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

Inactivation of IL11 Signaling Causes Craniosynostosis, Delayed Tooth Eruption, and Supernumerary Teeth

(2011) Pekka Nieminen et al.   AMERICAN JOURNAL OF HUMAN GENETICS

The smallest teeth in the world are caused by mutations in the PCNT gene

(2011) Piranit Kantaputra et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

WNT10A and isolated hypodontia

(2011) Piranit Kantaputra et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

Isolated oligodontia associated with mutations in EDARADD, AXIN2, MSX1, and PAX9 genes

(2011) Birgitta Bergendal et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

Wnt5a plays a crucial role in determining tooth size during murine tooth development

(2011) Jinglei Cai et al.   CELL AND TISSUE RESEARCH

Amelogenesis Imperfecta: Genotype-Phenotype Studies in 71 Families

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

Interactions between Shh, Sostdc1 and Wnt signaling and a new feedback loop for spatial patterning of the teeth

(2011) S.-W. Cho et al.   DEVELOPMENT

Molecular genetics of supernumerary tooth formation

(2011) Xiu-Ping Wang et al.   GENESIS

Tissue-specific roles of Axin2 in the inhibition and activation of Wnt signaling in the mouse embryo

(2011) L. Qian et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

Temtamy Preaxial Brachydactyly Syndrome Is Caused by Loss-of-Function Mutations in Chondroitin Synthase 1, a Potential Target of BMP Signaling

(2010) Yun Li et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Defining a New Candidate Gene for Amelogenesis Imperfecta: From Molecular Genetics to Biochemistry

(2010) Blanca Urzúa et al.   BIOCHEMICAL GENETICS

Revisiting the supernumerary: the epidemiological and molecular basis of extra teeth

(2010) P. S. Fleming et al.   BRITISH DENTAL JOURNAL

Inhibition of Wnt signaling by Wise (Sostdc1) and negative feedback from Shh controls tooth number and patterning

(2010) Y. Ahn et al.   DEVELOPMENT

Genetic interactions between Pax9 and Msx1 regulate lip development and several stages of tooth morphogenesis

(2010) Mitsushiro Nakatomi et al.   DEVELOPMENTAL BIOLOGY

Tbx1 regulates progenitor cell proliferation in the dental epithelium by modulating Pitx2 activation of p21

(2010) Huojun Cao et al.   DEVELOPMENTAL BIOLOGY

Splitting placodes: effects of bone morphogenetic protein and Activin on the patterning and identity of mouse incisors

(2010) Pauliina M. Munne et al.   EVOLUTION & DEVELOPMENT

Dentinogenesis imperfecta in children with osteogenesis imperfecta: a clinical and ultrastructural study

(2010) ALESSANDRA MAJORANA et al.   International Journal of Paediatric Dentistry

A dominant mutation etiologic for human tricho-dento-osseous syndrome impairs the ability of DLX3 to downregulate ΔNp63α

(2010) Antonella Di Costanzo et al.   JOURNAL OF CELLULAR PHYSIOLOGY

FAM83H Mutations Cause ADHCAI and Alter Intracellular Protein Localization

(2010) S.-K. Lee et al.   JOURNAL OF DENTAL RESEARCH

Making up the numbers: The molecular control of mammalian dental formula

(2010) Martyn T. Cobourne et al.   SEMINARS IN CELL & DEVELOPMENTAL BIOLOGY

The Etiology of Eruption Disorders—Further Evidence of a “Genetic Paradigm”

(2010) Sylvia A. Frazier-Bowers et al.   Seminars in Orthodontics

Mutations in CNNM4 Cause Recessive Cone-Rod Dystrophy with Amelogenesis Imperfecta

(2009) Bozena Polok et al.   AMERICAN JOURNAL OF HUMAN GENETICS

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

WNT10A Mutations Are a Frequent Cause of a Broad Spectrum of Ectodermal Dysplasias with Sex-Biased Manifestation Pattern in Heterozygotes

(2009) Axel Bohring et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Mutations in CNNM4 Cause Jalili Syndrome, Consisting of Autosomal-Recessive Cone-Rod Dystrophy and Amelogenesis Imperfecta

(2009) David A. Parry et al.   AMERICAN JOURNAL OF HUMAN GENETICS

A Common Variation in EDAR Is a Genetic Determinant of Shovel-Shaped Incisors

(2009) Ryosuke Kimura et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Mutations in the Beta Propeller WDR72 Cause Autosomal-Recessive Hypomaturation Amelogenesis Imperfecta

(2009) Walid El-Sayed et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Molecular aspects of hypohidrotic ectodermal dysplasia

(2009) Marja L. Mikkola   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

Ectodermal dysplasias: Clinical and molecular review

(2009) Átila F. Visinoni et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

Apc inhibition of Wnt signaling regulates supernumerary tooth formation during embryogenesis and throughout adulthood

(2009) X.-P. Wang et al.   DEVELOPMENT

Primary cilia regulate Shh activity in the control of molar tooth number

(2009) A. Ohazama et al.   DEVELOPMENT

Osteogenesis imperfecta: Recent findings shed new light on this once well-understood condition

(2009) Donald Basel et al.   GENETICS IN MEDICINE

Pathogenic mechanisms of tooth agenesis linked to paired domain mutations in human PAX9

(2009) Y. Wang et al.   HUMAN MOLECULAR GENETICS

Tricho-Rhino-Phalangeal Syndrome with Supernumerary Teeth

(2009) P. Kantaputra et al.   JOURNAL OF DENTAL RESEARCH

Dentin sialoprotein and dentin phosphoprotein have distinct roles in dentin mineralization

(2009) Shigeki Suzuki et al.   MATRIX BIOLOGY

Cellular and molecular basis of tooth eruption

(2009) GE Wise   Orthodontics & Craniofacial Research

Distinct Impacts of Eda and Edar Loss of Function on the Mouse Dentition

(2009) Cyril Charles et al.   PLoS One

Modulation ofFgf3dosage in mouse and men mirrors evolution of mammalian dentition

(2009) Cyril Charles et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

FAM83H Mutations in Families with Autosomal-Dominant Hypocalcified Amelogenesis Imperfecta

(2008) Jung-Wook Kim et al.   AMERICAN JOURNAL OF HUMAN GENETICS

PTHR1 Loss-of-Function Mutations in Familial, Nonsyndromic Primary Failure of Tooth Eruption

(2008) Eva Decker et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Expanding the phenotype of SPONASTRIME dysplasia to include short dental roots, hypogammaglobulinemia, and cataracts

(2008) Karen W. Gripp et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

DLX3 c.561_562delCT mutation causes attenuated phenotype of tricho-dento-osseous syndrome

(2008) J. Timothy Wright et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

The genetic basis of inherited anomalies of the teeth

(2008) Isabelle Bailleul-Forestier et al.   European Journal of Medical Genetics

Physiological implications of DLX homeoproteins in enamel formation

(2008) Frédéric Lézot et al.   JOURNAL OF CELLULAR PHYSIOLOGY

Hereditary dentine disorders: dentinogenesis imperfecta and dentine dysplasia

(2008) Martin J Barron et al.   Orphanet Journal of Rare Diseases

Lrp4 Modulates Extracellular Integration of Cell Signaling Pathways in Development

(2008) Atsushi Ohazama et al.   PLoS One

Wnt/β-catenin signaling directs multiple stages of tooth morphogenesis

(2007) Fei Liu et al.   DEVELOPMENTAL BIOLOGY