Autosomal-dominant hypoplastic form of amelogenesis imperfecta caused by an enamelin gene mutation at the exon-intron boundary.
about
Interventions for the restorative care of amelogenesis imperfecta in children and adolescentsProtein-mediated enamel mineralizationThe molecular etiologies and associated phenotypes of amelogenesis imperfectaNovel genetic linkage of rat Sp6 mutation to Amelogenesis imperfectaBodyweight assessment of enamelin null miceTarget gene analyses of 39 amelogenesis imperfecta kindredsAmelogenesis imperfecta caused by N-terminal enamelin point mutations in mice and men is driven by endoplasmic reticulum stress.Amelogenesis imperfecta due to a mutation of the enamelin gene: clinical case with genotype-phenotype correlations.Amelogenesis imperfecta and anterior open bite: Etiological, classification, clinical and management interrelationships.Exclusion of p63 as a candidate gene for autosomal-dominant amelogenesis imperfecta.Exclusion of known gene for enamel development in two Brazilian families with amelogenesis imperfecta.Amelogenesis imperfectaCharacterization of periodontal structures of enamelin-null mice.ENAM mutations with incomplete penetrance.MMP20 active-site mutation in hypomaturation amelogenesis imperfectaMultiple unerupted teeth with amelogenesis imperfecta in siblingsReview: extracellular matrix regulates tooth morphogenesis.Dietary change and adaptive evolution of enamelin in humans and among primates.Phenotype of ENAM mutations is dosage-dependentMiR-153 Regulates Amelogenesis by Targeting Endocytotic and Endosomal/lysosomal Pathways-Novel Insight into the Origins of Enamel Pathologies.Defining a new candidate gene for amelogenesis imperfecta: from molecular genetics to biochemistry.The cooperation of enamelin and amelogenin in controlling octacalcium phosphate crystal morphology.DENTAL ENAMEL FORMATION AND IMPLICATIONS FOR ORAL HEALTH AND DISEASE.Amelogenesis imperfecta: review of diagnostic findings and treatment concepts.Novel FAM83H mutations in patients with amelogenesis imperfecta.Altered enamelin phosphorylation site causes amelogenesis imperfecta.Tooth enamel proteins enamelin and amelogenin cooperate to regulate the growth morphology of octacalcium phosphate crystals.Clinical and molecular analysis of the enamelin gene ENAM in Colombian families with autosomal dominant amelogenesis imperfecta.A transgenic animal model resembling amelogenesis imperfecta related to ameloblastin overexpression.Significance of genetic variations in developmental enamel defects of primary dentition in Polish children.Esthetic treatment of a diffuse amelogenesis imperfecta using pressed lithium disilicate and feldspathic ceramic restorations: 5-year follow up.Hypoplastic AI with Highly Variable Expressivity Caused by ENAM Mutations.Exclusion of candidate genes in seven Turkish families with autosomal recessive amelogenesis imperfecta.
P2860
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P2860
Autosomal-dominant hypoplastic form of amelogenesis imperfecta caused by an enamelin gene mutation at the exon-intron boundary.
description
2002 nî lūn-bûn
@nan
2002 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած
@hyw
2002 թվականի նոյեմբերին հրատարակված գիտական հոդված
@hy
2002年の論文
@ja
2002年論文
@yue
2002年論文
@zh-hant
2002年論文
@zh-hk
2002年論文
@zh-mo
2002年論文
@zh-tw
2002年论文
@wuu
name
Autosomal-dominant hypoplastic ...... n at the exon-intron boundary.
@ast
Autosomal-dominant hypoplastic ...... n at the exon-intron boundary.
@en
Autosomal-dominant hypoplastic ...... n at the exon-intron boundary.
@nl
type
label
Autosomal-dominant hypoplastic ...... n at the exon-intron boundary.
@ast
Autosomal-dominant hypoplastic ...... n at the exon-intron boundary.
@en
Autosomal-dominant hypoplastic ...... n at the exon-intron boundary.
@nl
prefLabel
Autosomal-dominant hypoplastic ...... n at the exon-intron boundary.
@ast
Autosomal-dominant hypoplastic ...... n at the exon-intron boundary.
@en
Autosomal-dominant hypoplastic ...... n at the exon-intron boundary.
@nl
P2093
P1476
Autosomal-dominant hypoplastic ...... n at the exon-intron boundary.
@en
P2093
P304
P356
10.1177/154405910208101103
P407
P577
2002-11-01T00:00:00Z