Evidence map›Paper›PMID 34950447›Full record

ArticleToxicology research2021

Towards a reporting guideline for developmental and reproductive toxicology testing in

Monique van der Voet, Marc Teunis, Johanna Louter-van de Haar, Nienke Stigter, Diksha Bhalla, Martijn Rooseboom, Kimberley E Wever, Cyrille Krul, Raymond Pieters, Marjolein Wildwater and 1 more

Open access · hybridAbstract read
In one paragraph

Article in Toxicology research, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.4field-weighted citation impact, top 46% 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

4 citing papers in PubMed, 11 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Reproductive-Toxicity-Related Endpoints inJournal of developmental biology · 2023
    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 5 institutions in 3 countries.

Monique van der VoetVivaltes, 1704 NA, Heerhugowaard the Netherlands.
Marc TeunisUtrecht University of Applied Sciences, Innovative testing in Life Sciences & Chemistry, 3584 CH, Utrecht, the Netherlands.
Johanna Louter-van de HaarUtrecht University of Applied Sciences, Innovative testing in Life Sciences & Chemistry, 3584 CH, Utrecht, the Netherlands.
Nienke StigterUtrecht University of Applied Sciences, Innovative testing in Life Sciences & Chemistry, 3584 CH, Utrecht, the Netherlands.
Diksha BhallaKU Leuven, Centre of Microbial and Plant Genetics, Faculty of Bioscience Engineering, 3001, Leuven, Belgium.
Martijn RooseboomToxicology group Shell International B.V., 2596 HR, The Hague, the Netherlands.
Kimberley E WeverRadboud University Medical Center, Radboud Institute for Health Sciences, Department for Health Evidence, 6525 GA, Nijmegen, the Netherlands.
Cyrille KrulUtrecht University of Applied Sciences, Innovative testing in Life Sciences & Chemistry, 3584 CH, Utrecht, the Netherlands.
Raymond PietersUtrecht University of Applied Sciences, Innovative testing in Life Sciences & Chemistry, 3584 CH, Utrecht, the Netherlands.
Marjolein WildwaterVivaltes, 1704 NA, Heerhugowaard the Netherlands.
Vera van NoortKU Leuven, Centre of Microbial and Plant Genetics, Faculty of Bioscience Engineering, 3001, Leuven, Belgium.ORCID https://orcid.org/0000-0002-8436-6602
University of Applied Sciences Utrecht · NLKU Leuven · BELeiden University · NLRadboud University Nijmegen · NLShell (Netherlands) · NL

Funding

National Centre for the Replacement, Refinement and Reduction of Animals in Research NC/C012103/1National Centre for the Replacement, Refinement and Reduction of Animals in Research NC/C012202/1National Centre for the Replacement, Refinement and Reduction of Animals in Research NC/C017101/1
6 · The paper itself

Abstract

Implementation of reliable methodologies allowing Reduction, Refinement, and Replacement (3Rs) of animal testing is a process that takes several decades and is still not complete. Reliable methods are essential for regulatory hazard assessment of chemicals where differences in test protocol can influence the test outcomes and thus affect the confidence in the predictive value of the organisms used as an alternative for mammals. Although test guidelines are common for mammalian studies, they are scarce for non-vertebrate organisms that would allow for the 3Rs of animal testing. Here, we present a set of 30 reporting criteria as the basis for such a guideline for Developmental and Reproductive Toxicology (DART) testing in the nematode

Indexed as

developmental and reproductive toxicology (DART)new approach methodologies (NAMs)reductionrefinement and replacement (3Rs)

Identifiers

PMID34950447
PMCPMC8692742
OpenAlexW4200196663

What OpenQuestion holds

Textmetadata
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.