Mutation inSSUH2Causes Autosomal-Dominant Dentin Dysplasia Type I

Accelerated enamel mineralization in Dspp mutant mice

(2016) Kostas Verdelis et al.   MATRIX BIOLOGY

Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology

(2015) Sue Richards et al.   GENETICS IN MEDICINE

Single Nucleotide Differences (SNDs) Continue to Contaminate the dbSNP Database With Consequences for Human Genomics and Health

(2015) Jonathan W. Arthur et al.   HUMAN MUTATION

An Overview of Molecular and Genetic Alterations in Selected Benign Odontogenic Disorders

(2014) Robert J. Cabay   ARCHIVES OF PATHOLOGY & LABORATORY MEDICINE

Isolated dentinogenesis imperfecta and dentin dysplasia: revision of the classification

(2014) Muriel de La Dure-Molla et al.   EUROPEAN JOURNAL OF HUMAN GENETICS

Dentin Sialophosphoprotein: A Regulatory Protein for Dental Pulp Stem Cell Identity and Fate

(2014) Shiliang Guo et al.   STEM CELLS AND DEVELOPMENT

Developmental disorders of the dentition: An update

(2013) Ophir D. Klein et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART C-SEMINARS IN MEDICAL GENETICS

The Rescue of Dentin Matrix Protein 1 (DMP1)-deficient Tooth Defects by the Transgenic Expression of Dentin Sialophosphoprotein (DSPP) Indicates That DSPP Is a Downstream Effector Molecule of DMP1 in Dentinogenesis

(2013) Monica Prasad Gibson et al.   JOURNAL OF BIOLOGICAL CHEMISTRY

Molecular patterning of the mammalian dentition

(2013) Yu Lan et al.   SEMINARS IN CELL & DEVELOPMENTAL BIOLOGY

Tooth shape formation and tooth renewal: evolving with the same signals

(2012) J. Jernvall et al.   DEVELOPMENT

Roles of Bmp4 during tooth morphogenesis and sequential tooth formation

(2012) S. Jia et al.   DEVELOPMENT

Signaling Networks Regulating Tooth Organogenesis and Regeneration, and the Specification of Dental Mesenchymal and Epithelial Cell Lineages

(2012) M. Jussila et al.   Cold Spring Harbor Perspectives in Biology

Diseases of the tooth: the genetic and molecular basis of inherited anomalies affecting the dentition

(2012) Martyn T. Cobourne et al.   Wiley Interdisciplinary Reviews-Developmental Biology

Homozygosity Mapping and Candidate Prioritization Identify Mutations, Missed by Whole-Exome Sequencing, in SMOC2, Causing Major Dental Developmental Defects

(2011) Agnès Bloch-Zupan et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Functional Mutation of SMAC/DIABLO, Encoding a Mitochondrial Proapoptotic Protein, Causes Human Progressive Hearing Loss DFNA64

(2011) Jing Cheng et al.   AMERICAN JOURNAL OF HUMAN GENETICS

The role of runt-related transcription factor 2 (Runx2) in the late stage of odontoblast differentiation and dentin formation

(2011) Shiting Li et al.   BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS

Genetic basis for tooth malformations: from mice to men and back again

(2011) TA Mitsiadis et al.   CLINICAL GENETICS

How Proteins Form Disulfide Bonds

(2010) Matthieu Depuydt et al.   ANTIOXIDANTS & REDOX SIGNALING

Small intestinal mucosa expression of putative chaperone fls485

(2010) Andrea Reinartz et al.   BMC GASTROENTEROLOGY

Mutant DLX 3 disrupts odontoblast polarization and dentin formation

(2010) S.J. Choi et al.   DEVELOPMENTAL BIOLOGY

bmp2b and bmp4 are dispensable for zebrafish tooth development

(2010) Sarah B. Wise et al.   DEVELOPMENTAL DYNAMICS

The Canonical BMP Signaling Pathway Plays a Crucial Part in Stimulation of Dentin Sialophosphoprotein Expression by BMP-2

(2010) Young-Dan Cho et al.   JOURNAL OF BIOLOGICAL CHEMISTRY

Developmental defects and neuromuscular alterations due to mitofusin 2 gene (MFN2) silencing in zebrafish: a new model for Charcot-Marie-Tooth type 2A neuropathy

(2010) Andrea Vettori et al.   NEUROMUSCULAR DISORDERS

Oligodontia Is Caused by Mutation in LTBP3, the Gene Encoding Latent TGF-β Binding Protein 3

(2009) Abdul Noor et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Loss-of-Function Mutations in the PRPS1 Gene Cause a Type of Nonsyndromic X-linked Sensorineural Deafness, DFN2

(2009) Xuezhong Liu et al.   AMERICAN JOURNAL OF HUMAN GENETICS