Evidence map›Paper›PMID 38892284›Full record

ArticleInternational journal of molecular sciences2024

Genetic Alterations of

Brunna Letícia Olivera Santana, Mariana Braccialli de Loyola, Ana Cristina Moura Gualberto, Fabio Pittella-Silva

Abstract read
PubMed Full text at PMC Publisher
In one paragraph

Article in International journal of molecular sciences, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Identification of Epigenetic Regulator-Associated Genes in Keloid Disease Through Integrated Bulk and Single-Cell Transcriptomics With RT-qPCR Validation.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2026
    Article
  2. Review
  3. Article
  4. 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

4 authors.

Brunna Letícia Olivera SantanaLaboratory of Molecular Pathology of Cancer, Faculty of Healthy Sciences, University of Brasília, Federal District, Brasília 70910-900, Brazil.
Mariana Braccialli de LoyolaLaboratory of Molecular Pathology of Cancer, Faculty of Healthy Sciences, University of Brasília, Federal District, Brasília 70910-900, Brazil.ORCID 0000-0002-7816-764X
Ana Cristina Moura GualbertoLaboratory of Molecular Pathology of Cancer, Faculty of Healthy Sciences, University of Brasília, Federal District, Brasília 70910-900, Brazil.
Fabio Pittella-SilvaLaboratory of Molecular Pathology of Cancer, Faculty of Healthy Sciences, University of Brasília, Federal District, Brasília 70910-900, Brazil.ORCID 0000-0002-9644-7098

Funding

Foundation for Research Support of the Federal District 00193-00001029/2021-95 and 00193-00002146/2023-38
6 · The paper itself

Abstract

SMYD4 is a member of the SMYD family that has lysine methyltransferase function. Little is known about the roles of

Indexed as

MutationNeoplasmsBiomarkers, TumorDNA Copy Number VariationsGene Expression Regulation, NeoplasticHistone-Lysine N-MethyltransferaseHumansBiomarkers, TumorHistone-Lysine N-Methyltransferaseepigeneticsin silico analysisprotein methyltransferaseSMYD4SMYD familysolid tumors

Identifiers

PMID38892284
PMCPMC11172816

What OpenQuestion holds

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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.