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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...
Autores principales: | Uchida, Shinichi, Mori, Takayasu, Susa, Koichiro, Sohara, Eisei |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2023
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Materias: | |
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 |
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