Evidence map›Paper›PMID 28374058›Full record

ReviewMammalian genome : official journal of the International Mammalian Genome Society2017

Control of gene editing by manipulation of DNA repair mechanisms.

Eric Danner, Sanum Bashir, Saniye Yumlu, Wolfgang Wurst, Benedikt Wefers, Ralf Kühn

Abstract readReview
PubMed Publisher
In one paragraph

Review in Mammalian genome : official journal of the International Mammalian Genome Society, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 42 papers.

0numbers the graph read from it
0cells of the map it votes in
42citing papers in PubMed
3.1field-weighted citation impact, top 8% 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

42 citing papers in PubMed, 71 citations in OpenAlex.

  1. Article
  2. Article
  3. Reinforced Defenses:International journal of molecular sciences · 2025
    Review
  4. Article
  5. Article
  6. Article
  7. CRISPR-Mediated Viral Gene Knock-In for Studying Viral-Host Interactions.Methods in molecular biology (Clifton, N.J.) · 2025
    Article
  8. Review
  9. Review
  10. Article
  11. Allele-specific CRISPR-Cas9 editing of dominant epidermolysis bullosa simplex in human epidermal stem cells.Molecular therapy : the journal of the American Society of Gene Therapy · 2024
    Article
  12. Review
  13. Article
  14. Genetic manipulation of betta fish.bioRxiv : the preprint server for biology · 2023
    Article
  15. Genetic manipulation of betta fish.Frontiers in genome editing · 2023
    Article
  16. Genome Editing Using Cas9 Ribonucleoprotein Is Effective for IntroducingInternational journal of molecular sciences · 2022
    Article
  17. Article
  18. Article
  19. Review
  20. Article
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

6 authors at 2 institutions in 1 country.

Eric DannerMax-Delbrück-Centrum für Molekulare Medizin, Robert-Rössle-Str. 10, 13125, Berlin, Germany.
Sanum BashirMax-Delbrück-Centrum für Molekulare Medizin, Robert-Rössle-Str. 10, 13125, Berlin, Germany.
Saniye YumluMax-Delbrück-Centrum für Molekulare Medizin, Robert-Rössle-Str. 10, 13125, Berlin, Germany.
Wolfgang WurstDeutsches Zentrum für Neurodegenerative Erkrankungen e. V. (DZNE), Feodor-Lynen-Str. 17, 81377, Munich, Germany.
Benedikt WefersDeutsches Zentrum für Neurodegenerative Erkrankungen e. V. (DZNE), Feodor-Lynen-Str. 17, 81377, Munich, Germany.
Ralf KühnMax-Delbrück-Centrum für Molekulare Medizin, Robert-Rössle-Str. 10, 13125, Berlin, Germany. ralf.kuehn@mdc-berlin.de.ORCID http://orcid.org/0000-0003-1694-9803
Max Delbrück Center · DEGerman Center for Neurodegenerative Diseases · DE

Funding

BMBF VIP 03V0261
6 · The paper itself

Abstract

DNA double-strand breaks (DSBs) are produced intentionally by RNA-guided nucleases to achieve genome editing through DSB repair. These breaks are repaired by one of two main repair pathways, classic non-homologous end joining (c-NHEJ) and homology-directed repair (HDR), the latter being restricted to the S/G2 phases of the cell cycle and notably less frequent. Precise genome editing applications rely on HDR, with the abundant c-NHEJ formed mutations presenting a barrier to achieving high rates of precise sequence modifications. Here, we give an overview of HDR- and c-NHEJ-mediated DSB repair in gene editing and summarize the current efforts to promote HDR over c-NHEJ.

Indexed as

DNA RepairGene EditingAnimalsBiomarkersCRISPR-Cas SystemsDNA End-Joining RepairGene Knock-In TechniquesGene Knockout TechniquesGenetic TestingHomologous RecombinationHumansRecombinational DNA RepairSignal TransductionBiomarkersGene EditingHomologous RecombinationHomologous Recombination PathwayRepair TemplateU2OS Cell

Identifiers

PMID28374058
OpenAlexW2604576157

What OpenQuestion holds

Textmetadata
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.