DLX3 mutation associated with autosomal dominant amelogenesis imperfecta with taurodontism
about
Tricho-dento-osseous syndrome: diagnosis and dental managementDlx genes, p63, and ectodermal dysplasias.Mutations in CNNM4 cause Jalili syndrome, consisting of autosomal-recessive cone-rod dystrophy and amelogenesis imperfectaThe molecular etiologies and associated phenotypes of amelogenesis imperfectaMalformations of the tooth root in humansPERP regulates enamel formation via effects on cell-cell adhesion and gene expressionNovel genetic linkage of rat Sp6 mutation to Amelogenesis imperfectaNeural crest deletion of Dlx3 leads to major dentin defects through down-regulation of DsppDoes enamelin have pleiotropic effects on organs other than the teeth? Lessons from a phenotyping screen of two enamelin-mutant mouse linesReassessing the Dlx code: the genetic regulation of branchial arch skeletal pattern and developmentAmelogenesis imperfecta caused by N-terminal enamelin point mutations in mice and men is driven by endoplasmic reticulum stress.Unexpected identification of a recurrent mutation in the DLX3 gene causing amelogenesis imperfecta.MMP-20 is predominately a tooth-specific enzyme with a deep catalytic pocket that hydrolyzes type V collagenDLX3 interacts with GCM1 and inhibits its transactivation-stimulating activity in a homeodomain-dependent manner in human trophoblast-derived cells.New roles and mechanism of action of BMP4 in postnatal tooth cytodifferentiationImmortalized mouse floxed Bmp2 dental papilla mesenchymal cell lines preserve odontoblastic phenotype and respond to BMP2.Genes and related proteins involved in amelogenesis imperfecta.Exclusion of p63 as a candidate gene for autosomal-dominant amelogenesis imperfecta.Amelogenesis imperfectaDevelopment and characterization of a mouse floxed Bmp2 osteoblast cell line that retains osteoblast genotype and phenotype.Amelogenesis imperfecta: Report of a case and review of literatureThe use of mouse models to investigate shear bond strength in amelogenesis imperfecta.Morphological analyses and a novel de novo DLX3 mutation associated with tricho-dento-osseous syndrome in a Chinese family.Bmp2 deletion causes an amelogenesis imperfecta phenotype via regulating enamel gene expressionDLX4 is associated with orofacial clefting and abnormal jaw development.MicroRNA 665 Regulates Dentinogenesis through MicroRNA-Mediated Silencing and Epigenetic MechanismsA Novel Homozygous WDR72 Mutation in Two Siblings with Amelogenesis Imperfecta and Mild Short Stature.A targeted next-generation sequencing assay for the molecular diagnosis of genetic disorders with orodental involvementDevelopmental biology and genetics of dental malformations.Taurodontism in deciduous molars.Msx and dlx homeogene expression in epithelial odontogenic tumorsMouse models of tooth abnormalities.Taurodontism: a review of the condition and endodontic treatment challenges.Immortalized mouse dental papilla mesenchymal cells preserve odontoblastic phenotype and respond to bone morphogenetic protein 2.Distal cis-regulatory elements are required for tissue-specific expression of enamelin (Enam).Developmental disorders of the dentition: an update.Deletion of amelotin exons 3-6 is associated with amelogenesis imperfecta.Multilevel complex interactions between genetic, epigenetic and environmental factors in the aetiology of anomalies of dental development.Defining a new candidate gene for amelogenesis imperfecta: from molecular genetics to biochemistry.Diseases of the tooth: the genetic and molecular basis of inherited anomalies affecting the dentition.
P2860
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P2860
DLX3 mutation associated with autosomal dominant amelogenesis imperfecta with taurodontism
description
2005 nî lūn-bûn
@nan
2005 թուականի Մարտին հրատարակուած գիտական յօդուած
@hyw
2005 թվականի մարտին հրատարակված գիտական հոդված
@hy
2005年の論文
@ja
2005年学术文章
@wuu
2005年学术文章
@zh-cn
2005年学术文章
@zh-hans
2005年学术文章
@zh-my
2005年学术文章
@zh-sg
2005年學術文章
@yue
name
DLX3 mutation associated with ...... s imperfecta with taurodontism
@ast
DLX3 mutation associated with ...... s imperfecta with taurodontism
@en
DLX3 mutation associated with ...... s imperfecta with taurodontism
@nl
type
label
DLX3 mutation associated with ...... s imperfecta with taurodontism
@ast
DLX3 mutation associated with ...... s imperfecta with taurodontism
@en
DLX3 mutation associated with ...... s imperfecta with taurodontism
@nl
prefLabel
DLX3 mutation associated with ...... s imperfecta with taurodontism
@ast
DLX3 mutation associated with ...... s imperfecta with taurodontism
@en
DLX3 mutation associated with ...... s imperfecta with taurodontism
@nl
P2093
P3181
P356
P1476
DLX3 mutation associated with ...... s imperfecta with taurodontism
@en
P2093
David Amor
Mary MacDougall
Michael Escamilla
Michael J Aldred
TingTing Gu
P304
P3181
P356
10.1002/AJMG.A.30521
P407
P577
2005-03-01T00:00:00Z