Evidence map›Paper›PMID 26898344›Full record

ArticleScientific reports2016

Induction of site-specific chromosomal translocations in embryonic stem cells by CRISPR/Cas9.

Junfeng Jiang, Li Zhang, Xingliang Zhou, Xi Chen, Guanyi Huang, Fengsheng Li, Ruizhe Wang, Nancy Wu, Youzhen Yan, Chang Tong and 4 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
4.2field-weighted citation impact, top 6% 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

23 citing papers in PubMed, 50 citations in OpenAlex.

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  8. Variability in Genome Editing Outcomes: Challenges for Research Reproducibility and Clinical Safety.Molecular therapy : the journal of the American Society of Gene Therapy · 2020
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  20. Applications of Alternative Nucleases in the Age of CRISPR/Cas9.International journal of molecular sciences · 2017
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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

14 authors at 3 institutions in 2 countries.

Junfeng JiangResearch Center of Developmental Biology, Histology and Embryology Department, Second Military Medical University, Shanghai, 200433, China.
Li ZhangEli and Edythe Broad Center for Regenerative Medicine and Stem Cell Research at USC, Department of Stem Cell Biology &Regenerative Medicine, Keck School of Medicine, University of Southern California, Los Angeles, CA, USA.
Xingliang ZhouEli and Edythe Broad Center for Regenerative Medicine and Stem Cell Research at USC, Department of Stem Cell Biology &Regenerative Medicine, Keck School of Medicine, University of Southern California, Los Angeles, CA, USA.
Xi ChenEli and Edythe Broad Center for Regenerative Medicine and Stem Cell Research at USC, Department of Stem Cell Biology &Regenerative Medicine, Keck School of Medicine, University of Southern California, Los Angeles, CA, USA.
Guanyi HuangEli and Edythe Broad Center for Regenerative Medicine and Stem Cell Research at USC, Department of Stem Cell Biology &Regenerative Medicine, Keck School of Medicine, University of Southern California, Los Angeles, CA, USA.
Fengsheng LiEli and Edythe Broad Center for Regenerative Medicine and Stem Cell Research at USC, Department of Stem Cell Biology &Regenerative Medicine, Keck School of Medicine, University of Southern California, Los Angeles, CA, USA.
Ruizhe WangEli and Edythe Broad Center for Regenerative Medicine and Stem Cell Research at USC, Department of Stem Cell Biology &Regenerative Medicine, Keck School of Medicine, University of Southern California, Los Angeles, CA, USA.
Nancy WuEli and Edythe Broad Center for Regenerative Medicine and Stem Cell Research at USC, Department of Stem Cell Biology &Regenerative Medicine, Keck School of Medicine, University of Southern California, Los Angeles, CA, USA.
Youzhen YanEli and Edythe Broad Center for Regenerative Medicine and Stem Cell Research at USC, Department of Stem Cell Biology &Regenerative Medicine, Keck School of Medicine, University of Southern California, Los Angeles, CA, USA.
Chang TongEli and Edythe Broad Center for Regenerative Medicine and Stem Cell Research at USC, Department of Stem Cell Biology &Regenerative Medicine, Keck School of Medicine, University of Southern California, Los Angeles, CA, USA.
Sankalp SrivastavaEli and Edythe Broad Center for Regenerative Medicine and Stem Cell Research at USC, Department of Stem Cell Biology &Regenerative Medicine, Keck School of Medicine, University of Southern California, Los Angeles, CA, USA.
Yue WangResearch Center of Developmental Biology, Histology and Embryology Department, Second Military Medical University, Shanghai, 200433, China.
Houqi LiuResearch Center of Developmental Biology, Histology and Embryology Department, Second Military Medical University, Shanghai, 200433, China.
Qi-Long YingEli and Edythe Broad Center for Regenerative Medicine and Stem Cell Research at USC, Department of Stem Cell Biology &Regenerative Medicine, Keck School of Medicine, University of Southern California, Los Angeles, CA, USA.
Broad Center · USUniversity of Southern California · USSecond Military Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Chromosomal translocation is the most common form of chromosomal abnormality and is often associated with congenital genetic disorders, infertility, and cancers. The lack of cellular and animal models for chromosomal translocations, however, has hampered our ability to understand the underlying disease mechanisms and to develop new therapies. Here, we show that site-specific chromosomal translocations can be generated in mouse embryonic stem cells (mESCs) via CRISPR/Cas9. Mouse ESCs carrying translocated chromosomes can be isolated and expanded to establish stable cell lines. Furthermore, chimeric mice can be generated by injecting these mESCs into host blastocysts. The establishment of ESC-based cellular and animal models of chromosomal translocation by CRISPR/Cas9 provides a powerful platform for understanding the effect of chromosomal translocation and for the development of new therapeutic strategies.

Indexed as

CRISPR-Cas SystemsEmbryonic Stem CellsTranslocation, GeneticAnimalsCell LineMiceMice, TransgenicModels, AnimalModels, Genetic

Identifiers

PMID26898344
PMCPMC4761995
OpenAlexW2406621791

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.