Evidence map›Paper›PMID 19998274›Full record

ArticleHepatology (Baltimore, Md.)2010

Highly efficient generation of human hepatocyte-like cells from induced pluripotent stem cells.

Karim Si-Tayeb, Fallon K Noto, Masato Nagaoka, Jixuan Li, Michele A Battle, Christine Duris, Paula E North, Stephen Dalton, Stephen A Duncan

Erratum issuedAbstract read
In one paragraph

Article in Hepatology (Baltimore, Md.), 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 645 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
645citing papers in PubMed, 1 pooled it
–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

645 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Review
  3. Article
  4. Article
  5. Review
  6. Article
  7. Review
  8. Review
  9. A CYP3A7 metabolically competent human induced pluripotent stem cell-derived hepatocyte-like cell (hHLCDrug metabolism and disposition: the biological fate of chemicals · 2026
    Article
  10. Article
  11. Article
  12. Article
  13. Review
  14. [Advances in the construction and application of a novel liver organoid model for hepatitis B virus infection].Zhonghua gan zang bing za zhi = Zhonghua ganzangbing zazhi = Chinese journal of hepatology · 2026
    Review
  15. Haematologica · 2026
    Article
  16. Review
  17. Article
  18. Review
  19. Article
  20. Article

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

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

9 authors.

Karim Si-TayebDepartment of Cell Biology, Division of Pediatric Pathology, Medical College of Wisconsin, Milwaukee, WI 53226, USA.
Fallon K Noto
Masato Nagaoka
Jixuan Li
Michele A Battle
Christine Duris
Paula E North
Stephen Dalton
Stephen A Duncan

Funding

UNDERSTANDING MECHANISMS OF hESC SELF-RENEWAL AND CELL FATE COMMITMENTP01GM085354 · NIGMS · UNIVERSITY OF GEORGIA · PI DALTON, STEPHEN · 2008 to 2018
$18.3M
Role of GATA4 and GATA6 in Controlling Heart DevelopmentP01HL089471 · NHLBI · MEDICAL COLLEGE OF WISCONSIN · PI NORTH, PAULA E. · 2009 to 2013
$7.9M
TRANSCRIPTIONAL REGULAT OF MAMMALIAN HEPATIC DEVELOPMENTR01DK055743 · NIDDK · MEDICAL COLLEGE OF WISCONSIN · PI DUNCAN, STEPHEN A · 2000 to 2014
$4.6M
Modeling liver metabolism with patient-specific iPS derived hepatocytesRC1DK087377 · NIDDK · MEDICAL COLLEGE OF WISCONSIN · PI DUNCAN, STEPHEN A, GROMPE, MARKUS · 2009 to 2010
$999k
NHLBI NIH HHS P01 HL089471NIDDK NIH HHS R01 DK055743NIDDK NIH HHS RC1 DK087377NIGMS NIH HHS P01 GM085354
6 · The paper itself

Abstract

unlabelledThere exists a worldwide shortage of donor livers available for orthotropic liver transplantation and hepatocyte transplantation therapies. In addition to their therapeutic potential, primary human hepatocytes facilitate the study of molecular and genetic aspects of human hepatic disease and development and provide a platform for drug toxicity screens and identification of novel pharmaceuticals with potential to treat a wide array of metabolic diseases. The demand for human hepatocytes, therefore, heavily outweighs their availability. As an alternative to using donor livers as a source of primary hepatocytes, we explored the possibility of generating patient-specific human hepatocytes from induced pluripotent stem (iPS) cells.

conclusionWe demonstrate that mouse iPS cells retain full potential for fetal liver development and describe a procedure that facilitates the efficient generation of highly differentiated human hepatocyte-like cells from iPS cells that display key liver functions and can integrate into the hepatic parenchyma in vivo.

Indexed as

AnimalsCell DifferentiationHepatocytesHumansInduced Pluripotent Stem CellsMice

Identifiers

PMID19998274
PMCPMC2946078

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.