Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Single-Nucleotide Variants in microRNAs Sequences or in their Target Genes Might Influence the Risk of Epilepsy: A Review.

Cellular and molecular neurobiology - 1 Aug 2022

Buainain Renata Parissi, Boschiero Matheus Negri, Camporeze Bruno, de Aguiar Paulo Henrique Pires, Marson Fernando Augusto Lima, Ortega Manoela Marques

Abstract excerpt

Single-nucleotide variant (SNV) is a single base mutation at a specific location in the genome and may play an import role in epilepsy pathophysiology. The aim of this study was to review case-control studies that have investigated the relationship between SNVs within microRNAs (miRs) sequences or in their target genes and epilepsy susceptibility from January 1, 2010 to October 31, 2020. Nine case-control studies...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Case-Control Studies
Share to Epilepsy

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Gene Frequency

Share to Genetic Predisposition to Disease

Share to Genotype

Share to MicroRNAs

Share to Nucleotides

Share to Polymorphism, Single Nucleotide

Source

Identifiers

PMID: 33666796
DOI: 10.1007/s10571-021-01058-7

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Single-Nucleotide Variants in microRNAs Sequences or in their Target Genes Might Influence the Risk of Epilepsy: A Review.PMID 33666796Read ↗

The single nucleotide variant n.60G>C in the microRNA-146a associated with susceptibility to drug-resistant epilepsy.Semantic proximity Read ↗

Single-Base Gene Variants in MIR-146A and SCN1A Genes Related to the Epileptogenic Process in Drug-Responsive and Drug-Resistant Temporal Lobe Epilepsy-A Preliminary Study in a Brazilian Cohort Sample.Semantic proximity Read ↗

A functional polymorphism of the microRNA-146a gene is associated with susceptibility to drug-resistant epilepsy and seizures frequency.Semantic proximity Read ↗

A functional SNP in miR-146a and genetic susceptibility to drug-resistant epilepsy.Semantic proximity Read ↗

Association of the genetic polymorphisms in pre-microRNAs with risk of childhood epilepsy in a Chinese population.Semantic proximity Read ↗

Association Between Single-Nucleotide Polymorphism (SNP) in miR-146a, miR-196a2, and miR-499 and Risk of Ischemic Stroke: A Meta-Analysis.Semantic proximity Read ↗

Association of Tag SNPs and Rare CNVs of the MIR155HG/miR-155 Gene with Epilepsy in the Chinese Han Population.Semantic proximity Read ↗

A functional SNP catalog of overlapping miRNA-binding sites in genes implicated in prion disease and other neurodegenerative disorders.Semantic proximity Read ↗

Genome-wide identification of m6A-associated single nucleotide polymorphisms in complex diseases of nervous system.Semantic proximity Read ↗

Associations of microRNA single nucleotide polymorphisms and disease risk and pathophysiology.Semantic proximity Read ↗

Association between the three functional miR-146a single-nucleotide polymorphisms, rs2910164, rs57095329, and rs2431697, and autoimmune disease susceptibility: A meta-analysis.Semantic proximity Read ↗

Relationship between genetic variant in pre-microRNA-146a and genetic predisposition to temporal lobe epilepsy: a case-control study.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.