Hereditary Dentin Defects
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概要
- 論文の詳細を見る
- 2007-05-01
著者
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Kim J.-w.
Seoul National University School Of Dentistry Department Of Pediatric Dentistry & Dental Researc
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SIMMER J.
Department of Biologic and Materials Science, University of Michigan School of Dentistry, Dental Res
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Simmer J.
Department Of Biologic And Materials Science University Of Michigan School Of Dentistry Dental Resea
関連論文
- Premature Stop Codon in MMP20 Causing Amelogenesis Imperfecta
- Processing of Ameloblastin by MMP-20
- Hereditary Dentin Defects
- Fam83h is Associated with Intracellular Vesicles and ADHCAI
- Amelogenin is a Cell Adhesion Protein
- Amelogenin p. M1T and p. W4S Mutations Underlying Hypoplastic X-linked Amelogenesis Imperfecta
- Mmp-20 and Klk4 Cleavage Site Preferences for Amelogenin Sequences
- DPPI May Activate KLK4 during Enamel Formation
- Cleavage Site Specificity of MMP-20 for Secretory-stage Ameloblastin
- Splicing Determines the Glycosylation State of Ameloblastin
- Overlapping DSPP Mutations Cause Dentin Dysplasia and Dentinogenesis Imperfecta
- Altered Enamelin Phosphorylation Site Causes Amelogenesis Imperfecta
- ENAM Mutations in Autosomal-dominant Amelogenesis Imperfecta
- Novel WDR72 Mutation and Cytoplasmic Localization
- Regulation of Dental Enamel Shape and Hardness
- Transgenic Rescue of Enamel Phenotype in Ambn Null Mice
- Novel MSX1 Frameshift Causes Autosomal-dominant Oligodontia
- FAM83H Mutations Cause ADHCAI and Alter Intracellular Protein Localization