Evidence map›Paper›PMID 32670545›Full record

ArticleCell & bioscience2020

Genome editing of CCR5 by AsCpf1 renders CD4

Zhepeng Liu, Jin Liang, Shuliang Chen, Kewu Wang, Xianhao Liu, Beibei Liu, Yang Xia, Mingxiong Guo, Xiaoshi Zhang, Guihong Sun and 1 more

Abstract read
In one paragraph

Article in Cell & bioscience, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing 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

19 citing papers in PubMed.

  1. Review
  2. Article
  3. Review
  4. CRISPR-Cpf1 system and its applications in animal genome editing.Molecular genetics and genomics : MGG · 2024
    Review
  5. Review
  6. Article
  7. Article
  8. Review
  9. Therapeutic Application of Genome Editing Technologies in Viral Diseases.International journal of molecular sciences · 2022
    Review
  10. Article
  11. Review
  12. Review
  13. Review
  14. Review
  15. Article
  16. Review
  17. Review
  18. Review
  19. 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.

Zhepeng Liu *Department of Biotherapy Research Center, Sun Yat-sen University Cancer Center, 651 Dongfeng East Road, Guangzhou, Guangdong 510060 People's Republic of China.
Jin Liang *Department of Oncology, The First Affiliated Hospital of Shenzhen University, The Second People's Hospital of Shenzhen, 3002 Sungang West Road, Shenzhen, 518035 People's Republic of China.
Shuliang ChenSchool of Basic Medical Sciences, Wuhan University, Wuhan, 430071 People's Republic of China.
Kewu WangDepartment of Oncology, The Second People's Hospital of Wuhu, Wuhu, 242401 People's Republic of China.
Xianhao LiuDepartment of Oncology, The First Affiliated Hospital of Shenzhen University, The Second People's Hospital of Shenzhen, 3002 Sungang West Road, Shenzhen, 518035 People's Republic of China.
Beibei LiuDepartment of Oncology, The First Affiliated Hospital of Shenzhen University, The Second People's Hospital of Shenzhen, 3002 Sungang West Road, Shenzhen, 518035 People's Republic of China.
Yang XiaDepartment of Oncology, The First Affiliated Hospital of Shenzhen University, The Second People's Hospital of Shenzhen, 3002 Sungang West Road, Shenzhen, 518035 People's Republic of China.
Mingxiong GuoCollege of Life Sciences, Wuhan University, Wuhan, 430071 People's Republic of China.
Xiaoshi ZhangDepartment of Biotherapy Research Center, Sun Yat-sen University Cancer Center, 651 Dongfeng East Road, Guangzhou, Guangdong 510060 People's Republic of China.
Guihong SunSchool of Basic Medical Sciences, Wuhan University, Wuhan, 430071 People's Republic of China.
Geng TianDepartment of Oncology, The First Affiliated Hospital of Shenzhen University, The Second People's Hospital of Shenzhen, 3002 Sungang West Road, Shenzhen, 518035 People's Republic of China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe chemokine receptor CCR5 is one of the co-receptor of HIV-1 infection. People with homozygous

resultsHere, we demonstrated that CRISPR/AsCpf1 could ablate the main co-receptor of HIV-1 infection-

conclusionsOur study provides a basis for a possible application of

Indexed as

CCR5CRISPR/AsCpf1HIV-1HIV-1 resistanceSelective advantage

Identifiers

PMID32670545
PMCPMC7346486

What OpenQuestion holds

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Registered trials

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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.