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Regulation of Dental Enamel Shape and Hardness

Journal of Dental Research, 2010-10, Vol.89 (10), p.1024-1038

2010

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Hereditary Dentin Defects

Journal of Dental Research, 2007-05, Vol.86 (5), p.392-399

2007

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MMP-20 mutation in autosomal recessive pigmented hypomaturation amelogenesis imperfecta

Journal of medical genetics, 2005-03, Vol.42 (3), p.271-275

2005

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Leucine-rich Amelogenin Peptides Regulate Mineralization in vitro

Journal of dental research, 2011-09, Vol.90 (9), p.1091-1097

2011

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Mmp-20 and Klk4 Cleavage Site Preferences for Amelogenin Sequences

Journal of dental research, 2009-09, Vol.88 (9), p.823-828

2009

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Cleavage Site Specificity of MMP-20 for Secretory-stage Ameloblastin

Journal of dental research, 2010-08, Vol.89 (8), p.785-790

2010

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Altered Enamelin Phosphorylation Site Causes Amelogenesis Imperfecta

Journal of dental research, 2010-07, Vol.89 (7), p.695-699

2010

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Overlapping DSPP Mutations Cause Dentin Dysplasia and Dentinogenesis Imperfecta

Journal of dental research, 2008-12, Vol.87 (12), p.1108-1111

2008

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FAM83H Mutations Cause ADHCAI and Alter Intracellular Protein Localization

Journal of dental research, 2011-03, Vol.90 (3), p.377-381

2011

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Transgenic Rescue of Enamel Phenotype in Ambn Null Mice

Journal of dental research, 2010-12, Vol.89 (12), p.1414-1420

2010

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ENAM Mutations in Autosomal-dominant Amelogenesis Imperfecta

Journal of dental research, 2005-03, Vol.84 (3), p.278-282

2005

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Novel WDR72 Mutation and Cytoplasmic Localization

Journal of dental research, 2010-12, Vol.89 (12), p.1378-1382

2010

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Novel MSX1 Frameshift Causes Autosomal-dominant Oligodontia

Journal of dental research, 2006-03, Vol.85 (3), p.267-271

2006

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The Structural Biology of the Developing Dental Enamel Matrix

Journal of structural biology, 1999-06, Vol.126 (3), p.270-299

1999

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Fam83h is Associated with Intracellular Vesicles and ADHCAI

Journal of dental research, 2009-11, Vol.88 (11), p.991-996

2009

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Developmental biology and genetics of dental malformations

Orthodontics & craniofacial research, 2007-05, Vol.10 (2), p.45-52

2007

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Processing of Ameloblastin by MMP-20

Journal of dental research, 2007-02, Vol.86 (2), p.153-157

2007

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Premature Stop Codon in MMP20 Causing Amelogenesis Imperfecta

Journal of dental research, 2008-01, Vol.87 (1), p.56-59

2008

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DPPI May Activate KLK4 during Enamel Formation

Journal of dental research, 2009-04, Vol.88 (4), p.323-327

2009

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FAM83H and Autosomal Dominant Hypocalcified Amelogenesis Imperfecta

Journal of dental research, 2021-03, Vol.100 (3), p.293-301

2021

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A novel splice acceptor mutation in the DSPP gene causing dentinogenesis imperfecta type II

Human genetics, 2004-08, Vol.115 (3), p.248-254

2004

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Phenotypic Variation in Dentinogenesis Imperfecta/Dentin Dysplasia Linked to 4q21

Journal of dental research, 2006-04, Vol.85 (4), p.329-333

2006

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Biomimetic Enamel Regeneration Mediated by Leucine-Rich Amelogenin Peptide

Journal of dental research, 2017-05, Vol.96 (5), p.524-530

2017

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WDR72 Mutations Associated with Amelogenesis Imperfecta and Acidosis

Journal of dental research, 2019-05, Vol.98 (5), p.541-548

2019

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Amelogenin is a Cell Adhesion Protein

Journal of dental research, 2002-07, Vol.81 (7), p.497-500

2002

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Regulation of Dental Enamel Shape and Hardness

Hereditary Dentin Defects

MMP-20 mutation in autosomal recessive pigmented hypomaturation amelogenesis imperfecta

Leucine-rich Amelogenin Peptides Regulate Mineralization in vitro

Mmp-20 and Klk4 Cleavage Site Preferences for Amelogenin Sequences

Cleavage Site Specificity of MMP-20 for Secretory-stage Ameloblastin

Altered Enamelin Phosphorylation Site Causes Amelogenesis Imperfecta

Overlapping DSPP Mutations Cause Dentin Dysplasia and Dentinogenesis Imperfecta

FAM83H Mutations Cause ADHCAI and Alter Intracellular Protein Localization

Transgenic Rescue of Enamel Phenotype in Ambn Null Mice

ENAM Mutations in Autosomal-dominant Amelogenesis Imperfecta

Novel WDR72 Mutation and Cytoplasmic Localization

Novel MSX1 Frameshift Causes Autosomal-dominant Oligodontia

The Structural Biology of the Developing Dental Enamel Matrix

Fam83h is Associated with Intracellular Vesicles and ADHCAI

Developmental biology and genetics of dental malformations

Processing of Ameloblastin by MMP-20

Premature Stop Codon in MMP20 Causing Amelogenesis Imperfecta

DPPI May Activate KLK4 during Enamel Formation

FAM83H and Autosomal Dominant Hypocalcified Amelogenesis Imperfecta

A novel splice acceptor mutation in the DSPP gene causing dentinogenesis imperfecta type II

Phenotypic Variation in Dentinogenesis Imperfecta/Dentin Dysplasia Linked to 4q21

Biomimetic Enamel Regeneration Mediated by Leucine-Rich Amelogenin Peptide

WDR72 Mutations Associated with Amelogenesis Imperfecta and Acidosis

Amelogenin is a Cell Adhesion Protein

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