Evidence map›Paper›PMID 34435363›Full record

ArticleJournal of anatomy2022

The venous system of E14.5 mouse embryos-reference data and examples for diagnosing malformations in embryos with gene deletions.

Stefan H Geyer, Barbara Maurer-Gesek, Lukas F Reissig, Julia Rose, Fabrice Prin, Robert Wilson, Antonella Galli, Catherine Tudor, Jacqueline K White, Timothy J Mohun and 1 more

Open access · hybridAbstract read
In one paragraph

Article in Journal of anatomy, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
0.8field-weighted citation impact, top 29% 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

9 citing papers in PubMed, 12 citations in OpenAlex.

  1. Article
  2. Article
  3. Three-dimensional structural and metric characterisation of cardioids.Frontiers in cell and developmental biology · 2024
    Article
  4. Review
  5. Article
  6. Author reply.Journal of anatomy · 2022
    Article
  7. Article
  8. Article
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

11 authors at 3 institutions in 2 countries.

Stefan H GeyerDivision of Anatomy, MIC, BioImaging Austria/CMI, Medical University of Vienna, Vienna, Austria.ORCID 0000-0003-2283-4439
Barbara Maurer-GesekDivision of Anatomy, MIC, BioImaging Austria/CMI, Medical University of Vienna, Vienna, Austria.
Lukas F ReissigDivision of Anatomy, MIC, BioImaging Austria/CMI, Medical University of Vienna, Vienna, Austria.ORCID 0000-0001-5833-8176
Julia RoseDivision of Anatomy, MIC, BioImaging Austria/CMI, Medical University of Vienna, Vienna, Austria.
Fabrice PrinCrick Advanced Light Microscopy Facility, The Francis Crick Institute, London, UK.
Robert WilsonThe Francis Crick Institute, London, UK.
Antonella GalliWellcome Trust Sanger Institute, Wellcome Genome Campus, Cambridge, UK.
Catherine TudorWellcome Trust Sanger Institute, Wellcome Genome Campus, Cambridge, UK.
Jacqueline K WhiteWellcome Trust Sanger Institute, Wellcome Genome Campus, Cambridge, UK.
Timothy J MohunThe Francis Crick Institute, London, UK.
Wolfgang J WeningerDivision of Anatomy, MIC, BioImaging Austria/CMI, Medical University of Vienna, Vienna, Austria.ORCID 0000-0003-0575-0073
Medical University of Vienna · ATThe Francis Crick Institute · GBWellcome Sanger Institute · GB

Funding

Cancer Research UK FC001117Medical Research Council FC001117Wellcome TrustWellcome Trust 100160Wellcome Trust FC001117
6 · The paper itself

Abstract

Approximately one-third of randomly produced knockout mouse lines produce homozygous offspring, which fail to survive the perinatal period. The majority of these die around or after embryonic day (E)14.5, presumably from cardiovascular insufficiency. For diagnosing structural abnormalities underlying death and diseases and for researching gene function, the phenotype of these individuals has to be analysed. This makes the creation of reference data, which define normal anatomy and normal variations the highest priority. While such data do exist for the heart and arteries, they are still missing for the venous system. Here we provide high-quality descriptive and metric information on the normal anatomy of the venous system of E14.5 embryos. Using high-resolution digital volume data and 3D models from 206 genetically normal embryos, bred on the C57BL/6N background, we present precise descriptive and metric information of the venous system as it presents itself in each of the six developmental stages of E14.5. The resulting data shed new light on the maturation and remodelling of the venous system at transition of embryo to foetal life and provide a reference that can be used for detecting venous abnormalities in mutants. To explore this capacity, we analysed the venous phenotype of embryos from 7 knockout lines (Atp11a, Morc2a, 1700067K01Rik, B9d2, Oaz1, Celf4 and Coro1c). Careful comparisons enabled the diagnosis of not only simple malformations, such as dual inferior vena cava, but also complex and subtle abnormalities, which would have escaped diagnosis in the absence of detailed, stage-specific referenced data.

Indexed as

Embryo, MammalianAnimalsFemaleGene DeletionMiceMice, Inbred C57BLMice, KnockoutPhenotypePregnancyDMDDembryoHREMmousemutantphenotypingvenous system

Identifiers

PMID34435363
PMCPMC8655187
OpenAlexW3193996807

What OpenQuestion holds

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LicenceCC BY
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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.