Evidence map›Paper›PMID 21540845›Full record

ReviewNature cell biology2011

Harnessing the potential of induced pluripotent stem cells for regenerative medicine.

Sean M Wu, Konrad Hochedlinger

Erratum issued Registry-linked trialAbstract readReview
In one paragraph

Review in Nature cell biology, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. It is linked to trial NCT01432847 (Generation of Induced Pluripotent Stem), which is not on this map. Cited by 238 papers.

0numbers the graph read from it
0cells of the map it votes in
238citing 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.

NCT01432847 recruitingnot on this map

Generation of Induced Pluripotent Stem (iPS) Cell Lines From Somatic Cells of Participants With Eye Diseases and From Somatic Cells of Matched Controls

TypeobservationalSponsorNational Eye Institute (NEI)Ran2011Enrolled930ConditionsRetinal Disease, AMD, Retinal Degeneration, Retinitis Pigmentosa
3 · Its place in the literature

Who cites it

238 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. Review
  5. Article
  6. Review
  7. Article
  8. Review
  9. Review
  10. Article
  11. Bioreactors, scaffolds and microcarriers andFrontiers in nutrition · 2023
    Review
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Review
  18. Review
  19. Review
  20. Review

178 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

  • Erratum issued
5 · Who and what money

Authors and funding

2 authors.

Sean M WuCardiovascular Research Center, Division of Cardiology, Massachusetts General Hospital, Boston 02114, Massachusetts, USA. smwu@partners.org
Konrad Hochedlinger

Funding

Human Pluripotent Stem Cell and Progenitor Models of Cardiac and Blood DiseasesU01HL100408 · NHLBI · MASSACHUSETTS GENERAL HOSPITAL · PI COWAN, CHAD ALBERT, MELTON, DOUGLAS A · 2009 to 2015
$8.9M
Induced pluripotent stem cells in the understanding and treatment of heart diseaseU01HL099776 · NHLBI · STANFORD UNIVERSITY · PI LONGAKER, MICHAEL T, WU, JOSEPH C. · 2009 to 2015
$8.2M
Transcription Factor Induced ReprogrammingR01HD058013 · NICHD · MASSACHUSETTS GENERAL HOSPITAL · PI HOCHEDLINGER, KONRAD · 2010 to 2019
$4.4M
Reprogramming of somatic cells by defined factorsDP2OD003266 · OD · MASSACHUSETTS GENERAL HOSPITAL · PI HOCHEDLINGER, KONRAD · 2007 to 2007
$2.6M
Generation of functional organs via developmental chimerismDP2OD004411 · OD · STANFORD UNIVERSITY · PI WU, SEAN M · 2008 to 2008
$2.5M
Cardiac Progenitor Cells in Development and DiseaseK08HL081086 · NHLBI · MASSACHUSETTS GENERAL HOSPITAL · PI WU, SEAN M · 2005 to 2010
$657k
Howard Hughes Medical InstituteNHLBI NIH HHS HL081086NHLBI NIH HHS HL100408NHLBI NIH HHS K08 HL081086NHLBI NIH HHS U01 HL099776NHLBI NIH HHS U01 HL100408NICHD NIH HHS HD058013NICHD NIH HHS R01 HD058013NIH HHS DP2 OD003266NIH HHS DP2 OD004411NIH HHS OD003266NIH HHS OD004411
6 · The paper itself

Abstract

The discovery of methods to convert somatic cells into induced pluripotent stem cells (iPSCs) through expression of a small combination of transcription factors has raised the possibility of producing custom-tailored cells for the study and treatment of numerous diseases. Indeed, iPSCs have already been derived from patients suffering from a large variety of disorders. Here we review recent progress that has been made in establishing iPSC-based disease models, discuss associated technical and biological challenges, and highlight possible solutions to overcome these barriers. We believe that a better understanding of the molecular basis of pluripotency, cellular reprogramming and lineage-specific differentiation of iPSCs is necessary for progress in regenerative medicine.

Indexed as

Regenerative MedicineAnimalsCell TransplantationClinical Trials as TopicDrug DiscoveryHumansMicePluripotent Stem Cells

Identifiers

PMID21540845
PMCPMC3617981

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

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.