Fangsheng Fu
Guangxi Key Laboratory Of Regenerative Medicine
Nanning, China
Nanning, China
Last Updated: 09/26/2026
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Found 9 publications
Tiliroside is a new potential therapeutic drug for osteoporosis in mice.
Journal: Journal of cellular physiology
Published: February 06, 2024
Chrysin Protects Against Titanium Particle-Induced Osteolysis by Attenuating Osteoclast Formation and Function by Inhibiting NF-κB and MAPK Signaling.
Journal: Frontiers in pharmacology
Published: October 11, 2021
Ellagic acid protects ovariectomy-induced bone loss in mice by inhibiting osteoclast differentiation and bone resorption.
Journal: Journal of cellular physiology
Published: May 20, 2019
Daphnetin attenuates LPS-induced osteolysis and RANKL mediated osteoclastogenesis through suppression of ERK and NFATc1 pathways.
Journal: Journal of cellular physiology
Published: December 07, 2018
Tiliroside is a new potential therapeutic drug for osteoporosis in mice.
Journal: Journal of cellular physiology
Published: November 26, 2018
Pectolinarigenin prevents bone loss in ovariectomized mice and inhibits RANKL-induced osteoclastogenesis via blocking activation of MAPK and NFATc1 signaling.
Journal: Journal of cellular physiology
Published: November 13, 2018
Salidroside promotes rat spinal cord injury recovery by inhibiting inflammatory cytokine expression and NF-κB and MAPK signaling pathways.
Journal: Journal of cellular physiology
Published: November 12, 2018
Diosmetin inhibits osteoclast formation and differentiation and prevents LPS-induced osteolysis in mice.
Journal: Journal of cellular physiology
Published: September 09, 2018
Scutellarein inhibits RANKL-induced osteoclast formation in vitro and prevents LPS-induced bone loss in vivo.
Journal: Journal of cellular physiology
Published: September 07, 2018
Showing 1-9 of 9
Last Updated: 09/26/2026