Evidence map›Paper›PMID 22669657›Full record

ArticleMethods in molecular biology (Clifton, N.J.)2012

Caenorhabditis elegans as a model in developmental toxicology.

Windy A Boyd, Marjolein V Smith, Jonathan H Freedman

Open access · greenAbstract read
In one paragraph

Article in Methods in molecular biology (Clifton, N.J.), 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 84 papers.

0numbers the graph read from it
0cells of the map it votes in
84citing papers in PubMed
2.7field-weighted citation impact, top 13% 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

84 citing papers in PubMed, 155 citations in OpenAlex.

  1. Article
  2. DivergenteLife · 2026
    Article
  3. Article
  4. Review
  5. Natural variation suggests candidate genes underlying Caenorhabditis elegans susceptibility to diverse toxicants.Toxicological sciences : an official journal of the Society of Toxicology · 2026
    Article
  6. Progeny effects of rotenone exposure depend on parental toxicity.Toxicological sciences : an official journal of the Society of Toxicology · 2026
    Article
  7. Article
  8. High-Throughput Toxicity Screening withEnvironmental science & technology · 2026
    Review
  9. Article
  10. Natural variation suggests candidate genes underlyingbioRxiv : the preprint server for biology · 2025
    Article
  11. Article
  12. Article
  13. Article
  14. Screening for toxicity of azole fungicides inmicroPublication biology · 2025
    Article
  15. IntegratingFrontiers in pharmacology · 2025
    Article
  16. Article
  17. Review
  18. Review
  19. Article
  20. Quantitative tests of albendazole resistance in beta-tubulin mutants.bioRxiv : the preprint server for biology · 2024
    Article

24 more citing papers are in PubMed but not listed here.

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 2 institutions in 1 country.

Windy A BoydBiomolecular Screening Branch, National Toxicology Program, National Institute of Environmental Health Sciences, NIH, Research Triangle Park, NC, USA.
Marjolein V Smith
Jonathan H Freedman
National Institute of Environmental Health Sciences · USSRA International (United States) · US

Funding

NTP MediumThroughput C. elegans Screening FacilityZIAES102046 · NIEHS · NATIONAL INSTITUTE OF ENVIRONMENTAL HEALTH SCIENCES · PI FREEDMAN, JONATHAN H · 2009 to 2013
$13.6M
Comparative Genomic Responses to Environmental StressorsZIAES102045 · NIEHS · NATIONAL INSTITUTE OF ENVIRONMENTAL HEALTH SCIENCES · PI FREEDMAN, JONATHAN H · 2009 to 2014
$6.9M
NTP High Throughput C. elegans Screening CoreZ01ES102046 · NIEHS · NATIONAL INSTITUTE OF ENVIRONMENTAL HEALTH SCIENCES · PI FREEDMAN, JONATHAN H · 2006 to 2008
$3.1M
Intramural NIH HHS Z01 ES102046Intramural NIH HHS ZIA ES102045Intramural NIH HHS ZIA ES102046
6 · The paper itself

Abstract

A number of practical advantages have made the nematode Caenorhabditis elegans a useful model for genetic and developmental biological research. These same advantages, along with conservation of disease and stress response pathways, availability of mutant and transgenic strains, and wealth of biological information, have led to the increased use of C. elegans in toxicological studies. Although the potential to study the mechanisms of developmental toxicology in C. elegans is promising, embryonic and larval growth tests to identify compounds that affect the nematode have remained the primary use of C. elegans in developmental toxicology. Here, we describe a C. elegans larval growth and development assay for medium- and high-throughput screening using the COPAS Biosort flow cytometer and provide descriptions of the data and subsequent analysis.

Indexed as

Disease Models, AnimalAnimalsCadmium ChlorideCaenorhabditis elegansCulture TechniquesHumansLarvaTeratogensTeratologyToxicity TestsCadmium ChlorideTeratogens

Identifiers

PMID22669657
PMCPMC3513774
OpenAlexW1539869680

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.