Evidence map›Paper›PMID 31738163›Full record

ArticleeLife2019

Persistent epigenetic memory impedes rescue of the telomeric phenotype in human ICF iPSCs following DNMT3B correction.

Shir Toubiana, Miriam Gagliardi, Mariarosaria Papa, Roberta Manco, Maty Tzukerman, Maria R Matarazzo, Sara Selig

Open access · goldAbstract read
In one paragraph

Article in eLife, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
1.2field-weighted citation impact, top 21% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

15 citing papers in PubMed, 26 citations in OpenAlex.

  1. MAM-STAT3-Driven Mitochondrial CaAdvanced science (Weinheim, Baden-Wurttemberg, Germany) · 2025
    Article
  2. Review
  3. Article
  4. ICF1-Syndrome-AssociatedBiomolecules · 2023
    Article
  5. The aberrant epigenome ofGenome research · 2023
    Article
  6. Review
  7. Article
  8. Article
  9. Review
  10. The makings of TERRA R-loops at chromosome ends.Cell cycle (Georgetown, Tex.) · 2021
    Review
  11. Correction of Heritable Epigenetic Defects Using Editing Tools.International journal of molecular sciences · 2021
    Review
  12. Article
  13. Cardiac Fibroblasts and Myocardial Regeneration.Frontiers in bioengineering and biotechnology · 2021
    Review
  14. Article
  15. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors at 2 institutions in 2 countries.

Shir Toubiana *Molecular Medicine Laboratory, Rappaport Faculty of Medicine, Technion, Haifa, Israel.ORCID 0000-0003-3001-5281
Miriam Gagliardi *Institute of Genetics and Biophysics, ABT CNR, Naples, Italy.ORCID 0000-0003-0156-3705
Mariarosaria PapaInstitute of Genetics and Biophysics, ABT CNR, Naples, Italy.ORCID 0000-0002-2467-4187
Roberta MancoInstitute of Genetics and Biophysics, ABT CNR, Naples, Italy.ORCID 0000-0003-2888-3442
Maty TzukermanMolecular Medicine Laboratory, Rappaport Faculty of Medicine, Technion, Haifa, Israel.ORCID 0000-0002-9080-2511
Maria R MatarazzoInstitute of Genetics and Biophysics, ABT CNR, Naples, Italy.ORCID 0000-0002-8192-4322
Sara SeligMolecular Medicine Laboratory, Rappaport Faculty of Medicine, Technion, Haifa, Israel.ORCID 0000-0001-5759-9948
Institute of Genetics and Biophysics · ITTechnion – Israel Institute of Technology · IL

Funding

Israel Science Foundation 1362/17MIUR/CNR Epigenomics Flagship Project (EPIGEN)PON/MISE 2014-2020 FESR F/050011/01-02/X32Telethon GGP15209
6 · The paper itself

Abstract

DNA methyltransferase 3B (DNMT3B) is the major DNMT that methylates mammalian genomes during early development. Mutations in human

Indexed as

DNA (Cytosine-5-)-MethyltransferasesDNA MethylationDNA Methyltransferase 3BEpigenesis, GeneticFaceGenomeHistonesHumansInduced Pluripotent Stem CellsMutationPrimary Immunodeficiency DiseasesPromoter Regions, GeneticTelomereDNA (Cytosine-5-)-MethyltransferasesDNA Methyltransferase 3Bhistone H3 trimethyl Lys4HistonesDNA methylationDNMT3Bhumanhuman biologyICF syndromemedicineregenerative medicinestem cellssubtelomeretelomere

Identifiers

PMID31738163
PMCPMC6897513
OpenAlexW2988079525

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.