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Craniofacial Microsomia and Variants in Genes Related to Retinoic Acid, Endothelin, and Phenotypically Overlapping Syndromes
Background: Craniofacial microsomia (CFM) is the second most common facial congenital anomaly. It involves asymmetric underdevelopment of facial skeletal bones and soft tissues, mostly the lower face and ear. Aberration ...
Attenuation of Articular Cartilage Degeneration by the Genetic Deletion of HtrA1 in Mice
Objective To investigate whether the genetic deletion of the serine protease, high temperature requirement protein A1 (HtrA1), will attenuate the progression of articular cartilage degeneration in mouse osteoarthritis ...
The Longitudinal Effects of Orthodontic Therapy on the Obstructive Apnea Hypopnea Index (AHI).
Objectives: To evaluate the cross-sectional relationship between sleep apnea and dental model measurements, cephalometric measurements (skeletal, dental, airway) and sleep-disordered breathing (SDB) questionnaires, in a ...