Enamel malformations associated with a defined dentin sialophosphoprotein mutation in two families.
about
Intrinsically disordered proteins and biomineralization.Novel PAX9 and COL1A2 missense mutations causing tooth agenesis and OI/DGI without skeletal abnormalities.Ameloblast transcriptome changes from secretory to maturation stages.The molecular basis of hereditary enamel defects in humans.The dentin phosphoprotein repeat region and inherited defects of dentin.Detection of a Novel DSPP Mutation by NGS in a Population Isolate in Madagascar.Accelerated enamel mineralization in Dspp mutant mice.Phenotype and genotype analyses in seven families with dentinogenesis imperfecta or dentin dysplasia.Dentinogenesis imperfecta type II- genotype and phenotype analyses in three Danish families.Whole exome sequencing identifies an AMBN missense mutation causing severe autosomal-dominant amelogenesis imperfecta and dentin disorders
P2860
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P2860
Enamel malformations associated with a defined dentin sialophosphoprotein mutation in two families.
description
2011 nî lūn-bûn
@nan
2011年の論文
@ja
2011年論文
@yue
2011年論文
@zh-hant
2011年論文
@zh-hk
2011年論文
@zh-mo
2011年論文
@zh-tw
2011年论文
@wuu
2011年论文
@zh
2011年论文
@zh-cn
name
Enamel malformations associate ...... tein mutation in two families.
@ast
Enamel malformations associate ...... tein mutation in two families.
@en
type
label
Enamel malformations associate ...... tein mutation in two families.
@ast
Enamel malformations associate ...... tein mutation in two families.
@en
prefLabel
Enamel malformations associate ...... tein mutation in two families.
@ast
Enamel malformations associate ...... tein mutation in two families.
@en
P2093
P2860
P1476
Enamel malformations associate ...... otein mutation in two families
@en
P2093
Hui-Chen Chan
James P Simmer
Jan C-C Hu
Jung-Wook Kim
Karen A Uston
Rachel N Milkovich
Sudha Rajderkar
P2860
P304
P356
10.1111/J.1600-0722.2011.00874.X
P478
119 Suppl 1
P577
2011-12-01T00:00:00Z