Evidence map›Paper›PMID 32335893›Full record

ArticleBritish journal of pharmacology2020

B

Bruna da Silva Soley, Leonardo Martins Silva, Daniel Augusto Gasparin Bueno Mendes, André Báfica, João Bosco Pesquero, Michael Bader, Deborah A Witherden, Wendy L Havran, João B Calixto, Michel Fleith Otuki and 1 more

Open access · bronzeAbstract read
In one paragraph

Article in British journal of pharmacology, 2020. 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
0.8field-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, 15 citations in OpenAlex.

  1. Review
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  4. γδ T cells: origin and fate, subsets, diseases and immunotherapy.Signal transduction and targeted therapy · 2023
    Review
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  7. BBritish journal of pharmacology · 2020
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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

11 authors at 5 institutions in 3 countries.

Bruna da Silva SoleyDepartment of Pharmacology, Federal University of Parana, Curitiba, Brazil.
Leonardo Martins SilvaDepartment of Biophysics, Federal University of São Paulo, São Paulo, Brazil.
Daniel Augusto Gasparin Bueno MendesDepartment of Microbiology, Immunology and Parasitology, Federal University of Santa Catarina, Florianópolis, Brazil.
André BáficaDepartment of Microbiology, Immunology and Parasitology, Federal University of Santa Catarina, Florianópolis, Brazil.
João Bosco PesqueroDepartment of Biophysics, Federal University of São Paulo, São Paulo, Brazil.
Michael BaderMax Delbrück Center for Molecular Medicine (MDC), Berlin, Germany.
Deborah A WitherdenImmunology and Microbiology, Scripps Research Institute, La Jolla, California, USA.
Wendy L HavranImmunology and Microbiology, Scripps Research Institute, La Jolla, California, USA.
João B CalixtoCenter of Innovation and Preclinical Studies (CIENP), Florianópolis, Brazil.
Michel Fleith OtukiDepartment of Pharmacology, Federal University of Parana, Curitiba, Brazil.
Daniela Almeida CabriniDepartment of Pharmacology, Federal University of Parana, Curitiba, Brazil.
Universidade Federal do Paraná · BRScripps Research Institute · USUniversidade Federal de Santa Catarina · BRUniversidade Federal de São Paulo · BRCharité - Universitätsmedizin Berlin · DE

Funding

Conselho Nacional de Desenvolvimento Científico e Tecnológico 157002/2018-7Conselho Nacional de Desenvolvimento Científico e Tecnológico 203667/2018-2Conselho Nacional de Desenvolvimento Científico e Tecnológico 445822/2014-7INCT-INOVAMED 465430/2014-7
6 · The paper itself

Abstract

background and purposeThe entire kallikrein-kinin system is present in the skin, and it is thought to exert a relevant role in cutaneous diseases, including psoriasis. The present study was designed to evaluate the relevance of kinin receptors in the development and progression of a model of psoriasis in mice. EXPERIMENTAL APPROACH: The effects of kinin B KEY

resultsBoth kinin receptors were up-regulated following 6 days of imiquimod treatment. Kinin B CONCLUSIONS AND IMPLICATIONS: Kinins exerted critical roles in imiquimod-induced psoriasis. Both B

Indexed as

KininsPsoriasisAnimalsCD8-Positive T-LymphocytesMiceMice, Inbred C57BLReceptor, Bradykinin B1Receptor, Bradykinin B2KininsReceptor, Bradykinin B1Receptor, Bradykinin B2

Identifiers

PMID32335893
PMCPMC7348090
OpenAlexW3017797134

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.