Paper · 40469445
The evolution of the therapeutic concept 'GIP receptor antagonism'.
Koefoed-Hansen F and 5 others. Front Endocrinol (Lausanne), 2025. Cited by 9 papers, by iCite.
11 sourcespapers-2026-11-12-0.1.0
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ConductScience Library. The evolution of the therapeutic concept 'GIP receptor antagonism'. Papers, record 40469445. Release papers-2026-11-12-0.1.0, 12 Nov 2026. https://conductscience.org/library/papers/40469445
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Paper
PubMed's record of the paper, with iCite's citation figures. No abstract is shown.
Topics4
NLM's MeSH indexing of the paper, its major topics first.
| MeSH term | Major |
|---|---|
| Receptors, Gastrointestinal Hormone | Major topic |
| Gastric Inhibitory Polypeptide | Major topic |
| Humans | |
| Animals |
Source PubMed
Grants0
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.
None in this release.
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.
References119
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 | 28,237,651 | GIP(3-30)NH2 is a potent competitive antagonist of the GIP receptor and effectively inhibits GIP-mediated insulin, glucagon, and somatostatin release. | Biochem Pharmacol | 2017 | https://conductscience.org/library/papers/28237651 | PubMed |
| 2 | 27,186,353 | Alternative form of glucose-dependent insulinotropic polypepide and its physiology. | J Diabetes Investig | 2016 | https://conductscience.org/library/papers/27186353 | PubMed |
| 3 | 4,749,457 | Stimulation of insulin secretion by gastric inhibitory polypeptide in man. | J Clin Endocrinol Metab | 1973 | https://conductscience.org/library/papers/4749457 | PubMed |
| 4 | 36,509,857 | Beyond the pancreas: contrasting cardiometabolic actions of GIP and GLP1. | Nat Rev Endocrinol | 2023 | https://conductscience.org/library/papers/36509857 | PubMed |
| 5 | 36,400,403 | Discovery of a potent GIPR peptide antagonist that is effective in rodent and human systems. | Mol Metab | 2022 | https://conductscience.org/library/papers/36400403 | PubMed |
| 6 | 21,593,115 | Incretin hormone and insulin responses to oral versus intravenous lipid administration in humans. | J Clin Endocrinol Metab | 2011 | https://conductscience.org/library/papers/21593115 | PubMed |
| 7 | 22,522,617 | Xenin-25 amplifies GIP-mediated insulin secretion in humans with normal and impaired glucose tolerance but not type 2 diabetes. | Diabetes | 2012 | https://conductscience.org/library/papers/22522617 | PubMed |
| 8 | 24,446,656 | A functional amino acid substitution in the glucose-dependent insulinotropic polypeptide receptor (GIPR) gene is associated with lower bone mineral density and increased fracture risk. | J Clin Endocrinol Metab | 2014 | https://conductscience.org/library/papers/24446656 | PubMed |
| 9 | 29,378,179 | Human GIP(3-30)NH2 inhibits G protein-dependent as well as G protein-independent signaling and is selective for the GIP receptor with high-affinity binding to primate but not rodent GIP receptors. | Biochem Pharmacol | 2018 | https://conductscience.org/library/papers/29378179 | PubMed |
| 10 | 34,210,852 | Sequencing of 640,000 exomes identifies GPR75 variants associated with protection from obesity. | Science | 2021 | https://conductscience.org/library/papers/34210852 | PubMed |
1 to 10 of 119
See all 119 referencesCited by7
The papers in our copy of PubMed whose reference list names this one, newest first. iCite, which reads more sources, counts 9 citations.
| PMID | Title | Journal | Year | In Papers | Source |
|---|---|---|---|---|---|
| 42,603,240 | Effect of tirzepatide and semaglutide on blood pressure: A systematic review and meta-analysis. | Endocrine | 2026 | https://conductscience.org/library/papers/42603240 | PubMed |
| 42,525,756 | Altered Gi signaling in enteroendocrine K cells in vivo causes pronounced changes in glucose homeostasis. | Sci Adv | 2026 | https://conductscience.org/library/papers/42525756 | PubMed |
| 42,373,095 | Reproducibility of Splanchnic Blood Flow Measured Using Phase-Contrast MRI. | NMR Biomed | 2026 | https://conductscience.org/library/papers/42373095 | PubMed |
| 42,307,179 | The evolving therapeutic landscape of gut-pancreatic peptide signalling in metabolic disorders: from mono- to multi-agonist therapies. | Biosci Rep | 2026 | https://conductscience.org/library/papers/42307179 | PubMed |
| 41,973,737 | Clinical Potential of GIP in Type 2 Diabetes and Obesity. | Diabetes Care | 2026 | https://conductscience.org/library/papers/41973737 | PubMed |
| 41,596,254 | The Role of Glucose-Dependent Insulinotropic Polypeptide (GIP) in Bone Metabolism. | Int J Mol Sci | 2026 | https://conductscience.org/library/papers/41596254 | PubMed |
| 40,943,066 | Recent Updates on Diabetes and Bone. | Int J Mol Sci | 2025 | https://conductscience.org/library/papers/40943066 | PubMed |
Genes3
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 |
|---|---|---|---|---|
| GIP | 2,695 | PubTator's text mining | https://conductscience.org/library/genes/2695 | NCBI Gene |
| GLP1R | 2,740 | PubTator's text mining | https://conductscience.org/library/genes/2740 | NCBI Gene |
| INS | 3,630 | PubTator's text mining | https://conductscience.org/library/genes/3630 | 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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