Evidence map›Paper›PMID 25349456›Full record

ReviewPhilosophical transactions of the Royal Society of London. Series B, Biological sciences2014

The molecular underpinnings of totipotency.

Sophie M Morgani, Joshua M Brickman

Abstract readReview
In one paragraph

Review in Philosophical transactions of the Royal Society of London. Series B, Biological sciences, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. 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
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  4. Prenatal and postnatal MRI imaging findings of intracranial parasitic fetus: a case report.Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery · 2021
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  6. Review
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  11. Review
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  14. Review
  15. Transient bursts of Zscan4 expression are accompanied by the rapid derepression of heterochromatin in mouse embryonic stem cells.DNA research : an international journal for rapid publication of reports on genes and genomes · 2015
    Article
  16. From pluripotency to differentiation: laying foundations for the body pattern in the mouse embryo.Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2014
    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

2 authors.

Sophie M MorganiThe Danish Stem Cell Centre-DanStem, University of Copenhagen, 3B Blegdamsvej, Copenhagen 2200, Denmark.
Joshua M BrickmanThe Danish Stem Cell Centre-DanStem, University of Copenhagen, 3B Blegdamsvej, Copenhagen 2200, Denmark joshua.brickman@sund.ku.dk.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Embryonic stem (ES) cells are characterized by their functional potency and capacity to self-renew in culture. Historically, ES cells have been defined as pluripotent, able to make the embryonic but not the extraembryonic lineages (such as the yolk sac and the placenta). The functional capacity of ES cells has been judged based on their ability to contribute to all somatic lineages when they are introduced into an embryo. However, a number of recent reports have suggested that under certain conditions, ES cells, and other reprogrammed cell lines, can also contribute to the extraembryonic lineages and, therefore, can be said to be totipotent. Here, we consider the molecular basis for this totipotent state, its transcriptional signature and the signalling pathways that define it.

Indexed as

AnimalsCell LineageCell ProliferationChromatinEmbryonic Stem CellsGene Regulatory NetworksMiceModels, BiologicalSignal TransductionTotipotent Stem CellsChromatinembryonic stem cellsendodermpluripotencytotipotencytrophoblast

Identifiers

PMID25349456
PMCPMC4216470

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.