Evidence map›Paper›PMID 28776665›Full record

ArticleJournal of anatomy2017

Morphology, topology and dimensions of the heart and arteries of genetically normal and mutant mouse embryos at stages S21-S23.

Stefan H Geyer, Lukas F Reissig, Markus Hüsemann, Cordula Höfle, Robert Wilson, Fabrice Prin, Dorota Szumska, Antonella Galli, David J Adams, Jacqui White and 2 more

Open access · hybridAbstract read
In one paragraph

Article in Journal of anatomy, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
0.9field-weighted citation impact, top 26% 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

12 citing papers in PubMed, 21 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Review
  6. Article
  7. Article
  8. Article
  9. Cardiac multi-scale investigation of the right and left ventricleCardiovascular diagnosis and therapy · 2020
    Review
  10. TheBiology open · 2019
    Article
  11. Article
  12. Review
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

12 authors at 4 institutions in 2 countries.

Stefan H GeyerDivision of Anatomy & MIC, Medical University of Vienna, Vienna, Austria.ORCID http://orcid.org/0000-0003-2283-4439
Lukas F ReissigDivision of Anatomy & MIC, Medical University of Vienna, Vienna, Austria.
Markus HüsemannDivision of Anatomy & MIC, Medical University of Vienna, Vienna, Austria.
Cordula HöfleDivision of Anatomy & MIC, Medical University of Vienna, Vienna, Austria.
Robert WilsonThe Francis Crick Institute, London, UK.
Fabrice PrinThe Francis Crick Institute, London, UK.
Dorota SzumskaWellcome Trust Centre for Human Genetics, Oxford, UK.
Antonella GalliWellcome Trust Sanger Institute, Cambridge, UK.
David J AdamsWellcome Trust Sanger Institute, Cambridge, UK.
Jacqui WhiteWellcome Trust Sanger Institute, Cambridge, UK.
Timothy J MohunThe Francis Crick Institute, London, UK.
Wolfgang J WeningerDivision of Anatomy & MIC, Medical University of Vienna, Vienna, Austria.
Medical University of Vienna · ATThe Francis Crick Institute · GBWellcome Sanger Institute · GBCentre for Human Genetics · GB

Funding

Wellcome Trust 100160Wellcome Trust FC001117Wellcome Trust FC001157
6 · The paper itself

Abstract

Accurate identification of abnormalities in the mouse embryo depends not only on comparisons with appropriate, developmental stage-matched controls, but also on an appreciation of the range of anatomical variation that can be expected during normal development. Here we present a morphological, topological and metric analysis of the heart and arteries of mouse embryos harvested on embryonic day (E)14.5, based on digital volume data of whole embryos analysed by high-resolution episcopic microscopy (HREM). By comparing data from 206 genetically normal embryos, we have analysed the range and frequency of normal anatomical variations in the heart and major arteries across Theiler stages S21-S23. Using this, we have identified abnormalities in these structures among 298 embryos from mutant mouse lines carrying embryonic lethal gene mutations produced for the Deciphering the Mechanisms of Developmental Disorders (DMDD) programme. We present examples of both commonly occurring abnormal phenotypes and novel pathologies that most likely alter haemodynamics in these genetically altered mouse embryos. Our findings offer a reference baseline for identifying accurately abnormalities of the heart and arteries in embryos that have largely completed organogenesis.

Indexed as

MutationAnimalsArteriesEmbryo, MammalianFemaleHeartMiceMice, Inbred C57BLMyocardiumcardiovascular systemdeciphering the mechanisms of developmental disordersembryohigh resolution episcopic microscopymousemutant

Identifiers

PMID28776665
PMCPMC5603791
OpenAlexW2743458358

What OpenQuestion holds

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LicenceCC BY
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.