Relationship of phenotype and genotype in X-linked amelogenesis imperfecta.
about
Protein-mediated enamel mineralizationHuman and mouse enamel phenotypes resulting from mutation or altered expression of AMEL, ENAM, MMP20 and KLK4Phenotypic variation in FAM83H-associated amelogenesis imperfectaThe molecular etiologies and associated phenotypes of amelogenesis imperfectaPartial rescue of the amelogenin null dental enamel phenotypeDental enamel development: proteinases and their enamel matrix substratesTarget gene analyses of 39 amelogenesis imperfecta kindredsAnalyses of MMP20 Missense Mutations in Two Families with Hypomaturation Amelogenesis ImperfectaA mutation in the mouse Amelx tri-tyrosyl domain results in impaired secretion of amelogenin and phenocopies human X-linked amelogenesis imperfectaAmelogenesis imperfecta due to a mutation of the enamelin gene: clinical case with genotype-phenotype correlations.Mouse genetic background influences the dental phenotype.Preferential and selective degradation and removal of amelogenin adsorbed on hydroxyapatites by MMP20 and KLK4 in vitro.CRAC channelopathies.Treatment of early caries lesions using biomimetic self-assembling peptides--a clinical safety trialPerturbed amelogenin secondary structure leads to uncontrolled aggregation in amelogenesis imperfecta mutant proteins.Amelogenesis imperfecta in two families with defined AMELX deletions in ARHGAP6.Amelogenesis imperfectaNovel FAM83H mutations in Turkish families with autosomal dominant hypocalcified amelogenesis imperfecta.The molecular basis of hereditary enamel defects in humans.Transcriptional factor DLX3 promotes the gene expression of enamel matrix proteins during amelogenesis.Amelogenesis imperfecta: genotype-phenotype studies in 71 families.Rescue of the murine amelogenin null phenotype with two amelogenin transgenes.MMP20 active-site mutation in hypomaturation amelogenesis imperfectaLongitudinal analysis of heritability for dental caries traitsThe role of amelogenin during enamel-crystallite growth and organization in vivo.Origin, splicing, and expression of rodent amelogenin exon 8.Phenotype of ENAM mutations is dosage-dependentM180 amelogenin processed by MMP20 is sufficient for decussating murine enamel.Molecular genetics of ameloblast cell lineage.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.Amelogenesis imperfecta: an introduction.Diseases of the tooth: the genetic and molecular basis of inherited anomalies affecting the dentition.DENTAL ENAMEL FORMATION AND IMPLICATIONS FOR ORAL HEALTH AND DISEASE.Ca2+ transport and signalling in enamel cells.Amelogenin Affects Brushite Crystal Morphology and Promotes Its Phase Transformation to Monetite.The promise of human induced pluripotent stem cells in dental research.Shear bond strength of dentin and deproteinized enamel of amelogenesis imperfecta mouse incisors.Phenotype-genotype correlations in mouse models of amelogenesis imperfecta caused by Amelx and Enam mutations.Association between AMELX polymorphisms and dental caries in Koreans.
P2860
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P2860
Relationship of phenotype and genotype in X-linked amelogenesis imperfecta.
description
2003 nî lūn-bûn
@nan
2003 թուականի Յունուարին հրատարակուած գիտական յօդուած
@hyw
2003 թվականի հունվարին հրատարակված գիտական հոդված
@hy
2003年の論文
@ja
2003年論文
@yue
2003年論文
@zh-hant
2003年論文
@zh-hk
2003年論文
@zh-mo
2003年論文
@zh-tw
2003年论文
@wuu
name
Relationship of phenotype and genotype in X-linked amelogenesis imperfecta.
@ast
Relationship of phenotype and genotype in X-linked amelogenesis imperfecta.
@en
type
label
Relationship of phenotype and genotype in X-linked amelogenesis imperfecta.
@ast
Relationship of phenotype and genotype in X-linked amelogenesis imperfecta.
@en
prefLabel
Relationship of phenotype and genotype in X-linked amelogenesis imperfecta.
@ast
Relationship of phenotype and genotype in X-linked amelogenesis imperfecta.
@en
P2093
P356
P1476
Relationship of phenotype and genotype in X-linked amelogenesis imperfecta.
@en
P2093
Crawford PJ
P356
10.1080/713713640
P478
44 Suppl 1
P577
2003-01-01T00:00:00Z