New Function of RUNX2 in Regulating Osteoclast Differentiation via the AKT/NFATc1/CTSK Axis

Xin, YJ; Liu, Y; Liu, DD; Li, J; Zhang, CY; Wang, YX; Zheng, SG

Zheng, SG (corresponding author), Peking Univ, Dept Prevent Dent, Sch & Hosp Stomatol, Beijing, Peoples R China.; Wang, YX; Zheng, SG (corresponding author), Natl Clin Res Ctr Oral Dis, Beijing, Peoples R China.; Wang, YX; Zheng, SG (corresponding author), Natl Engn Lab Digital & Mat Technol Stomatol, Beijing, Peoples R China.; Wang, YX; Zheng, SG (corresponding author), Beijing Key Lab Digital Stomatol, Beijing, Peoples R China.; Wang, YX (corresponding author), Peking Univ, Sch & Hosp Stomatol, Cent Lab, Dept Oral & Maxillofacial Surg, Beijing, Peoples R China.

CALCIFIED TISSUE INTERNATIONAL, 2020; 106 (5): 553

Abstract

Cleidocranial dysplasia is an autosomal dominant skeletal disorder resulting from RUNX2 mutations. The influence of RUNX2 mutations on osteoclastogene......

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