Evidence map›Paper›PMID 31930701›Full record

ArticleJournal of cellular and molecular medicine2020

Modified level of miR-376a is associated with Parkinson's disease.

Masoud Baghi, Mahsa Rostamian Delavar, Elaheh Yadegari, Maryam Peymani, David Pozo, Mohammad Hossein Nasr-Esfahani, Kamran Ghaedi

Open access · goldAbstract read
In one paragraph

Article in Journal of cellular and molecular medicine, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed, 2 pooled it
2.2field-weighted citation impact, top 11% 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

25 citing papers in PubMed, 2 syntheses or guidelines pooled it, 37 citations in OpenAlex.

  1. The Role of miRNAs in Parkinson's Disease: A Systematic Review.International journal of molecular sciences · 2025
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  20. MiR-193b deregulation is associated with Parkinson's disease.Journal of cellular and molecular medicine · 2021
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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 at 3 institutions in 2 countries.

Masoud BaghiDepartment of Cell and Molecular Biology and Microbiology, Faculty of Biological Science and Technology, University of Isfahan, Isfahan, Iran.ORCID 0000-0001-7622-0905
Mahsa Rostamian DelavarDepartment of Cell and Molecular Biology and Microbiology, Faculty of Biological Science and Technology, University of Isfahan, Isfahan, Iran.ORCID 0000-0001-7966-3365
Elaheh YadegariDepartment of Cell and Molecular Biology and Microbiology, Faculty of Biological Science and Technology, University of Isfahan, Isfahan, Iran.ORCID 0000-0002-0513-4193
Maryam PeymaniDepartment of Cellular Biotechnology, Cell Science Research Center, Royan Institute for Biotechnology, Isfahan, Iran.ORCID 0000-0001-5075-5661
David PozoCABIMER, Andalusian Center for Molecular Biology and Regenerative Medicine, Sevilla, Spain.ORCID 0000-0002-3732-4960
Mohammad Hossein Nasr-EsfahaniDepartment of Cellular Biotechnology, Cell Science Research Center, Royan Institute for Biotechnology, Isfahan, Iran.ORCID 0000-0003-1983-3435
Kamran GhaediDepartment of Cell and Molecular Biology and Microbiology, Faculty of Biological Science and Technology, University of Isfahan, Isfahan, Iran.ORCID 0000-0002-9790-5644
Royan Institute · IRCentro Andaluz de Biología Molecular y Medicina Regenerativa · ESUniversity of Isfahan · IR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Parkinson's disease (PD) is a frequent progressive neurodegenerative disorder. Impaired mitochondrial function is a major feature of sporadic PD. Some susceptibility or causative genes detected in PD are strongly associated with mitochondrial dysfunction including PGC1α, TFAM and GSK3β. microRNAs (miRNAs) are non-coding RNAs whose altered levels are proven in disparate PD models and human brains. Therefore, the aim of this study was to detect modulations of miRs upstream of PGC1α, TFAM and GSK3β in association with PD onset and progress. In this study, a total of 33 PD subjects and 25 healthy volunteers were recruited. Candidate miRNA (miR-376a) was selected through target prediction tools and literature survey. Chronic and acute in vitro PD models were created by MPP

Indexed as

AgedApoptosisBiomarkersCase-Control StudiesCell LineCell Line, TumorDNA-Binding ProteinsDown-RegulationFemaleHumansLeukocytes, MononuclearMaleMicroRNAsMiddle AgedMitochondriaParkinson DiseaseBiomarkersDNA-Binding ProteinsMicroRNAsMIRN376C microRNA, humanPeroxisome Proliferator-Activated Receptor Gamma Coactivator 1-alphaGSK3βmiR-376amitochondrial transcription factor AParkinson's diseasePGC1α

Identifiers

PMID31930701
PMCPMC7028860
OpenAlexW3000228962

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.