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Title
WNT10B
mutations associated with isolated dental anomalies
Authors
Keywords
-
Journal
CLINICAL GENETICS
Volume 93, Issue 5, Pages 992-999
Publisher
Wiley
Online
2018-01-24
DOI
10.1111/cge.13218
References
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Related references
Note: Only part of the references are listed.- Mutations in WNT10B Are Identified in Individuals with Oligodontia
- (2016) Ping Yu et al. AMERICAN JOURNAL OF HUMAN GENETICS
- Functional Study of Ectodysplasin-A Mutations Causing Non-Syndromic Tooth Agenesis
- (2016) Wenjing Shen et al. PLoS One
- Loss-of-Function Mutations in the WNT Co-receptor LRP6 Cause Autosomal-Dominant Oligodontia
- (2015) Maarten P.G. Massink et al. AMERICAN JOURNAL OF HUMAN GENETICS
- GREMLIN 2 Mutations and Dental Anomalies
- (2015) P.N. Kantaputra et al. JOURNAL OF DENTAL RESEARCH
- The I-TASSER Suite: protein structure and function prediction
- (2015) Jianyi Yang et al. NATURE METHODS
- Tricho-odonto-onycho-dermal dysplasia andWNT10Amutations
- (2014) P. Kantaputra et al. AMERICAN JOURNAL OF MEDICAL GENETICS PART A
- WNT10Amutations also associated with agenesis of the maxillary permanent canines, a separate entity
- (2013) P. Kantaputra et al. AMERICAN JOURNAL OF MEDICAL GENETICS PART A
- Novel homozygous mutations in the WNT10B gene underlying autosomal recessive split hand/foot malformation in three consanguineous families
- (2013) Abdul Aziz et al. GENE
- β-catenin is Required in Odontoblasts for Tooth Root Formation
- (2013) T.H. Kim et al. JOURNAL OF DENTAL RESEARCH
- Candidate Gene Analysis of Tooth Agenesis Identifies Novel Mutations in Six Genes and Suggests Significant Role for WNT and EDA Signaling and Allele Combinations
- (2013) Sirpa Arte et al. PLoS One
- The ectodysplasin pathway: from diseases to adaptations
- (2013) Alexa Sadier et al. TRENDS IN GENETICS
- Wnt/β-Catenin Signaling and Disease
- (2012) Hans Clevers et al. CELL
- Mutations inWNT10Aare present in more than half of isolated hypodontia cases
- (2012) Marie-José van den Boogaard et al. JOURNAL OF MEDICAL GENETICS
- Structural Basis of Wnt Recognition by Frizzled
- (2012) C. Y. Janda et al. SCIENCE
- WNT10A and isolated hypodontia
- (2011) Piranit Kantaputra et al. AMERICAN JOURNAL OF MEDICAL GENETICS PART A
- A novel homozygous missense mutation in WNT10B in familial split-hand/foot malformation
- (2011) S Khan et al. CLINICAL GENETICS
- Homozygous nonsense mutation in WNT10B and sporadic split-hand/foot malformation (SHFM) with autosomal recessive inheritance
- (2010) Ariane Blattner et al. AMERICAN JOURNAL OF MEDICAL GENETICS PART A
- Phenotypic analysis of Arg227 mutations of TP63 with emphasis on dental phenotype and micturition difficulties in EEC syndrome
- (2010) Warissara Sripathomsawat et al. AMERICAN JOURNAL OF MEDICAL GENETICS PART A
- Inhibition of Wnt signaling by Wise (Sostdc1) and negative feedback from Shh controls tooth number and patterning
- (2010) Y. Ahn et al. DEVELOPMENT
- Cooperation between the transcription factors p63 and IRF6 is essential to prevent cleft palate in mice
- (2010) Helen A. Thomason et al. JOURNAL OF CLINICAL INVESTIGATION
- Genome-Wide Profiling of p63 DNA–Binding Sites Identifies an Element that Regulates Gene Expression during Limb Development in the 7q21 SHFM1 Locus
- (2010) Evelyn N. Kouwenhoven et al. PLoS Genetics
- Apc inhibition of Wnt signaling regulates supernumerary tooth formation during embryogenesis and throughout adulthood
- (2009) X.-P. Wang et al. DEVELOPMENT
- Reciprocal Requirements for EDA/EDAR/NF-κB and Wnt/β-Catenin Signaling Pathways in Hair Follicle Induction
- (2009) Yuhang Zhang et al. DEVELOPMENTAL CELL
- Homozygous WNT10b mutation and complex inheritance in Split-Hand/Foot Malformation
- (2008) Sibel Aylin Ugur et al. HUMAN MOLECULAR GENETICS
- Phenome connections
- (2008) Martin Oti et al. TRENDS IN GENETICS
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