Evidence map›Paper›PMID 21527744›Full record

ReviewCirculation research2011

Derivation of human induced pluripotent stem cells for cardiovascular disease modeling.

Kamileh Narsinh, Kazim H Narsinh, Joseph C Wu

Open access · bronzeAbstract readReview
In one paragraph

Review in Circulation research, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 43 papers.

0numbers the graph read from it
0cells of the map it votes in
43citing papers in PubMed
4.9field-weighted citation impact, top 4% 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

43 citing papers in PubMed, 70 citations in OpenAlex.

  1. A Hypoxia-reoxygenation Injury Model in Self-assembling Human Cardioids.Journal of visualized experiments : JoVE · 2026
    Article
  2. Article
  3. Article
  4. Review
  5. Review
  6. Review
  7. Gene Therapy Approaches to Biological Pacemakers.Journal of cardiovascular development and disease · 2018
    Review
  8. Article
  9. Article
  10. Review
  11. Review
  12. Article
  13. Review
  14. Review
  15. Article
  16. Review
  17. Article
  18. Article
  19. Article
  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 at 1 institution in 1 country.

Kamileh NarsinhDepartment of Medicine, Stanford University School of Medicine, Stanford, CA, USA.
Kazim H Narsinh
Joseph C Wu
University of California, Los Angeles · US

Funding

09: Inducing Pluripotency with MiRNAs: New Paradigm Shif in Cell ReprogrammingDP2OD004437 · OD · STANFORD UNIVERSITY · PI WU, JOSEPH C. · 2008 to 2008
$2.4M
Nanostructuring and Molecular Imaging of Engineered Cardiovascular TissuesR33HL089027 · NHLBI · STANFORD UNIVERSITY · PI WU, JOSEPH C. · 2009 to 2011
$2.3M
Nanostructuring and Molecular Imaging of Engineered Cardiovascular TissuesR21HL089027 · NHLBI · STANFORD UNIVERSITY · PI WU, JOSEPH C. · 2007 to 2008
$777k
Biological Insights into Dynamics of Stem Cell Differentiation and MisbehaviorR21HL091453 · NHLBI · STANFORD UNIVERSITY · PI WU, JOSEPH C. · 2008 to 2009
$719k
Howard Hughes Medical InstituteNHLBI NIH HHS HL089027NHLBI NIH HHS HL091453NHLBI NIH HHS R21 HL091453NHLBI NIH HHS R33 HL089027NIH HHS DP2 OD004437NIH HHS DP2OD004437
6 · The paper itself

Abstract

The successful derivation of human induced pluripotent stem cells (hiPSCs) by dedifferentiation of somatic cells offers significant potential to overcome obstacles in the field of cardiovascular disease. hiPSC derivatives offer incredible potential for new disease models and regenerative medicine therapies. However, many questions remain regarding the optimal starting materials and methods to enable safe, efficient derivation of hiPSCs suitable for clinical applications. Initial reprogramming experiments were carried out using lentiviral or retroviral gene delivery methods. More recently, various nonviral methods that avoid permanent and random transgene insertion have emerged as alternatives. These include transient DNA transfection using plasmids or minicircles, protein transduction, or RNA transfection. In addition, several small molecules have been found to significantly augment hiPSC derivation efficiency, allowing the use of a fewer number of genes during pluripotency induction. We review these various methods for the derivation of hiPSCs, focusing on their ultimate clinical applicability, with an emphasis on their potential for use as cardiovascular therapies and disease-modeling platforms.

Indexed as

Cardiovascular DiseasesCell DedifferentiationHumansMyocytes, CardiacPluripotent Stem Cells

Identifiers

PMID21527744
PMCPMC3098466
OpenAlexW2127725721

What OpenQuestion holds

Textmetadata
LicenceTDM
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.