Results 101 to 110 of about 7,940 (235)
Emerging therapeutic strategies targeting bone signaling pathways in periodontitis
Journal of Periodontal Research, Volume 60, Issue 2, Page 101-120, February 2025.Anti‐resorptive, immunomodulatory, and emerging therapeutic approaches to treat periodontal disease and promote resolution of inflammation. Abstract Periodontitis is a multifactorial immune‐mediated disease exacerbated by dysregulated alveolar bone homeostasis. Timely intervention is crucial for disease management to prevent tooth loss. To successfully
Araceli Valverde +3 more
wiley +1 more source
Study on frequency of dental developmental alterations in a MEXICAN school-based population [PDF]
, 2016 Background: The aim of this study was to know the distribution of dental developmental alterations in the population requesting stomatological attention at the Admission and Diagnosis Clinic of our institution in Mexico City.
Garcés Ortíz, Maricela +3 more
core +1 more source
Constitutive expression of spliced X-box binding protein 1 inhibits dentin formation in mice
Frontiers in PhysiologyUpon endoplasmic reticulum (ER) stress, inositol-requiring enzyme 1 (IRE1) is activated, which subsequently converts an unspliced X-box binding protein 1 (XBP1U) mRNA to a spliced mRNA that encodes a potent XBP1S transcription factor.
Qian Xu +5 more
doaj +1 more source
Genetic Aspects of Dentinogenesis Imperfecta
Journal of Dentistry Indonesia, 1998 Dentinogenesis Imperfecta (DI) is a hereditary, simple autosomal dominant disorder showing abnormalities in the dentin of the developing teeth and occurring at a rate of about 1 in 8000 births. The expression of DI shows a high penetrance and a low mutation rate.
Hedijanti Joenoes, Elza Ibrahim Auerkari
openaire +3 more sources
Managing Large Perforated Internal Root Resorption With Partial Pulpectomy: A Case Report
Clinical Case Reports, Volume 13, Issue 1, January 2025.ABSTRACT Internal root resorption (IRR) is a complex and often asymptomatic dental condition that can severely compromise tooth vitality and function. This case report presents the successful management of a perforated large IRR lesion in a 49‐year‐old female using an ultraconservative approach involving partial pulpectomy (PP) using calcium‐enriched ...
Saeed Asgary
wiley +1 more source
Intrafibrillar Mineral May be Absent in Dentinogenesis Imperfecta Type II (DI-II) [PDF]
, 2001 J.H. Kinney +5 more
openalex +3 more sources
Dentinogenesis imperfecta: The Genetic Causes and Outcomes [PDF]
, 2021 Dentinogenesis imperfecta (DI) is a genetic disorder characterized by dentin discoloration, tooth development irregularities, and decreased tooth strength. This autosomal dominant disorder is identified in individuals of all ages.
Johnson, Sydney P, Ms.
core +1 more source
Indian Journal of Dental Research, 2019 Dentinogenesis Imperfecta and dentin dysplasia are genetic oral diseases inherited in a simple autosomal dominant mode, with high penetrance and a low mutation rate.
Nikita Gulati +3 more
doaj +1 more source
Imperfecta Dentinogenesis: a case report
Revista Estomatología, 2017 Summary: Introduction: Dentinogenesis imperfecta (DI) is an inherited dental diaseasein which dental crowns are affected. DI originates by defects on the histo-differenciation stage ofodontogenesis, constituting a localized mesodermal dysplasia characterized by an expressedalteration of dentin proteins.
Claudia Ponce de León +2 more
openaire +2 more sources
A novel DSPP mutation causes dentinogenesis imperfecta type II in a large Mongolian family [PDF]
, 2010 Background Several studies have shown that the clinical phenotypes of dentinogenesis imperfecta type II (DGI-II) may be caused by mutations in dentin sialophosphoprotein (DSPP).
AC Acevedo +28 more
core +3 more sources