טוען...
Polycystins as components of large multiprotein complexes of polycystin interactors
Naturally occurring mutations in two separate genes, PKD1 and PKD2, are responsible for the vast majority of all cases of autosomal dominant polycystic kidney disease (ADPKD), one of the most common genetic diseases affecting 1 in 1000 Americans. The hallmark of ADPKD is the development of epithelia...
שמור ב:
| הוצא לאור ב: | Cell Signal |
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| Main Authors: | , |
| פורמט: | Artigo |
| שפה: | Inglês |
| יצא לאור: |
2020
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| נושאים: | |
| גישה מקוונת: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7269800/ https://ncbi.nlm.nih.gov/pubmed/32305669 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.cellsig.2020.109640 |
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