Evidence map›Paper›PMID 28634472›Full record

ArticleFrontiers in microbiology2017

Antifungal Activity against Filamentous Fungi of Ts1, a Multifunctional Toxin from

Welligton M Santussi, Karla C F Bordon, Ana P N Rodrigues Alves, Camila T Cologna, Suraia Said, Eliane C Arantes

Open access · goldAbstract read
PubMed Full text at PMC Publisher
In one paragraph

Article in Frontiers in microbiology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
0.9field-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

8 citing papers in PubMed, 22 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Review
  5. Article
  6. Antifungal activity ofToxicon: X · 2022
    Article
  7. Article
  8. 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

6 authors at 1 institution in 1 country.

Welligton M SantussiLaboratory of Animal Toxins, Department of Physics and Chemistry, School of Pharmaceutical Sciences of Ribeirão Preto, University of São PauloRibeirão Preto, Brazil.
Karla C F BordonLaboratory of Animal Toxins, Department of Physics and Chemistry, School of Pharmaceutical Sciences of Ribeirão Preto, University of São PauloRibeirão Preto, Brazil.
Ana P N Rodrigues AlvesLaboratory of Animal Toxins, Department of Physics and Chemistry, School of Pharmaceutical Sciences of Ribeirão Preto, University of São PauloRibeirão Preto, Brazil.
Camila T ColognaLaboratory of Animal Toxins, Department of Physics and Chemistry, School of Pharmaceutical Sciences of Ribeirão Preto, University of São PauloRibeirão Preto, Brazil.
Suraia SaidLaboratory of Industrial Enzymology, Department of Pharmaceutical Sciences, School of Pharmaceutical Sciences of Ribeirão Preto, University of São PauloRibeirão Preto, Brazil.
Eliane C ArantesLaboratory of Animal Toxins, Department of Physics and Chemistry, School of Pharmaceutical Sciences of Ribeirão Preto, University of São PauloRibeirão Preto, Brazil.
Universidade de São Paulo · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Antimicrobial peptides (AMPs) are ubiquitous and multipotent components of the innate immune defense arsenal used by both prokaryotic and eukaryotic organisms. The search for new AMPs has increased in recent years, due to the growing development of microbial resistance to therapeutical drugs. In this work, we evaluate the effects of

Indexed as

antifungal drugsantimicrobial peptidesantimycoticcysteine-rich antifungal proteinsdefensinsdrosomycinfungiTityus serrulatus

Identifiers

PMID28634472
PMCPMC5459920
OpenAlexW2622229804

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.