Evidence map›Paper›PMID 34916302›Full record

ArticleGenes & development2022

Functional rejuvenation of aged neural stem cells by Plagl2 and anti-Dyrk1a activity.

Takashi Kaise, Masahiro Fukui, Risa Sueda, Wenhui Piao, Mayumi Yamada, Taeko Kobayashi, Itaru Imayoshi, Ryoichiro Kageyama

Erratum issuedOpen access · diamondAbstract read
In one paragraph

Article in Genes & development, 2022. 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 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing 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

14 citing papers in PubMed, 24 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Review
  6. Review
  7. Review
  8. Article
  9. Article
  10. Review
  11. Article
  12. Review
  13. Article
  14. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

8 authors at 1 institution in 1 country.

Takashi KaiseInstitute for Frontier Life and Medical Sciences, Kyoto University, Kyoto 606-8507, Japan.
Masahiro FukuiInstitute for Frontier Life and Medical Sciences, Kyoto University, Kyoto 606-8507, Japan.
Risa SuedaInstitute for Frontier Life and Medical Sciences, Kyoto University, Kyoto 606-8507, Japan.
Wenhui PiaoInstitute for Frontier Life and Medical Sciences, Kyoto University, Kyoto 606-8507, Japan.
Mayumi YamadaInstitute for Frontier Life and Medical Sciences, Kyoto University, Kyoto 606-8507, Japan.
Taeko KobayashiInstitute for Frontier Life and Medical Sciences, Kyoto University, Kyoto 606-8507, Japan.
Itaru ImayoshiInstitute for Frontier Life and Medical Sciences, Kyoto University, Kyoto 606-8507, Japan.
Ryoichiro KageyamaInstitute for Frontier Life and Medical Sciences, Kyoto University, Kyoto 606-8507, Japan.
Kyoto University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The regenerative potential of neural stem cells (NSCs) declines during aging, leading to cognitive dysfunctions. This decline involves up-regulation of senescence-associated genes, but inactivation of such genes failed to reverse aging of hippocampal NSCs. Because many genes are up-regulated or down-regulated during aging, manipulation of single genes would be insufficient to reverse aging. Here we searched for a gene combination that can rejuvenate NSCs in the aged mouse brain from nuclear factors differentially expressed between embryonic and adult NSCs and their modulators. We found that a combination of inducing the zinc finger transcription factor gene

Indexed as

Neural Stem CellsRejuvenationAnimalsHippocampusMiceNeurogenesisNeuronsadult neurogenesisaged brainAscl1ATAC-seqChIP-seqDyrk1alentivirusmouseneural stem cellPlagl2

Identifiers

PMID34916302
PMCPMC8763050
OpenAlexW4200161324

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.