Evidence map›Paper›PMID 25098353›Full record

ReviewCellular and molecular life sciences : CMLS2014

DLK1-DIO3 imprinted cluster in induced pluripotency: landscape in the mist.

Leonidas Benetatos, George Vartholomatos, Eleftheria Hatzimichael

Abstract readReview
In one paragraph

Review in Cellular and molecular life sciences : CMLS, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
–field-weighted citation impact
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

24 citing papers in PubMed.

  1. Article
  2. Article
  3. TET3 protects theiScience · 2025
    Article
  4. Article
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  6. DLK1/DIO3 locus upregulation by a β-catenin-dependent enhancer drives cell proliferation and liver tumorigenesis.Molecular therapy : the journal of the American Society of Gene Therapy · 2024
    Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Review
  13. Article
  14. Loss of TSC complex enhances gluconeogenesis via upregulation ofProceedings of the National Academy of Sciences of the United States of America · 2020
    Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. 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

3 authors.

Leonidas BenetatosBlood Bank, Selefkeias 2, Preveza General Hospital, 48100, Preveza, Greece, benetatosleon@yahoo.com.
George Vartholomatos
Eleftheria Hatzimichael

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

DLK1-DIO3 represents an imprinted cluster which genes are involved in physiological cell biology as early as the stem cell level and in the pathogenesis of several diseases. Transcription factor-mediated induced pluripotent cells (iPSCs) are considered an unlimited source of patient-specific hematopoietic stem cells for clinical application in patient-tailored regenerative medicine. However, to date there is no marker established able to distinguish embryonic stem cell-equivalent iPSCs or safe human iPSCs. Recent findings suggest that the DLK1-DIO3 locus possesses the potential to represent such a marker but there are also contradictory data. This review aims to report the current data on the topic describing both sides of the coin.

Indexed as

Calcium-Binding ProteinsCarcinogenesisEpigenesis, GeneticGenomic ImprintingHumansInduced Pluripotent Stem CellsIntercellular Signaling Peptides and ProteinsIodide PeroxidaseMembrane ProteinsMicroRNAsTranscription FactorsCalcium-Binding ProteinsDLK1 protein, humanIntercellular Signaling Peptides and ProteinsIodide PeroxidaseMembrane ProteinsMicroRNAsTranscription Factors

Identifiers

PMID25098353
PMCPMC11113449

What OpenQuestion holds

Textmetadata
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.