Altered enamelin phosphorylation site causes amelogenesis imperfecta.
about
A secretory kinase complex regulates extracellular protein phosphorylationA Single Kinase Generates the Majority of the Secreted PhosphoproteomeProtein-mediated enamel mineralizationSecreted protein kinasesStress response pathways in ameloblasts: implications for amelogenesis and dental fluorosisDental 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 kindredsAmelogenesis imperfecta caused by N-terminal enamelin point mutations in mice and men is driven by endoplasmic reticulum stress.FAM20A Gene Mutation: Amelogenesis or Ectopic Mineralization?Ecto-protein kinases and phosphatases: an emerging field for translational medicine.Characterization of periodontal structures of enamelin-null mice.ENAM mutations with incomplete penetrance.Proteomic database mining opens up avenues utilizing extracellular protein phosphorylation for novel therapeutic applications.Genetic basis for tooth malformations: from mice to men and back again.Phosphorylation of substrates destined for secretion by the Fam20 kinases.An inductive signalling network regulates mammalian tooth morphogenesis with implications for tooth regeneration.Effect of etching on bonding of a self-etch adhesive to dentine affected by amelogenesis imperfecta.Amelogenesis Imperfecta; Genes, Proteins, and Pathways.Neanderthal and Denisova tooth protein variants in present-day humans.Phosphorylation of serine96 of histidine-rich calcium-binding protein by the Fam20C kinase functions to prevent cardiac arrhythmia.FAM20C functions intracellularly within both ameloblasts and odontoblasts in vivo.Clinical and molecular analysis of the enamelin gene ENAM in Colombian families with autosomal dominant amelogenesis imperfecta.Molecular characterization of amelogenesis imperfecta in Chinese patients.Evolutionary Analysis of the Mammalian Tuftelin Sequence Reveals Features of Functional Importance.The importance of a potential phosphorylation site in enamelin on enamel formation.Claudin-16 Deficiency Impairs Tight Junction Function in Ameloblasts, Leading to Abnormal Enamel Formation.Dental Caries and Enamelin Haplotype
P2860
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P2860
Altered enamelin phosphorylation site causes amelogenesis imperfecta.
description
2010 nî lūn-bûn
@nan
2010年の論文
@ja
2010年論文
@yue
2010年論文
@zh-hant
2010年論文
@zh-hk
2010年論文
@zh-mo
2010年論文
@zh-tw
2010年论文
@wuu
2010年论文
@zh
2010年论文
@zh-cn
name
Altered enamelin phosphorylation site causes amelogenesis imperfecta.
@en
type
label
Altered enamelin phosphorylation site causes amelogenesis imperfecta.
@en
prefLabel
Altered enamelin phosphorylation site causes amelogenesis imperfecta.
@en
P2093
P2860
P356
P1476
Altered enamelin phosphorylation site causes amelogenesis imperfecta
@en
P2093
A Oikonomopoulou
A S Richardson
J P Simmer
P2860
P304
P356
10.1177/0022034510365662
P407
P577
2010-05-03T00:00:00Z