Evidence map›Paper›PMID 42531125›Full record

ArticleSTAR protocols2026

Protocol to stress human primary pancreatic islets with diabetogenic factors for subsequent single-cell RNA sequencing.

Daniel A Veronese-Paniagua, Marlie M Maestas, Jared P Taylor, Hubert M Tse, Jeffrey R Millman

Abstract read
In one paragraph

Article in STAR protocols, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

5 authors.

Daniel A Veronese-PaniaguaRoy and Diana Vagelos Division of Biology and Biomedical Sciences, Washington University School of Medicine, St. Louis, MO 63110, USA; Division of Endocrinology, Metabolism, and Lipid Research, Washington University School of Medicine, St. Louis, MO 63110, USA.
Marlie M MaestasRoy and Diana Vagelos Division of Biology and Biomedical Sciences, Washington University School of Medicine, St. Louis, MO 63110, USA; Division of Endocrinology, Metabolism, and Lipid Research, Washington University School of Medicine, St. Louis, MO 63110, USA.
Jared P TaylorDepartment of Microbiology, University of Alabama at Birmingham, Birmingham, AL 35294, USA.
Hubert M TseDepartment of Microbiology, Molecular Genetics and Immunology, The University of Kansas Medical Center, Kansas City, KS 66160, USA. Electronic address: htse@kumc.edu.
Jeffrey R MillmanRoy and Diana Vagelos Division of Biology and Biomedical Sciences, Washington University School of Medicine, St. Louis, MO 63110, USA; Division of Endocrinology, Metabolism, and Lipid Research, Washington University School of Medicine, St. Louis, MO 63110, USA. Electronic address: jmillman@wustl.edu.

Funding

Washington University Center for Cellular ImagingP30CA091842 · NCI · WASHINGTON UNIVERSITY · PI TIMOTHY J. EBERLEIN · 2001 to 2026
$128.0M
WU P&FP30DK020579 · NIDDK · WASHINGTON UNIVERSITY · PI Clay F. Semenkovich · 2013 to 2026
$27.1M
Determining the mechanism of IFIH1 disease-associated variants on beta-cell and immune responses in Type 1 diabetesR01DK127497 · NIDDK · UNIVERSITY OF KANSAS MEDICAL CENTER · PI MATHEWS, CLAYTON E, MILLMAN, JEFFREY ROBERT · 2020 to 2023
$4.7M
STUDYING THE ROLE OF THE MICROENVIRONMENT ON DIFFERENTIATION AND MATURATION OF BETA CELLSR01DK114233 · NIDDK · WASHINGTON UNIVERSITY · PI Jeffrey Robert Millman · 2017 to 2026
$3.6M
Beta-cell responses to oxidative stress and Type 1 diabetesR01DK126456 · NIDDK · UNIVERSITY OF KANSAS MEDICAL CENTER · PI HUNTER, CHAD S, TSE, HUBERT M · 2021 to 2025
$2.3M
Uncovering the Interplay Among Pancreatic Tissue Types, Inflammation, and Genotypes in Type 1 DiabetesR01DK138469 · NIDDK · WASHINGTON UNIVERSITY · PI Jeffrey Robert Millman, HUBERT M TSE · 2024 to 2026
$811k
NCI NIH HHS P30 CA091842NIDDK NIH HHS P30 DK020579NIDDK NIH HHS R01 DK114233NIDDK NIH HHS R01 DK126456NIDDK NIH HHS R01 DK127497NIDDK NIH HHS R01 DK138469
6 · The paper itself

Abstract

Type 1 diabetes (T1D) is an autoimmune disease that destroys insulin-secreting pancreatic β cells. Using human islets is instrumental to understanding the initiation and progression of T1D. Here, we present a protocol for treating cadaveric primary human islets with inflammatory, immune, and viral stressors. We detail Coxsackievirus B3 expansion, primary islet cell culture, and treatment with diabetogenic stressors, followed by procedures for single-cell RNA sequencing analysis. For complete execution details, please refer to Maestas et al.

Indexed as

BioinformaticsGenomicsImmunologyMolecular BiologyRNAseqSequencingSingle Cell

Identifiers

PMID42531125
PMCPMC13452298

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.