专题:dental development and anomalies

This cluster of papers explores the molecular mechanisms, genetic regulation, and signaling pathways involved in tooth development, morphogenesis, and anomalies such as hypodontia and ectodermal dysplasia. It delves into the role of epithelial-mesenchymal interactions, stem cell niches, and key signaling pathways like Wnt/ß-catenin in shaping the dentition.
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Patient experiences with orthodontic retention and retainers: A scoping review

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Adverse Outcomes After Mandibular Distraction Osteogenesis in Robin Sequence

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Familial Tooth Agenesis in Lebanese Patients: Clinical Characterization and Whole-Exome Identification of Rare CACNA2D2 and TRIO Variants

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Dens Invaginatus as a Biomechanical Risk Modifier in Dental Trauma: Finite Element Analysis

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Loss of PTH 1 receptor signaling in periodontal cells drives cementum dysfunction and molar ankylosis in mice

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Orthodontic perspective on treatment recommendations for missing maxillary incisors: A contemporary guideline

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Single‐Cell Virtual Perturbation Screening Identifies STAT3 as a Key Regulator of Dentinogenesis

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ACP4 Variants in Hypoplastic Amelogenesis Imperfecta

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Molar incisor hypomineralisation (MIH) and hypomineralised second primary molars (HSPM): do we need to alter terminology and definition? A scoping review

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Effectiveness of single versus double attachments in the correction of premolar rotation in adult patients: A retrospective study

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