Nucleotide variants of genes encoding components of the Wnt signalling pathway and the risk of non-syndromic tooth agenesis

Genetic basis of non-syndromic anomalies of human tooth number

(2012) Gabriella Galluccio et al.   ARCHIVES OF ORAL BIOLOGY

Association ofDVL2andAXIN2gene polymorphisms with cleft lip with or without cleft palate in a polish population

(2012) Adrianna Mostowska et al.   BIRTH DEFECTS RESEARCH PART A-CLINICAL AND MOLECULAR TERATOLOGY

Genotype and haplotype analysis of WNT genes in non-syndromic cleft lip with or without cleft palate

(2012) Adrianna Mostowska et al.   EUROPEAN JOURNAL OF ORAL SCIENCES

Mutations inWNT10Aare present in more than half of isolated hypodontia cases

(2012) Marie-José van den Boogaard et al.   JOURNAL OF MEDICAL GENETICS

WNT secretion and signalling in human disease

(2012) Patrick Herr et al.   TRENDS IN MOLECULAR MEDICINE

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

Studies with Wnt genes and nonsyndromic cleft lip and palate

(2010) Renato Menezes et al.   BIRTH DEFECTS RESEARCH PART A-CLINICAL AND MOLECULAR TERATOLOGY

Dvl2 Promotes Intestinal Length and Neoplasia in the ApcMin Mouse Model for Colorectal Cancer

(2010) C. Metcalfe et al.   CANCER RESEARCH

Two families confirm Schöpf-Schulz-Passarge syndrome as a discrete entity within the WNT10A phenotypic spectrum

(2010) M Castori et al.   CLINICAL GENETICS

Wnt/β-catenin Signaling in Oral Tissue Development and Disease

(2010) F. Liu et al.   JOURNAL OF DENTAL RESEARCH

Dental agenesis: genetic and clinical perspectives

(2010) P. J. De Coster et al.   JOURNAL OF ORAL PATHOLOGY & MEDICINE

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

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

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

Wnt/β-Catenin Signaling: Components, Mechanisms, and Diseases

(2009) Bryan T. MacDonald et al.   DEVELOPMENTAL CELL

WNT10A missense mutation associated with a complete Odonto-Onycho-Dermal Dysplasia syndrome

(2009) Sadia Nawaz et al.   EUROPEAN JOURNAL OF HUMAN GENETICS

Tooth Agenesis: from Molecular Genetics to Molecular Dentistry

(2009) E. Matalova et al.   JOURNAL OF DENTAL RESEARCH

Axis inhibition protein 2 (AXIN2) polymorphisms and tooth agenesis

(2008) N. Callahan et al.   ARCHIVES OF ORAL BIOLOGY

Regulation of cell–cell adhesion by the cadherin–catenin complex

(2008) W. James Nelson   BIOCHEMICAL SOCIETY TRANSACTIONS

The genetic basis of inherited anomalies of the teeth

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

Variation in WNT genes is associated with non-syndromic cleft lip with or without cleft palate

(2008) Brett T. Chiquet et al.   HUMAN MOLECULAR GENETICS

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

(2007) Fei Liu et al.   DEVELOPMENTAL BIOLOGY