Evidence map›Paper›PMID 18519804›Full record

ArticleFASEB journal : official publication of the Federation of American Societies for Experimental Biology2008

Levamisole resistance resolved at the single-channel level in Caenorhabditis elegans.

Hai Qian, Alan P Robertson, Jo Anne Powell-Coffman, Richard J Martin

Abstract read
In one paragraph

Article in FASEB journal : official publication of the Federation of American Societies for Experimental Biology, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 49 papers.

0numbers the graph read from it
0cells of the map it votes in
49citing papers in PubMed
1.2field-weighted citation impact, top 25% 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

49 citing papers in PubMed, 89 citations in OpenAlex.

  1. Article
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  5. Review
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  8. Article
  9. Praziquantel activates a native cation current inFrontiers in parasitology · 2023
    Article
  10. Allele specific PCR for a major marker of levamisole resistance in Haemonchus contortus.International journal for parasitology. Drugs and drug resistance · 2022
    Article
  11. Benzimidazoles cause lethality by inhibiting the function of Caenorhabditis elegans neuronal beta-tubulin.International journal for parasitology. Drugs and drug resistance · 2022
    Article
  12. Article
  13. An extracellular scaffolding complex confers unusual rectification upon an ionotropic acetylcholine receptor inProceedings of the National Academy of Sciences of the United States of America · 2022
    Article
  14. Article
  15. Towards the development of phytoextract based healthy ageing cognitive booster formulation, explored throughThe Nucleus : an international journal of cytology and allied topics · 2022
    Article
  16. Frontiers in toxicology · 2022
    Article
  17. Article
  18. Article
  19. Action of Carvacrol onPharmaceuticals (Basel, Switzerland) · 2021
    Article
  20. 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

4 authors at 1 institution in 1 country.

Hai QianDepartment of Biomedical Sciences, Iowa State University, Ames, IA 50011, USA.
Alan P Robertson
Jo Anne Powell-Coffman
Richard J Martin
Iowa State University · US

Funding

RESISTANCE &MODULATION OF LEVAMISOLE RECEPTOR CHANNELSR01AI047194 · NIAID · IOWA STATE UNIVERSITY · PI MARTIN, RICHARD JOHN · 2001 to 2021
$5.8M
NIAID NIH HHS R01 AI047194
6 · The paper itself

Abstract

Sydney Brenner promoted Caenorhabditis elegans as a model organism, and subsequent investigations pursued resistance to the nicotinic anthelmintic drug levamisole in C. elegans at a genetic level. These studies have advanced our understanding of genes associated with neuromuscular transmission and resistance to the antinematodal drug. In lev-8 and lev-1 mutant C. elegans, levamisole resistance is associated with reductions in levamisole-activated whole muscle cell currents. Although lev-8 and lev-1 are known to code for nicotinic acetylcholine receptor (nAChR) subunits, an explanation for why these currents get smaller is not available. In wild-type adults, nAChRs aggregate at neuromuscular junctions and are not accessible for single-channel recording. Here we describe a use of LEV-10 knockouts, in which aggregation is lost, to make in situ recordings of nAChR channel currents. Our observations provide an explanation for levamisole resistance produced by LEV-8 and LEV-1 mutants at the single-channel level.

Indexed as

Drug ResistanceAnimalsCaenorhabditis elegansCaenorhabditis elegans ProteinsIon ChannelsLevamisoleMembrane ProteinsPatch-Clamp TechniquesReceptors, NicotinicCaenorhabditis elegans ProteinsIon ChannelsLEV-10 protein, C elegansLev-1 protein, C elegansLev-8 protein, C elegansLevamisoleMembrane ProteinsReceptors, Nicotinic

Identifiers

PMID18519804
PMCPMC2518249
OpenAlexW2116394768

What OpenQuestion holds

Textmetadata
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.