Evidence map›Paper›PMID 21879736›Full record

ReviewMolecular pharmaceutics2011

Human pluripotent stem cell-based approaches for myocardial repair: from the electrophysiological perspective.

Ellen Poon, Chi-Wing Kong, Ronald A Li

Abstract readReview
In one paragraph

Review in Molecular pharmaceutics, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
–field-weighted citation impact
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

28 citing papers in PubMed.

  1. Article
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  3. Review
  4. Article
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  8. Article
  9. Review
  10. Article
  11. Review
  12. Article
  13. Review
  14. Review
  15. Strategies and Challenges to Myocardial Replacement Therapy.Stem cells translational medicine · 2016
    Review
  16. Review
  17. Review
  18. Article
  19. Review
  20. 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

3 authors.

Ellen PoonStem Cell & Regenerative Medicine Consortium, LKS Faculty of Medicine, University of Hong Kong, Pokfulam, Hong Kong.
Chi-Wing Kong
Ronald A Li

Funding

Molecular Physiology of the Pacemaker ChannelsR01HL072857 · NHLBI · UNIVERSITY OF CALIFORNIA AT DAVIS · PI LI, RONALD A · 2004 to 2013
$3.4M
NHLBI NIH HHS R01 HL072857NHLBI NIH HHS R01HL72857
6 · The paper itself

Abstract

Heart diseases are a leading cause of mortality worldwide. Terminally differentiated adult cardiomyocytes (CMs) lack the innate ability to regenerate. Their malfunction or significant loss can lead to conditions from cardiac arrhythmias to heart failure. For myocardial repair, cell- and gene-based therapies offer promising alternatives to donor organ transplantation. Human embryonic stem cells (hESCs) can self-renew while maintaining their pluripotency. Direct reprogramming of adult somatic cells to become pluripotent hES-like cells (also known as induced pluripotent stem cells or iPSCs) has been achieved. Both hESCs and iPSCs have been successfully differentiated into genuine human CMs. In this review, we describe our current knowledge of the structure-function properties of hESC/iPSC-CMs, with an emphasis on their electrophysiology and Ca(2+) handling, along with the hurdles faced and potential solutions for translating into clinical and other applications (e.g., disease modeling, cardiotoxicity and drug screening).

Indexed as

Electrophysiological PhenomenaRegenerationAnimalsEmbryonic Stem CellsHeartHumansInduced Pluripotent Stem CellsMicroRNAsMuscle DevelopmentMyocardial InfarctionMyocytes, CardiacPluripotent Stem CellsSinoatrial NodeTissue EngineeringMicroRNAs

Identifiers

PMID21879736
PMCPMC3362797

What OpenQuestion holds

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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.