Evidence map›Paper›PMID 30145115›Full record

ArticleCell systems2018

A Chromatin Basis for Cell Lineage and Disease Risk in the Human Pancreas.

H Efsun Arda, Jennifer Tsai, Yenny R Rosli, Paul Giresi, Rita Bottino, William J Greenleaf, Howard Y Chang, Seung K Kim

Open access · bronzeAbstract read
In one paragraph

Article in Cell systems, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed, 2 pooled it
9.9field-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

34 citing papers in PubMed, 2 syntheses or guidelines pooled it, 57 citations in OpenAlex.

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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

8 authors at 3 institutions in 1 country.

H Efsun ArdaDepartment of Developmental Biology, Stanford University School of Medicine, 279 Campus Drive, Stanford, CA 94305, USA.
Jennifer TsaiDepartment of Developmental Biology, Stanford University School of Medicine, 279 Campus Drive, Stanford, CA 94305, USA.
Yenny R RosliDepartment of Developmental Biology, Stanford University School of Medicine, 279 Campus Drive, Stanford, CA 94305, USA.
Paul GiresiCenter for Personal Dynamic Regulomes, 269 Campus Drive CCSR 2145, Stanford, CA 94305, USA.
Rita BottinoInstitute of Cellular Therapeutics, Allegheny Health Network, 320 East North Avenue, Pittsburgh, PA 15212, USA.
William J GreenleafDepartment of Genetics, Stanford University School of Medicine, 279 Campus Drive West Beckman Center, B-257, Stanford, CA 94305, USA; Chan Zuckerberg Biohub, San Francisco, CA 94158, USA.
Howard Y ChangCenter for Personal Dynamic Regulomes, 269 Campus Drive CCSR 2145, Stanford, CA 94305, USA; Program in Epithelial Biology, Stanford University School of Medicine, 269 Campus Drive CCSR 2145, Stanford, CA 94305, USA.
Seung K KimDepartment of Developmental Biology, Stanford University School of Medicine, 279 Campus Drive, Stanford, CA 94305, USA; Department of Medicine, Stanford University School of Medicine, 279 Campus Drive, Stanford, CA 94305, USA; Stanford Diabetes Research Center, Stanford University School of Medicine, 279 Campus Drive, Stanford, CA 94305, USA. Electronic address: seungkim@stanford.edu.
Stanford University · USAllegheny Health Network · USDynamic Systems (United States) · US

Funding

Vanderbilt Diabetes Research CenterP30DK020593 · NIDDK · VANDERBILT UNIVERSITY MEDICAL CENTER · PI ALVIN C POWERS · 2012 to 2026
$29.3M
Stanford Islet Research CoreP30DK116074 · NIDDK · STANFORD UNIVERSITY · PI Seung K Kim · 2017 to 2026
$19.5M
Special EquipmentP50HG007735 · NHGRI · STANFORD UNIVERSITY · PI CHANG, HOWARD Y · 2014 to 2018
$15.2M
Molecular Mechanisms of Physiologic Beta Cell Growth in Juvenile Human PancreasUC4DK104211 · NIDDK · VANDERBILT UNIVERSITY MEDICAL CENTER · PI KIM, SEUNG K, POWERS, ALVIN C · 2014 to 2015
$4.0M
Epigenetic and Genetic Control of Human and Murine Beta Cell Development and FateU01DK089532 · NIDDK · STANFORD UNIVERSITY · PI KIM, SEUNG K · 2010 to 2014
$3.4M
CAR T cell targeting of human isletsUC4DK116252 · NIDDK · STANFORD UNIVERSITY · PI KIM, SEUNG K, MEYER, EVERETT · 2017 to 2017
$1.4M
Howard Hughes Medical InstituteNHGRI NIH HHS P50 HG007735NIDDK NIH HHS P30 DK020593NIDDK NIH HHS P30 DK116074NIDDK NIH HHS U01 DK089532NIDDK NIH HHS UC4 DK104211NIDDK NIH HHS UC4 DK116252
6 · The paper itself

Abstract

Understanding the genomic logic that underlies cellular diversity and developmental potential in the human pancreas will accelerate the growth of cell replacement therapies and reveal genetic risk mechanisms in diabetes. Here, we identified and characterized thousands of chromatin regions governing cell-specific gene regulation in human pancreatic endocrine and exocrine lineages, including islet β cells, α cells, duct, and acinar cells. Our findings have captured cellular ontogenies at the chromatin level, identified lineage-specific regulators potentially acting on these sites, and uncovered hallmarks of regulatory plasticity between cell types that suggest mechanisms to regenerate β cells from pancreatic endocrine or exocrine cells. Our work shows that disease risk variants related to pancreas are significantly enriched in these regulatory regions and reveals previously unrecognized links between endocrine and exocrine pancreas in diabetes risk.

Indexed as

Cell DifferentiationCell LineageCell PlasticityCells, CulturedChromatinChromatin Assembly and DisassemblyDiabetes MellitusGene Expression RegulationHomeodomain ProteinsHumansInsulin-Secreting CellsOrgan SpecificityPancreasPancreas, ExocrinePolymorphism, Single NucleotideRegenerationChromatinHomeodomain ProteinsATAC-seqcell lineagechromatindevelopmentdiabetesenhancergenomicshistone modificationisletpancreas

Identifiers

PMID30145115
PMCPMC6347013
OpenAlexW2888208343

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.