Evidence map›Paper›PMID 33807610›Full record

ArticleInternational journal of molecular sciences2021

Allele-Specific Knockout by CRISPR/Cas to Treat Autosomal Dominant Retinitis Pigmentosa Caused by the G56R Mutation in NR2E3.

Michalitsa Diakatou, Gregor Dubois, Nejla Erkilic, Carla Sanjurjo-Soriano, Isabelle Meunier, Vasiliki Kalatzis

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed, 1 pooled it
2.5field-weighted citation impact, top 10% 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

23 citing papers in PubMed, 1 synthesis or guideline pooled it, 36 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Review
  4. Article
  5. Article
  6. Characterization of NiCas12b for In Vivo Genome Editing.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2024
    Article
  7. Review
  8. Review
  9. Article
  10. Review
  11. Review
  12. Article
  13. Review
  14. Article
  15. Article
  16. Genetic dissection of non-syndromic retinitis pigmentosa.Indian journal of ophthalmology · 2022
    Review
  17. CRISPR-AsCas12a Efficiently Corrects aThe CRISPR journal · 2022
    Article
  18. Human organoids in basic research and clinical applications.Signal transduction and targeted therapy · 2022
    Review
  19. Retinal organoids as models for development and diseases.Cell regeneration (London, England) · 2021
    Review
  20. Retinal Organoid Technology: Where Are We Now?International journal of molecular sciences · 2021
    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

6 authors at 1 institution in 1 country.

Michalitsa DiakatouINM, University of Montpellier, Inserm, 34091 Montpellier, France.
Gregor DuboisINM, University of Montpellier, Inserm, 34091 Montpellier, France.
Nejla ErkilicINM, University of Montpellier, Inserm, 34091 Montpellier, France.
Carla Sanjurjo-SorianoINM, University of Montpellier, Inserm, 34091 Montpellier, France.
Isabelle MeunierINM, University of Montpellier, Inserm, 34091 Montpellier, France.ORCID 0000-0003-3407-5265
Vasiliki KalatzisINM, University of Montpellier, Inserm, 34091 Montpellier, France.ORCID 0000-0002-9626-8807
Inserm · FR

Funding

Laboratoire d'Excellence EpiGenMed ANR-10-LABX-12-01
6 · The paper itself

Abstract

Retinitis pigmentosa (RP) is an inherited retinal dystrophy that causes progressive vision loss. The G56R mutation in NR2E3 is the second most common mutation causing autosomal dominant (ad) RP, a transcription factor that is essential for photoreceptor development and maintenance. The G56R variant is exclusively responsible for all cases of

Indexed as

AllelesAnimalsBase SequenceCell LineChlorocebus aethiopsClustered Regularly Interspaced Short Palindromic RepeatsCOS CellsGene EditingGenes, DominantHEK293 CellsHumansInduced Pluripotent Stem CellsMutationOrphan Nuclear ReceptorsRetinaRetinitis PigmentosaOrphan Nuclear Receptorsallele-specificautosomal dominant retinitis pigmentosaCRISPR/Casinherited retinal dystrophiesiPSCknockoutNR2E3photoreceptorretinal organoidsrod-cone dystrophy

Identifiers

PMID33807610
PMCPMC7961898
OpenAlexW3135708836

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.