A mutation in the mouse Amelx tri-tyrosyl domain results in impaired secretion of amelogenin and phenocopies human X-linked amelogenesis imperfecta
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UTX and UTY demonstrate histone demethylase-independent function in mouse embryonic developmentScube3 is expressed in multiple tissues during development but is dispensable for embryonic survival in the mouseWDR72 models of structure and function: a stage-specific regulator of enamel mineralizationA solution NMR investigation into the impaired self-assembly properties of two murine amelogenins containing the point mutations T21→I or P41→TEndoplasmic reticulum stress in amelogenesis imperfecta and phenotypic rescue using 4-phenylbutyrate.Amelogenesis 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?Transcription factor FoxO1 is essential for enamel biomineralization.Amelogenesis imperfecta in two families with defined AMELX deletions in ARHGAP6.Enamel malformations associated with a defined dentin sialophosphoprotein mutation in two families.Improved protocol to purify untagged amelogenin - Application to murine amelogenin containing the equivalent P70→T point mutation observed in human amelogenesis imperfectaRetinoic Acid Excess Impairs Amelogenesis Inducing Enamel Defects.Tooth evolution and dental defects: from genetic regulation network to micro-RNA fine-tuning.Folding, assembly, and aggregation of recombinant murine amelogenins with T21I and P41T point mutations.Modeling craniofacial and skeletal congenital birth defects to advance therapies.Amelogenesis Imperfecta; Genes, Proteins, and Pathways.Ameloblastin peptide encoded by exon 5 interacts with amelogenin N-terminus.The Unfolded Protein Response in Amelogenesis and Enamel Pathologies.Hypomaturation amelogenesis imperfecta due to WDR72 mutations: a novel mutation and ultrastructural analyses of deciduous teeth.Preparative SDS PAGE as an Alternative to His-Tag Purification of Recombinant AmelogeninPhenotype-genotype correlations in mouse models of amelogenesis imperfecta caused by Amelx and Enam mutations.[Enamel: a unique self-assembling in mineral world].Ablation of Runx2 in Ameloblasts Suppresses Enamel Maturation in Tooth Development.
P2860
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P2860
A mutation in the mouse Amelx tri-tyrosyl domain results in impaired secretion of amelogenin and phenocopies human X-linked amelogenesis imperfecta
description
2010 nî lūn-bûn
@nan
2010 թուականի Յունուարին հրատարակուած գիտական յօդուած
@hyw
2010 թվականի հունվարին հրատարակված գիտական հոդված
@hy
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
name
A mutation in the mouse Amelx ...... linked amelogenesis imperfecta
@ast
A mutation in the mouse Amelx ...... linked amelogenesis imperfecta
@en
A mutation in the mouse Amelx ...... linked amelogenesis imperfecta
@en-gb
type
label
A mutation in the mouse Amelx ...... linked amelogenesis imperfecta
@ast
A mutation in the mouse Amelx ...... linked amelogenesis imperfecta
@en
A mutation in the mouse Amelx ...... linked amelogenesis imperfecta
@en-gb
prefLabel
A mutation in the mouse Amelx ...... linked amelogenesis imperfecta
@ast
A mutation in the mouse Amelx ...... linked amelogenesis imperfecta
@en
A mutation in the mouse Amelx ...... linked amelogenesis imperfecta
@en-gb
P2093
P2860
P50
P356
P1476
A mutation in the mouse Amelx ...... linked amelogenesis imperfecta
@en
P2093
Aleksandr Mironov
C Adrian Shuttleworth
Charlotte Hunt
Joanne Maycock
Michael J Dixon
Nicola J Kingswell
Roger C Shore
P2860
P304
P356
10.1093/HMG/DDQ001
P577
2010-01-12T00:00:00Z