Identification of a mutation in DLX3 associated with tricho-dento-osseous (TDO) syndrome
about
Tricho-dento-osseous syndrome: diagnosis and dental managementBP1, a homeodomain-containing isoform of DLX4, represses the beta-globin geneDlx genes, p63, and ectodermal dysplasias.Phosphorylation of murine homeodomain protein Dlx3 by protein kinase C.Bone morphogenetic protein-2 (BMP-2) transactivates Dlx3 through Smad1 and Smad4: alternative mode for Dlx3 induction in mouse keratinocytesDlx3 is a crucial regulator of hair follicle differentiation and cyclingThe molecular etiologies and associated phenotypes of amelogenesis imperfectaMalformations of the tooth root in humansTooth and scale morphogenesis in shark: an alternative process to the mammalian enamel knot system.A role for the homeobox protein Distal-less 3 in the activation of the glycoprotein hormone alpha subunit gene in choriocarcinoma cellsSmad6 represses Dlx3 transcriptional activity through inhibition of DNA bindingNeural crest deletion of Dlx3 leads to major dentin defects through down-regulation of DsppPlacental failure in mice lacking the homeobox gene Dlx3Unexpected identification of a recurrent mutation in the DLX3 gene causing amelogenesis imperfecta.DLX3 mutation in a new family and its phenotypic variations.A common DLX3 gene mutation is responsible for tricho-dento-osseous syndrome in Virginia and North Carolina families.DLX3 interacts with GCM1 and inhibits its transactivation-stimulating activity in a homeodomain-dependent manner in human trophoblast-derived cells.Mammalian Dlx homeobox gene control of craniofacial and inner ear morphogenesis.Molecular genetics of the hair follicle: the state of the art.The impact of molecular genetics on oral health paradigms.Tricho-dento-osseous syndrome and amelogenesis imperfecta with taurodontism are genetically distinct conditions.Molecular evolution of the homeodomain family of transcription factorsp63 in skin development and ectodermal dysplasias.Ectodermal dysplasias: a new clinical-genetic classificationEctodermal dysplasias: not only 'skin' deep.Mutant DLX 3 disrupts odontoblast polarization and dentin formation.Regulation of the Dlx3 homeobox gene upon differentiation of mouse keratinocytes.The Dlx3 protein harbors basic residues required for nuclear localization, transcriptional activity and binding to Msx1.Immortalized mouse floxed Bmp2 dental papilla mesenchymal cell lines preserve odontoblastic phenotype and respond to BMP2.Hypomaturation amelogenesis imperfecta caused by a novel SLC24A4 mutation.Genes and related proteins involved in amelogenesis imperfecta.Exclusion of p63 as a candidate gene for autosomal-dominant amelogenesis imperfecta.Molecular-pathogenetic classification of genetic disorders of the skeleton.Amelogenesis imperfectaThe homeobox gene DLX4 promotes generation of human induced pluripotent stem cells.Development and characterization of a mouse floxed Bmp2 osteoblast cell line that retains osteoblast genotype and phenotype.The molecular basis of hereditary enamel defects in humans.Genetically altered mouse models: the good, the bad, and the ugly.Transcriptional factor DLX3 promotes the gene expression of enamel matrix proteins during amelogenesis.SUMOylation of DLX3 by SUMO1 promotes its transcriptional activity.
P2860
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P2860
Identification of a mutation in DLX3 associated with tricho-dento-osseous (TDO) syndrome
description
1998 nî lūn-bûn
@nan
1998 թուականի Մարտին հրատարակուած գիտական յօդուած
@hyw
1998 թվականի մարտին հրատարակված գիտական հոդված
@hy
1998年の論文
@ja
1998年論文
@yue
1998年論文
@zh-hant
1998年論文
@zh-hk
1998年論文
@zh-mo
1998年論文
@zh-tw
1998年论文
@wuu
name
Identification of a mutation in DLX3 associated with tricho-dento-osseous (TDO) syndrome
@ast
Identification of a mutation in DLX3 associated with tricho-dento-osseous (TDO) syndrome
@en
Identification of a mutation in DLX3 associated with tricho-dento-osseous (TDO) syndrome
@en-gb
Identification of a mutation in DLX3 associated with tricho-dento-osseous (TDO) syndrome
@nl
type
label
Identification of a mutation in DLX3 associated with tricho-dento-osseous (TDO) syndrome
@ast
Identification of a mutation in DLX3 associated with tricho-dento-osseous (TDO) syndrome
@en
Identification of a mutation in DLX3 associated with tricho-dento-osseous (TDO) syndrome
@en-gb
Identification of a mutation in DLX3 associated with tricho-dento-osseous (TDO) syndrome
@nl
prefLabel
Identification of a mutation in DLX3 associated with tricho-dento-osseous (TDO) syndrome
@ast
Identification of a mutation in DLX3 associated with tricho-dento-osseous (TDO) syndrome
@en
Identification of a mutation in DLX3 associated with tricho-dento-osseous (TDO) syndrome
@en-gb
Identification of a mutation in DLX3 associated with tricho-dento-osseous (TDO) syndrome
@nl
P2093
P3181
P356
P1476
Identification of a mutation in DLX3 associated with tricho-dento-osseous (TDO) syndrome
@en
P2093
D W Bowden
J T Wright
M J Pettenati
P3181
P356
10.1093/HMG/7.3.563
P407
P577
1998-03-01T00:00:00Z