Novel ENAM mutation responsible for autosomal recessive amelogenesis imperfecta and localised enamel defects
about
Novel FAM20A mutations in hypoplastic amelogenesis imperfectaHuman and mouse enamel phenotypes resulting from mutation or altered expression of AMEL, ENAM, MMP20 and KLK4Amelogenesis imperfecta in a new animal model--a mutation in chromosome 5 (human 4q21)Novel genetic linkage of rat Sp6 mutation to Amelogenesis imperfectaEnamel defects and ameloblast-specific expression in Enam knock-out/lacz knock-in miceDental enamel development: proteinases and their enamel matrix substratesBodyweight assessment of enamelin null miceCell proliferation and apoptosis in enamelin null miceTarget gene analyses of 39 amelogenesis imperfecta kindredsENAM Mutations in Autosomal-dominant Amelogenesis ImperfectaAmelogenesis 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.Genes and related proteins involved in amelogenesis imperfecta.Exclusion of p63 as a candidate gene for autosomal-dominant amelogenesis imperfecta.Amelogenesis imperfectaCharacterization of periodontal structures of enamelin-null mice.ENAM mutations with incomplete penetrance.Amelogenesis imperfecta: Report of a case and review of literatureMMP20 active-site mutation in hypomaturation amelogenesis imperfectaA Novel Homozygous WDR72 Mutation in Two Siblings with Amelogenesis Imperfecta and Mild Short Stature.Dietary change and adaptive evolution of enamelin in humans and among primates.Developmental biology and genetics of dental malformations.Enamel formation and amelogenesis imperfecta.Phenotype of ENAM mutations is dosage-dependentPangolin genomes and the evolution of mammalian scales and immunity.Candidate gene strategy reveals ENAM mutations.MiR-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.Diseases of the tooth: the genetic and molecular basis of inherited anomalies affecting the dentition.The genetic basis of dental anomalies and its relation to orthodonticsDeletion of Slc26a1 and Slc26a7 Delays Enamel Mineralization in Mice.Abrogation of epithelial BMP2 and BMP4 causes Amelogenesis Imperfecta by reducing MMP20 and KLK4 expression.Missense Mutation in Fam83H Gene in Iranian Patients with Amelogenesis Imperfecta.Neanderthal and Denisova tooth protein variants in present-day humans.Altered enamelin phosphorylation site causes amelogenesis imperfecta.Clinical and molecular analysis of the enamelin gene ENAM in Colombian families with autosomal dominant amelogenesis imperfecta.Epithelial fibroblast growth factor receptor 1 regulates enamel formation.Simple recessive mutation in ENAM is associated with amelogenesis imperfecta in Italian Greyhounds.How do enamelysin and kallikrein 4 process the 32-kDa enamelin?Significance of genetic variations in developmental enamel defects of primary dentition in Polish children.
P2860
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P2860
Novel ENAM mutation responsible for autosomal recessive amelogenesis imperfecta and localised enamel defects
description
2003 nî lūn-bûn
@nan
2003 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած
@hyw
2003 թվականի դեկտեմբերին 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
Novel ENAM mutation responsibl ...... a and localised enamel defects
@ast
Novel ENAM mutation responsibl ...... a and localised enamel defects
@en
Novel ENAM mutation responsibl ...... a and localised enamel defects
@nl
type
label
Novel ENAM mutation responsibl ...... a and localised enamel defects
@ast
Novel ENAM mutation responsibl ...... a and localised enamel defects
@en
Novel ENAM mutation responsibl ...... a and localised enamel defects
@nl
prefLabel
Novel ENAM mutation responsibl ...... a and localised enamel defects
@ast
Novel ENAM mutation responsibl ...... a and localised enamel defects
@en
Novel ENAM mutation responsibl ...... a and localised enamel defects
@nl
P2093
P3181
P356
P1476
Novel ENAM mutation responsibl ...... a and localised enamel defects
@en
P2093
M D Michalec
P3181
P356
10.1136/JMG.40.12.900
P407
P577
2003-12-01T00:00:00Z