Sentence examples for most craniofacial bone from inspiring English sources

These advances unfortunately have not lead to rapid application of using BMP osteoinductive protein therapy for reconstructing most craniofacial bone defects, with clinical case series beginning to be reported only for limited small-sized defects.

In addition, mouse genome informatics mammalian phenotype analysis to determine overrepresented mouse phenotypes (Chen et al., 2013) identifies abnormal craniofacial bone development as the most enriched phenotype in the 4-hr PDGF target genes.

This is a reflection of the complexity and unique characteristics of most craniofacial defects, which will likely require a more robust osteoinductive signal than delivering recombinant protein on a scaffold for clinically meaningful bone regeneration.

Fang, F. et al. Neural crest-specific TSC1 deletion in mice leads to sclerotic craniofacial bone lesion.

Craniofacial bone loss caused by trauma, cancer resection, or congenital diseases significantly impacts patients' facial appearance.

The results showed that craniofacial bone remodeling occurred around both Mg and AZ31 screws.

In this chapter, we review various 3DP methods and their application in craniofacial bone tissue engineering.

Research has shown promise of using bone marrow mesenchymal stem cells (BMSCs) for craniofacial bone regeneration; yet little is known about the differences of BMSCs from limb and craniofacial bones.

The purpose of this study was to evaluate the clinical application of individual craniofacial bone fabrications using computer-assisted design (CAD computer-assisted manufaCAD computer-assisted the reconstruction of craniofacial bone defects.

More recently, injectable and mouldable cements as well as scaffolds for craniofacial bone tissue engineering have been developed.

In the craniofacial bone field, fibrin sealants are used as coagulant and adhesive tools to stabilize grafts during surgery.