👤 Felix Faas
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Articles
articles
Characterization of genetic variants of GIPR reveals a contribution of β-arrestin to metabolic phenotypes.
🤍
Hüsün S Kizilkaya
,
Kimmie V Sørensen
,
Jakob S Madsen
+32 more
· 2024 · Nature metabolism · Nature
· added 2026-04-24
Hüsün S Kizilkaya
,
Kimmie V Sørensen
,
Jakob S Madsen
,
Peter Lindquist
,
Jonathan D Douros
,
Jette Bork-Jensen
,
Alessandro Berghella
,
Peter A Gerlach
,
Lærke S Gasbjerg
,
Jacek Mokrosiński
,
Stephanie A Mowery
,
Patrick J Knerr
,
Brian Finan
,
Jonathan E Campbell
,
David A D'Alessio
,
Diego Perez-Tilve
,
Felix Faas
,
Signe Mathiasen
,
Jørgen Rungby
,
Henrik T Sørensen
,
Allan Vaag
,
Jens S Nielsen
,
Jens-Christian Holm
,
Jeannet Lauenborg
,
Peter Damm
,
Oluf Pedersen
,
Allan Linneberg
,
Bolette Hartmann
,
Jens J Holst
,
Torben Hansen
,
Shane C Wright
,
Volker M Lauschke
,
Niels Grarup
,
Alexander S Hauser
,
Mette M Rosenkilde
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Incretin-based therapies are highly successful in combatting obesity and type 2 diabetes
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DOI:
10.1038/s42255-024-01061-4
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GIPR
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