Huabing Qi

A Pro253Arg mutation in fibroblast growth factor receptor 2 (Fgfr2) causes skeleton malformation mimicking human Apert syndrome by affecting both chondrogenesis and osteogenesis

Liangjun Yin, Xiaolan Du, Cuiling Li et al. · Bone · 2007 · 141 citations

Developmental Biology, Bone Morphogenic Protein, Bone Repair +9

Mechanical loading regulates human MSC differentiation in a multi-layer hydrogel for osteochondral tissue engineering

Neven J. Steinmetz, Elizabeth A. Aisenbrey, Kristofer K. Westbrook et al. · Acta Biomaterialia · 2015 · 115 citations

Tissue Engineering, Mechanobiology, Regenerative Medicine +14

Gain-of-function mutation in FGFR3 in mice leads to decreased bone mass by affecting both osteoblastogenesis and osteoclastogenesis

Nan Su, Qingfang Sun, Chao Li et al. · Human Molecular Genetics · 2010 · 98 citations · Full text

FGFR3/fibroblast growth factor receptor 3 inhibits autophagy through decreasing the ATG12–ATG5 conjugate, leading to the delay of cartilage development in achondroplasia

Xiaofeng Wang, Huabing Qi, Quan Wang et al. · Autophagy · 2015 · 86 citations · Full text

Atg12–atg5 Conjugate, Cell Growth, Osteoporosis +17

FGFR3 deficiency enhances CXCL12-dependent chemotaxis of macrophages via upregulating CXCR7 and aggravates joint destruction in mice

Liang Kuang, Jiangyi Wu, Nan Su et al. · Annals of the Rheumatic Diseases · 2019 · 78 citations