Evidence map›Paper›PMID 23615030›Full record

ArticleOpen biology2013

A new role for muscle segment homeobox genes in mammalian embryonic diapause.

Jeeyeon Cha, Xiaofei Sun, Amanda Bartos, Jane Fenelon, Pavine Lefèvre, Takiko Daikoku, Geoff Shaw, Robert Maxson, Bruce D Murphy, Marilyn B Renfree and 1 more

Open access · goldAbstract read
In one paragraph

Article in Open biology, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
2.8field-weighted citation impact, top 9% 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

22 citing papers in PubMed, 53 citations in OpenAlex.

  1. SAV1 in Cooperation With FKBP52 Participates in Implantation.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
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  14. Homeobox genes for embryo implantation: From mouse to human.Animal models and experimental medicine · 2018
    Review
  15. Article
  16. Article
  17. Article
  18. Uterine inactivation of muscle segment homeobox (Msx) genes alters epithelial cell junction proteins during embryo implantation.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2016
    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

11 authors at 4 institutions in 3 countries.

Jeeyeon ChaDivision of Reproductive Sciences, Cincinnati Children's Research Foundation, Cincinnati, OH 45229, USA.
Xiaofei Sun
Amanda Bartos
Jane Fenelon
Pavine Lefèvre
Takiko Daikoku
Geoff Shaw
Robert Maxson
Bruce D Murphy
Marilyn B Renfree
Sudhansu K Dey
Cincinnati Children's Hospital Medical Center · USUniversité de Montréal · CAUniversity of Melbourne · AUUniversity of Southern California · US

Funding

Medical Scientist Training ProgramT32GM063483 · NIGMS · UNIVERSITY OF CINCINNATI · PI KHURANA HERSHEY, GURJIT K. · 2002 to 2022
$6.7M
Molecular signaling in uterine receptivity to implantationR01HD068524 · NICHD · CINCINNATI CHILDRENS HOSP MED CTR · PI Xiaofei Sun · 2011 to 2026
$5.3M
TWIST AND Msx2 IN BOUNDARY FORMATION AND CRANIOSYNOSTOSISR01DE016320 · NIDCR · UNIVERSITY OF SOUTHERN CALIFORNIA · PI MAXSON, ROBERT E. · 2005 to 2014
$3.9M
Endocannabinoid Signaling During Early PregnancyR37DA006668 · NIDA · VANDERBILT UNIVERSITY · PI DEY, SUDHANSU K · 2003 to 2012
$3.8M
ASPECTS OF BLASTOCYST IMPLANTATIONR37HD012304 · NICHD · VANDERBILT UNIVERSITY · PI DEY, SUDHANSU K · 1999 to 2010
$2.9M
MARIJUANA EFFECTS ON EARLY PREGNANCYR01DA006668 · NIDA · UNIVERSITY OF KANSAS MEDICAL CENTER · PI DEY, SUDHANSU K · 1990 to 2019
$2.1M
Premature Uterine Ageing and Preterm DeliveryF30AG040858 · NIA · CINCINNATI CHILDRENS HOSP MED CTR · PI CHA, JEEYEON · 2011 to 2014
$184k
ROLE OF HISTAMINE IN EARLY PREGNANCYR01HD012304 · NICHD · UNIVERSITY OF KANSAS MEDICAL CENTER · PI DEY, SUDHANSU K · 1985 to 1998
–
NIA NIH HHS F30AG040858NICHD NIH HHS HD068524NICHD NIH HHS HD12304NICHD NIH HHS R01 HD068524NIDA NIH HHS DA06668NIDCR NIH HHS R01 DE016320NIGMS NIH HHS T32 GM063483
6 · The paper itself

Abstract

Mammalian embryonic diapause is a phenomenon defined by the temporary arrest in blastocyst growth and metabolic activity within the uterus which synchronously becomes quiescent to blastocyst activation and implantation. This reproductive strategy temporally uncouples conception from parturition until environmental or maternal conditions are favourable for the survival of the mother and newborn. The underlying molecular mechanism by which the uterus and embryo temporarily achieve quiescence, maintain blastocyst survival and then resume blastocyst activation with subsequent implantation remains unknown. Here, we show that uterine expression of Msx1 or Msx2, members of an ancient, highly conserved homeobox gene family, persists in three unrelated mammalian species during diapause, followed by rapid downregulation with blastocyst activation and implantation. Mice with uterine inactivation of Msx1 and Msx2 fail to achieve diapause and reactivation. Remarkably, the North American mink and Australian tammar wallaby share similar expression patterns of MSX1 or MSX2 as in mice-it persists during diapause and is rapidly downregulated upon blastocyst activation and implantation. Evidence from mouse studies suggests that the effects of Msx genes in diapause are mediated through Wnt5a, a known transcriptional target of uterine Msx. These studies provide strong evidence that the Msx gene family constitutes a common conserved molecular mediator in the uterus during embryonic diapause to improve female reproductive fitness.

Indexed as

AnimalsBlastocystDown-RegulationEmbryo ImplantationEmbryonic DevelopmentFemaleHomeodomain ProteinsMiceMinkMSX1 Transcription FactorUterusWnt-5a ProteinWnt ProteinsHomeodomain ProteinsMsx1 protein, mouseMSX1 Transcription FactorMSX2 proteinWnt-5a ProteinWnt5a protein, mouseWnt Proteins

Identifiers

PMID23615030
PMCPMC3718335
OpenAlexW2139510123

What OpenQuestion holds

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Registered trials

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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.