Evidence map›Paper›PMID 28992755›Full record

ArticleStem cells and development2017

Drug-Mediated Shortening of Action Potentials in LQTS2 Human Induced Pluripotent Stem Cell-Derived Cardiomyocytes.

Gary Duncan, Karl Firth, Vinoj George, Minh Duc Hoang, Andrew Staniforth, Godfrey Smith, Chris Denning

Open access · hybridAbstract read
In one paragraph

Article in Stem cells and development, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.2field-weighted citation impact, top 18% 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

13 citing papers in PubMed, 23 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Review
  5. Review
  6. Article
  7. 14-3-3 protein regulation of excitation-contraction coupling.Pflugers Archiv : European journal of physiology · 2022
    Review
  8. Article
  9. Cardiac hERG KHandbook of experimental pharmacology · 2021
    Article
  10. Article
  11. Review
  12. Article
  13. 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

7 authors at 3 institutions in 1 country.

Gary Duncan1 Department of Stem Cell Biology, Centre of Biomolecular Sciences, University of Nottingham , Nottingham, United Kingdom .
Karl Firth1 Department of Stem Cell Biology, Centre of Biomolecular Sciences, University of Nottingham , Nottingham, United Kingdom .
Vinoj George1 Department of Stem Cell Biology, Centre of Biomolecular Sciences, University of Nottingham , Nottingham, United Kingdom .
Minh Duc Hoang1 Department of Stem Cell Biology, Centre of Biomolecular Sciences, University of Nottingham , Nottingham, United Kingdom .
Andrew Staniforth3 Department of Cardiovascular Medicine, Queen's Medical Centre , Nottingham, United Kingdom .
Godfrey Smith4 Institute of Cardiovascular and Medical Sciences, University of Glasgow , Glasgow, United Kingdom .
Chris Denning1 Department of Stem Cell Biology, Centre of Biomolecular Sciences, University of Nottingham , Nottingham, United Kingdom .
University of Nottingham · GBQueen's Medical Centre · GBUniversity of Glasgow · GB

Funding

British Heart Foundation PG/09/027/27141British Heart Foundation PG/14/59/31000British Heart Foundation RG/11/19/29264British Heart Foundation RG/14/1/30588British Heart Foundation RG/15/6/31436British Heart Foundation SP/15/9/31605Medical Research Council MR/M017354/1National Centre for the Replacement, Refinement and Reduction of Animals in Research NC/C013202/1National Centre for the Replacement, Refinement and Reduction of Animals in Research NC/K000225/1
6 · The paper itself

Abstract

Cardiomyocytes (CMs) derived from human induced pluripotent stem cells (hiPSCs) are now a well-established modality for modeling genetic disorders of the heart. This is especially so for long QT syndrome (LQTS), which is caused by perturbation of ion channel function, and can lead to fainting, malignant arrhythmias and sudden cardiac death. LQTS2 is caused by mutations in KCNH2, a gene whose protein product contributes to I

Indexed as

Action PotentialsAdrenergic beta-AntagonistsCell DifferentiationCells, CulturedERG1 Potassium ChannelFemaleFibroblastsHumansInduced Pluripotent Stem CellsLong QT SyndromeMyocytes, CardiacPropranololYoung AdultAdrenergic beta-AntagonistsERG1 Potassium ChannelKCNH2 protein, humanPropranololcardiomyocyteselectrophysiologyHERGhuman induced pluripotent stem cellslong QT syndromePPAR delta

Identifiers

PMID28992755
PMCPMC5706629
OpenAlexW2763450878

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.