Evidence map›Paper›PMID 35159383›Full record

ReviewCells2022

The Biogenesis of miRNAs and Their Role in the Development of Amyotrophic Lateral Sclerosis.

Jinmeng Liu, Fenghua Zhou, Yingjun Guan, Fandi Meng, Zhenhan Zhao, Qi Su, Weiwei Bao, Xuemei Wang, Jiantao Zhao, Zijun Huo and 4 more

Open access · goldAbstract readReview
In one paragraph

Review in Cells, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed, 1 pooled it
5.1field-weighted citation impact, top 4% 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

32 citing papers in PubMed, 1 synthesis or guideline pooled it, 42 citations in OpenAlex.

  1. Pooled it
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  17. Role of miRNAs in Brain Development.MicroRNA (Shariqah, United Arab Emirates) · 2024
    Review
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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

14 authors at 2 institutions in 2 countries.

Jinmeng LiuLaboratory of Biochemistry and Molecular Biology, School of Basic Medical Sciences, Weifang Medical University, Weifang 261053, China.ORCID 0000-0002-6041-2723
Fenghua ZhouNeurologic Disorders and Regenerative Repair Laboratory, Weifang Medical University, Weifang 261053, China.
Yingjun GuanNeurologic Disorders and Regenerative Repair Laboratory, Weifang Medical University, Weifang 261053, China.
Fandi MengDepartment of Histology and Embryology, School of Basic Medical Sciences, Weifang Medical University, Weifang 261053, China.
Zhenhan ZhaoDepartment of Histology and Embryology, School of Basic Medical Sciences, Weifang Medical University, Weifang 261053, China.
Qi SuDepartment of Histology and Embryology, School of Basic Medical Sciences, Weifang Medical University, Weifang 261053, China.
Weiwei BaoDepartment of Histology and Embryology, School of Basic Medical Sciences, Weifang Medical University, Weifang 261053, China.
Xuemei WangDepartment of Histology and Embryology, School of Basic Medical Sciences, Weifang Medical University, Weifang 261053, China.
Jiantao ZhaoDepartment of Histology and Embryology, School of Basic Medical Sciences, Weifang Medical University, Weifang 261053, China.
Zijun HuoDepartment of Histology and Embryology, School of Basic Medical Sciences, Weifang Medical University, Weifang 261053, China.
Lingyun ZhangNeurologic Disorders and Regenerative Repair Laboratory, Weifang Medical University, Weifang 261053, China.
Shuanhu ZhouDepartment of Orthopedic Surgery, Brigham and Women's Hospital, Harvard Medical School, Boston, MA 02115, USA.ORCID 0000-0003-4745-5347
Yanchun ChenNeurologic Disorders and Regenerative Repair Laboratory, Weifang Medical University, Weifang 261053, China.ORCID 0000-0003-4740-9228
Xin WangDepartment of Neurosurgery, Brigham and Women's Hospital, Harvard Medical School, Boston, MA 02115, USA.
Weifang Medical University · CNBrigham and Women's Hospital · US

Funding

Key Project of Shandong Province Higher Educational Science and Technology Program of China J18KZ013National Natural Science Foundation of China 81871006Shandong Province Natural Science Foundation of China ZR2020MH150 and ZR2020MH149Support Program for Youth Innovation Technology in Colleges and Universities of Shandong Province of China Grant No. 2019KJK004The Brigham and Women's Hospital BRI Fund to Sustain Research Excellence (to X.W.) N/A
6 · The paper itself

Abstract

Amyotrophic lateral sclerosis (ALS) is a neurodegenerative disease that affects upper and lower motor neurons. As there is no effective treatment for ALS, it is particularly important to screen key gene therapy targets. The identifications of microRNAs (miRNAs) have completely changed the traditional view of gene regulation. miRNAs are small noncoding single-stranded RNA molecules involved in the regulation of post-transcriptional gene expression. Recent advances also indicate that miRNAs are biomarkers in many diseases, including neurodegenerative diseases. In this review, we summarize recent advances regarding the mechanisms underlying the role of miRNAs in ALS pathogenesis and its application to gene therapy for ALS. The potential of miRNAs to target diverse pathways opens a new avenue for ALS therapy.

Indexed as

Amyotrophic Lateral SclerosisMicroRNAsNeurodegenerative DiseasesBiomarkersHumansMotor NeuronsBiomarkersMicroRNAsamyotrophic lateral sclerosisbiomarkermiRNAsneurodegenerationnoncoding RNAtherapy

Identifiers

PMID35159383
PMCPMC8833997
OpenAlexW4210825399

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.