Evidence map›Paper›PMID 28874577›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2017

Gabriel S Salzman, Shu Zhang, Ankit Gupta, Akiko Koide, Shohei Koide, Demet Araç

Open access · bronzeAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 59 papers.

0numbers the graph read from it
0cells of the map it votes in
59citing papers in PubMed
3.2field-weighted citation impact, top 7% 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

59 citing papers in PubMed, 86 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Adhesion G protein-coupled receptors.Pharmacological reviews · 2026
    Review
  5. Self-cleavage-dependent and -independent functions ofProceedings of the National Academy of Sciences of the United States of America · 2026
    Article
  6. Article
  7. Article
  8. Review
  9. Article
  10. Review
  11. The far extracellular CUB domain of the adhesion GPCR ADGRG6/GPR126 is a key regulator of receptor signaling.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  12. Engineering antibody-drug conjugates targeting an adhesion GPCR, CD97.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Review
  18. Article
  19. Article
  20. Article
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

6 authors at 3 institutions in 1 country.

Gabriel S SalzmanBiophysical Sciences Program, The University of Chicago, Chicago, IL 60637.
Shu ZhangDepartment of Biochemistry and Molecular Biology, The University of Chicago, Chicago, IL 60637.
Ankit GuptaPerlmutter Cancer Center, New York University Langone Medical Center, New York, NY 10016.
Akiko KoidePerlmutter Cancer Center, New York University Langone Medical Center, New York, NY 10016.
Shohei KoidePerlmutter Cancer Center, New York University Langone Medical Center, New York, NY 10016; Shohei.Koide@nyumc.org arac@uchicago.edu.
Demet AraçDepartment of Biochemistry and Molecular Biology, The University of Chicago, Chicago, IL 60637; Shohei.Koide@nyumc.org arac@uchicago.edu.
University of Chicago · USNYU Langone Health · USNew York University · US

Funding

Synthetic Antigen Binder CoreU54GM087519 · NIGMS · UNIVERSITY OF CHICAGO · PI NAKAMOTO, ROBERT K. · 2010 to 2017
$31.9M
Molecular And Cellular Biology Training ProgramT32GM007183 · NIGMS · UNIVERSITY OF CHICAGO · PI GLICK, BENJAMIN S, RICE, PHOEBE A · 1985 to 2021
$23.9M
Graduate Program in Biophysical Sciences at the University of Chicago - Renewal 0T32EB009412 · NIBIB · UNIVERSITY OF CHICAGO · PI ENGEL, GREGORY S, SOSNICK, TOBIN R · 2009 to 2023
$4.9M
Structural and Functional Studies of Adhesion GPCRsR01GM120322 · NIGMS · UNIVERSITY OF CHICAGO · PI ARAC-OZKAN, DEMET · 2016 to 2020
$1.7M
Modulation and molecular mechanisms of GPR56 functionF30GM116455 · NIGMS · UNIVERSITY OF CHICAGO · PI SALZMAN, GABRIEL · 2015 to 2017
$146k
NIBIB NIH HHS T32 EB009412NIGMS NIH HHS F30 GM116455NIGMS NIH HHS R01 GM120322NIGMS NIH HHS T32 GM007183NIGMS NIH HHS U54 GM087519
6 · The paper itself

Abstract

Adhesion G protein-coupled receptors (aGPCRs) play critical roles in diverse biological processes, including neurodevelopment and cancer progression. aGPCRs are characterized by large and diverse extracellular regions (ECRs) that are autoproteolytically cleaved from their membrane-embedded signaling domains. Although ECRs regulate receptor function, it is not clear whether ECRs play a direct regulatory role in G-protein signaling or simply serve as a protective cap for the activating "

Indexed as

ProteolysisSignal TransductionAnimalsCell LineHumansPeptidesProtein DomainsReceptors, G-Protein-CoupledSpodopteraADGRG1 protein, humanPeptidesReceptors, G-Protein-Coupledadhesion GPCRallosterycell signalingmonobodyprotein engineering

Identifiers

PMID28874577
PMCPMC5617296
OpenAlexW2751716123

What OpenQuestion holds

Textmetadata
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.