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STAT Signaling in Polycystic Kidney Disease

The most common form of polycystic kidney disease (PKD) in humans is caused by mutations in the PKD1 gene coding for polycystin1 (PC1). Among the many identified or proposed functions of PC1 is its ability to regulate the activity of transcription factors of the STAT family. Most STAT proteins that...

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Bibliografske podrobnosti
izdano v:Cell Signal
Main Authors: Strubl, Sebastian, Torres, Jacob A., Spindt, Alison K., Pellegrini, Hannah, Liebau, Max C., Weimbs, Thomas
Format: Artigo
Jezik:Inglês
Izdano: 2020
Teme:
Online dostop:https://ncbi.nlm.nih.gov/pmc/articles/PMC7269822/
https://ncbi.nlm.nih.gov/pubmed/32325185
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.cellsig.2020.109639
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