A Novel Splicing Mutation Alters DSPP Transcription and Leads to Dentinogenesis Imperfecta Type II
, 2011 Jun Zhang +11 more
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Phenotype and molecular characterizations of a family with dentinogenesis imperfecta shields type II with a novel DSPP mutation [PDF]
, 2021 Qin Du +11 more
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Whole Exome Sequencing Identifies a Novel COL1A1 Missense Mutation Causing Dentinogenesis Imperfecta Type I Without Skeletal Abnormalities [PDF]
, 2021 Yuting Zeng +6 more
openalex +1 more source
Dentinogenesis imperfecta type II dentin: nanostructural mechanics analysis [PDF]
Jia Gao +10 more
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Antimicrobial Peptide‐ and Dentin Matrix‐Functionalized Hydrogel for Vital Pulp Therapy via Synergistic Bacteriostasis, Immunomodulation, and Dentinogenesis (Adv. Healthcare Mater. 18/2024) [PDF]
Zhuo Xie +8 more
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Dental Management of a Child with Dentinogenesis Imperfecta: A Case Report
Frontiers in Dentistry, 2016 Dentinogenesis imperfecta (DI) is a hereditary dentin defect caused by an autosomal dominant mutation in dentin sialophosphoprotein gene. Defective dentin development results in discolored teeth that are prone to wear and fracture.
Najmeh Akhlaghi +2 more
doaj
Role of the
, 2013 Monica Prasad Gibson +10 more
openalex +2 more sources
An Aesthetic and Economic Approach of Smile Designing for a Patient With Dentinogenesis Imperfecta: A Rare Case Entity [PDF]
Arunoday Kumar +4 more
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Beyond the diagnosis: Unraveling <i>DSPP</i> genotype-phenotype correlations in dentin dysplasia and dentinogenesis imperfecta. [PDF]
Jpn Dent Sci RevBoonyakanog A +8 more
europepmc +1 more source