Disease Info Card

Dentin Dysplasia

Information about Dentin Dysplasia: 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 Dentin Dysplasia

Most recent studies have shown that Dentin Dysplasia shares some biological mechanisms with abscess, amelogenesis-imperfecta, calcinosis, congenital-abnormality, dental-caries, dental-enamel-hypoplasia, dental-pulp-calcification, dentin-dyspalsia-shields-type-2, dentin-dysplasia-type-i, dentinogenesis-imperfecta, developmental-absence-of-tooth, dysplasia, hypodontia, hypoplasia, odontodysplasia, osteogenesis-imperfecta, rickets, tooth-abnormalities, tooth-diseases, tooth-loss.

Among the many pathways, these few ones have gauged particular interests from scientists studying Dentin Dysplasia, and have been seen in publications frequently: Amelogenesis, Bone Mineralization, Bone Resorption, Cell Adhesion, Cell Differentiation, Cell Migration, Dentin Mineralization, Dentinogenesis, Glycosylation, Immune Response, Innervation, Localization, Odontoblast Differentiation, Odontogenesis, Pathogenesis, Protein Processing, Root Development, Secretion, Tooth Eruption, Tooth Mineralization

Quite a number of genes have been found to play important roles in Dentin Dysplasia, such as AKR1C2, AMBN, ATP2A2, AXIN2, COL1A2, DMP1, DMTF1, DSG1, DSP, DSPP, ENAM, IBSP, KLK4, MEPE, MMP20, MSX1, SPP1. 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.