Evidence map›Paper›PMID 34833137›Full record

ArticleLife (Basel, Switzerland)2021

An Episomal CRISPR/Cas12a System for Mediating Efficient Gene Editing.

Nannan Duan, Shuqing Tang, Baitao Zeng, Zhiqing Hu, Qian Hu, Lingqian Wu, Miaojin Zhou, Desheng Liang

Open access · goldAbstract read
In one paragraph

Article in Life (Basel, Switzerland), 2021. 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
0.4field-weighted citation impact, top 40% 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

4 citing papers in PubMed, 7 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  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

8 authors at 1 institution in 1 country.

Nannan DuanCenter for Medical Genetics, School of Life Sciences, Central South University, Changsha 410078, China.
Shuqing TangCenter for Medical Genetics, School of Life Sciences, Central South University, Changsha 410078, China.
Baitao ZengCenter for Medical Genetics, School of Life Sciences, Central South University, Changsha 410078, China.
Zhiqing HuCenter for Medical Genetics, School of Life Sciences, Central South University, Changsha 410078, China.
Qian HuCenter for Medical Genetics, School of Life Sciences, Central South University, Changsha 410078, China.
Lingqian WuCenter for Medical Genetics, School of Life Sciences, Central South University, Changsha 410078, China.
Miaojin ZhouCenter for Medical Genetics, School of Life Sciences, Central South University, Changsha 410078, China.ORCID 0000-0002-6636-6000
Desheng LiangCenter for Medical Genetics, School of Life Sciences, Central South University, Changsha 410078, China.
Central South University · CN

Funding

China Postdoctoral Science Foundation 2020TQ0362National Key Research and Development Program of China 2016YFC0905102National Key Research and Development Program of China 2017YFC1001802National Natural Science Foundation of China 81770200National Natural Science Foundation of China 81902150National Natural Science Foundation of China 82101957
6 · The paper itself

Abstract

(1) Background: Gene editing technology, as represented by CRISPR is a powerful tool used in biomedical science. However, the editing efficiency of such technologies, especially in induced pluripotent stem cells (iPSCs) and other types of stem cells, is low which hinders its application in regenerative medicine; (2) Methods: A gene-editing system, COE, was designed and constructed based on CRISPR/Cas12a and Orip/EBNA1, and its editing efficiency was evaluated in human embryonic kidney 293T (HEK-293T) cells with flow cytometry and restriction fragment length polymorphism (RFLP) analysis. The COE was nucleofected into iPSCs, then, the editing efficiency was verified by a polymerase chain reaction and Sanger sequencing; (3) Results: With the extension of time, COE enables the generation of up to 90% insertion or deletion rates in HEK-293T cells. Furthermore, the deletion of a 2.5 kb fragment containing Exon 51 of the dystrophin gene (

Indexed as

CRISPR/Cas12aDMDgene editingiPSCsOrip/EBNA1

Identifiers

PMID34833137
PMCPMC8620414
OpenAlexW3211702824

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.