Evidence map›Paper›PMID 36212827›Full record

ArticleFrontiers in microbiology2022

First generation of multifunctional peptides derived from latarcin-3a from

Luiz Filipe Ramalho Nunes de Moraes, Patrícia Souza E Silva, Tábata Camila Pereira Leite Pereira, Thiago Antônio Almeida Rodrigues, Breno Emanuel Farias Frihling, Rosiane Andrade da Costa, Heron Fernandes Vieira Torquato, Cauê Santos Lima, Edgar Julian Paredes-Gamero, Ludovico Migliolo

Open access · goldAbstract read
In one paragraph

Article in Frontiers in microbiology, 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
1.1field-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

9 citing papers in PubMed, 9 citations in OpenAlex.

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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

10 authors at 3 institutions in 1 country.

Luiz Filipe Ramalho Nunes de MoraesS-Inova Biotech, Programa de Pós-Graduação em Biotecnologia, Universidade Católica Dom Bosco, Campo Grande, MS, Brazil.
Patrícia Souza E SilvaS-Inova Biotech, Programa de Pós-Graduação em Biotecnologia, Universidade Católica Dom Bosco, Campo Grande, MS, Brazil.
Tábata Camila Pereira Leite PereiraS-Inova Biotech, Programa de Pós-Graduação em Biotecnologia, Universidade Católica Dom Bosco, Campo Grande, MS, Brazil.
Thiago Antônio Almeida RodriguesS-Inova Biotech, Programa de Pós-Graduação em Biotecnologia, Universidade Católica Dom Bosco, Campo Grande, MS, Brazil.
Breno Emanuel Farias FrihlingS-Inova Biotech, Programa de Pós-Graduação em Biotecnologia, Universidade Católica Dom Bosco, Campo Grande, MS, Brazil.
Rosiane Andrade da CostaPrograma de Pós-Graduação em Ciências Genômica e Biotecnologia, Universidade Católica de Brasília, Brasília, DF, Brazil.
Heron Fernandes Vieira TorquatoPrograma de Pós-Graduação em Biotecnologia, Universidade Federal de Mato Grosso do Sul, Campo Grande, MS, Brazil.
Cauê Santos LimaPrograma de Pós-Graduação em Biotecnologia, Universidade Federal de Mato Grosso do Sul, Campo Grande, MS, Brazil.
Edgar Julian Paredes-GameroPrograma de Pós-Graduação em Biotecnologia, Universidade Federal de Mato Grosso do Sul, Campo Grande, MS, Brazil.
Ludovico MiglioloS-Inova Biotech, Programa de Pós-Graduação em Biotecnologia, Universidade Católica Dom Bosco, Campo Grande, MS, Brazil.
Universidade Católica Dom Bosco · BRUniversidade Federal de Mato Grosso do Sul · BRUniversidade Católica de Brasília · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The need for discovering new compounds that can act selectively on pathogens is becoming increasingly evident, given the number of deaths worldwide due to bacterial infections or tumor cells. New multifunctional biotechnological tools are being sought, including compounds present in spider venoms, which have high biotechnological potential. The present work aims to perform the rational design and functional evaluation of synthetic peptides derived from

Indexed as

antimicrobial peptidesantitumordrug designresistant bacteriaspider

Identifiers

PMID36212827
PMCPMC9532841
OpenAlexW4296744718

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.