Evidence map›Paper›PMID 36440631›Full record

ArticleDevelopment (Cambridge, England)2022

Transposon control as a checkpoint for tissue regeneration.

Krista M Angileri, Nornubari A Bagia, Cedric Feschotte

Open access · bronzeAbstract read
In one paragraph

Article in Development (Cambridge, England), 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.3field-weighted citation impact, top 20% 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

11 citing papers in PubMed, 16 citations in OpenAlex.

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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 at 1 institution in 1 country.

Krista M AngileriDepartment of Molecular Biology and Genetics, Cornell University, 526 Campus Rd, Ithaca, NY 14850, USA.ORCID 0000-0002-8251-5563
Nornubari A BagiaDepartment of Molecular Biology and Genetics, Cornell University, 526 Campus Rd, Ithaca, NY 14850, USA.
Cedric FeschotteDepartment of Molecular Biology and Genetics, Cornell University, 526 Campus Rd, Ithaca, NY 14850, USA.ORCID 0000-0002-8772-6976
Cornell University · US

Funding

Genomic and Physiological Impact of Transposable Elements.R35GM122550 · NIGMS · CORNELL UNIVERSITY · PI Cedric Feschotte · 2017 to 2026
$4.4M
NIGMS NIH HHS R35 GM122550NIH HHS GM122550
6 · The paper itself

Abstract

Tissue regeneration requires precise temporal control of cellular processes such as inflammatory signaling, chromatin remodeling and proliferation. The combination of these processes forms a unique microenvironment permissive to the expression, and potential mobilization of, transposable elements (TEs). Here, we develop the hypothesis that TE activation creates a barrier to tissue repair that must be overcome to achieve successful regeneration. We discuss how uncontrolled TE activity may impede tissue restoration and review mechanisms by which TE activity may be controlled during regeneration. We posit that the diversification and co-evolution of TEs and host control mechanisms may contribute to the wide variation in regenerative competency across tissues and species.

Indexed as

DNA Transposable ElementsEvolution, MolecularDNA Transposable ElementsInflammationProliferationRegenerative biologyStem cellsTransposable elements

Identifiers

PMID36440631
PMCPMC10655923
OpenAlexW4310215792

What Socratic 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 Socratic graph.