Evidence map›Paper›PMID 28408975›Full record

ReviewF1000Research2017

X chromosome inactivation: new players in the initiation of gene silencing.

Ines Pinheiro, Edith Heard

Abstract readReview
In one paragraph

Review in F1000Research, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing 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

20 citing papers in PubMed.

  1. Article
  2. A previously unreportedDigital journal of ophthalmology : DJO · 2025
    Article
  3. Revisiting the consequences of deleting the X inactivation center.Proceedings of the National Academy of Sciences of the United States of America · 2021
    Article
  4. Review
  5. Article
  6. Biological Function of Long Non-coding RNA (LncRNA) Xist.Frontiers in cell and developmental biology · 2021
    Review
  7. Article
  8. Architectural RNA in chromatin organization.Biochemical Society transactions · 2020
    Review
  9. Article
  10. Review
  11. Article
  12. Review
  13. Review
  14. Extensive cellular heterogeneity of X inactivation revealed by single-cell allele-specific expression in human fibroblasts.Proceedings of the National Academy of Sciences of the United States of America · 2018
    Article
  15. The genetic basis of disease.Essays in biochemistry · 2018
    Review
  16. Article
  17. Changes in the position and volume of inactive X chromosomes during the G0/G1 transition.Chromosome research : an international journal on the molecular, supramolecular and evolutionary aspects of chromosome biology · 2018
    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

2 authors.

Ines PinheiroMammalian Developmental Epigenetics Group (équipe labellisée La Ligue), Institut Curie, PSL Research University, CNRS UMR3215, INSERM U934, 26 Rue d'Ulm, 11 75248 Paris Cedex 05, France.ORCID 0000-0002-8342-7266
Edith HeardMammalian Developmental Epigenetics Group (équipe labellisée La Ligue), Institut Curie, PSL Research University, CNRS UMR3215, INSERM U934, 26 Rue d'Ulm, 11 75248 Paris Cedex 05, France.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

X chromosome inactivation (XCI) is a dosage compensation process that was adopted by female mammals to balance gene dosage between XX females and XY males. XCI starts with the upregulation of the non-coding RNA Xist, after which most X-linked genes are silenced and acquire a repressive chromatin state. Even though the chromatin marks of the inactive X have been fairly well described, the mechanisms responsible for the initiation of XCI remain largely unknown. In this review, we discuss recent developments that revealed unexpected factors playing a role in XCI and that might be of crucial importance to understand the mechanisms responsible for the very first steps of this chromosome-wide gene-silencing event.

Indexed as

chromatinepigeneticsX chromosome inactivationXCIXist RNAX-linked genes

Identifiers

PMID28408975
PMCPMC5373419

What OpenQuestion holds

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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.