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This study was designed to evaluate the bone response to surface immobilized BPs on implants inserted in tibiae of ovariectomized (OVX) rats.
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We demonstrated that eldecalcitol enhanced bone formation dose-dependently and exerted a synergistic effect on the cortical bone response to mechanical loading at the endocortical surface.
Compared to the periosteal surface, the preferential endocortical bone response to loading and to eldecalcitol treatment may be due to the lack of a direct pad effect and to the lower induced mechanical strain (stimulus).
To evaluate the early bone response to plateau root form dental implants with 4 different surface treatments.
Introduction: Bone response to orthodontic loading was compared around 2 different types of osseointegrated implants (porous surfaced and machined threaded) to determine the effect of implant surface geometry on regional bone remodeling.
Introduction: Bone response to orthodontic loading was compared histomorphometrically around 2 different types of osseointegrated implants (porous surfaced and machined threaded) to determine their suitability for orthodontic anchorage.
Lin, C. et al. Sclerostin mediates bone response to mechanical unloading through antagonizing Wnt/beta-catenin signaling.
A rat tibial model with bilateral placement of titanium alloy implants was employed to analyze the bones' response to polyelectrolyte surfaces in vivo.
The objective of this study was to investigate bone responses to titanium implants surface-roughened by sandblasted and double-etched treatments in a rabbit model.
Future investigations on various coating processes will have to include clinical trials to get better understanding of bone responses to coated-implant surfaces, as well as studies on coupling of calcium orthophosphate coatings, layers and films with drugs, growth factors and cells.
While males and females have similar responses to surface roughness, they differ in production of local factors regulating bone resorption and in the magnitude of the response 1 α,25(OH)2D3.
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