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Dysfunctional oleoylethanolamide signaling in a mouse model of Prader-Willi syndrome
Prader-Willi syndrome (PWS), the leading genetic cause of obesity, is characterized by a striking hyperphagic behavior that can lead to obesity, type-2 diabetes, cardiovascular disease and death. The molecular mechanism underlying impaired satiety in PWS is unknown. Oleoylethanolamide (OEA) is alipi...
Enregistré dans:
| Publié dans: | Pharmacol Res |
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| Auteurs principaux: | , , , , , , |
| Format: | Artigo |
| Langue: | Inglês |
| Publié: |
2016
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| Sujets: | |
| Accès en ligne: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5922435/ https://ncbi.nlm.nih.gov/pubmed/28007570 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.phrs.2016.12.024 |
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