Evidence map›Paper›PMID 37298068›Full record

ArticleInternational journal of molecular sciences2023

In-Frame Deletion of Dystrophin Exons 8-50 Results in DMD Phenotype.

Tatiana V Egorova, Ivan I Galkin, Oleg A Velyaev, Svetlana G Vassilieva, Irina M Savchenko, Vyacheslav A Loginov, Marina A Dzhenkova, Diana S Korshunova, Olga S Kozlova, Dmitry N Ivankov and 1 more

Open access · goldAbstract read
PubMed Full text at PMC Publisher
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 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing 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

8 citing papers in PubMed, 7 citations in OpenAlex.

  1. Article
  2. Article
  3. Genome-wide association testing beyond SNPs.Nature reviews. Genetics · 2025
    Review
  4. Review
  5. Incidental finding of aFrontiers in pediatrics · 2025
    Article
  6. Review
  7. Review
  8. Frontiers in neurology · 2023
    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 at 3 institutions in 1 country.

Tatiana V EgorovaLaboratory of Modeling and Therapy of Hereditary Diseases, Institute of Gene Biology Russian Academy of Sciences, Moscow 119334, Russia.ORCID 0000-0002-3346-3242
Ivan I GalkinMarlin Biotech LLC, Sochi 354340, Russia.
Oleg A VelyaevLaboratory of Modeling and Therapy of Hereditary Diseases, Institute of Gene Biology Russian Academy of Sciences, Moscow 119334, Russia.
Svetlana G VassilievaLaboratory of Modeling and Therapy of Hereditary Diseases, Institute of Gene Biology Russian Academy of Sciences, Moscow 119334, Russia.
Irina M SavchenkoLaboratory of Modeling and Therapy of Hereditary Diseases, Institute of Gene Biology Russian Academy of Sciences, Moscow 119334, Russia.
Vyacheslav A LoginovLaboratory of Modeling and Therapy of Hereditary Diseases, Institute of Gene Biology Russian Academy of Sciences, Moscow 119334, Russia.
Marina A DzhenkovaLaboratory of Modeling and Therapy of Hereditary Diseases, Institute of Gene Biology Russian Academy of Sciences, Moscow 119334, Russia.
Diana S KorshunovaCore Facilities, Institute of Gene Biology Russian Academy of Sciences, Moscow 119334, Russia.
Olga S KozlovaLaboratory of Modeling and Therapy of Hereditary Diseases, Institute of Gene Biology Russian Academy of Sciences, Moscow 119334, Russia.
Dmitry N IvankovCenter for Molecular and Cellular Biology, Skolkovo Institute of Science and Technology, Moscow 121205, Russia.
Anna V PolikarpovaLaboratory of Modeling and Therapy of Hereditary Diseases, Institute of Gene Biology Russian Academy of Sciences, Moscow 119334, Russia.
Institute of Gene Biology · RULomonosov Moscow State University · RUSkolkovo Institute of Science and Technology · RU

Funding

Russian Science Foundation 21-75-00084
6 · The paper itself

Abstract

Mutations that prevent the production of proteins in the

Indexed as

DystrophinMuscular Dystrophy, DuchenneAnimalsExonsGene DeletionMiceMice, Inbred CBAPhenotypeDystrophinBecker muscular dystrophyBMDCRISPR–Cas9DMDdystrophingenome editingmouse model

Identifiers

PMID37298068
PMCPMC10252864
OpenAlexW4377822075

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.