Evidence map›Paper›PMID 32330446›Full record

ArticleStem cell reports2020

Myogenic Progenitor Cell Lineage Specification by CRISPR/Cas9-Based Transcriptional Activators.

Jennifer B Kwon, Ashish Vankara, Adarsh R Ettyreddy, Joel D Bohning, Charles A Gersbach

Open access · goldAbstract read
In one paragraph

Article in Stem cell reports, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
1.3field-weighted citation impact, top 21% 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

18 citing papers in PubMed, 25 citations in OpenAlex.

  1. Review
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  8. Advancing in vivo reprogramming with synthetic biology.Current opinion in biotechnology · 2024
    Review
  9. Article
  10. Review
  11. Article
  12. Review
  13. Article
  14. Available In Vitro Models for Human Satellite Cells from Skeletal Muscle.International journal of molecular sciences · 2021
    Review
  15. Article
  16. Review
  17. Review
  18. Neuromuscular Development and Disease: Learning FromFrontiers in cell and developmental biology · 2021
    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

5 authors at 2 institutions in 1 country.

Jennifer B KwonUniversity Program in Genetics and Genomics, Duke University Medical Center, Durham, NC 27710, USA; Center for Advanced Genomic Technologies, Duke University, Durham, NC 27708, USA.
Ashish VankaraCenter for Advanced Genomic Technologies, Duke University, Durham, NC 27708, USA; Department of Biomedical Engineering, Duke University, Durham, NC 27708, USA.
Adarsh R EttyreddyCenter for Advanced Genomic Technologies, Duke University, Durham, NC 27708, USA; Department of Biomedical Engineering, Duke University, Durham, NC 27708, USA.
Joel D BohningCenter for Advanced Genomic Technologies, Duke University, Durham, NC 27708, USA; Department of Biomedical Engineering, Duke University, Durham, NC 27708, USA.
Charles A GersbachCenter for Advanced Genomic Technologies, Duke University, Durham, NC 27708, USA; Department of Biomedical Engineering, Duke University, Durham, NC 27708, USA; Department of Surgery, Duke University Medical Center, Durham, NC 27710, USA. Electronic address: charles.gersbach@duke.edu.
Duke University · USApplied Genetic Technologies (United States) · US

Funding

Training Program in Developmental & Stem Cell BiologyT32HD040372 · NICHD · DUKE UNIVERSITY · PI Terry H Lechler · 2001 to 2026
$8.9M
Vascular, Cardiac, and Lung Alveolar Human Microphysiological Systems for SARS-CoV-2 Drug ScreeningUH3TR002142 · NCATS · DUKE UNIVERSITY · PI TRUSKEY, GEORGE A · 2019 to 2021
$4.0M
University Training Program in Biomolecular and Tissue EngineeringT32GM144291 · NIGMS · DUKE UNIVERSITY · PI Charles A. Gersbach, Tatiana Segura · 2022 to 2026
$2.6M
Engineering Morphogenetic Factors for Enhanced Genetic ReprogrammingDP2OD008586 · OD · DUKE UNIVERSITY · PI GERSBACH, CHARLES A. · 2011 to 2011
$2.4M
Evolving High Potency AAV Vectors for Neuromuscular Genome EditingUG3AR075336 · NIAMS · DUKE UNIVERSITY · PI ASOKAN, ARAVIND · 2018 to 2020
$2.1M
Microphysiological Human Tissue Systems for Monitoring of Genome Editing OutcomesU01HL156348 · NHLBI · DUKE UNIVERSITY · PI BURSAC, NENAD, GERSBACH, CHARLES A. · 2020 to 2022
$2.0M
CRISPR/Cas9-Based Gene Editing for the Correction of Duchenne Muscular DystrophyR01AR069085 · NIAMS · DUKE UNIVERSITY · PI GERSBACH, CHARLES A. · 2016 to 2020
$1.7M
Epigenome Editing Technologies for Treating Diverse DiseaseU01AI146356 · NIAID · DUKE UNIVERSITY · PI GERSBACH, CHARLES A. · 2019 to 2022
$1.6M
Microphysiological Human Tissue Systems for Monitoring of Genome Editing OutcomesU01EB028901 · NIBIB · DUKE UNIVERSITY · PI BURSAC, NENAD, GERSBACH, CHARLES A. · 2019 to 2019
$668k
Enhancing Neuronal Reprogramming with Epigenome EditingR21NS103007 · NINDS · DUKE UNIVERSITY · PI GERSBACH, CHARLES A. · 2018 to 2019
$427k
Combinatorial biomimetic systems to enable high-throughput evaluation and expansion of genome-edited dystrophic muscle stem cellsR21AR072265 · NIAMS · CORNELL UNIVERSITY · PI COSGROVE, BENJAMIN DAVID · 2018 to 2019
$397k
NCATS NIH HHS UH3 TR002142NHLBI NIH HHS U01 HL156348NIAID NIH HHS U01 AI146356NIAMS NIH HHS R01 AR069085NIAMS NIH HHS R21 AR072265NIAMS NIH HHS UG3 AR075336NIBIB NIH HHS U01 EB028901NIGMS NIH HHS T32 GM144291NIH HHS DP2 OD008586NINDS NIH HHS R21 NS103007
6 · The paper itself

Abstract

Engineered CRISPR/Cas9-based transcriptional activators can potently and specifically activate endogenous fate-determining genes to direct differentiation of pluripotent stem cells. Here, we demonstrate that endogenous activation of the PAX7 transcription factor results in stable epigenetic remodeling and differentiates human pluripotent stem cells into skeletal myogenic progenitor cells. Compared with exogenous overexpression of PAX7 cDNA, we find that endogenous activation results in the generation of more proliferative myogenic progenitors that can maintain PAX7 expression over multiple passages in serum-free conditions while preserving the capacity for terminal myogenic differentiation. Transplantation of human myogenic progenitors derived from endogenous activation of PAX7 into immunodeficient mice resulted in a greater number of human dystrophin

Indexed as

Cell LineageAnimalsCell DifferentiationCells, CulturedCellular Reprogramming TechniquesCRISPR-Cas SystemsDystrophinEpigenesis, GeneticFemaleGene EditingHEK293 CellsHumansInduced Pluripotent Stem CellsInfant, NewbornMaleMiceDystrophinPAX7 protein, humanPAX7 Transcription FactorCRISPRdifferentiationepigenome editingiPSCsmyoblastsmyogenesispluripotentsatellite cells

Identifiers

PMID32330446
PMCPMC7221109
OpenAlexW3019444898

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.