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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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Foilsithe in:Cell Signal
Main Authors: Strubl, Sebastian, Torres, Jacob A., Spindt, Alison K., Pellegrini, Hannah, Liebau, Max C., Weimbs, Thomas
Formáid: Artigo
Teanga:Inglês
Foilsithe: 2020
Ábhair:
Rochtain Ar Líne: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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