Evidence map›Paper›PMID 23630303›Full record

ArticleDiabetes2013

Development of the human pancreas from foregut to endocrine commitment.

Rachel E Jennings, Andrew A Berry, Rebecca Kirkwood-Wilson, Neil A Roberts, Thomas Hearn, Rachel J Salisbury, Jennifer Blaylock, Karen Piper Hanley, Neil A Hanley

Open access · hybridAbstract read
In one paragraph

Article in Diabetes, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 165 papers.

0numbers the graph read from it
0cells of the map it votes in
165citing papers in PubMed
17.1field-weighted citation impact, top 1% 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

165 citing papers in PubMed, 312 citations in OpenAlex.

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  19. Pancreatic organogenesis mapped through space and time.Experimental & molecular medicine · 2025
    Article
  20. Review

105 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

9 authors at 3 institutions in 1 country.

Rachel E JenningsCentre for Endocrinology and Diabetes, Institute of Human Development, Faculty of Medical & Human Sciences, Manchester Academic Health Sciences Centre, University of Manchester, Manchester, U.K.
Andrew A Berry
Rebecca Kirkwood-Wilson
Neil A Roberts
Thomas Hearn
Rachel J Salisbury
Jennifer Blaylock
Karen Piper Hanley
Neil A Hanley
Manchester Academic Health Science Centre · GBNational Health Service · GBSouthampton General Hospital · GB

Funding

Medical Research Council G1100420Medical Research Council MR/J003352/1Wellcome Trust 088566Wellcome Trust WT088566MAWellcome Trust WT097820MF
6 · The paper itself

Abstract

Knowledge of human pancreas development underpins our interpretation and exploitation of human pluripotent stem cell (PSC) differentiation toward a β-cell fate. However, almost no information exists on the early events of human pancreatic specification in the distal foregut, bud formation, and early development. Here, we have studied the expression profiles of key lineage-specific markers to understand differentiation and morphogenetic events during human pancreas development. The notochord was adjacent to the dorsal foregut endoderm during the fourth week of development before pancreatic duodenal homeobox-1 detection. In contrast to the published data from mouse embryos, during human pancreas development, we detected only a single-phase of Neurogenin 3 (NEUROG3) expression and endocrine differentiation from approximately 8 weeks, before which Nirenberg and Kim homeobox 2.2 (NKX2.2) was not observed in the pancreatic progenitor cell population. In addition to revealing a number of disparities in timing between human and mouse development, these data, directly assembled from human tissue, allow combinations of transcription factors to define sequential stages and differentiating pancreatic cell types. The data are anticipated to provide a useful reference point for stem cell researchers looking to differentiate human PSCs in vitro toward the pancreatic β-cell so as to model human development or enable drug discovery and potential cell therapy.

Indexed as

Cell DifferentiationAnimalsBasic Helix-Loop-Helix ProteinsCell LineageEndocrine SystemFemaleGene Expression Regulation, DevelopmentalHomeobox Protein Nkx-2.2Homeodomain ProteinsHumansImmunohistochemistryInsulin-Secreting CellsMiceNerve Tissue ProteinsNuclear ProteinsPancreasBasic Helix-Loop-Helix ProteinsHomeobox Protein Nkx-2.2Homeodomain ProteinsNerve Tissue ProteinsNEUROG3 protein, humanNeurog3 protein, mousenkx2.2b protein, zebrafishNKX2-2 protein, humanNkx2-2 protein, mouseNuclear ProteinsTranscription FactorsZebrafish Proteins

Identifiers

PMID23630303
PMCPMC3781486
OpenAlexW2115389601

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.