Evidence map›Paper›PMID 31833031›Full record

ArticleMolecular biology reports2020

Establishment of a conditional Nomo1 mouse model by CRISPR/Cas9 technology.

Ignacio García-Tuñón, Elena Vuelta, Laura Lozano, María Herrero, Lucía Méndez, Javier Palomero-Hernandez, María Pérez-Caro, Jessica Pérez-García, Rogelio González-Sarmiento, Manuel Sánchez-Martín

Open access · hybridAbstract read
PubMed Publisher
In one paragraph

Article in Molecular biology reports, 2020. 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
0.6field-weighted citation impact, top 32% 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, 9 citations in OpenAlex.

  1. Article
  2. RecurrentCancers · 2022
    Article
  3. Reply to Zhao et al.: NOMO1 is a potential target gene of MRTFB.Proceedings of the National Academy of Sciences of the United States of America · 2020
    Article
  4. MRTFB regulates the expression of NOMO1 in colon.Proceedings of the National Academy of Sciences of the United States of America · 2020
    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

10 authors at 1 institution in 1 country.

Ignacio García-TuñónIBSAL (Instituto de Investigación Biomédica de Salamanca), Salamanca, Spain.
Elena VueltaServicio de Transgénesis, Nucleus, Universidad de Salamanca, Salamanca, Spain.
Laura LozanoServicio de Transgénesis, Nucleus, Universidad de Salamanca, Salamanca, Spain.
María HerreroServicio de Transgénesis, Nucleus, Universidad de Salamanca, Salamanca, Spain.
Lucía MéndezServicio de Transgénesis, Nucleus, Universidad de Salamanca, Salamanca, Spain.
Javier Palomero-HernandezServicio de Transgénesis, Nucleus, Universidad de Salamanca, Salamanca, Spain.
María Pérez-CaroBanco de ADN, Nucleus, Universidad de Salamanca, Salamanca, Spain.
Jessica Pérez-GarcíaIBSAL (Instituto de Investigación Biomédica de Salamanca), Salamanca, Spain.
Rogelio González-SarmientoIBSAL (Instituto de Investigación Biomédica de Salamanca), Salamanca, Spain.
Manuel Sánchez-MartínIBSAL (Instituto de Investigación Biomédica de Salamanca), Salamanca, Spain. adolsan@usal.es.ORCID http://orcid.org/0000-0001-8370-1336
Universidad de Salamanca · ES

Funding

Instituto de Salud Carlos III PI16/01920
6 · The paper itself

Abstract

The Nomo1 gene mediates a wide range of biological processes of importance in embryonic development. Accordingly, constitutive perturbation of Nomo1 function may result in myriad developmental defects that trigger embryonic lethality. To extend our understanding of Nomo1 function in postnatal stages and in a tissue-specific manner, we generated a conditional knockout mouse model of Nomo1. To achieve this, we used clustered regularly interspaced short palindromic repeats (CRISPR)/Cas9 technology in C57Bl/6J mouse zygotes to generate a new mouse model in which exon 3 of the Nomo1 gene is specifically flanked (or floxed) by LoxP sites (Nomo1

Indexed as

AllelesAnimalsBase SequenceClustered Regularly Interspaced Short Palindromic RepeatsCRISPR-Associated Protein 9Disease Models, AnimalExonsIntegrasesMembrane ProteinsMice, Inbred C57BLMice, TransgenicMosaicismMutationNodal ProteinRNA, Guide, CRISPR-Cas SystemsCre recombinaseCRISPR-Associated Protein 9IntegrasesMembrane ProteinsNodal ProteinNomo1 protein, mouseRNA, Guide, CRISPR-Cas SystemsConditional Mouse ModelCRISPR/Cas9Knock outNOMO1

Identifiers

PMID31833031
OpenAlexW2996175928

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.