Evidence map›Paper›PMID 34160809›Full record

ArticleMethods in molecular biology (Clifton, N.J.)2021

In Vivo Silencing/Overexpression of lncRNAs by CRISPR/Cas System.

Marianna Vitiello, Laura Poliseno, Pier Paolo Pandolfi

Abstract read
PubMed Publisher
In one paragraph

Article in Methods in molecular biology (Clifton, N.J.), 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
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

2 citing papers in PubMed.

  1. Review
  2. 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.

Marianna VitielloOncogenomics Unit, CRL-ISPRO, Pisa, Italy.
Laura PolisenoOncogenomics Unit, CRL-ISPRO, Pisa, Italy. laura.poliseno@cnr.it.
Pier Paolo PandolfiDepartment of Molecular Biotechnologies & Health Sciences, Molecular Biotechnology Center, University of Turin, Turin, Italy. PierPaolo.PandolfiDeRinaldis@renown.org.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Long noncoding RNAs (lncRNAs) are implicated in several biological processes and it has been observed that their expression is altered in several diseases. The generation of animal models where selective silencing or overexpression of lncRNAs can be attained is crucial for their biological characterization, since it offers the opportunity to analyze their function at the tissue specific or organismal level. CRISPR/Cas technology is a newly developed tool that allows to easily manipulate the mouse genome, in turn allowing to discover lncRNAs functions in an in vivo context. Here, we provide an overview of how CRISPR/Cas technology can be used to generate transgenic mouse models in which lncRNAs can be studied.

Indexed as

CRISPR-Cas SystemsGene EditingGene ExpressionGene SilencingAdult Stem CellsAnimalsGene TargetingMiceMice, TransgenicMicroinjectionsRNA, Long NoncodingRNA, Long NoncodingCRISPR/Cas systemGenetically engineered mouse modellncRNA

Identifiers

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.