Evidence map›Paper›PMID 23907190›Full record

ArticleNature cell biology2013

Linking HSCs to their youth.

Eric M Pietras, Emmanuelle Passegué

Erratum issuedAbstract readNewsComment
PubMed Publisher
In one paragraph

Article in Nature cell biology, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing 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

16 citing papers in PubMed.

  1. Article
  2. Germline bi-allelicHaematologica · 2024
    Article
  3. Article
  4. Review
  5. Article
  6. Article
  7. Review
  8. Review
  9. Article
  10. Review
  11. Review
  12. Article
  13. Article
  14. Article
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  16. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

2 authors.

Eric M Pietras
Emmanuelle Passegué

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Fetal haematopoietic stem cells (HSCs) self-renew extensively to build the blood system from scratch. The protein Lin28b negatively regulates the microRNA let-7 to keep levels of its target Hmga2 high, hence conferring high self-renewal potential to fetal HSCs. This regulatory circuit can be experimentally modulated to boost the lower self-renewal activity of quiescent adult HSCs.

Indexed as

AnimalsDNA-Binding ProteinsHematopoietic Stem CellsHMGA2 ProteinMicroRNAsRNA-Binding ProteinsDNA-Binding ProteinsHMGA2 ProteinLIN28B protein, humanMicroRNAsmirnlet7 microRNA, mouseRNA-Binding Proteins

Identifiers

PMID23907190

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.