Evidence map›Paper›PMID 35198566›Full record

ReviewFrontiers in cell and developmental biology2021

Strategies for High-Efficiency Mutation Using the CRISPR/Cas System.

Shuying Feng, Zilong Wang, Aifang Li, Xin Xie, Junjie Liu, Shuxuan Li, Yalan Li, Baiyan Wang, Lina Hu, Lianhe Yang and 1 more

Abstract readReview
In one paragraph

Review in Frontiers in cell and developmental biology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
–field-weighted citation impact
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

12 citing papers in PubMed.

  1. Review
  2. Review
  3. Review
  4. Optimization of a CRISPR-Cas9Frontiers in plant science · 2025
    Article
  5. Article
  6. CRISPR/Cas9: a powerful tool in colorectal cancer research.Journal of experimental & clinical cancer research : CR · 2023
    Review
  7. Review
  8. Article
  9. Article
  10. Review
  11. Article
  12. Selecting for CRISPR-Edited Knock-In Cells.International journal of molecular sciences · 2022
    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

11 authors.

Shuying FengMedical College, Henan University of Chinese Medicine, Zhengzhou, China.
Zilong WangMedical College, Henan University of Chinese Medicine, Zhengzhou, China.
Aifang LiMedical College, Henan University of Chinese Medicine, Zhengzhou, China.
Xin XieMedical College, Henan University of Chinese Medicine, Zhengzhou, China.
Junjie LiuMedical College, Henan University of Chinese Medicine, Zhengzhou, China.
Shuxuan LiMedical College, Henan University of Chinese Medicine, Zhengzhou, China.
Yalan LiMedical College, Henan University of Chinese Medicine, Zhengzhou, China.
Baiyan WangMedical College, Henan University of Chinese Medicine, Zhengzhou, China.
Lina HuMedical College, Henan University of Chinese Medicine, Zhengzhou, China.
Lianhe YangMedical College, Henan University of Chinese Medicine, Zhengzhou, China.
Tao GuoDepartment of Pharmacy, Henan University of Chinese Medicine, Zhengzhou, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Clustered regularly interspaced short palindromic repeats (CRISPR)-associated systems have revolutionized traditional gene-editing tools and are a significant tool for ameliorating gene defects. Characterized by high target specificity, extraordinary efficiency, and cost-effectiveness, CRISPR/Cas systems have displayed tremendous potential for genetic manipulation in almost any organism and cell type. Despite their numerous advantages, however, CRISPR/Cas systems have some inherent limitations, such as off-target effects, unsatisfactory efficiency of delivery, and unwanted adverse effects, thereby resulting in a desire to explore approaches to address these issues. Strategies for improving the efficiency of CRISPR/Cas-induced mutations, such as reducing off-target effects, improving the design and modification of sgRNA, optimizing the editing time and the temperature, choice of delivery system, and enrichment of sgRNA, are comprehensively described in this review. Additionally, several newly emerging approaches, including the use of Cas variants, anti-CRISPR proteins, and mutant enrichment, are discussed in detail. Furthermore, the authors provide a deep analysis of the current challenges in the utilization of CRISPR/Cas systems and the future applications of CRISPR/Cas systems in various scenarios. This review not only serves as a reference for improving the maturity of CRISPR/Cas systems but also supplies practical guidance for expanding the applicability of this technology.

Indexed as

CRISPR/Cas systemhighly efficientmutantoff-target effectoptimized strategies

Identifiers

PMID35198566
PMCPMC8860194

What OpenQuestion holds

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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.