Evidence map›Paper›PMID 31350390›Full record

ArticleNature communications2019

Single cell analysis of human foetal liver captures the transcriptional profile of hepatobiliary hybrid progenitors.

Joe M Segal, Deniz Kent, Daniel J Wesche, Soon Seng Ng, Maria Serra, Bénédicte Oulès, Gozde Kar, Guy Emerton, Samuel J I Blackford, Spyros Darmanis and 13 more

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 66 papers.

0numbers the graph read from it
0cells of the map it votes in
66citing papers in PubMed
6.1field-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

66 citing papers in PubMed, 130 citations in OpenAlex.

  1. Article
  2. A CYP3A7 metabolically competent human induced pluripotent stem cell-derived hepatocyte-like cell (hHLCDrug metabolism and disposition: the biological fate of chemicals · 2026
    Article
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  11. Organoids in biliary atresia.World journal of pediatric surgery · 2025
    Review
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  16. Review
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  20. Article

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

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

23 authors at 4 institutions in 2 countries.

Joe M SegalCentre for Stem Cells and Regenerative Medicine & Institute for Liver Studies, King's College London, London, WC2R 2LS, UK. joe.segal@kcl.ac.uk.ORCID http://orcid.org/0000-0003-2079-2722
Deniz KentCentre for Stem Cells and Regenerative Medicine & Institute for Liver Studies, King's College London, London, WC2R 2LS, UK.
Daniel J WescheInstitute for Stem Cell Biology and Regenerative Medicine, Stanford University School of Medicine, Stanford, CA, 94305, USA.
Soon Seng NgCentre for Stem Cells and Regenerative Medicine & Institute for Liver Studies, King's College London, London, WC2R 2LS, UK.ORCID http://orcid.org/0000-0001-9851-1447
Maria SerraCentre for Stem Cells and Regenerative Medicine & Institute for Liver Studies, King's College London, London, WC2R 2LS, UK.
Bénédicte OulèsCentre for Stem Cells and Regenerative Medicine & Institute for Liver Studies, King's College London, London, WC2R 2LS, UK.ORCID http://orcid.org/0000-0001-8269-4306
Gozde KarWellcome Trust Sanger Institute, Hinxton, CB10 1SA, UK.
Guy EmertonWellcome Trust Sanger Institute, Hinxton, CB10 1SA, UK.
Samuel J I BlackfordCentre for Stem Cells and Regenerative Medicine & Institute for Liver Studies, King's College London, London, WC2R 2LS, UK.ORCID http://orcid.org/0000-0001-5890-0624
Spyros DarmanisSchool of Engineering, Stanford University, Stanford, 94350, CA, USA.
Rosa MiquelCentre for Stem Cells and Regenerative Medicine & Institute for Liver Studies, King's College London, London, WC2R 2LS, UK.
Tu Vinh LuongCentre for Stem Cells and Regenerative Medicine & Institute for Liver Studies, King's College London, London, WC2R 2LS, UK.
Ryo YamamotoInstitute for Stem Cell Biology and Regenerative Medicine, Stanford University School of Medicine, Stanford, CA, 94305, USA.
Andrew BonhamInstitute for Stem Cell Biology and Regenerative Medicine, Stanford University School of Medicine, Stanford, CA, 94305, USA.
Wayel JassemInstitute of Liver Studies, Kings College Hospital, London, SE4 9RS, UK.
Nigel HeatonInstitute of Liver Studies, Kings College Hospital, London, SE4 9RS, UK.
Alessandra VigilanteCentre for Stem Cells and Regenerative Medicine & Institute for Liver Studies, King's College London, London, WC2R 2LS, UK.
Aileen KingDepartment of Diabetes, King's College London, London, SE1 1UL, UK.
Rocio SanchoCentre for Stem Cells and Regenerative Medicine & Institute for Liver Studies, King's College London, London, WC2R 2LS, UK.ORCID http://orcid.org/0000-0002-4894-5391
Sarah TeichmannWellcome Trust Sanger Institute, Hinxton, CB10 1SA, UK.ORCID http://orcid.org/0000-0002-6294-6366
Stephen R QuakeSchool of Engineering, Stanford University, Stanford, 94350, CA, USA.
Hiromitsu NakauchiInstitute for Stem Cell Biology and Regenerative Medicine, Stanford University School of Medicine, Stanford, CA, 94305, USA.
S Tamir RashidCentre for Stem Cells and Regenerative Medicine & Institute for Liver Studies, King's College London, London, WC2R 2LS, UK. tamir.rashid@kcl.ac.uk.
King's College London · GBStanford University · USWellcome Sanger Institute · GBKing's College Hospital · GB

Funding

Translational Incubator CoreU19AI109662 · NIAID · STANFORD UNIVERSITY · PI GLENN, JEFFREY S · 2014 to 2019
$28.6M
The PIP2-virus interface and PI 4-kinase: novel biology and validation targetsR01AI099245 · NIAID · STANFORD UNIVERSITY · PI GLENN, JEFFREY S · 2012 to 2016
$5.2M
Medical Research Council MR/L006537/1Medical Research Council MR/S000011/1NIAID NIH HHS R01 AI099245NIAID NIH HHS U19 AI109662
6 · The paper itself

Abstract

The liver parenchyma is composed of hepatocytes and bile duct epithelial cells (BECs). Controversy exists regarding the cellular origin of human liver parenchymal tissue generation during embryonic development, homeostasis or repair. Here we report the existence of a hepatobiliary hybrid progenitor (HHyP) population in human foetal liver using single-cell RNA sequencing. HHyPs are anatomically restricted to the ductal plate of foetal liver and maintain a transcriptional profile distinct from foetal hepatocytes, mature hepatocytes and mature BECs. In addition, molecular heterogeneity within the EpCAM

Indexed as

Transcription, GeneticAntigens, NeoplasmCell Adhesion MoleculesEpithelial Cell Adhesion MoleculeFetusHepatocytesHumansLiverSingle-Cell AnalysisStem CellsAntigens, NeoplasmCell Adhesion MoleculesEPCAM protein, humanEpithelial Cell Adhesion MoleculeTACSTD2 protein, human

Identifiers

PMID31350390
PMCPMC6659636
OpenAlexW2963310788

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.