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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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Detalhes bibliográficos
Publicado no:Cell Signal
Main Authors: Strubl, Sebastian, Torres, Jacob A., Spindt, Alison K., Pellegrini, Hannah, Liebau, Max C., Weimbs, Thomas
Formato: Artigo
Idioma:Inglês
Publicado em: 2020
Assuntos:
Acesso em linha: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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