Evidence map›Paper›PMID 36835061›Full record

ArticleInternational journal of molecular sciences2023

High-Efficiency CRISPR/Cas9-Mediated Correction of a Homozygous Mutation in Achromatopsia-Patient-Derived iPSCs.

Laura Siles, Paula Gaudó, Esther Pomares

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2023. 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
1.1field-weighted citation impact, top 23% 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. Reporter Alleles in hiPSCs: Visual Cues on Development and Disease.International journal of molecular sciences · 2024
    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

3 authors at 1 institution in 1 country.

Laura SilesFundació de Recerca de l'Institut de Microcirurgia Ocular, 08035 Barcelona, Spain.
Paula GaudóFundació de Recerca de l'Institut de Microcirurgia Ocular, 08035 Barcelona, Spain.
Esther PomaresFundació de Recerca de l'Institut de Microcirurgia Ocular, 08035 Barcelona, Spain.ORCID 0000-0002-3818-3303
Instituto de Microcirugía Ocular · ES

Funding

Fundació Bancària La Caixa LCF/PR/PR17/11120006Private donation Fi-201401
6 · The paper itself

Abstract

Achromatopsia is an autosomal recessive disorder, in which cone photoreceptors undergo progressive degeneration, causing color blindness and poor visual acuity, among other significant eye affectations. It belongs to a group of inherited retinal dystrophies that currently have no treatment. Although functional improvements have been reported in several ongoing gene therapy studies, more efforts and research should be carried out to enhance their clinical application. In recent years, genome editing has arisen as one of the most promising tools for personalized medicine. In this study, we aimed to correct a homozygous

Indexed as

Color Vision DefectsCRISPR-Cas SystemsGene EditingHumansInduced Pluripotent Stem CellsMutationTranscription Activator-Like Effector NucleasesTranscription Activator-Like Effector NucleasesachromatopsiaCRISPR/Cas9gene editinginherited retinal dystrophies

Identifiers

PMID36835061
PMCPMC9964936
OpenAlexW4320493001

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.