Evidence map›Paper›PMID 25045544›Full record

ArticleCase reports in dentistry2014

Amelogenesis imperfecta and screening of mutation in amelogenin gene.

Fernanda Veronese Oliveira, Carla Vecchione Gurgel, Tatiana Yuriko Kobayashi, Thiago José Dionísio, Lucimara Teixeira Neves, Carlos Ferreira Santos, Maria Aparecida Andrade Moreira Machado, Thais Marchini Oliveira

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PubMed Full text at PMC Publisher
In one paragraph

Article in Case reports in dentistry, 2014. 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
0.3field-weighted citation impact, top 40% 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

0 citing papers in PubMed, 4 citations in OpenAlex.

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

8 authors at 1 institution in 1 country.

Fernanda Veronese OliveiraDepartment of Pediatric Dentistry, Orthodontics and Community Health, Bauru School of Dentistry, University of São Paulo, Alameda Octávio Pinheiro Brisolla, No. 9-75, 17012-901 Bauru, SP, Brazil.
Carla Vecchione GurgelDepartment of Pediatric Dentistry, Orthodontics and Community Health, Bauru School of Dentistry, University of São Paulo, Alameda Octávio Pinheiro Brisolla, No. 9-75, 17012-901 Bauru, SP, Brazil.
Tatiana Yuriko KobayashiDepartment of Pediatric Dentistry, Orthodontics and Community Health, Bauru School of Dentistry, University of São Paulo, Alameda Octávio Pinheiro Brisolla, No. 9-75, 17012-901 Bauru, SP, Brazil.
Thiago José DionísioDepartment of Biological Sciences, Bauru School of Dentistry, University of São Paulo, Alameda Octávio Pinheiro Brisolla, No. 9-75, 17012-901 Bauru, SP, Brazil.
Lucimara Teixeira NevesDepartment of Biological Sciences, Bauru School of Dentistry, University of São Paulo, Alameda Octávio Pinheiro Brisolla, No. 9-75, 17012-901 Bauru, SP, Brazil ; Hospital for the Rehabilitation of Craniofacial Anomalies, University of São Paulo, Rua Silvio Marchione, No. 3-20, 17012-900 Bauru, SP, Brazil.
Carlos Ferreira SantosDepartment of Biological Sciences, Bauru School of Dentistry, University of São Paulo, Alameda Octávio Pinheiro Brisolla, No. 9-75, 17012-901 Bauru, SP, Brazil.
Maria Aparecida Andrade Moreira MachadoDepartment of Pediatric Dentistry, Orthodontics and Community Health, Bauru School of Dentistry, University of São Paulo, Alameda Octávio Pinheiro Brisolla, No. 9-75, 17012-901 Bauru, SP, Brazil.
Thais Marchini OliveiraDepartment of Pediatric Dentistry, Orthodontics and Community Health, Bauru School of Dentistry, University of São Paulo, Alameda Octávio Pinheiro Brisolla, No. 9-75, 17012-901 Bauru, SP, Brazil ; Hospital for the Rehabilitation of Craniofacial Anomalies, University of São Paulo, Rua Silvio Marchione, No. 3-20, 17012-900 Bauru, SP, Brazil.ORCID 0000-0003-3460-3144
Universidade de São Paulo · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The aim of this study was to report the clinical findings and the screening of mutations of amelogenin gene of a 7-year-old boy with amelogenesis imperfecta (AI). The genomic DNA was extracted from saliva of patient and his family, followed by PCR and direct DNA sequencing. The c.261C>T mutation was found in samples of mother, father, and brother, but the mutation was not found in the sequence of the patient. This mutation is a silent mutation and a single-nucleotide polymorphism (rs2106416). Thus, it is suggested that the mutation found was not related to the clinical presence of AI. Further research is necessary to examine larger number of patients and genes related to AI.

Identifiers

PMID25045544
PMCPMC4089840
OpenAlexW2029983017

What OpenQuestion holds

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Registered trials

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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.