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Demineralization-remineralization dynamics in teeth and bonePhenotype characterization and DSPP mutational analysis of three Brazilian dentinogenesis imperfecta type II families.Porcine dentin sialoprotein glycosylation and glycosaminoglycan attachmentsImmortalized mouse floxed Bmp2 dental papilla mesenchymal cell lines preserve odontoblastic phenotype and respond to BMP2.Dentinogenesis imperfecta type I: A case report with literature review on nomenclature system.Potential Role of Dentin Sialoprotein by Inducing Dental Pulp Mesenchymal Stem Cell Differentiation and Mineralization for Dental Tissue Repair.Astacin proteases cleave dentin sialophosphoprotein (Dspp) to generate dentin phosphoprotein (Dpp).Variability of systemic and oro-dental phenotype in two families with non-lethal Raine syndrome with FAM20C mutations.Bmp2 is required for odontoblast differentiation and pulp vasculogenesis.Enamel malformations associated with a defined dentin sialophosphoprotein mutation in two families.Dentin phosphoprotein (DPP) activates integrin-mediated anchorage-dependent signals in undifferentiated mesenchymal cells.Dentin dysplasia type I-novel findings in deciduous and permanent teethGenetic studies of craniofacial anomalies: clinical implications and applicationsThe dentin phosphoprotein repeat region and inherited defects of dentin.Dentin sialophosphoprotein and dentin matrix protein-1: Two highly phosphorylated proteins in mineralized tissuesDSPP Is Essential for Normal Development of the Dental-Craniofacial Complex.Detection of a Novel DSPP Mutation by NGS in a Population Isolate in Madagascar.A DSPP mutation causing dentinogenesis imperfecta and characterization of the mutational effect.Invited commentary: The need for human genetics and genomics in dental school curricula.Gene evolution and functions of extracellular matrix proteins in teethAcidic domain in dentin phosphophoryn facilitates cellular uptake: implications in targeted protein delivery.Porcine dentin sialophosphoprotein: length polymorphisms, glycosylation, phosphorylation, and stability.SCPP gene evolution and the dental mineralization continuum.Hereditary dentine disorders: dentinogenesis imperfecta and dentine dysplasia.Dentin sialoprotein and dentin phosphoprotein have distinct roles in dentin mineralizationA dentin sialophosphoprotein mutation that partially disrupts a splice acceptor site causes type II dentin dysplasiaSchwartz-Jampel syndrome: a review of the literature and case report.The role of fetuin-A in physiological and pathological mineralization.Isolated dentinogenesis imperfecta and dentin dysplasia: revision of the classification.Phenotype and genotype analyses in seven families with dentinogenesis imperfecta or dentin dysplasia.A comprehensive analysis of normal variation and disease-causing mutations in the human DSPP gene.Rough endoplasmic reticulum trafficking errors by different classes of mutant dentin sialophosphoprotein (DSPP) cause dominant negative effects in both dentinogenesis imperfecta and dentin dysplasia by entrapping normal DSPP.Novel dentin phosphoprotein frameshift mutations in dentinogenesis imperfecta type II.Functional splicing assay of DSPP mutations in hereditary dentin defects.Dentinogenesis imperfecta type II- genotype and phenotype analyses in three Danish families.Identification of the DSPP mutation in a new kindred and phenotype-genotype correlation.Structural and Morphometric Comparison of Lower Incisors in PACAP-Deficient and Wild-Type Mice.Frameshift mutations in dentin phosphoprotein and dependence of dentin disease phenotype on mutation location
P2860
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P2860
description
2007 nî lūn-bûn
@nan
2007年の論文
@ja
2007年論文
@yue
2007年論文
@zh-hant
2007年論文
@zh-hk
2007年論文
@zh-mo
2007年論文
@zh-tw
2007年论文
@wuu
2007年论文
@zh
2007年论文
@zh-cn
name
Disorders of human dentin
@ast
Disorders of human dentin
@en
type
label
Disorders of human dentin
@ast
Disorders of human dentin
@en
prefLabel
Disorders of human dentin
@ast
Disorders of human dentin
@en
P2860
P356
P1433
P1476
Disorders of human dentin
@en
P2093
P Suzanne Hart
Thomas C Hart
P2860
P356
10.1159/000102682
P577
2007-01-01T00:00:00Z