3 results match your criteria: "School of Dental Medicine Tufts University[Affiliation]"
Bioengineering (Basel)
November 2024
Clinical Research Laboratory, Dentistry School, Universidade Federal Fluminense, Niteroi 24220-140, Brazil.
Dental implants are essential for the prosthetic rehabilitation of edentulous patients, requiring adequate bone volume and density for osseointegration and load support. The posterior region of the maxilla, commonly deficient in bone quality and quantity, represents a clinical challenge. This case series reports an analysis involving 69 dental implants in the atrophic maxilla of nine patients.
View Article and Find Full Text PDFMaterials (Basel)
January 2023
Department of Prosthodontics, School of Dental Medicine Tufts University, Boston, MA 02111, USA.
The aim of this in vitro study was to investigate the effect of hydrogen peroxide (HO) on the surface properties of various zirconia-based dental implant materials and the response of human alveolar bone osteoblasts. For this purpose, discs of two zirconia-based materials with smooth and roughened surfaces were immersed in 20% HO for two hours. Scanning electron and atomic force microscopy showed no topographic changes after HO-treatment.
View Article and Find Full Text PDFJ Invest Dermatol
October 2008
Division of Cancer Biology and Tissue Engineering, Department of Oral and Maxillofacial Pathology, School of Dental Medicine Tufts University, Boston, Massachusetts 02111, USA.
The link between loss of cell-cell adhesion, the activation of cell migration, and the behavior of intraepithelial (IE) tumor cells during the early stages of skin cancer progression is not well understood. The current study characterized the migratory behavior of a squamous cell carcinoma cell line (HaCaT-II-4) upon E-cadherin suppression in both 2D, monolayer cultures and within human skin equivalents that mimic premalignant disease. The migratory behavior of tumor cells was first analyzed in 3D tissue context by developing a model that mimics transepithelial tumor cell migration.
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