Evidence map›Paper›PMID 37894981›Full record

ReviewInternational journal of molecular sciences2023

Recent Advances in In Vivo Somatic Cell Gene Modification in Newborn Pups.

Shingo Nakamura, Kazunori Morohoshi, Emi Inada, Yoko Sato, Satoshi Watanabe, Issei Saitoh, Masahiro Sato

Open access · goldAbstract readReview
In one paragraph

Review 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 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.3field-weighted citation impact, top 36% 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

1 citing paper in PubMed, 2 citations in OpenAlex.

  1. 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

7 authors at 6 institutions in 1 country.

Shingo NakamuraDivision of Biomedical Engineering, National Defense Medical College Research Institute, Tokorozawa 359-8513, Japan.ORCID 0000-0001-6084-0958
Kazunori MorohoshiDivision of Biomedical Engineering, National Defense Medical College Research Institute, Tokorozawa 359-8513, Japan.
Emi InadaDepartment of Pediatric Dentistry, Graduate School of Medical and Dental Sciences, Kagoshima University, Kagoshima 890-8544, Japan.
Yoko SatoGraduate School of Public Health, Shizuoka Graduate University of Public Health, Aoi-ku, Shizuoka 420-0881, Japan.
Satoshi WatanabeInstitute of Livestock and Grassland Science, NARO, Tsukuba 305-0901, Japan.
Issei SaitohDepartment of Pediatric Dentistry, Asahi University School of Dentistry, Mizuho 501-0296, Japan.ORCID 0000-0002-7451-0666
Masahiro SatoDepartment of Genome Medicine, National Center for Child Health and Development, Setagaya-ku, Tokyo 157-8535, Japan.ORCID 0000-0003-1334-2950
National Defense Medical College · JPAsahi University · JPInstitute of Livestock and Grassland Science · JPKagoshima University · JPNational Center For Child Health and Development · JPUniversity of Shizuoka · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Germline manipulation at the zygote stage using the CRISPR/Cas9 system has been extensively employed for creating genetically modified animals and maintaining established lines. However, this approach requires a long and laborious task. Recently, many researchers have attempted to overcome these limitations by generating somatic mutations in the adult stage through tail vein injection or local administration of CRISPR reagents, as a new strategy called "in vivo somatic cell genome editing". This approach does not require manipulation of early embryos or strain maintenance, and it can test the results of genome editing in a short period. The newborn is an ideal stage to perform in vivo somatic cell genome editing because it is immune-privileged, easily accessible, and only a small amount of CRISPR reagents is required to achieve somatic cell genome editing throughout the entire body, owing to its small size. In this review, we summarize in vivo genome engineering strategies that have been successfully demonstrated in newborns. We also report successful in vivo genome editing through the neonatal introduction of genome editing reagents into various sites in newborns (as exemplified by intravenous injection via the facial vein), which will be helpful for creating models for genetic diseases or treating many genetic diseases.

Indexed as

CRISPR-Cas SystemsGene EditingAnimalsAnimals, NewbornZygoteCRISPR/Cas9genetically modified animalgenome editingin vivo genome engineeringnewbornsomatic mutation

Identifiers

PMID37894981
PMCPMC10607593
OpenAlexW4387738063

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.