Evidence map›Paper›PMID 28417998›Full record

ArticleNature methods2017

Marker-free coselection for CRISPR-driven genome editing in human cells.

Daniel Agudelo, Alexis Duringer, Lusiné Bozoyan, Caroline C Huard, Sophie Carter, Jeremy Loehr, Dafni Synodinou, Mathieu Drouin, Jayme Salsman, Graham Dellaire and 2 more

Abstract read
PubMed Publisher
In one paragraph

Article in Nature methods, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 107 papers.

0numbers the graph read from it
0cells of the map it votes in
107citing papers in PubMed
9.3field-weighted citation impact, top 1% 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

107 citing papers in PubMed, 189 citations in OpenAlex.

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  7. Identification of PKN2 and MOB4 as Coordinators of Collective Cell Migration.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
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47 more citing papers are in PubMed but not listed here.

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

12 authors at 3 institutions in 1 country.

Daniel AgudeloCentre Hospitalier Universitaire de Québec Research Center-Université Laval, Quebec City, Quebec, Canada.
Alexis DuringerCentre Hospitalier Universitaire de Québec Research Center-Université Laval, Quebec City, Quebec, Canada.
Lusiné BozoyanCentre Hospitalier Universitaire de Québec Research Center-Université Laval, Quebec City, Quebec, Canada.
Caroline C HuardCentre Hospitalier Universitaire de Québec Research Center-Université Laval, Quebec City, Quebec, Canada.
Sophie CarterCentre Hospitalier Universitaire de Québec Research Center-Université Laval, Quebec City, Quebec, Canada.ORCID http://orcid.org/0000-0002-9817-0029
Jeremy LoehrCentre Hospitalier Universitaire de Québec Research Center-Université Laval, Quebec City, Quebec, Canada.
Dafni SynodinouCentre Hospitalier Universitaire de Québec Research Center-Université Laval, Quebec City, Quebec, Canada.
Mathieu DrouinResearch and Development, Héma-Québec, Quebec City, Quebec, Canada.
Jayme SalsmanDepartment of Pathology, Dalhousie University, Halifax, Nova Scotia, Canada.
Graham DellaireDepartment of Pathology, Dalhousie University, Halifax, Nova Scotia, Canada.ORCID http://orcid.org/0000-0002-3466-6316
Josée LaganièreResearch and Development, Héma-Québec, Quebec City, Quebec, Canada.ORCID http://orcid.org/0000-0003-0775-3331
Yannick DoyonCentre Hospitalier Universitaire de Québec Research Center-Université Laval, Quebec City, Quebec, Canada.ORCID http://orcid.org/0000-0002-3889-9563
Centre hospitalier universitaire de Québec · CAHéma-Québec · CADalhousie University · CA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Targeted genome editing enables the creation of bona fide cellular models for biological research and may be applied to human cell-based therapies. Therefore, broadly applicable and versatile methods for increasing its efficacy in cell populations are highly desirable. We designed a simple and robust coselection strategy for enrichment of cells with either nuclease-driven nonhomologous end joining (NHEJ) or homology-directed repair (HDR) events by harnessing the multiplexing capabilities of CRISPR-Cas9 and Cpf1 systems. Selection for dominant alleles of the ubiquitous sodium/potassium pump (Na

Indexed as

Mutagenesis, Site-DirectedCells, CulturedCRISPR-Cas SystemsDNA RepairGene EditingGenetic MarkersHumansGenetic Markers

Identifiers

PMID28417998
OpenAlexW2607021366

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.