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The native TRPP2-dependent channel of murine renal primary cilia
Autosomal dominant polycystic kidney disease (ADPKD) is the most common life-threatening monogenic renal disease. ADPKD results from mutations in either of two proteins: polycystin-1 (also known as PC1 or PKD1) or transient receptor potential cation channel, subfamily P, member 2 (TRPP2, also known...
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| Publicado en: | Am J Physiol Renal Physiol |
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| Autores principales: | , |
| Formato: | Artigo |
| Lenguaje: | Inglês |
| Publicado: |
American Physiological Society
2017
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| Materias: | |
| Acceso en línea: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5283891/ https://ncbi.nlm.nih.gov/pubmed/27760766 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1152/ajprenal.00272.2016 |
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