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Activation of AQP2 water channels without vasopressin: therapeutic strategies for congenital nephrogenic diabetes insipidus

Congenital nephrogenic diabetes insipidus (NDI) is characterized by defective urine concentrating ability. Symptomatic polyuria is present from birth, even with normal release of the antidiuretic hormone vasopressin by the pituitary. Over the last two decades, the aquaporin-2 (AQP2) gene has been cl...

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Dades bibliogràfiques
Publicat a:Clin Exp Nephrol
Autors principals: Ando, Fumiaki, Uchida, Shinichi
Format: Artigo
Idioma:Inglês
Publicat: Springer Singapore 2018
Matèries:
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC5956045/
https://ncbi.nlm.nih.gov/pubmed/29478202
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s10157-018-1544-8
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