Adenosine methylation as a molecular imprint defining the fate of RNA
inferred← citeshttps://doi.org/10.1002/1878-0261.12593openalex-snapshot
Loss of RDM1 enhances hepatocellular carcinoma progression via p53 and Ras/Raf/ERK pathways
inferred← citeshttps://doi.org/10.1002/9781119692799.ch7openalex-snapshot
METHODS FOR MAPPING OF NUCLEIC ACIDS EPIGENETIC MODIFICATIONS AND ITS CLINIC APPLICATIONS
inferred← citeshttps://doi.org/10.1002/9783527840458.ch12openalex-snapshot
Drugging the Epitranscriptome
inferred← citeshttps://doi.org/10.1002/advs.202001563openalex-snapshot
Novel Insights into Adipogenesis from the Perspective of Transcriptional and RNA N6‐Methyladenosine‐Mediated Post‐Transcriptional Regulation
inferred← citeshttps://doi.org/10.1002/advs.202400133openalex-snapshot
PCBP1/2 and TDP43 Function as NAT10 Adaptors to Mediate mRNA ac 4 C Formation in Mammalian Cells
inferred← citeshttps://doi.org/10.1002/advs.202407013openalex-snapshot
Deciphering 3'UTR Mediated Gene Regulation Using Interpretable Deep Representation Learning
inferred← citeshttps://doi.org/10.1002/advs.202510075openalex-snapshot
Comprehensive Profiling of N 6 ‐methyladnosine (m 6 A) Readouts Reveals Novel m 6 A Readers That Regulate Human Embryonic Stem Cell Differentiation
inferred← citeshttps://doi.org/10.1002/ajmg.a.38089openalex-snapshot
Novel LINS1 missense mutation in a family with non‐syndromic intellectual disability
inferred← citeshttps://doi.org/10.1002/ange.201410647openalex-snapshot
High‐Resolution N6‐Methyladenosine (m6A) Map Using Photo‐Crosslinking‐Assisted m6A Sequencing
inferred← citeshttps://doi.org/10.1002/anie.201410647openalex-snapshot
High‐Resolution N6‐Methyladenosine (m6A) Map Using Photo‐Crosslinking‐Assisted m6A Sequencing
inferred← citeshttps://doi.org/10.1002/arch.22005openalex-snapshot
RNA methyltransferase BmMettl3 and BmMettl14 in silkworm (Bombyx mori) and the regulation of silkworm embryonic development
inferred← citeshttps://doi.org/10.1002/art.42629openalex-snapshot
METTL14‐Mediated m6A Modification of TNFAIP3 Involved in Inflammation in Patients With Active Rheumatoid Arthritis
inferred← citeshttps://doi.org/10.1002/asia.202200367openalex-snapshot
Mechanisms and Strategies for Determining m6A RNA Modification Sites by Natural and Engineered m6A Effector Proteins
inferred← citeshttps://doi.org/10.1002/bies.201700093openalex-snapshot
mRNA Traffic Control Reviewed: N6‐Methyladenosine (m6A) Takes the Driver's Seat
inferred← citeshttps://doi.org/10.1002/biot.202400078openalex-snapshot
Overexpression of YTHDF3 increases the specific productivity of the recombinant protein in CHO cells by promoting the translation process
inferred← citeshttps://doi.org/10.1002/bip.23403openalex-snapshot
Mechanisms of epitranscriptomic gene regulation
inferred← citeshttps://doi.org/10.1002/cam4.2360openalex-snapshot
Reduced m6A modification predicts malignant phenotypes and augmented Wnt/PI3K‐Akt signaling in gastric cancer
inferred← citeshttps://doi.org/10.1002/cam4.4157openalex-snapshot
MicroRNA‐501‐3p inhibits the proliferation of kidney cancer cells by targeting WTAP
inferred← citeshttps://doi.org/10.1002/cam4.4913openalex-snapshot
Comprehensive analyses indicated the association between m6A related long non‐coding RNAs and various pathways in glioma
inferred← citeshttps://doi.org/10.1002/cam4.70771openalex-snapshot
METTL3 , an Independent Adverse Prognostic Factor for AML , Promotes the Development of AML by Modulating the PGC ‐1α– MAPK Pathway and PGC ‐1α–Antioxidant System Axis
inferred← citeshttps://doi.org/10.1002/cbf.70039openalex-snapshot
Mettl14 and Mettl3 Work Cooperatively to Regulate Retinal Development
inferred← citeshttps://doi.org/10.1002/cbic.201402449openalex-snapshot
miRNA and Methylation: A Multifaceted Liaison
inferred← citeshttps://doi.org/10.1002/chem.201804043openalex-snapshot
Mapping N6‐Methyladenosine (m6A) in RNA: Established Methods, Remaining Challenges, and Emerging Approaches
inferred← citeshttps://doi.org/10.1002/chem.202501788openalex-snapshot
Structural Control of RNA Demethylation: G‐Quadruplex Proximity Suppresses ALKBH5 Activity
inferred← citeshttps://doi.org/10.1002/cmdc.202000011openalex-snapshot
Small‐Molecule Inhibitors of METTL3, the Major Human Epitranscriptomic Writer
inferred← citeshttps://doi.org/10.1002/ctm2.525openalex-snapshot
RNA N6‐methyladenosine modification in the lethal teamwork of cancer stem cells and the tumor immune microenvironment: Current landscape and therapeutic potential
inferred← citeshttps://doi.org/10.1002/ctm2.553openalex-snapshot
Interplay of m6A and histone modifications contributes to temozolomide resistance in glioblastoma
inferred← citeshttps://doi.org/10.1002/ctm2.765openalex-snapshot
m6A hypomethylation of DNMT3B regulated by ALKBH5 promotes intervertebral disc degeneration via E4F1 deficiency
inferred← citeshttps://doi.org/10.1002/ddr.21910openalex-snapshot
Discovery of substituted indole derivatives as allosteric inhibitors of m 6 A‐RNA methyltransferase, METTL3 ‐14 complex
inferred← citeshttps://doi.org/10.1002/hep.28885openalex-snapshot
METTL14 suppresses the metastatic potential of hepatocellular carcinoma by modulating N 6‐methyladenosine‐dependent primary MicroRNA processing
inferred← citeshttps://doi.org/10.1002/hep.29683openalex-snapshot
RNA N6‐methyladenosine methyltransferase‐like 3 promotes liver cancer progression through YTHDF2‐dependent posttranscriptional silencing of SOCS2
inferred← citeshttps://doi.org/10.1002/iid3.70089openalex-snapshot
N6‐Methyladenosine Modification on the Function of Female Reproductive Development and Related Diseases
inferred← citeshttps://doi.org/10.1002/ijch.202300178openalex-snapshot
Recent Advance in the Study on 5‐Formylcytosine (f5C) RNA Modification
inferred← citeshttps://doi.org/10.1002/ijch.202400014openalex-snapshot
Unraveling the RNA Tapestry: A Symphony of Innovations in m6A Research Technology
inferred← citeshttps://doi.org/10.1002/jcb.25957openalex-snapshot
NSUN2-Mediated m5C Methylation and METTL3/METTL14-Mediated m6A Methylation Cooperatively Enhance p21 Translation
inferred← citeshttps://doi.org/10.1002/jcb.25967openalex-snapshot
Regulatory Role of N6-methyladenosine (m6A) Methylation in RNA Processing and Human Diseases
inferred← citeshttps://doi.org/10.1002/jcla.23866openalex-snapshot
Translation role of circRNAs in cancers
inferred← citeshttps://doi.org/10.1002/jcp.26507openalex-snapshot
Increased N6‐methyladenosine causes infertility is associated with FTO expression
inferred← citeshttps://doi.org/10.1002/jcp.28014openalex-snapshot
A dynamic reversible RNA N6‐methyladenosine modification: current status and perspectives
inferred← citeshttps://doi.org/10.1002/jcp.29531openalex-snapshot
Contributions and prognostic values of m6A RNA methylation regulators in non‐small‐cell lung cancer
inferred← citeshttps://doi.org/10.1002/jcp.30608openalex-snapshot
Regulation of cancer progression by circRNA and functional proteins
inferred← citeshttps://doi.org/10.1002/jcp.30733openalex-snapshot
The emerging roles of the interaction between m6A modification and c‐Myc in driving tumorigenesis and development
inferred← citeshttps://doi.org/10.1002/jcp.31289openalex-snapshot
The reduction of the m 6 A methyltransferase METTL3 in granulosa cells is related to the follicular cysts in pigs
inferred← citeshttps://doi.org/10.1002/jgm.3255openalex-snapshot
METTL3 polymorphisms and Wilms tumor susceptibility in Chinese children: A five‐center case–control study
inferred← citeshttps://doi.org/10.1002/jnr.24763openalex-snapshot
Epitranscriptomic m6A regulation following spinal cord injury
inferred← citeshttps://doi.org/10.1002/lipd.12023openalex-snapshot
Curcumin Attenuates Lipopolysaccharide‐Induced Hepatic Lipid Metabolism Disorder by Modification of m6A RNA Methylation in Piglets
inferred← citeshttps://doi.org/10.1002/mco2.70341openalex-snapshot
RNA Modifications in Health and Disease
inferred← citeshttps://doi.org/10.1002/nadc.201590093openalex-snapshot
Biochemie 2014
inferred← citeshttps://doi.org/10.1002/pld3.239openalex-snapshot
N6‐methyladenosine and RNA secondary structure affect transcript stability and protein abundance during systemic salt stress in Arabidopsis
inferred← citeshttps://doi.org/10.1002/pro.3456openalex-snapshot
The N‐terminal methyltransferase homologs NRMT1 and NRMT2 exhibit novel regulation of activity through heterotrimer formation
inferred← citeshttps://doi.org/10.1002/rmv.1983openalex-snapshot
RNA epitranscriptomics: Regulation of infection of RNA and DNA viruses by N 6 ‐methyladenosine (m 6 A)
inferred← citeshttps://doi.org/10.1002/smsc.202400308openalex-snapshot
m6A Ribonucleic Acid Methylation in Fibrotic Diseases of Visceral Organs
inferred← citeshttps://doi.org/10.1002/stem.2085openalex-snapshot
The Current State of Naïve Human Pluripotency
inferred← citeshttps://doi.org/10.1002/wrna.1375openalex-snapshot
Translating the epitranscriptome
inferred← citeshttps://doi.org/10.1002/wrna.1459openalex-snapshot
Emerging roles of RNA‐binding proteins in diabetes and their therapeutic potential in diabetic complications
inferred← citeshttps://doi.org/10.1002/wrna.1489openalex-snapshot
RNA methylation in nuclear pre‐mRNA processing
inferred← citeshttps://doi.org/10.1002/wrna.1507openalex-snapshot
Dynamic and reversible RNA N6‐methyladenosine methylation
inferred← citeshttps://doi.org/10.1002/wrna.1547openalex-snapshot
mRNA methylation in cell senescence
inferred← citeshttps://doi.org/10.1002/wrna.1618openalex-snapshot
A birds'‐eye view of the activity and specificity of the mRNA m6A methyltransferase complex
inferred← citeshttps://doi.org/10.1002/wrna.1673openalex-snapshot
Division of labor in epitranscriptomics: What have we learnt from the structures of eukaryotic and viral multimeric RNA methyltransferases?
inferred← citeshttps://doi.org/10.1002/wrna.1681openalex-snapshot
RNA methyltransferase METTL16 : Targets and function
inferred← citeshttps://doi.org/10.1002/wrna.1810openalex-snapshot
Ghost authors revealed: The structure and function of human N6 ‐methyladenosine RNA methyltransferases
inferred← citeshttps://doi.org/10.1007/978-1-4939-3591-8_8openalex-snapshot
Single-Turnover Kinetics of Methyl Transfer to tRNA by Methyltransferases
inferred← citeshttps://doi.org/10.1007/978-1-4939-6807-7_19openalex-snapshot
Methylated mRNA Nucleotides as Regulators for Ribosomal Translation
inferred← citeshttps://doi.org/10.1007/978-1-4939-6807-7_6openalex-snapshot
Detection and Quantification of N 6-Methyladenosine in Messenger RNA by TLC
inferred← citeshttps://doi.org/10.1007/978-1-4939-8808-2_4openalex-snapshot
HAMR: High-Throughput Annotation of Modified Ribonucleotides
inferred← citeshttps://doi.org/10.1007/978-3-030-14760-0_11openalex-snapshot
Chemical RNA Modifications: The Plant Epitranscriptome
inferred← citeshttps://doi.org/10.1007/978-3-030-14792-1_13openalex-snapshot
Functions and Dynamics of Methylation in Eukaryotic mRNA
inferred← citeshttps://doi.org/10.1007/978-3-030-14792-1_14openalex-snapshot
The Role of mRNA m6A in Regulation of Gene Expression
inferred← citeshttps://doi.org/10.1007/978-3-030-14792-1_15openalex-snapshot
m6A mRNA Methylation in the Mammalian Brain: Distribution, Function and Implications for Brain Functions
inferred← citeshttps://doi.org/10.1007/978-3-030-17086-8_2openalex-snapshot
Chemical Modifications and Their Role in Long Non-coding RNAs
inferred← citeshttps://doi.org/10.1007/978-3-030-33923-4_8openalex-snapshot
Epigenetics of Somatic Cell Reprogramming
inferred← citeshttps://doi.org/10.1007/978-3-030-71612-7_10openalex-snapshot
Roles of m6A RNA Modification in Normal Development and Disease
inferred← citeshttps://doi.org/10.1007/978-3-030-71612-7_11openalex-snapshot
N6-Methyladenosine in the Heart
inferred← citeshttps://doi.org/10.1007/978-3-031-33278-4_12openalex-snapshot
The Part Breast Milk Plays in Epigenetic Programming
inferred← citeshttps://doi.org/10.1007/978-3-032-08824-6_4openalex-snapshot
Epigenetic Regulation of miRNAs in Cancer
inferred← citeshttps://doi.org/10.1007/978-3-032-23085-0_1openalex-snapshot
Applications of Epigenetics to Forensic Sciences. Introduction
inferred← citeshttps://doi.org/10.1007/978-3-319-16769-5_9openalex-snapshot
RNA Methylation in the Control of Stem Cell Activity and Epidermal Differentiation
inferred← citeshttps://doi.org/10.1007/978-3-319-90695-9_15openalex-snapshot
Engineering of Human-Induced Pluripotent Stem Cells for Precise Disease Modeling
inferred← citeshttps://doi.org/10.1007/978-981-13-1568-8_2openalex-snapshot
RNome and Chromatin Dynamics
inferred← citeshttps://doi.org/10.1007/978-981-13-7342-8_4openalex-snapshot
RNA N 6-Methyladenosine Modification in Normal and Malignant Hematopoiesis
inferred← citeshttps://doi.org/10.1007/978-981-95-7295-3_11openalex-snapshot
mRNA Biomarkers and Their Analytical Methods
inferred← citeshttps://doi.org/10.1007/978-981-99-7471-9_7openalex-snapshot
N6-Methyladenosine RNA Modification in Normal and Malignant Hematopoiesis
inferred← citeshttps://doi.org/10.1007/s00011-023-01695-2openalex-snapshot
The potential role of N6-methyladenosine modification of LncRNAs in contributing to the pathogenesis of chronic glomerulonephritis
inferred← citeshttps://doi.org/10.1007/s00018-015-2125-6openalex-snapshot
Epigenetic regulation of early neural fate commitment
inferred← citeshttps://doi.org/10.1007/s00018-016-2428-2openalex-snapshot
More than just scanning: the importance of cap-independent mRNA translation initiation for cellular stress response and cancer
inferred← citeshttps://doi.org/10.1007/s00018-017-2602-1openalex-snapshot
Mechanisms of protein homeostasis (proteostasis) maintain stem cell identity in mammalian pluripotent stem cells
inferred← citeshttps://doi.org/10.1007/s00018-021-03823-9openalex-snapshot
Epigenetic regulations in mammalian spermatogenesis: RNA-m6A modification and beyond
inferred← citeshttps://doi.org/10.1007/s00018-024-05261-9openalex-snapshot
Dynamic changes in RNA m6A and 5 hmC influence gene expression programs during macrophage differentiation and polarisation
inferred← citeshttps://doi.org/10.1007/s00299-023-03046-1openalex-snapshot
The emerging role of epitranscriptome in shaping stress responses in plants
inferred← citeshttps://doi.org/10.1007/s00401-016-1590-9openalex-snapshot
Epigenetic regulation in Parkinson’s disease
inferred← citeshttps://doi.org/10.1007/s00432-018-2796-0openalex-snapshot
Novel positioning from obesity to cancer: FTO, an m6A RNA demethylase, regulates tumour progression
inferred← citeshttps://doi.org/10.1007/s00432-024-05785-4openalex-snapshot
The emerging role and mechanism of HMGA2 in breast cancer
inferred← citeshttps://doi.org/10.1007/s00439-026-02818-5openalex-snapshot
Human YTHDC2 mutations disturb RNA homeostasis of oocytes and early embryos
inferred← citeshttps://doi.org/10.1007/s00441-022-03667-0openalex-snapshot
Epigenetics as “conductor” in “orchestra” of pluripotent states
inferred← citeshttps://doi.org/10.1007/s00535-023-02015-5openalex-snapshot
VIRMA facilitates intrahepatic cholangiocarcinoma progression through epigenetic augmentation of TMED2 and PARD3B mRNA stabilization
inferred← citeshttps://doi.org/10.1007/s10565-021-09627-8openalex-snapshot
RNA methylation in mammalian development and cancer
inferred← citeshttps://doi.org/10.1007/s10571-021-01168-2openalex-snapshot
N6-Methyladenosine Methylation of mRNA in Cell Senescence
inferred← citeshttps://doi.org/10.1007/s10585-022-10169-4openalex-snapshot
FTO mediated ERBB2 demethylation promotes tumor progression in esophageal squamous cell carcinoma cells
inferred← citeshttps://doi.org/10.1007/s11033-026-11740-yopenalex-snapshot
Function and regulatory mechanism of RNA-binding protein IGF2BP2 in obesity and cancers
inferred← citeshttps://doi.org/10.1007/s11427-017-9193-9openalex-snapshot
RNA methylation regulates hematopoietic stem/progenitor cell specification
inferred← citeshttps://doi.org/10.1007/s11427-021-2038-5openalex-snapshot
rtcisE2F promotes the self-renewal and metastasis of liver tumor-initiating cells via N6-methyladenosine-dependent E2F3/E2F6 mRNA stability
inferred← citeshttps://doi.org/10.1007/s11427-023-2526-2openalex-snapshot
Dynamic RNA methylation modifications and their regulatory role in mammalian development and diseases
inferred← citeshttps://doi.org/10.1007/s11434-014-0695-6openalex-snapshot
Dynamic m 6 A modification and its emerging regulatory role in mRNA splicing
inferred← citeshttps://doi.org/10.1007/s11684-018-0654-8openalex-snapshot
RNA m6A modification and its function in diseases
inferred← citeshttps://doi.org/10.1007/s12013-024-01280-2openalex-snapshot
The Functions of N-methyladenosine (m6A) Modification on HIV-1 mRNA
inferred← citeshttps://doi.org/10.1007/s12015-019-09894-3openalex-snapshot
Deciphering the Epitranscriptomic Signatures in Cell Fate Determination and Development
inferred← citeshttps://doi.org/10.1007/s12015-022-10444-7openalex-snapshot
METTLing in Stem Cell and Cancer Biology
inferred← citeshttps://doi.org/10.1007/s12031-018-1037-yopenalex-snapshot
Analysis of Housekeeping Genes for Accurate Normalization of qPCR Data During Early Postnatal Brain Development
inferred← citeshttps://doi.org/10.1007/s12033-016-9947-9openalex-snapshot
N 6-Methyladenosine (m6A) Methylation in mRNA with A Dynamic and Reversible Epigenetic Modification
inferred← citeshttps://doi.org/10.1007/s12033-018-00149-zopenalex-snapshot
Understanding m6A Function Through Uncovering the Diversity Roles of YTH Domain-Containing Proteins
inferred← citeshttps://doi.org/10.1007/s12033-020-00269-5openalex-snapshot
m6A RNA Methylation: Ramifications for Gene Expression and Human Health
inferred← citeshttps://doi.org/10.1007/s12035-018-1138-1openalex-snapshot
m6A RNA Methylation Controls Neural Development and Is Involved in Human Diseases
inferred← citeshttps://doi.org/10.1007/s12035-024-04555-0openalex-snapshot
Global Co-regulatory Cross Talk Between m6A and m5C RNA Methylation Systems Coordinate Cellular Responses and Brain Disease Pathways
inferred← citeshttps://doi.org/10.1007/s12035-024-04614-6openalex-snapshot
Mechanism of N6-Methyladenosine Modification in the Pathogenesis of Depression
inferred← citeshttps://doi.org/10.1007/s12104-018-9826-3openalex-snapshot
1H, 15N, 13C backbone resonance assignment of human Alkbh5
inferred← citeshttps://doi.org/10.1007/s12185-023-03576-0openalex-snapshot
RNA modifications in hematological malignancies
inferred← citeshttps://doi.org/10.1007/s12265-021-10108-wopenalex-snapshot
N6-Adenosine Methylation (m6A) RNA Modification: an Emerging Role in Cardiovascular Diseases
inferred← citeshttps://doi.org/10.1007/s12374-020-09239-5openalex-snapshot
m6A mRNA Modification as a New Layer of Gene Regulation in Plants
inferred← citeshttps://doi.org/10.1007/s12519-016-0020-3openalex-snapshot
An epigenetic view of developmental diseases: new targets, new therapies
inferred← citeshttps://doi.org/10.1007/s12672-022-00595-xopenalex-snapshot
Systematic analysis of the expression profile and prognostic significance of m6A regulators and PD-L1 in hepatocellular carcinoma
inferred← citeshttps://doi.org/10.1007/s12672-023-00759-3openalex-snapshot
The therapeutic targets of N6-methyladenosine (m6A) modifications on tumor radioresistance
inferred← citeshttps://doi.org/10.1007/s13238-018-0518-7openalex-snapshot
Solution structure of the RNA recognition domain of METTL3-METTL14 N6-methyladenosine methyltransferase
inferred← citeshttps://doi.org/10.1007/s13238-020-00733-7openalex-snapshot
Mapping the epigenetic modifications of DNA and RNA
inferred← citeshttps://doi.org/10.1007/s13258-016-0507-2openalex-snapshot
Epitranscriptome: m6A and its function in stem cell biology
inferred← citeshttps://doi.org/10.1007/s13402-023-00839-0openalex-snapshot
Modulation of miR-146b by N6-methyladenosine modification remodels tumor-associated macrophages and enhances anti-PD-1 therapy in colorectal cancer
inferred← citeshttps://doi.org/10.1016/b978-0-12-800802-7.00002-2openalex-snapshot
RNA Epigenetics (Epitranscriptomics)
inferred← citeshttps://doi.org/10.1016/b978-0-12-805388-1.00004-3openalex-snapshot
The Epigenetics of Noncoding RNA
inferred← citeshttps://doi.org/10.1016/b978-0-12-814085-7.00001-5openalex-snapshot
Epigenetic processes and DNA repair in embryonic stem cells
inferred← citeshttps://doi.org/10.1016/b978-0-12-814085-7.00002-7openalex-snapshot
The epigenetics of pluripotent stem cells
inferred← citeshttps://doi.org/10.1016/b978-0-12-821785-6.00003-7openalex-snapshot
Role of RNA epigenetics in development
inferred← citeshttps://doi.org/10.1016/b978-0-12-822258-4.00003-1openalex-snapshot
RNA modifications in cardiovascular disease—An experimental and computational perspective
inferred← citeshttps://doi.org/10.1016/b978-0-323-85652-2.00019-1openalex-snapshot
Metabolic regulation in urological tumors: Interplay with epigenetics and epitranscriptomics
inferred← citeshttps://doi.org/10.1016/b978-0-323-89774-7.00020-0openalex-snapshot
RNA m6A modification and microRNAs
inferred← citeshttps://doi.org/10.1016/b978-0-323-91305-8.00007-7openalex-snapshot
Role of post-transcriptional gene regulation in hematological malignancies
inferred← citeshttps://doi.org/10.1016/b978-0-323-91909-8.00010-4openalex-snapshot
The Epigenetics of Noncoding RNA
inferred← citeshttps://doi.org/10.1016/bs.acr.2018.11.001openalex-snapshot
Hypoxia-inducible factors promote breast cancer stem cell specification and maintenance in response to hypoxia or cytotoxic chemotherapy
inferred← citeshttps://doi.org/10.1016/bs.acr.2020.05.001openalex-snapshot
Epigenetic regulation of cancer stem cell and tumorigenesis
inferred← citeshttps://doi.org/10.1016/bs.aivir.2022.01.002openalex-snapshot
Control of animal virus replication by RNA adenosine methylation
inferred← citeshttps://doi.org/10.1016/bs.enz.2017.03.004openalex-snapshot
Reading the Epitranscriptome
inferred← citeshttps://doi.org/10.1016/bs.enz.2017.03.008openalex-snapshot
Impact of RNA Modifications and RNA-Modifying Enzymes on Eukaryotic Ribonucleases
inferred← citeshttps://doi.org/10.1016/bs.mie.2015.03.005openalex-snapshot
Probing RNA Modification Status at Single-Nucleotide Resolution in Total RNA
inferred← citeshttps://doi.org/10.1016/bs.mie.2015.03.012openalex-snapshot
High-Resolution Mapping of N6-Methyladenosine in Transcriptome and Genome Using a Photo-Crosslinking-Assisted Strategy
inferred← citeshttps://doi.org/10.1016/bs.pmbts.2018.04.010openalex-snapshot
Neuroepigenetics of Schizophrenia
inferred← citeshttps://doi.org/10.1016/j.ab.2016.01.014openalex-snapshot
DRME: Count-based differential RNA methylation analysis at small sample size scenario
inferred← citeshttps://doi.org/10.1016/j.aca.2024.342474openalex-snapshot
Specific quantitative detection of N6-methyladenosine at single-base resolution by extension-based isothermal exponential amplification reaction (E-IEXPAR)
inferred← citeshttps://doi.org/10.1016/j.ajur.2020.05.009openalex-snapshot
Molecular and epigenetic pathogenesis of germ cell tumors
inferred← citeshttps://doi.org/10.1016/j.apsb.2018.06.001openalex-snapshot
N6-Methyladenosine modification: a novel pharmacological target for anti-cancer drug development
inferred← citeshttps://doi.org/10.1016/j.archger.2026.106402openalex-snapshot
m(6)A RNA Methylation in aging and age-related diseases
inferred← citeshttps://doi.org/10.1016/j.arr.2014.12.008openalex-snapshot
Protein synthesis as an integral quality control mechanism during ageing
inferred← citeshttps://doi.org/10.1016/j.aspen.2023.102126openalex-snapshot
m6A writer gene fl(2)d regulates the metamorphosis of silkworm Bombyx mori
inferred← citeshttps://doi.org/10.1016/j.bbagrm.2018.09.010openalex-snapshot
It's complicated… m6A-dependent regulation of gene expression in cancer
inferred← citeshttps://doi.org/10.1016/j.bbagrm.2018.10.008openalex-snapshot
Human ALKBH3-induced m1A demethylation increases the CSF-1 mRNA stability in breast and ovarian cancer cells
inferred← citeshttps://doi.org/10.1016/j.bbagrm.2018.10.013openalex-snapshot
Steering pluripotency and differentiation with N6-methyladenosine RNA modification
inferred← citeshttps://doi.org/10.1016/j.bbagrm.2018.12.001openalex-snapshot
The role of RNA adenosine demethylases in the control of gene expression
inferred← citeshttps://doi.org/10.1016/j.bbagrm.2018.12.008openalex-snapshot
Readers of the m6A epitranscriptomic code
inferred← citeshttps://doi.org/10.1016/j.bbagrm.2019.07.003openalex-snapshot
Small changes, big implications: The impact of m6A RNA methylation on gene expression in pluripotency and development
inferred← citeshttps://doi.org/10.1016/j.bbagrm.2023.194967openalex-snapshot
N6-methyladenosine (m6A) methylation in kidney diseases: Mechanisms and therapeutic potential
inferred← citeshttps://doi.org/10.1016/j.bbamcr.2022.119316openalex-snapshot
Hypoxia Induced ALKBH5 Prevents Spontaneous Abortion by Mediating M6a-Demethylation of SMAD1/5 mRNAs
inferred← citeshttps://doi.org/10.1016/j.bbcan.2021.188609openalex-snapshot
The RNA m6A writer METTL14 in cancers: Roles, structures, and applications
inferred← citeshttps://doi.org/10.1016/j.bbcan.2022.188691openalex-snapshot
The role of m6A modification in pediatric cancer
inferred← citeshttps://doi.org/10.1016/j.bbcan.2025.189299openalex-snapshot
Emerging importance of m6A modification in liver cancer and its potential therapeutic role
inferred← citeshttps://doi.org/10.1016/j.bbrc.2016.05.124openalex-snapshot
tRNA modification profiles of the fast-proliferating cancer cells
inferred← citeshttps://doi.org/10.1016/j.bbrc.2018.12.043openalex-snapshot
Differential m6A methylomes between two major life stages allows potential regulations in Trypanosoma brucei
inferred← citeshttps://doi.org/10.1016/j.bbrc.2019.08.107openalex-snapshot
Crystal structure of human YTHDC2 YTH domain
inferred← citeshttps://doi.org/10.1016/j.bbrc.2020.04.138openalex-snapshot
Regulation of autophagy in leukocytes through RNA N6-adenosine methylation in chronic kidney disease patients
inferred← citeshttps://doi.org/10.1016/j.bbrc.2020.06.153openalex-snapshot
RNA N6-methyladenosine demethylase FTO regulates PD-L1 expression in colon cancer cells
inferred← citeshttps://doi.org/10.1016/j.bbrc.2021.12.013openalex-snapshot
Structural basis for METTL6-mediated m3C RNA methylation
inferred← citeshttps://doi.org/10.1016/j.bbrc.2022.01.123openalex-snapshot
Destabilization of DNA and RNA G-quadruplex structures formed by GGA repeat due to N6-methyladenine modification
inferred← citeshttps://doi.org/10.1016/j.bcp.2019.113697openalex-snapshot
Methylation of adenosine at the N6 position post-transcriptionally regulates hepatic P450s expression
inferred← citeshttps://doi.org/10.1016/j.bcp.2023.115873openalex-snapshot
Emerging role of m6A modification in fibrotic diseases and its potential therapeutic effect
inferred← citeshttps://doi.org/10.1016/j.bcp.2024.116419openalex-snapshot
Inhibition of KIAA1429/HK1 axis enhances the sensitivity of liver cancer cells to sorafenib by regulating the Warburg effect
inferred← citeshttps://doi.org/10.1016/j.bcp.2024.116576openalex-snapshot
Biological functions of the m6A reader YTHDF2 and its role in central nervous system disorders
inferred← citeshttps://doi.org/10.1016/j.biochi.2015.02.012openalex-snapshot
MicroRNA regulation of stem cell differentiation and diseases of the bone and adipose tissue: Perspectives on miRNA biogenesis and cellular transcriptome
inferred← citeshttps://doi.org/10.1016/j.biopha.2019.108613openalex-snapshot
The role of m6A RNA methylation in cancer
inferred← citeshttps://doi.org/10.1016/j.biopha.2023.114298openalex-snapshot
m6A modification in inflammatory bowel disease provides new insights into clinical applications
inferred← citeshttps://doi.org/10.1016/j.biopha.2023.114846openalex-snapshot
N6-methyladenosine (m6A) in cancer stem cell: From molecular mechanisms to therapeutic implications
inferred← citeshttps://doi.org/10.1016/j.biopha.2023.115192openalex-snapshot
Insights into the role of N6-methyladenosine in ferroptosis
inferred← citeshttps://doi.org/10.1016/j.biopha.2024.117331openalex-snapshot
m6A modification in non-coding RNAs: Mechanisms and potential therapeutic implications in fibrosis
inferred← citeshttps://doi.org/10.1016/j.bios.2023.115645openalex-snapshot
RNA methylation-driven assembly of fluorescence-encoded nanostructures for sensitive detection of m6A modification writer METTL3/14 complex in human breast tissues
inferred← citeshttps://doi.org/10.1016/j.biotechadv.2020.107656openalex-snapshot
Advances in the profiling of N6-methyladenosine (m6A) modifications
inferred← citeshttps://doi.org/10.1016/j.bmc.2019.03.057openalex-snapshot
Unveiling the druggable RNA targets and small molecule therapeutics
inferred← citeshttps://doi.org/10.1016/j.bmc.2023.117373openalex-snapshot
Targeting m6A binding protein YTHDFs for cancer therapy
inferred← citeshttps://doi.org/10.1016/j.bmc.2026.118686openalex-snapshot
Synthesis and mechanistic insights of carbazole-based inhibitors targeting FTO by spectroscopic characterization and molecular simulation
inferred← citeshttps://doi.org/10.1016/j.bpj.2018.10.004openalex-snapshot
Active Site Breathing of Human Alkbh5 Revealed by Solution NMR and Accelerated Molecular Dynamics
inferred← citeshttps://doi.org/10.1016/j.canlet.2023.216246openalex-snapshot
TROP2 translation mediated by dual m6A/m7G RNA modifications promotes bladder cancer development
inferred← citeshttps://doi.org/10.1016/j.cbpa.2015.10.024openalex-snapshot
RNA epigenetics — chemical messages for posttranscriptional gene regulation
inferred← citeshttps://doi.org/10.1016/j.ccell.2016.11.017openalex-snapshot
FTO Plays an Oncogenic Role in Acute Myeloid Leukemia as a N 6 -Methyladenosine RNA Demethylase
inferred← citeshttps://doi.org/10.1016/j.ccell.2017.02.013openalex-snapshot
m 6 A Demethylase ALKBH5 Maintains Tumorigenicity of Glioblastoma Stem-like Cells by Sustaining FOXM1 Expression and Cell Proliferation Program
inferred← citeshttps://doi.org/10.1016/j.ccell.2017.03.010openalex-snapshot
Messenger RNA Methylation Regulates Glioblastoma Tumorigenesis
inferred← citeshttps://doi.org/10.1016/j.ccell.2019.03.006openalex-snapshot
Small-Molecule Targeting of Oncogenic FTO Demethylase in Acute Myeloid Leukemia
inferred← citeshttps://doi.org/10.1016/j.ccell.2020.02.004openalex-snapshot
m6A Modification in Coding and Non-coding RNAs: Roles and Therapeutic Implications in Cancer
inferred← citeshttps://doi.org/10.1016/j.ccell.2020.10.004openalex-snapshot
YTHDF3 Induces the Translation of m6A-Enriched Gene Transcripts to Promote Breast Cancer Brain Metastasis
inferred← citeshttps://doi.org/10.1016/j.ccell.2022.10.004openalex-snapshot
The m6A reader IGF2BP2 regulates glutamine metabolism and represents a therapeutic target in acute myeloid leukemia
inferred← citeshttps://doi.org/10.1016/j.ceb.2014.06.006openalex-snapshot
Role of RNA methyltransferases in tissue renewal and pathology
inferred← citeshttps://doi.org/10.1016/j.cell.2014.08.005openalex-snapshot
Emerging Roles of RNA Modification: m6A and U-Tail
inferred← citeshttps://doi.org/10.1016/j.cell.2015.05.014openalex-snapshot
N6-methyladenosine Modulates Messenger RNA Translation Efficiency
inferred← citeshttps://doi.org/10.1016/j.cell.2015.08.011openalex-snapshot
HNRNPA2B1 Is a Mediator of m6A-Dependent Nuclear RNA Processing Events
showing the first 200 of 1292
Editorial review for independent work. ICSAC — the Institute for Complexity Science and Advanced Computing — runs a structured editorial panel for researchers publishing outside journals, and publishes on CiteStamp rails. Submission is free and goes through ORCID: icsacinstitute.org/submit.