Evidence map›Paper›PMID 28335859›Full record

ReviewCurrent topics in developmental biology2017

Making It New Again: Insight Into Liver Development, Regeneration, and Disease From Zebrafish Research.

Shuang Wang, Sophie R Miller, Elke A Ober, Kirsten C Sadler

Abstract readReview
In one paragraph

Review in Current topics in developmental biology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed
6.3field-weighted citation impact, top 3% 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

34 citing papers in PubMed, 67 citations in OpenAlex.

  1. Article
  2. Article
  3. Flavone C-Glycosides fromNutrients · 2025
    Article
  4. Review
  5. Article
  6. Article
  7. Article
  8. Article
  9. Methods to Study Liver Disease Using Zebrafish Larvae.Methods in molecular biology (Clifton, N.J.) · 2024
    Article
  10. Using different zebrafish models to explore liver regeneration.Frontiers in cell and developmental biology · 2024
    Review
  11. Article
  12. Review
  13. Regulation of chromatin organization during animal regeneration.Cell regeneration (London, England) · 2023
    Review
  14. Article
  15. Article
  16. Article
  17. Article
  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

4 authors at 2 institutions in 3 countries.

Shuang WangIcahn School of Medicine at Mount Sinai, New York, NY, United States.
Sophie R MillerDanish Stem Cell Center (DanStem), University of Copenhagen, Copenhagen N, Denmark.
Elke A OberDanish Stem Cell Center (DanStem), University of Copenhagen, Copenhagen N, Denmark.
Kirsten C SadlerIcahn School of Medicine at Mount Sinai, New York, NY, United States; New York University Abu Dhabi, Abu Dhabi, United Arab Emirates. Electronic address: kirsten.edepli@nyu.edu.
Icahn School of Medicine at Mount Sinai · USUniversity of Copenhagen · DK

Funding

Role of Uhrf1 in Liver Development, Regeneration and CarciogenesisR01DK080789 · NIDDK · NEW YORK UNIVERSITY · PI Kirsten C Sadler Edepli · 2009 to 2026
$5.2M
Understanding fatty liver disease using the zebrafish mutant, foie grasR01AA018886 · NIAAA · NEW YORK UNIVERSITY · PI SADLER EDEPLI, KIRSTEN C · 2009 to 2017
$2.4M
NIAAA NIH HHS R01 AA018886NIDDK NIH HHS R01 DK080789
6 · The paper itself

Abstract

The adult liver of most vertebrates is predominantly comprised of hepatocytes. However, these cells must work in concert with biliary, stellate, vascular, and immune cells to accomplish the vast array of hepatic functions required for physiological homeostasis. Our understanding of liver development was accelerated as zebrafish emerged as an ideal vertebrate system to study embryogenesis. Through work in zebrafish and other models, it is now clear that the cells in the liver develop in a coordinated fashion during embryogenesis through a complex yet incompletely understood set of molecular guidelines. Zebrafish research has uncovered many key players that govern the acquisition of hepatic potential, cell fate, and plasticity. Although rare, some hepatobiliary diseases-especially biliary atresia-are caused by developmental defects; we discuss how research using zebrafish to study liver development has informed our understanding of and approaches to liver disease. The liver can be injured in response to an array of stressors including viral, mechanical/surgical, toxin-induced, immune-mediated, or inborn defects in metabolism. The liver has thus evolved the capacity to efficiently repair and regenerate. We discuss the emerging field of using zebrafish to study liver regeneration and highlight recent advances where zebrafish genetics and imaging approaches have provided novel insights into how cell plasticity contributes to liver regeneration.

Indexed as

Liver RegenerationAnimalsLiverLiver DiseasesModels, BiologicalZebrafishBiliary atresiaBiliary developmentHepatogenesisLiver developmentLiver regenerationZebrafish

Identifiers

PMID28335859
PMCPMC6450094
OpenAlexW2746799676

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.