Evidence map›Paper›PMID 21997775›Full record

ReviewStem cells (Dayton, Ohio)2012

Concise review: Pluripotency and the transcriptional inactivation of the female Mammalian X chromosome.

Alissa Minkovsky, Sanjeet Patel, Kathrin Plath

Open access · bronzeAbstract readReview
In one paragraph

Review in Stem cells (Dayton, Ohio), 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed
2.4field-weighted citation impact, top 11% 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

30 citing papers in PubMed, 55 citations in OpenAlex.

  1. Using Organoids to Model Sex Differences in the Human Brain.Biological psychiatry global open science · 2024
    Review
  2. Article
  3. Article
  4. Article
  5. Establishment of bovine expanded potential stem cells.Proceedings of the National Academy of Sciences of the United States of America · 2021
    Article
  6. Article
  7. Manipulating the Epigenome in Nuclear Transfer Cloning: Where, When and How.International journal of molecular sciences · 2020
    Review
  8. Review
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Review
  18. Review
  19. Review
  20. Two novel DXZ4-associated long noncoding RNAs show developmental changes in expression coincident with heterochromatin formation at the human (Homo sapiens) macrosatellite repeat.Chromosome research : an international journal on the molecular, supramolecular and evolutionary aspects of chromosome biology · 2015
    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

3 authors at 1 institution in 1 country.

Alissa MinkovskyDepartment of Biological Chemistry, Jonsson Comprehensive Cancer Center, David Geffen School of Medicine, University of California Los Angeles, Los Angeles, California, USA.
Sanjeet Patel
Kathrin Plath
University of California, Los Angeles · US

Funding

PREDOCTORAL TRAINING PROGRAM IN GENETIC MECHANISMS AT UCT32GM007104 · NIGMS · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI GOBER, JAMES W · 1985 to 2011
$3.6M
CHROMATIN AND EPIGENETIC INHERITANCEDP2OD001686 · OD · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI PLATH, KATHRIN · 2007 to 2007
$2.3M
Aging and the Developmental Regulation of X Chromosome InactivationF30AG039179 · NIA · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI KEEGAN, ALISSA F · 2011 to 2014
$110k
NIA NIH HHS F30 AG039179NIGMS NIH HHS GM07104NIGMS NIH HHS T32 GM007104NIH HHS DP2 OD001686NIH HHS DP2OD001686
6 · The paper itself

Abstract

X chromosome inactivation (XCI) is a striking example of developmentally regulated, wide-range heterochromatin formation that is initiated during early embryonic development. XCI is a mechanism of dosage compensation unique to placental mammals whereby one X chromosome in every diploid cell of the female organism is transcriptionally silenced to equalize X-linked gene levels to XY males. In the embryo, XCI is random with respect to whether the maternal or paternal X chromosome is inactivated and is established in epiblast cells on implantation of the blastocyst. Conveniently, ex vivo differentiation of mouse embryonic stem cells recapitulates random XCI and permits mechanistic dissection of this stepwise process that leads to stable epigenetic silencing. Here, we focus on recent studies in mouse models characterizing the molecular players of this female-specific process with an emphasis on those relevant to the pluripotent state. Further, we will summarize advances characterizing XCI states in human pluripotent cells, where surprising differences from the mouse process may have far-reaching implications for human pluripotent cell biology.

Indexed as

AnimalsBlastocystDosage Compensation, GeneticEmbryo, MammalianEmbryonic DevelopmentEmbryonic Stem CellsFemaleGene Expression Regulation, DevelopmentalHumansMaleMicePluripotent Stem CellsRNA, Long NoncodingRNA, UntranslatedX ChromosomeX Chromosome InactivationRNA, Long NoncodingRNA, UntranslatedXIST non-coding RNA

Identifiers

PMID21997775
PMCPMC3251695
OpenAlexW2056403943

What OpenQuestion holds

Textmetadata
LicenceTDM
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.