Evidence map›Paper›PMID 33070670›Full record

ArticleAdipocyte2020

CRISPR/Cas9-mediated gene knockout in human adipose stem/progenitor cells.

Markus Mandl, Heike Ritthammer, Asim Ejaz, Sonja A Wagner, Florian M Hatzmann, Saphira Baumgarten, Hans P Viertler, Marit E Zwierzina, Monika Mattesich, Valerie Schiller and 5 more

Open access · goldAbstract read
In one paragraph

Article in Adipocyte, 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
0.3field-weighted citation impact, top 45% 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. Review
  2. Article
  3. Article
  4. 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

15 authors at 3 institutions in 2 countries.

Markus MandlDivision of Cell Metabolism and Differentiation Research, Research Institute for Biomedical Aging Research, University of Innsbruck , Austria.
Heike RitthammerDivision of Cell Metabolism and Differentiation Research, Research Institute for Biomedical Aging Research, University of Innsbruck , Austria.
Asim EjazDivision of Cell Metabolism and Differentiation Research, Research Institute for Biomedical Aging Research, University of Innsbruck , Austria.
Sonja A WagnerDivision of Cell Metabolism and Differentiation Research, Research Institute for Biomedical Aging Research, University of Innsbruck , Austria.
Florian M HatzmannDivision of Cell Metabolism and Differentiation Research, Research Institute for Biomedical Aging Research, University of Innsbruck , Austria.
Saphira BaumgartenDivision of Cell Metabolism and Differentiation Research, Research Institute for Biomedical Aging Research, University of Innsbruck , Austria.
Hans P ViertlerDivision of Cell Metabolism and Differentiation Research, Research Institute for Biomedical Aging Research, University of Innsbruck , Austria.
Marit E ZwierzinaInnsbruck Medical University , Innsbruck, Austria.
Monika MattesichInnsbruck Medical University , Innsbruck, Austria.
Valerie SchillerDivision of Cell Metabolism and Differentiation Research, Research Institute for Biomedical Aging Research, University of Innsbruck , Austria.
Tina RauchenwaldInnsbruck Medical University , Innsbruck, Austria.ORCID 0000-0002-7555-1582
Christian PlonerInnsbruck Medical University , Innsbruck, Austria.
Petra WaldeggerDivision of Cell Metabolism and Differentiation Research, Research Institute for Biomedical Aging Research, University of Innsbruck , Austria.
Gerhard PiererInnsbruck Medical University , Innsbruck, Austria.
Werner ZwerschkeDivision of Cell Metabolism and Differentiation Research, Research Institute for Biomedical Aging Research, University of Innsbruck , Austria.
Universität Innsbruck · ATInnsbruck Medical University · ATUniversity of Pittsburgh · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The CRISPR/Cas9 system is a powerful tool to generate a specific loss-of-function phenotype by gene knockout (KO). However, this approach is challenging in primary human cells. In this technical report, we present a reliable protocol to achieve a functional KO in the genome of human adipose stem/progenitor cells (ASCs). Using Sprouty1 (

Indexed as

CRISPR-Cas SystemsGene EditingGene Knockout TechniquesAdipose TissueBiomarkersCell DifferentiationCell LineGenes, ReporterGenetic VectorsHumansMutationRNA, Small InterferingStem CellsBiomarkersRNA, Small InterferingAdipose stem cellsageingCRISPR/Cas9genome editingloss-of-functionobesity

Identifiers

PMID33070670
PMCPMC7575003
OpenAlexW3092815006

What Socratic 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 Socratic graph.