The Molecular Basis of Hereditary Enamel Defects in Humans

Prevention of the Disrupted Enamel Phenotype in Slc4a4-Null Mice Using Explant Organ Culture Maintained in a Living Host Kidney Capsule

(2014) Xin Wen et al.   PLoS One

FAM20A Mutations Associated with Enamel Renal Syndrome

(2013) S.K. Wang et al.   JOURNAL OF DENTAL RESEARCH

Homozygous and Compound Heterozygous MMP20 Mutations in Amelogenesis Imperfecta

(2013) B. Gasse et al.   JOURNAL OF DENTAL RESEARCH

Mutations in ROGDI Cause Kohlschütter-Tönz Syndrome

(2012) Anna Schossig et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Gene-expression analysis of early- and late-maturation-stage rat enamel organ

(2012) Rodrigo S. Lacruz et al.   EUROPEAN JOURNAL OF ORAL SCIENCES

Enamel malformations associated with a defined dentin sialophosphoprotein mutation in two families

(2012) Shih-Kai Wang et al.   EUROPEAN JOURNAL OF ORAL SCIENCES

Amelogenesis Imperfecta: Genotype-Phenotype Studies in 71 Families

(2011) J. Timothy Wright et al.   CELLS TISSUES ORGANS

Requirements for ion and solute transport, and pH regulation during enamel maturation

(2011) Rodrigo S. Lacruz et al.   JOURNAL OF CELLULAR PHYSIOLOGY

Focal dermal hypoplasia: a case report and literature review

(2011) Christiana Murakami et al.   ORAL SURGERY ORAL MEDICINE ORAL PATHOLOGY ORAL RADIOLOGY AND ENDODONTICS

Gene expression and dental enamel structure in developing mouse incisor

(2010) Amer Sehic et al.   EUROPEAN JOURNAL OF ORAL SCIENCES

p63 in Skin Development and Ectodermal Dysplasias

(2010) Maranke I. Koster   JOURNAL OF INVESTIGATIVE DERMATOLOGY

Ameloblast differentiation in the human developing tooth: Effects of extracellular matrices

(2010) Pingping He et al.   MATRIX BIOLOGY