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Intron retention is regulated by altered MeCP2-mediated splicing factor recruitment

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What this work says

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

inferredcites →https://doi.org/10.1002/jcp.24067openalex-snapshot
Gadd45a and Gadd45b modulate innate immune functions of granulocytes and macrophages by differential regulation of p38 and JNK signaling
inferredcites →https://doi.org/10.1002/jemt.10299openalex-snapshot
S100A9/S100A8: Myeloid representatives of the S100 protein family as prominent players in innate immunity
inferredcites →https://doi.org/10.1006/excr.2001.5269openalex-snapshot
Nuclear Envelope and Chromatin Compositional Differences Comparing Undifferentiated and Retinoic Acid- and Phorbol Ester-Treated HL-60 Cells
inferredcites →https://doi.org/10.1016/j.ccr.2014.07.028openalex-snapshot
Gene Body Methylation Can Alter Gene Expression and Is a Therapeutic Target in Cancer
inferredcites →https://doi.org/10.1016/j.cell.2010.07.019openalex-snapshot
An Alternative Splicing Network Links Cell-Cycle Control to Apoptosis
inferredcites →https://doi.org/10.1016/j.cell.2013.03.011openalex-snapshot
Methylation-Dependent and -Independent Genomic Targeting Principles of the MBD Protein Family
inferredcites →https://doi.org/10.1016/j.cell.2013.06.052openalex-snapshot
Orchestrated Intron Retention Regulates Normal Granulocyte Differentiation
inferredcites →https://doi.org/10.1016/j.celrep.2013.01.010openalex-snapshot
Endogenous Purification Reveals GREB1 as a Key Estrogen Receptor Regulatory Factor
inferredcites →https://doi.org/10.1016/j.celrep.2014.12.046openalex-snapshot
The Alternative Splicing Regulator Tra2b Is Required for Somitogenesis and Regulates Splicing of an Inhibitory Wnt11b Isoform
inferredcites →https://doi.org/10.1016/j.celrep.2015.01.038openalex-snapshot
HP1 Is Involved in Regulating the Global Impact of DNA Methylation on Alternative Splicing
inferredcites →https://doi.org/10.1016/j.cmet.2014.12.002openalex-snapshot
Peroxisomal Lipid Synthesis Regulates Inflammation by Sustaining Neutrophil Membrane Phospholipid Composition and Viability
inferredcites →https://doi.org/10.1016/j.ctrv.2010.05.006openalex-snapshot
5-Azacytidine in myelodysplastic syndromes: A clinical practice guideline
inferredcites →https://doi.org/10.1016/j.molcel.2003.08.001openalex-snapshot
A Slow RNA Polymerase II Affects Alternative Splicing In Vivo
inferredcites →https://doi.org/10.1016/j.molcel.2014.08.022openalex-snapshot
BS69/ZMYND11 Reads and Connects Histone H3.3 Lysine 36 Trimethylation-Decorated Chromatin to Regulated Pre-mRNA Processing
inferredcites →https://doi.org/10.1016/j.stem.2014.06.018openalex-snapshot
Dnmt3a and Dnmt3b Have Overlapping and Distinct Functions in Hematopoietic Stem Cells
inferredcites →https://doi.org/10.1016/j.tcb.2011.04.004openalex-snapshot
Unraveling the enigma: progress towards understanding the coronin family of actin regulators
inferredcites →https://doi.org/10.1016/j.tig.2012.01.001openalex-snapshot
New connections between splicing and human disease
inferredcites →https://doi.org/10.1016/j.tig.2015.03.002openalex-snapshot
The alternative role of DNA methylation in splicing regulation
inferredcites →https://doi.org/10.1038/414929aopenalex-snapshot
Stimulatory effect of splicing factors on transcriptional elongation
inferredcites →https://doi.org/10.1038/cr.2013.110openalex-snapshot
Intragenic DNA methylation modulates alternative splicing by recruiting MeCP2 to promote exon recognition
inferredcites →https://doi.org/10.1038/nature10442openalex-snapshot
CTCF-promoted RNA polymerase II pausing links DNA methylation to splicing
inferredcites →https://doi.org/10.1038/nature13045openalex-snapshot
ZMYND11 links histone H3.3K36me3 to transcription elongation and tumour suppression
inferredcites →https://doi.org/10.1038/nature14046openalex-snapshot
Genome-wide characterization of the routes to pluripotency
inferredcites →https://doi.org/10.1038/nature14176openalex-snapshot
Genomic profiling of DNA methyltransferases reveals a role for DNMT3B in genic methylation
inferredcites →https://doi.org/10.1038/nbt.2398openalex-snapshot
Mapping recently identified nucleotide variants in the genome and transcriptome
inferredcites →https://doi.org/10.1038/ncomms5760openalex-snapshot
Human Tra2 proteins jointly control a CHEK1 splicing switch among alternative and constitutive target exons
inferredcites →https://doi.org/10.1038/ncomms7351openalex-snapshot
Epigenetic and transcriptional determinants of the human breast
inferredcites →https://doi.org/10.1038/ng.2836openalex-snapshot
Large conserved domains of low DNA methylation maintained by Dnmt3a
inferredcites →https://doi.org/10.1038/ng.3414openalex-snapshot
Intron retention is a widespread mechanism of tumor-suppressor inactivation
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.2012.016openalex-snapshot
Differential gene and transcript expression analysis of RNA-seq experiments with TopHat and Cufflinks
inferredcites →https://doi.org/10.1038/nrc3819openalex-snapshot
Poised epigenetic states and acquired drug resistance in cancer
inferredcites →https://doi.org/10.1038/nrg3230openalex-snapshot
Functions of DNA methylation: islands, start sites, gene bodies and beyond
inferredcites →https://doi.org/10.1038/nri1785openalex-snapshot
Neutrophils and immunity: challenges and opportunities
inferredcites →https://doi.org/10.1038/nsmb.1461openalex-snapshot
The splicing factor SC35 has an active role in transcriptional elongation
inferredcites →https://doi.org/10.1042/bsr20100124openalex-snapshot
A brain-derived MeCP2 complex supports a role for MeCP2 in RNA processing
inferredcites →https://doi.org/10.1073/pnas.0507856102openalex-snapshot
Regulation of RNA splicing by the methylation-dependent transcriptional repressor methyl-CpG binding protein 2
inferredcites →https://doi.org/10.1073/pnas.1310735110openalex-snapshot
RNA interference knockdown of DNA methyl-transferase 3 affects gene alternative splicing in the honey bee
inferredcites →https://doi.org/10.1073/pnas.1311839110openalex-snapshot
Differential splicing across immune system lineages
inferredcites →https://doi.org/10.1093/bioinformatics/bts635openalex-snapshot
STAR: ultrafast universal RNA-seq aligner
inferredcites →https://doi.org/10.1093/nar/gkv1168openalex-snapshot
A dynamic intron retention program enriched in RNA processing genes regulates gene expression during terminal erythropoiesis
inferredcites →https://doi.org/10.1093/nar/gkw591openalex-snapshot
Global intron retention mediated gene regulation during CD4+T cell activation
inferredcites →https://doi.org/10.1101/gad.188037.112openalex-snapshot
Coordinated regulation of neuronal mRNA steady-state levels through developmentally controlled intron retention
inferredcites →https://doi.org/10.1101/gr.101907.109openalex-snapshot
Dynamic changes in the human methylome during differentiation
inferredcites →https://doi.org/10.1101/gr.177790.114openalex-snapshot
Widespread intron retention in mammals functionally tunes transcriptomes
inferredcites →https://doi.org/10.1101/gr.7.10.986openalex-snapshot
The Significance of Digital Gene Expression Profiles
inferredcites →https://doi.org/10.1128/mcb.00379-10openalex-snapshot
MeCP2 Binds Cooperatively to Its Substrate and Competes with Histone H1 for Chromatin Binding Sites
inferredcites →https://doi.org/10.1182/blood-2002-04-1039openalex-snapshot
Regulation of neutrophil and eosinophil secondary granule gene expression by transcription factors C/EBPε and PU.1
inferredcites →https://doi.org/10.1182/blood-2016-01-692764openalex-snapshot
A dynamic intron retention program in the mammalian megakaryocyte and erythrocyte lineages
inferredcites →https://doi.org/10.1182/blood.v78.4.1069.1069openalex-snapshot
Retinoic acid-induced granulocytic differentiation of HL60 human promyelocytic leukemia cells is preceded by downregulation of autonomous generation of inositol lipid-derived second messengers
inferredcites →https://doi.org/10.1186/1756-8722-7-42openalex-snapshot
Identification of nuclear-enriched miRNAs during mouse granulopoiesis
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-2009-10-10-242openalex-snapshot
The SR protein family
inferredcites →https://doi.org/10.1186/s13059-014-0406-2openalex-snapshot
DNMT inhibitors reverse a specific signature of aberrant promoter DNA methylation and associated gene silencing in AML
inferredcites →https://doi.org/10.1186/s13059-017-1184-4openalex-snapshot
IRFinder: assessing the impact of intron retention on mammalian gene expression
inferredcites →https://doi.org/10.1186/s13072-016-0070-8openalex-snapshot
Changes of 5-hydroxymethylcytosine distribution during myeloid and lymphoid differentiation of CD34+ cells
inferredcites →https://doi.org/10.1186/s13073-015-0168-9openalex-snapshot
Widespread intron retention diversifies most cancer transcriptomes
inferredcites →https://doi.org/10.1189/jlb.0806516openalex-snapshot
ATF4 differentially regulates transcriptional activation of myeloid-specific genes by C/EBPε and C/EBPα
inferredcites →https://doi.org/10.1189/jlb.1109723openalex-snapshot
Adiponectin is produced by lymphocytes and is a negative regulator of granulopoiesis
inferredcites →https://doi.org/10.1196/annals.1410.001openalex-snapshot
Stress‐induced Alternative Splicing Modulations in Brain and Periphery
inferredcites →https://doi.org/10.15252/embj.201593235openalex-snapshot
TET‐catalyzed oxidation of intragenic 5‐methylcytosine regulates CTCF‐dependent alternative splicing
inferredcites →https://doi.org/10.4161/rna.26921openalex-snapshot
Chromatin context and ncRNA highlight targets of MeCP2 in brain

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.4680954openalex-extracted
inferred← citeshttps://doi.org/10.1002/1873-3468.13119openalex-snapshot
Regulation of alternative mRNA splicing: old players and new perspectives
inferred← citeshttps://doi.org/10.1002/9781119860914.ch18openalex-snapshot
The Emerging Roles of LIS 1 Biomechanics in Cellular and Cortical Homeostasis
inferred← citeshttps://doi.org/10.1002/advs.202203480openalex-snapshot
LAFITE Reveals the Complexity of Transcript Isoforms in Subcellular Fractions
inferred← citeshttps://doi.org/10.1002/alz.12254openalex-snapshot
Integrative functional genomic analysis of intron retention in human and mouse brain with Alzheimer's disease
inferred← citeshttps://doi.org/10.1002/wrna.1470openalex-snapshot
Intron retention in viruses and cellular genes: Detention, border controls and passports
inferred← citeshttps://doi.org/10.1002/wrna.1815openalex-snapshot
Regulation of alternative splicing: Functional interplay with epigenetic modifications and its implication to cancer
inferred← citeshttps://doi.org/10.1007/s00344-021-10360-zopenalex-snapshot
Difference Analysis of ClCYC2-Like Genes Expression and DNA Methylation Between the Two Types of Florets in Chrysanthemum lavandulifolium
inferred← citeshttps://doi.org/10.1007/s00436-022-07578-5openalex-snapshot
Acanthamoeba castellanii exhibits intron retention during encystment
inferred← citeshttps://doi.org/10.1007/s00439-021-02409-6openalex-snapshot
Differential fates of introns in gene expression due to global alternative splicing
inferred← citeshttps://doi.org/10.1016/b978-0-12-801238-3.11567-3openalex-snapshot
Computational Methods for Intron Retention Identification and Quantification
inferred← citeshttps://doi.org/10.1016/b978-0-12-813796-3.00009-2openalex-snapshot
Genetic and epigenetic influences on the phenotype of Rett syndrome
inferred← citeshttps://doi.org/10.1016/j.amolm.2024.100039openalex-snapshot
A canine mastocytoma with oncogenic c-kit activation by intra-exonic alternative splicing
inferred← citeshttps://doi.org/10.1016/j.biocel.2017.06.017openalex-snapshot
From intronization to intron loss: How the interplay between mRNA-associated processes can shape the architecture and the expression of eukaryotic genes
inferred← citeshttps://doi.org/10.1016/j.cellimm.2019.103996openalex-snapshot
Matters of life and death: How estrogen and estrogen receptor binding to the immunoglobulin heavy chain locus may influence outcomes of infection, allergy, and autoimmune disease
inferred← citeshttps://doi.org/10.1016/j.celrep.2025.116227openalex-snapshot
When the cell needs to respond to the environment: A chromatin-splicing love affair
inferred← citeshttps://doi.org/10.1016/j.envint.2022.107086openalex-snapshot
Secondhand smoke affects reproductive functions by altering the mouse testis transcriptome, and leads to select intron retention in Pde1a
inferred← citeshttps://doi.org/10.1016/j.immuni.2021.03.001openalex-snapshot
Atypical acute myeloid leukemia-specific transcripts generate shared and immunogenic MHC class-I-associated epitopes
inferred← citeshttps://doi.org/10.1016/j.jaut.2024.103306openalex-snapshot
Alternative splicing and intron retention: Their profiles and roles in cutaneous fibrosis of systemic sclerosis
inferred← citeshttps://doi.org/10.1016/j.jplph.2026.154868openalex-snapshot
Intron retention as a hub for splicing regulation in plant environmental adaptation and developmental programming
inferred← citeshttps://doi.org/10.1016/j.neulet.2024.137770openalex-snapshot
Chronic corticosterone exposure in rats induces sex-specific alterations in hypothalamic reelin fragments, MeCP2, and DNMT3a protein levels
inferred← citeshttps://doi.org/10.1016/j.omtn.2018.01.011openalex-snapshot
Antisense Oligonucleotide-Mediated Terminal Intron Retention of the SMN2 Transcript
inferred← citeshttps://doi.org/10.1016/j.omtn.2024.102202openalex-snapshot
Aberrant spliceosome activity via elevated intron retention and upregulation and phosphorylation of SF3B1 in chronic lymphocytic leukemia
inferred← citeshttps://doi.org/10.1016/j.scib.2026.07.025openalex-snapshot
Hierarchical regulation and molecular functions of co-transcriptional splicing
inferred← citeshttps://doi.org/10.1016/j.semcdb.2017.07.030openalex-snapshot
Challenges in defining the role of intron retention in normal biology and disease
inferred← citeshttps://doi.org/10.1016/j.tig.2020.10.008openalex-snapshot
Anything but Ordinary – Emerging Splicing Mechanisms in Eukaryotic Gene Regulation
inferred← citeshttps://doi.org/10.1016/j.tig.2022.06.001openalex-snapshot
The chromatin roots of abnormal splicing in autism
inferred← citeshttps://doi.org/10.1038/s12276-025-01407-2openalex-snapshot
Targeting the splicing factor SNRPB inhibits endometrial cancer progression by retaining the POLD1 intron
inferred← citeshttps://doi.org/10.1038/s41375-018-0021-4openalex-snapshot
We skip to work: alternative splicing in normal and malignant myelopoiesis
inferred← citeshttps://doi.org/10.1038/s41388-023-02692-9openalex-snapshot
Novel thrombospondin-1 transcript exhibits distinctive expression and activity in thyroid tumorigenesis
inferred← citeshttps://doi.org/10.1038/s41436-019-0516-zopenalex-snapshot
Aberrant DNA methylation as a diagnostic biomarker of diabetic embryopathy
inferred← citeshttps://doi.org/10.1038/s41467-018-04373-8openalex-snapshot
Intron retention and nuclear loss of SFPQ are molecular hallmarks of ALS
inferred← citeshttps://doi.org/10.1038/s41467-019-12642-3openalex-snapshot
Dissecting splicing decisions and cell-to-cell variability with designed sequence libraries
inferred← citeshttps://doi.org/10.1038/s41467-021-26084-3openalex-snapshot
Rett syndrome linked to defects in forming the MeCP2/Rbfox/LASR complex in mouse models
inferred← citeshttps://doi.org/10.1038/s41580-024-00739-7openalex-snapshot
Splicing regulation through biomolecular condensates and membraneless organelles
inferred← citeshttps://doi.org/10.1038/s41590-017-0028-4openalex-snapshot
RNA-binding proteins control gene expression and cell fate in the immune system
inferred← citeshttps://doi.org/10.1042/ebc20190056openalex-snapshot
DNA methylation analysis for screening and diagnostic testing in neurodevelopmental disorders
inferred← citeshttps://doi.org/10.1073/pnas.1722546115openalex-snapshot
Activity-dependent aberrations in gene expression and alternative splicing in a mouse model of Rett syndrome
inferred← citeshttps://doi.org/10.1073/pnas.2204179119openalex-snapshot
Truncated Tau caused by intron retention is enriched in Alzheimer’s disease cortex and exhibits altered biochemical properties
inferred← citeshttps://doi.org/10.1073/pnas.2309678120openalex-snapshot
Size matters: Fighting repeat expansion size in fragile X syndrome using antisense oligonucleotides
inferred← citeshttps://doi.org/10.1080/10985549.2025.2539755openalex-snapshot
Causes, Consequences and Challenges of Intron Retention in lncRNAs
inferred← citeshttps://doi.org/10.1080/15476286.2018.1465795openalex-snapshot
Modulating the expression of Chtop, a versatile regulator of gene-specific transcription and mRNA export
inferred← citeshttps://doi.org/10.1080/15476286.2020.1796052openalex-snapshot
Ctcf haploinsufficiency mediates intron retention in a tissue-specific manner
inferred← citeshttps://doi.org/10.1080/15476286.2024.2443876openalex-snapshot
EIciRNAs in focus: current understanding and future perspectives
inferred← citeshttps://doi.org/10.1080/15592294.2018.1514232openalex-snapshot
Age-dependent methylation in epigenetic clock CpGs is associated with G-quadruplex, co-transcriptionally formed RNA structures and tentative splice sites
inferred← citeshttps://doi.org/10.1093/nar/gkaa1154openalex-snapshot
Staying true to yourself: mechanisms of DNA methylation maintenance in mammals
inferred← citeshttps://doi.org/10.1093/nar/gkaa358openalex-snapshot
Structural disruption of exonic stem–loops immediately upstream of the intron regulates mammalian splicing
inferred← citeshttps://doi.org/10.1093/nar/gkaa435openalex-snapshot
Macrophage development and activation involve coordinated intron retention in key inflammatory regulators
inferred← citeshttps://doi.org/10.1093/nar/gkab437openalex-snapshot
CD44 alternative splicing senses intragenic DNA methylation in tumors via direct and indirect mechanisms
inferred← citeshttps://doi.org/10.1093/nar/gkab520openalex-snapshot
CTCF as a regulator of alternative splicing: new tricks for an old player
inferred← citeshttps://doi.org/10.1093/nar/gkac994openalex-snapshot
Increased chromatin accessibility facilitates intron retention in specific cell differentiation states
inferred← citeshttps://doi.org/10.1093/nar/gkz1068openalex-snapshot
The changing paradigm of intron retention: regulation, ramifications and recipes
inferred← citeshttps://doi.org/10.1093/nar/gkz1180openalex-snapshot
Dynamic changes in intron retention are tightly associated with regulation of splicing factors and proliferative activity during B-cell development
inferred← citeshttps://doi.org/10.1101/2021.01.27.428555openalex-snapshot
Diminished miRNA activity is associated with aberrant cytoplasmic intron retention in ALS pathogenesis
inferred← citeshttps://doi.org/10.1101/685651openalex-snapshot
CD44 alternative splicing is a sensor of intragenic DNA methylation in tumors
inferred← citeshttps://doi.org/10.1101/gr.276898.122openalex-snapshot
Physiological intron retaining transcripts in the cytoplasm abound during human motor neurogenesis
inferred← citeshttps://doi.org/10.1111/acel.12928openalex-snapshot
Increased intron retention is a post‐transcriptional signature associated with progressive aging and Alzheimer’s disease
inferred← citeshttps://doi.org/10.1111/acel.13276openalex-snapshot
Prevalent intron retention fine‐tunes gene expression and contributes to cellular senescence
inferred← citeshttps://doi.org/10.1111/imm.13435openalex-snapshot
Dynamic intron retention modulates gene expression in the monocytic differentiation pathway
inferred← citeshttps://doi.org/10.1111/jnc.15331openalex-snapshot
MECP2 and the biology of MECP2 duplication syndrome
inferred← citeshttps://doi.org/10.1111/nph.18692openalex-snapshot
SUMOylation regulates pre‐mRNA splicing to overcome DNA damage in fungi
inferred← citeshttps://doi.org/10.1111/nph.70736openalex-snapshot
Transcription elongation regulated by H2B deubiquitination and H2A .Z eviction enables fungal virulence
inferred← citeshttps://doi.org/10.1126/sciadv.adu8292openalex-snapshot
Synergistic intragenic epigenetic deregulation by IDH2 and SRSF2 mutations causes mis-splicing of key transcriptional regulators
inferred← citeshttps://doi.org/10.1142/s0219720023500208openalex-snapshot
Multi-omics data analysis reveals the biological implications of alternative splicing events in lung adenocarcinoma
inferred← citeshttps://doi.org/10.1158/0008-5472.c.6512560.v1openalex-snapshot
Data from Holding on to Junk Bonds: Intron Retention in Cancer and Therapy
inferred← citeshttps://doi.org/10.1158/0008-5472.can-20-1943openalex-snapshot
Holding on to Junk Bonds: Intron Retention in Cancer and Therapy
inferred← citeshttps://doi.org/10.1158/1541-7786.mcr-17-0227openalex-snapshot
Population-dependent Intron Retention and DNA Methylation in Breast Cancer
inferred← citeshttps://doi.org/10.1158/2643-3230.bcd-20-0224openalex-snapshot
ZBTB33 Is Mutated in Clonal Hematopoiesis and Myelodysplastic Syndromes and Impacts RNA Splicing
inferred← citeshttps://doi.org/10.1186/s12864-022-08609-2openalex-snapshot
Alternative splicing plays key roles in response to stress across different stages of fighting in the fish Betta splendens
inferred← citeshttps://doi.org/10.1186/s12915-023-01645-8openalex-snapshot
Associations between DNA methylation and gene regulation depend on chromatin accessibility during transgenerational plasticity
inferred← citeshttps://doi.org/10.1186/s12935-021-02429-2openalex-snapshot
Switched alternative splicing events as attractive features in lung squamous cell carcinoma
inferred← citeshttps://doi.org/10.1186/s13041-020-00695-1openalex-snapshot
MeCP2 gates spatial learning-induced alternative splicing events in the mouse hippocampus
inferred← citeshttps://doi.org/10.1186/s13046-019-1341-6openalex-snapshot
A central role for MeCP2 in the epigenetic repression of miR-200c during epithelial-to-mesenchymal transition of glioma
inferred← citeshttps://doi.org/10.1186/s13059-017-1339-3openalex-snapshot
Intron retention enhances gene regulatory complexity in vertebrates
inferred← citeshttps://doi.org/10.1186/s13578-021-00581-wopenalex-snapshot
Regulatory roles and mechanisms of alternative RNA splicing in adipogenesis and human metabolic health
inferred← citeshttps://doi.org/10.1186/s13578-026-01556-5openalex-snapshot
Regulation of oncogenic C-terminal truncated p53β protein isoform expression by SRSF3–UPF1 splicing and surveillance axis
inferred← citeshttps://doi.org/10.1242/jeb.157891openalex-snapshot
DNA methylation profiles in red blood cells of adult hens correlate with their rearing conditions
inferred← citeshttps://doi.org/10.1261/rna.066951.118openalex-snapshot
An important class of intron retention events in human erythroblasts is regulated by cryptic exons proposed to function as splicing decoys
inferred← citeshttps://doi.org/10.1261/rna.075028.120openalex-snapshot
Antisense targeting of decoy exons can reduce intron retention and increase protein expression in human erythroblasts
inferred← citeshttps://doi.org/10.1371/journal.pgen.1009087openalex-snapshot
Quantitative analysis questions the role of MeCP2 as a global regulator of alternative splicing
inferred← citeshttps://doi.org/10.1371/journal.pone.0200211openalex-snapshot
Alternative splicing of helicase-like transcription factor (Hltf): Intron retention-dependent activation of immune tolerance at the feto-maternal interface
inferred← citeshttps://doi.org/10.15698/mic2024.02.816openalex-snapshot
Replicative aging in yeast involves dynamic intron retention patterns associated with mRNA processing/export and protein ubiquitination
inferred← citeshttps://doi.org/10.20517/and.2023.13openalex-snapshot
Role of MeCP2 in oligodendrocyte lineage cells in Rett syndrome: review and inference
inferred← citeshttps://doi.org/10.21203/rs.3.rs-1622375/v1openalex-snapshot
Dysregulated Spliceosome Activity Involves Increased Intron Retention Plus Upregulation and Phosphorylation of SF3B1 in Chronic Lymphocytic Leukemia
inferred← citeshttps://doi.org/10.2217/epi-2018-0050openalex-snapshot
DNA methylation/hydroxymethylation regulate gene expression and alternative splicing during terminal granulopoiesis
inferred← citeshttps://doi.org/10.26508/lsa.202201593openalex-snapshot
IARA: a complete and curated atlas of the biogenesis of spliceosome machinery during RNA splicing
inferred← citeshttps://doi.org/10.3389/fgene.2020.00998openalex-snapshot
The Crosstalk Between Epigenetic Mechanisms and Alternative RNA Processing Regulation
inferred← citeshttps://doi.org/10.3389/fgene.2021.620859openalex-snapshot
MeCP2: The Genetic Driver of Rett Syndrome Epigenetics
inferred← citeshttps://doi.org/10.3389/fgene.2021.624290openalex-snapshot
The Molecular Functions of MeCP2 in Rett Syndrome Pathology
inferred← citeshttps://doi.org/10.3389/fncel.2019.00370openalex-snapshot
Interplay of LIS1 and MeCP2: Interactions and Implications With the Neurodevelopmental Disorders Lissencephaly and Rett Syndrome
inferred← citeshttps://doi.org/10.3389/freae.2026.1917394openalex-snapshot
MeCP2 functions as a DNA methylation reader in immune homeostasis and cancer
inferred← citeshttps://doi.org/10.3390/biomedicines9091268openalex-snapshot
Splice and Dice: Intronic microRNAs, Splicing and Cancer
inferred← citeshttps://doi.org/10.3390/cancers12123738openalex-snapshot
Widespread Aberrant Alternative Splicing despite Molecular Remission in Chronic Myeloid Leukaemia Patients
inferred← citeshttps://doi.org/10.3390/cancers14030560openalex-snapshot
Alternative Splicing, Epigenetic Modifications and Cancer: A Dangerous Triangle, or a Hopeful One?
inferred← citeshttps://doi.org/10.3390/cancers15235689openalex-snapshot
Pan-Cancer Profiling of Intron Retention and Its Clinical Significance in Diagnosis and Prognosis
inferred← citeshttps://doi.org/10.3390/genes16080986openalex-snapshot
Intron Retention: A Reemerging Paradigm in RNA Biology and Post-Transcriptional Gene Regulation
inferred← citeshttps://doi.org/10.3390/ijms20040937openalex-snapshot
Gene-Specific Intron Retention Serves as Molecular Signature that Distinguishes Melanoma from Non-Melanoma Cancer Cells in Greek Patients
inferred← citeshttps://doi.org/10.3390/ijms221910213openalex-snapshot
The Expanding Role of Alternative Splicing in Vascular Smooth Muscle Cell Plasticity
inferred← citeshttps://doi.org/10.3390/plants9070911openalex-snapshot
First Come, First Served: Sui Generis Features of the First Intron
inferred← citeshttps://doi.org/10.4103/1673-5374.265549openalex-snapshot
Increased intron retention is linked to Alzheimer’s disease
inferred← citeshttps://doi.org/10.4103/1673-5374.371359openalex-snapshot
Enrichment of novel Tau isoform with altered biochemical properties in Alzheimer’s disease
inferred← citeshttps://doi.org/10.64898/2026.02.19.706780openalex-snapshot
Intron Retention Controls Localization of lncRNAs PURPL and MALAT1 to Promote Cell Proliferation and Migration
inferred← citeshttps://doi.org/10.64898/2026.09.10.26362533openalex-snapshot
Mapping intronic mutational hotspots by in silico mutagenesis enables single antisense oligonucleotide correction of multiple variants
inferred← citeshttps://doi.org/10.70675/b9d2d0e4z8d00z4bcfza57bz31ca5ed1866copenalex-snapshot
Stratégies de stimulation du transport axonal endogène du Bdnf comme piste thérapeutique dans le syndrome de Rett
inferred← citeshttps://doi.org/10.70675/d05116ccz5de4z4d60z98ebz918144463fdbopenalex-snapshot
The Role of Convergent Transcription in Regulating Alternative Splicing : Targeted Epigenetic Modification via Repurposed CRISPR/Cas9 System and Its Impact on Alternative Splicing Modulation
inferred← citeshttps://doi.org/10.70675/f23d8d55z764cz4603za028zf9f54d767039openalex-snapshot
Biais de composition nucléotidique des gènes et épissage alternatif
inferred← citeshttps://doi.org/10.70675/f69d2875zfa9fz4465z917eza8e7b93935c6openalex-snapshot
Etude de la contribution de l'hormone adipocytaire leptine dans la pathogenèse du syndrome de Rett
inferred← citeshttps://doi.org/10.7554/elife.111394openalex-snapshot
Intron Retention Controls Localization of lncRNAs PURPL and MALAT1 to Promote Cell Proliferation and Migration
inferred← citeshttps://doi.org/10.7554/elife.111394.1openalex-snapshot
Intron Retention Controls Localization of lncRNAs PURPL and MALAT1 to Promote Cell Proliferation and Migration
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