Evidence map›Paper›PMID 33276684›Full record

ArticleInternational journal of molecular sciences2020

Length Polymorphism and Methylation Status of UPS29 Minisatellite of the

Irina O Suchkova, Elena V Borisova, Eugene L Patkin

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
1.6field-weighted citation impact, top 15% 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

3 citing papers in PubMed, 11 citations in OpenAlex.

  1. Review
  2. Complexity in Genetic Epilepsies: A Comprehensive Review.International journal of molecular sciences · 2023
    Review
  3. Article
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

3 authors at 2 institutions in 1 country.

Irina O SuchkovaLaboratory of Molecular Cytogenetics of Mammalian Development, Department of Molecular Genetics, Institute of Experimental Medicine of the Russian Academy of Sciences, St. Petersburg 197376, Russia.ORCID 0000-0003-2127-0459
Elena V BorisovaDepartment of Neurology, Clinic of Institute of Experimental Medicine, St. Petersburg 197376, Russia.
Eugene L PatkinLaboratory of Molecular Cytogenetics of Mammalian Development, Department of Molecular Genetics, Institute of Experimental Medicine of the Russian Academy of Sciences, St. Petersburg 197376, Russia.ORCID 0000-0002-6292-4167
Russian Academy of Sciences · RUInstitute of Experimental Medicine · RU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Epilepsy is a neurological disease with different clinical forms and inter-individuals heterogeneity, which may be associated with genetic and/or epigenetic polymorphisms of tandem-repeated noncoding DNA. These polymorphisms may serve as predictive biomarkers of various forms of epilepsy. ACAP3 is the protein regulating morphogenesis of neurons and neuronal migration and is an integral component of important signaling pathways. This study aimed to carry out an association analysis of the length polymorphism and DNA methylation of the UPS29 minisatellite of the

Indexed as

DNA MethylationMinisatellite RepeatsPolymorphism, GeneticAllelesBiomarkersEpilepsyFemaleGene FrequencyGenetic Association StudiesGenetic Predisposition to DiseaseGenotypeGTPase-Activating ProteinsHumansMaleMembrane Transport ProteinsMitochondrial ProteinsACAP3 protein, humanBiomarkersGTPase-Activating ProteinsMembrane Transport ProteinsMitochondrial ProteinsACAP3Arf GAPsassociation analysisbiomarkercentaurin beta 5CENTB5DNA methylationepilepsymethyl-sensitive PCRtandem repeats length polymorphismUPS29

Identifiers

PMID33276684
PMCPMC7730309
OpenAlexW3107495957

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.