Results 111 to 120 of about 5,434 (210)
Complete Overlay Denture for Pedodontic Patient with Severe Dentinogenesis Imperfecta
Dentinogenesis imperfecta (DI) is a hereditary condition that may affect both primary and permanent dentition and is characterized by abnormal dentin formation.
Suresh Rupesh
core +1 more source
The article presents the results of morphological and structural changes in the pulp using a combination drug composition for the treatment of acute focal pulpitis.
doaj
Expression of BSP-GFPtpz Transgene during Osteogenesis and Reparative Dentinogenesis
Bone sialoprotein (BSP) is a member of the SIBLING family with essential roles in skeletogenesis. In the developing teeth, although the expression and function of BSP in the formation of acellular cementum and periodontal attachment are well documented ...
Maye, P. +4 more
core +1 more source
Scap-Exo-Mediated Dspp Mrna Delivery Induces Bmmscs Specific Dentinogenesis
Aim or purpose: To investigate the use of exosomes derived from stem cells from apical papilla (SCAP-Exo) to deliver dentin sialophosphoprotein (DSPP) mRNA, promoting odontogenic differentiation of bone marrow mesenchymal stem cells (BMMSCs) and ...
Xueying Zhuang, Xu Chen
doaj +1 more source
A Novel Mutation in the DSPP Gene Associated with Dentinogenesis Imperfecta Type II
Hereditary dentin defects are divided into dentinogenesis imperfecta and dentin dysplasia. We identified a family segregating severe dentinogenesis imperfecta.
Jeon, D. +9 more
core +1 more source
Editorial: Cell-to-cell communications in tissue homeostasis and repair
Osamu Shimmi, Osamu Shimmi, Esko Kankuri
doaj +1 more source
Odontoblasts are cells specialized in dentin matrix deposition and the first line of defense when the dentin–pulp complex is injured by pathological processes, such as dental caries and trauma.
Carlos Alberto de Souza Costa +28 more
core +1 more source
<i>Dentinogenesis Imperfecta</i> in Primary Dentition: Case Report. [PDF]
Petrova L, Ustiča J, Čēma I.
europepmc +1 more source
Osteogenesis Imperfecta Type 4 With COL1A2 c.1135G>A (p.Gly379Arg) Variant: Unmodified by Concurrent ALPL c.1559delT (p.Leu520ArgfsTer86) Carrier Status: A Case Report. [PDF]
Nomura K +4 more
europepmc +1 more source

