Vasopressin receptor 2 mutations in the nephrogenic syndrome of inappropriate antidiuresis show different mechanisms of constitutive activation for G protein coupled receptors

Vasopressin receptor 2 (V2R) mutations causing the nephrogenic syndrome of inappropriate antidiuresis (NSIAD) can generate two constitutively active receptor phenotypes. One type results from residue substitutions in several V2R domains and is sensitive to vaptan inverse agonists. The other is only...

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Detalles Bibliográficos
Autores principales: Vezzi, Vanessa, Ambrosio, Caterina, Grò, Maria Cristina, Molinari, Paola, Süral, Gökçe, Costa, Tommaso, Onaran, H. Ongun, Cotecchia, Susanna
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7272623/
https://www.ncbi.nlm.nih.gov/pubmed/32499611
http://dx.doi.org/10.1038/s41598-020-65996-w

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7272623/
https://www.ncbi.nlm.nih.gov/pubmed/32499611
http://dx.doi.org/10.1038/s41598-020-65996-w

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