Evidence map›Paper›PMID 37839914›Full record

ReviewTrends in pharmacological sciences2023

Celiac disease: mechanisms and emerging therapeutics.

Harrison A Besser, Chaitan Khosla

Open access · greenAbstract readReview
In one paragraph

Review in Trends in pharmacological sciences, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
10.3field-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

24 citing papers in PubMed, 37 citations in OpenAlex.

  1. Review
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  19. Structural and mechanistic analysis of CaProceedings of the National Academy of Sciences of the United States of America · 2024
    Article
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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

2 authors at 1 institution in 1 country.

Harrison A BesserDepartment of Chemistry, Stanford University, Stanford, CA 94305, USA; Stanford Medical Scientist Training Program, Stanford University School of Medicine, Stanford, CA 94305, USA.
Chaitan KhoslaDepartment of Chemistry, Stanford University, Stanford, CA 94305, USA; Department of Chemical Engineering, Stanford University, Stanford, CA 94305, USA; Sarafan ChEM-H (Chemistry, Engineering and Medicine for Human Health), Stanford University, Stanford, CA 94305, USA. Electronic address: khosla@stanford.edu.
Stanford University · US

Funding

MEDICAL SCIENTIST TRAINING PROGRAMT32GM007365 · NIGMS · STANFORD UNIVERSITY · PI CHUA, KATRIN F · 1985 to 2021
$33.8M
Role of Transglutaminase 2 in Celiac SprueR01DK063158 · NIDDK · STANFORD UNIVERSITY · PI CHAITAN KHOSLA · 2003 to 2026
$11.2M
Medical Scientist Training ProgramT32GM145402 · NIGMS · STANFORD UNIVERSITY · PI Katrin F. Chua · 2022 to 2026
$10.0M
Localizing Pathogenically Relevant Transglutaminase 2 in Celiac DiseaseR01DK126487 · NIDDK · STANFORD UNIVERSITY · PI JABRI, BANA, KHOSLA, CHAITAN · 2021 to 2025
$1.8M
Gluten peptide presentation in celiac disease: investigating the role of transglutaminase 2 using novel chemical probesF30DK132903 · NIDDK · STANFORD UNIVERSITY · PI BESSER, HARRISON ANTHONY · 2022 to 2023
$80k
NIDDK NIH HHS F30 DK132903NIDDK NIH HHS R01 DK063158NIDDK NIH HHS R01 DK126487NIGMS NIH HHS T32 GM007365NIGMS NIH HHS T32 GM145402
6 · The paper itself

Abstract

Celiac disease (CeD) is a widespread, gluten-induced, autoimmune disorder that lacks any medicinal therapy. Towards the goal of developing non-dietary treatments for CeD, research has focused on elucidating its molecular and cellular etiology. A model of pathogenesis has emerged centered on interactions between three molecular families: specific class II MHC proteins on antigen-presenting cells (APCs), deamidated gluten-derived peptides, and T cell receptors (TCRs) on inflammatory CD4

Indexed as

Celiac DiseaseAntigen-Presenting CellsGlutensHumansReceptors, Antigen, T-CellT-LymphocytesGlutensReceptors, Antigen, T-Cellantigen-presenting cellsautoimmunityceliac diseaseclinical trialsglutenmajor histocompatibility complexT cellstherapeuticstransglutaminase

Identifiers

PMID37839914
PMCPMC10843302
OpenAlexW4387641222

What Socratic 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 Socratic graph.