Evidence map›Paper›PMID 41373738›Full record

ArticleInternational journal of molecular sciences2025

Role of the

Vinícius Santiago Dos Santos, Lucas Silva Mello, Luiz Felipe Azevedo Marques, Luana Rodrigues Silva, Carmen Sílvia Bertuzzo, José Dirceu Ribeiro, Fernando Augusto Lima Marson

Abstract read
In one paragraph

Article in International journal of molecular sciences, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

7 authors.

Vinícius Santiago Dos SantosLaboratory of Molecular Biology and Genetics, Postgraduate Program of Health Sciences, Postgraduate Program of Health Data Science, University of São Francisco (Universidade São Francisco-USF), Bragança Paulista 12916-900, SP, Brazil.ORCID 0009-0000-9549-6069
Lucas Silva MelloLaboratory of Molecular Biology and Genetics, Postgraduate Program of Health Sciences, Postgraduate Program of Health Data Science, University of São Francisco (Universidade São Francisco-USF), Bragança Paulista 12916-900, SP, Brazil.ORCID 0009-0006-9920-5058
Luiz Felipe Azevedo MarquesLaboratory of Molecular Biology and Genetics, Postgraduate Program of Health Sciences, Postgraduate Program of Health Data Science, University of São Francisco (Universidade São Francisco-USF), Bragança Paulista 12916-900, SP, Brazil.ORCID 0009-0008-5494-2171
Luana Rodrigues SilvaLaboratory of Molecular Biology and Genetics, Postgraduate Program of Health Sciences, Postgraduate Program of Health Data Science, University of São Francisco (Universidade São Francisco-USF), Bragança Paulista 12916-900, SP, Brazil.ORCID 0009-0003-7825-3761
Carmen Sílvia BertuzzoDepartment of Pediatrics, University of Campinas (Universidade de Campinas-Unicamp), Campinas 13083-970, SP, Brazil.ORCID 0000-0002-2813-2887
José Dirceu RibeiroDepartment of Pediatrics, University of Campinas (Universidade de Campinas-Unicamp), Campinas 13083-970, SP, Brazil.ORCID 0000-0002-3387-5642
Fernando Augusto Lima MarsonLaboratory of Molecular Biology and Genetics, Postgraduate Program of Health Sciences, Postgraduate Program of Health Data Science, University of São Francisco (Universidade São Francisco-USF), Bragança Paulista 12916-900, SP, Brazil.ORCID 0000-0003-4955-4234

Funding

Fundação de Amparo à Pesquisa do Estado de São Paulo 2024/20061-9Fundação de Amparo à Pesquisa do Estado de São Paulo 2024/2055-9National Council for Scientific and Technological Development 305906/2024-0National Council for Scientific and Technological Development 88887.823904/2023-00
6 · The paper itself

Abstract

Cystic fibrosis (CF) is a rare genetic disease caused by pathogenic variants in the

Indexed as

ADAM ProteinsCystic FibrosisLungPolymorphism, Single NucleotideAdolescentAdultChildCross-Sectional StudiesCystic Fibrosis Transmembrane Conductance RegulatorFemaleGenetic Predisposition to DiseaseGenotypeHumansMaleRespiratory Function TestsYoung AdultADAM33 protein, humanADAM ProteinsCFTR protein, humanCystic Fibrosis Transmembrane Conductance Regulatorairway remodelingcystic fibrosis phenotypegeneticgenetic association studiesmodifier genespolymorphismpulmonary function tests

Identifiers

PMID41373738
PMCPMC12692732

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.