Paper · 18445652
Beta-Arrestin-1 mediates glucagon-like peptide-1 signaling to insulin secretion in cultured pancreatic beta cells.
Sonoda N and 5 others. Proc Natl Acad Sci U S A, 2008. Cited by 195 papers, by iCite.
11 sourcespapers-2026-11-12-0.1.0
Cite this record
ConductScience Library. Beta-Arrestin-1 mediates glucagon-like peptide-1 signaling to insulin secretion in cultured pancreatic beta cells. Papers, record 18445652. Release papers-2026-11-12-0.1.0, 12 Nov 2026. https://conductscience.org/library/papers/18445652
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Paper
PubMed's record of the paper, with iCite's citation figures. No abstract is shown.
Topics19
NLM's MeSH indexing of the paper, its major topics first.
| MeSH term | Major |
|---|---|
| Arrestins | Major topic |
| Glucagon-Like Peptide 1 | Major topic |
| Insulin | Major topic |
| Insulin-Secreting Cells | Major topic |
| Signal Transduction | Major topic |
| Animals | |
| Cells, Cultured | |
| Cyclic AMP | |
| Endocytosis | |
| Glucagon-Like Peptide-1 Receptor | |
| Insulin Receptor Substrate Proteins | |
| Insulin Secretion | |
| Intracellular Signaling Peptides and Proteins | |
| Phosphoproteins | |
| Protein Binding | |
| Rats | |
| Receptors, Glucagon | |
| beta-Arrestin 1 | |
| beta-Arrestins |
Source PubMed
Grants7
Each grant PubMed's record writes, matched to the NIH project NIH's grant and paper links name for this paper, and each of those links the record does not write.
| Grant, as the record writes it | Agency | Country | NIH project | Stated by | Source |
|---|---|---|---|---|---|
| P01 DK074868 | NIDDK NIH HHS | United States | P01DK074868 | PubMed and NIH | NIH RePORTER |
| DK 033651 | NIDDK NIH HHS | United States | R01DK033651 | PubMed and NIH | NIH RePORTER |
| R01 DK033651 | NIDDK NIH HHS | United States | R01DK033651 | PubMed and NIH | NIH RePORTER |
| DK 074868 | NIDDK NIH HHS | United States | P01DK074868 | PubMed and NIH | NIH RePORTER |
| U54 HD012303 | NICHD NIH HHS | United States | U54HD012303 | PubMed and NIH | NIH RePORTER |
| R37 DK033651 | NIDDK NIH HHS | United States | R01DK033651 | PubMed and NIH | NIH RePORTER |
| R37DK033651 | NIH | NIH RePORTER |
Trials0
The trials whose ClinicalTrials.gov record lists the paper, and the trial numbers the paper's PubMed record names.
None in this release.
Comments and corrections0
PubMed's comments and corrections, NLM's own indexing: retractions first, then expressions of concern, errata and updates, and comments last.
None in this release.
References37
The papers the reference list in PubMed's record names, those in our copy of PubMed, in the list's order.
| Order | PMID | Title | Journal | Year | In Papers | Source |
|---|---|---|---|---|---|---|
| 1 | 17,289,847 | A role for beta-cell-expressed G protein-coupled receptor 119 in glycemic control by enhancing glucose-dependent insulin release. | Endocrinology | 2007 | https://conductscience.org/library/papers/17289847 | PubMed |
| 2 | 15,699,045 | Receptor-specific ubiquitination of beta-arrestin directs assembly and targeting of seven-transmembrane receptor signalosomes. | J Biol Chem | 2005 | https://conductscience.org/library/papers/15699045 | PubMed |
| 3 | 11,598,134 | Critical role of cAMP-GEFII--Rim2 complex in incretin-potentiated insulin secretion. | J Biol Chem | 2001 | https://conductscience.org/library/papers/11598134 | PubMed |
| 4 | 10,559,259 | Endothelin-1-induced GLUT4 translocation is mediated via Galpha(q/11) protein and phosphatidylinositol 3-kinase in 3T3-L1 adipocytes. | J Biol Chem | 1999 | https://conductscience.org/library/papers/10559259 | PubMed |
| 5 | 17,306,374 | Mechanisms of action of glucagon-like peptide 1 in the pancreas. | Pharmacol Ther | 2007 | https://conductscience.org/library/papers/17306374 | PubMed |
| 6 | 16,325,578 | A nuclear function of beta-arrestin1 in GPCR signaling: regulation of histone acetylation and gene transcription. | Cell | 2005 | https://conductscience.org/library/papers/16325578 | PubMed |
| 7 | 17,305,471 | Beta-arrestins and cell signaling. | Annu Rev Physiol | 2007 | https://conductscience.org/library/papers/17305471 | PubMed |
| 8 | 12,842,910 | cAMP promotes pancreatic beta-cell survival via CREB-mediated induction of IRS2. | Genes Dev | 2003 | https://conductscience.org/library/papers/12842910 | PubMed |
| 9 | 15,456,867 | beta-arrestin-1 competitively inhibits insulin-induced ubiquitination and degradation of insulin receptor substrate 1. | Mol Cell Biol | 2004 | https://conductscience.org/library/papers/15456867 | PubMed |
| 10 | 14,693,691 | Epac: A new cAMP-binding protein in support of glucagon-like peptide-1 receptor-mediated signal transduction in the pancreatic beta-cell. | Diabetes | 2004 | https://conductscience.org/library/papers/14693691 | PubMed |
1 to 10 of 37
See all 37 referencesCited by132
The papers in our copy of PubMed whose reference list names this one, newest first. iCite, which reads more sources, counts 195 citations.
| PMID | Title | Journal | Year | In Papers | Source |
|---|---|---|---|---|---|
| 42,947,790 | Insights from multi-omics on GLP-1 receptor agonists in type 2 diabetes and obesity. | Front Pharmacol | 2026 | https://conductscience.org/library/papers/42947790 | PubMed |
| 42,830,469 | Glucagon-Like Peptide-1 Agonists and Blood Pressure Regulation: Molecular Mechanisms and Cardiovascular Implications. | Pharmacol Res Perspect | 2026 | https://conductscience.org/library/papers/42830469 | PubMed |
| 42,651,699 | For Weight Loss: Why Do GLP-1 Agonists Work, and How Can We Make Them Work Better? | Biology (Basel) | 2026 | https://conductscience.org/library/papers/42651699 | PubMed |
| 42,487,666 | Personalization of incretin therapy: can GLP-1 and GIP receptor polymorphisms influence therapy response? | J Endocr Soc | 2026 | https://conductscience.org/library/papers/42487666 | PubMed |
| 42,198,465 | Multidimensional Predictors of Tirzepatide Efficacy: Clinical, Genetic, and Molecular Biomarkers for Glycemic, Weight, and Organ Protection. | Pharmaceuticals (Basel) | 2026 | https://conductscience.org/library/papers/42198465 | PubMed |
| 42,157,346 | Progressive loss of glycemic control during chronic DPP-4 inhibitor therapy despite preserved β-cell function: a case report suggesting acquired incretin resistance. | Cardiovasc Diabetol Endocrinol Rep | 2026 | https://conductscience.org/library/papers/42157346 | PubMed |
| 42,106,160 | Dietary Fiber and Glucagon-Like Peptide-1 Receptor Agonists in Obesity Management: Converging Mechanisms, Interactions, and Strategies for Durable Weight Control. | Adv Nutr | 2026 | https://conductscience.org/library/papers/42106160 | PubMed |
| 41,762,282 | Unravelling the novel insights between miR-7 and Parkinson's disease (PD). | Neurol Sci | 2026 | https://conductscience.org/library/papers/41762282 | PubMed |
| 41,735,212 | Efficacy of Dual Glucagon and GLP-1 Agonists as New Treatments for Type II Diabetes. | Mini Rev Med Chem | 2026 | https://conductscience.org/library/papers/41735212 | PubMed |
| 41,570,980 | Modelling G protein-biased agonism using GLP-1 receptor C-terminal mutations. | Mol Metab | 2026 | https://conductscience.org/library/papers/41570980 | PubMed |
1 to 10 of 132
See all 132 cited byGenes4
The genes the Gene search release ties to the paper: Swiss-Prot's references first, then PubTator's text mining.
| Gene | NCBI Gene ID | Linked by | In Genes | Source |
|---|---|---|---|---|
| ARRB1 | 408 | PubTator's text mining | https://conductscience.org/library/genes/408 | NCBI Gene |
| ARRB2 | 409 | PubTator's text mining | https://conductscience.org/library/genes/409 | NCBI Gene |
| GCG | 2,641 | PubTator's text mining | https://conductscience.org/library/genes/2641 | NCBI Gene |
| GLP1R | 2,740 | PubTator's text mining | https://conductscience.org/library/genes/2740 | NCBI Gene |
Drugs0
The drugs whose trials, in the Pipelines release, list the paper.
None in this release.
Data0
The data bank entries PubMed's record names. Trial numbers are under Trials.
None in this release.
Data dates
The date of each source this release read.
- Trials
- 2026-11-12
- Gene search
- 2026-11-11
- Pipelines
- 2026-09-18
Sources 11
- ChEMBL, through Open TargetsCC BY-SA 3.0
- ClinicalTrials.govNo license stated
- HGNCCC0
- iCiteCC BY 4.0
- NCBI GenePublic domain (US government)
- NIH RePORTER's grant and paper linksPublic domain
- Open TargetsCC0 1.0
- PMC's ID filePublic domain (US government)
- PubMedNLM's terms
- PubTator 3Public domain
- UniProtCC BY 4.0
Each source's terms
- ChEMBL, through Open TargetsCC BY-SA 3.0, for the parts from ChEMBL. Read on 8 Nov 2026 at https://platform-docs.opentargets.org/licence
- ClinicalTrials.govnone stated
- HGNCCC0: https://www.genenames.org/about/license/
- iCiteCC BY 4.0
- NCBI GeneNone named for the file. NCBI says information created by or for the US government on its site is in the public domain, and asks that NLM be acknowledged: https://www.ncbi.nlm.nih.gov/home/about/policies/
- NIH RePORTER's grant and paper linksPublic domain (NIH RePORTER)
- Open TargetsCC0 1.0. Open Targets asks that users cite its latest paper: Buniello et al. 2025, Open Targets Platform: facilitating therapeutic hypotheses building in drug discovery, Nucleic Acids Research 53(D1):D1467, PMID 39657122. Read on 8 Nov 2026 at https://platform-docs.opentargets.org/licence
- PMC's ID fileNone named for the file. NCBI says information created by or for the US government on its site is in the public domain, and asks that NLM be acknowledged: https://www.ncbi.nlm.nih.gov/home/about/policies/
- PubMedNLM's terms
- PubTator 3Public domain
- UniProtCC BY 4.0. UniProt's licence file: "All databases and documents in the UniProt FTP directory may be copied and redistributed freely, without advance permission, provided that this copyright statement is reproduced with each copy." UniProt asks that users cite its latest paper: The UniProt Consortium, UniProt: the Universal Protein Knowledgebase in 2025, Nucleic Acids Research 53:D609-D617, https://doi.org/10.1093/nar/gkae1010. Read on 9 Nov 2026 at https://www.uniprot.org/help/license
ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.
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