AQP2: Mutations Associated with Congenital Nephrogenic Diabetes Insipidus and Regulation by Post-Translational Modifications and Protein-Protein Interactions

As a rare hereditary disease, congenital nephrogenic diabetes insipidus (NDI) is clinically characterized by polyuria with hyposthenuria and polydipsia. NDI results from collecting duct principal cell hyporesponsiveness or insensitivity to the antidiuretic action of arginine vasopressin (AVP). The p...

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Detalles Bibliográficos
Autores principales: Gao, Chao, Higgins, Paul J., Zhang, Wenzheng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7599609/
https://www.ncbi.nlm.nih.gov/pubmed/32993088
http://dx.doi.org/10.3390/cells9102172

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7599609/
https://www.ncbi.nlm.nih.gov/pubmed/32993088
http://dx.doi.org/10.3390/cells9102172

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