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KLHL3 regulates paracellular chloride transport in the kidney by ubiquitination of claudin-8
A rare Mendelian syndrome—pseudohypoaldosteronism type II (PHA-II)—features hypertension, hyperkalemia, and metabolic acidosis. Genetic linkage studies and exome sequencing have identified four genes—with no lysine kinase 1 (wnk1), wnk4, Kelch-like 3 (KLHL3), and Cullin 3 (Cul3)—mutations of which a...
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| Publicado en: | Proc Natl Acad Sci U S A |
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| Main Authors: | , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado: |
National Academy of Sciences
2015
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| Assuntos: | |
| Acceso en liña: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4394310/ https://ncbi.nlm.nih.gov/pubmed/25831548 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1073/pnas.1421441112 |
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