NCC regulation by WNK signal cascade

With-no-lysine (K) (WNK) kinases have been identified as the causal genes for pseudohypoaldosteronism type II (PHAII), a rare hereditary hypertension condition characterized by hyperkalemia, hyperchloremic metabolic acidosis, and thiazide-hypersensitivity. We thought that clarifying the link between...

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Detalles Bibliográficos
Autores principales: Uchida, Shinichi, Mori, Takayasu, Susa, Koichiro, Sohara, Eisei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Physiology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9845728/
https://www.ncbi.nlm.nih.gov/pubmed/36685207
http://dx.doi.org/10.3389/fphys.2022.1081261

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9845728/
https://www.ncbi.nlm.nih.gov/pubmed/36685207
http://dx.doi.org/10.3389/fphys.2022.1081261

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