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Optimized GIP analogs promote body weight lowering in mice through GIPR agonism not antagonism
OBJECTIVE: Structurally-improved GIP analogs were developed to determine precisely whether GIP receptor (GIPR) agonism or antagonism lowers body weight in obese mice. METHODS: A series of peptide-based GIP analogs, including structurally diverse agonists and a long-acting antagonist, were generated...
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| Gepubliceerd in: | Mol Metab |
|---|---|
| Hoofdauteurs: | , , , , , , |
| Formaat: | Artigo |
| Taal: | Inglês |
| Gepubliceerd in: |
Elsevier
2018
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| Onderwerpen: | |
| Online toegang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6358549/ https://ncbi.nlm.nih.gov/pubmed/30578168 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.molmet.2018.12.001 |
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