Home Newsletters Mesenchymal Cell News Stat3 Loss in Mesenchymal Progenitors Causes Job Syndrome-Like Skeletal Defects by Reducing...

Stat3 Loss in Mesenchymal Progenitors Causes Job Syndrome-Like Skeletal Defects by Reducing Wnt/β-Catenin Signaling

By
Justin.choi
-
0
Researchers investigated the molecular mechanism whereby Stat3 regulates skeletal development and osteoblast differentiation.
[Proceedings of the National Academy of Sciences of the United States of America]

Sorry, but the selected Zotpress account can't be found.

Abstract

RELATED ARTICLES

Exit mobile version