Disease Info Card

Dentinogenesis Imperfecta

Information about Dentinogenesis Imperfecta: characteristics, related genes and pathways, plus antibodies you can use for research. This page is being enriched constantly, if you see some information you would like this page to include please send your suggestions to us.

Overview of Dentinogenesis Imperfecta

Most recent studies have shown that Dentinogenesis Imperfecta shares some biological mechanisms with amelogenesis-imperfecta, blue-sclera, congenital-abnormality, connective-tissue-diseases, dental-caries, dental-enamel-hypoplasia, dentin-dysplasia, developmental-absence-of-tooth, dwarfism, dysplasia, fracture, hereditary-diseases, hereditary-opalescent-dentin-(disorder), joint-laxity, malocclusion, osteogenesis-imperfecta, scleral-diseases, tooth-abnormalities, tooth-abrasion, tooth-diseases.

Among the many pathways, these few ones have gauged particular interests from scientists studying Dentinogenesis Imperfecta, and have been seen in publications frequently: Amelogenesis, Cell Adhesion, Chromosome Localization, Dentin Mineralization, Dentinogenesis, Excretion, Fertilization, Immune Response, Localization, Mastication, Odontoblast Differentiation, Odontogenesis, Osteoclast Differentiation, Pathogenesis, Pigmentation, Root Development, Secretion, Tooth Eruption, Tooth Mineralization, Transport

Quite a number of genes have been found to play important roles in Dentinogenesis Imperfecta, such as AKR1C2, ATP2A2, COL1A1, COL1A2, CRTAP, CXXC1, DMP1, DMTF1, DSG1, DSP, DSPP, ENAM, FKBP10, FN1, IBSP, MSX1, SLC4A1, SPP1, TNC. See what Boster has to offer for the research of these genes by clicking the gene name links below and view a more detailed info card/product listing for that gene.

In a later update, we will include information such as current drugs and therapy solutions as well as on-going and past clinical trials for this disease. Plesae stay updated.