Expression Levels of WNT Signaling Pathway Genes During Early Tooth Development

A novel frameshift mutation of DVL1 ‐induced Robinow syndrome: A case report and literature review

(2022) Ruolan Hu et al.   Molecular Genetics & Genomic Medicine

Novel Dental Anomaly–associated Mutations in WNT10A Protein Binding Sites

(2022) Piranit Kantaputra et al.   INTERNATIONAL DENTAL JOURNAL

Mutations in LRP5 and BMP4 are associated with mesiodens, tooth agenesis, root malformation, and oral exostoses

(2022) Piranit Nik Kantaputra et al.   CLINICAL GENETICS

Adenomatous Polyposis Coli (APC) in cell migration

(2022) Xingyuan Fang et al.   EUROPEAN JOURNAL OF CELL BIOLOGY

Mutations in LRP6 highlight the role of WNT signaling in oral exostoses and dental anomalies

(2022) Piranit Kantaputra et al.   ARCHIVES OF ORAL BIOLOGY

Mutational landscape of non-functional adrenocortical adenomas

(2022) Luming Wu et al.   ENDOCRINE-RELATED CANCER

The neuronal protein Neuroligin 1 promotes colorectal cancer progression by modulating the APC/β-catenin pathway

(2022) Margherita Pergolizzi et al.   JOURNAL OF EXPERIMENTAL & CLINICAL CANCER RESEARCH

The Wnt signaling cascade in the pathogenesis of osteoarthritis and related promising treatment strategies

(2022) Jinchao Cheng et al.   Frontiers in Physiology

G Protein-Coupled Estrogen Receptor Correlates With Dkk2 Expression and Has Prognostic Impact in Ovarian Cancer Patients

(2021) Patricia Fraungruber et al.   Frontiers in Endocrinology

Targeted next-generation sequencing (NGS) analysis of mutations in nonsyndromic tooth agenesis candidate genes

(2021) Gül Keskin et al.   Journal of Orofacial Orthopedics-Fortschritte der Kieferorthopadie

Investigation of a Novel LRP6 Variant Causing Autosomal-Dominant Tooth Agenesis

(2021) Yan-xia Huang et al.   Frontiers in Genetics

The Development of Dentin Microstructure Is Controlled by the Type of Adjacent Epithelium

(2021) Josef Lavicky et al.   JOURNAL OF BONE AND MINERAL RESEARCH

Correction: Analyses of oligodontia phenotypes and genetic etiologies

(2021) Mengqi Zhou et al.   International Journal of Oral Science

Synergistic Mutations of LRP6 and WNT10A in Familial Tooth Agenesis

(2021) Kuan-Yu Chu et al.   Journal of Personalized Medicine

FZD10 regulates cell proliferation and mediates Wnt1 induced neurogenesis in the developing spinal cord

(2020) Abdulmajeed Fahad Alrefaei et al.   PLoS One

A novel missense mutation of LRP6 identified by whole‐exome sequencing in a Chinese family with nonsyndromic tooth agenesis

(2020) Huijuan Wang et al.   Orthodontics & Craniofacial Research

Functional characterization of ATF1 , GREM2 AND WNT10B variants associated with tooth agenesis

(2020) Meredith Williams et al.   Orthodontics & Craniofacial Research

Selective activation of FZD7 promotes mesendodermal differentiation of human pluripotent stem cells

(2020) Diana Gumber et al.   eLife

WNT10A mutations causing oligodontia

(2019) Haemin Park et al.   ARCHIVES OF ORAL BIOLOGY

Schopf‐Schulz‐Passarge syndrome: a rare ectodermal dysplasia with a delayed diagnosis

(2019) Fathima F. Ismail et al.   INTERNATIONAL JOURNAL OF DERMATOLOGY

Advances of Wnt signalling pathway in dental development and potential clinical application

(2019) Xi Lu et al.   Organogenesis

Deleterious Variants in WNT10A, EDAR, and EDA Causing Isolated and Syndromic Tooth Agenesis: A Structural Perspective from Molecular Dynamics Simulations

(2019) Asia Parveen et al.   INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES

Molecular mechanisms for short root anomaly

(2019) Mengjia Yu et al.   ORAL DISEASES

EDA, EDAR, EDARADD and WNT10A allelic variants in patients with ectodermal derivative impairment in the Spanish population

(2019) María Carmen Martínez-Romero et al.   Orphanet Journal of Rare Diseases

WNT10B mutations associated with isolated dental anomalies

(2018) P.N. Kantaputra et al.   CLINICAL GENETICS

Novel mutations of the SERPINF1 and FKBP10 genes in Chinese families with autosomal recessive osteogenesis imperfecta

(2018) Hao Zhang et al.   INTERNATIONAL JOURNAL OF MOLECULAR MEDICINE

Genetic analysis: Wnt and other pathways in non-syndromic tooth agenesis

(2018) Miao Yu et al.   ORAL DISEASES

Identification of likely pathogenic and known variants in TSPEAR, LAMB3, BCOR, and WNT10A in four Turkish families with tooth agenesis

(2018) Renqian Du et al.   HUMAN GENETICS

Further evidence for the role of WNT10A, WNT10B, and GREM2 as candidate genes for isolated tooth agenesis

(2018) S. Magruder et al.   Orthodontics & Craniofacial Research

Distinct impacts of bi-allelic WNT10A mutations on the permanent and primary dentitions in odonto-onycho-dermal dysplasia

(2018) Miao Yu et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

WNT10A variants in relation to nonsyndromic hypodontia in eastern Slovak population

(2018) D. Grejtakova et al.   JOURNAL OF GENETICS

Novel mutations identified in patients with tooth agenesis by whole-exome sequencing

(2018) Kai Zhao et al.   ORAL DISEASES

The Role of Wnt Pathway in the Pathogenesis of OA and Its Potential Therapeutic Implications in the Field of Regenerative Medicine

(2018) Maria De Santis et al.   Biomed Research International

Al-Awadi-Raas-Rothschild syndrome with dental anomalies and a novel WNT7A mutation

(2017) Piranit Nik Kantaputra et al.   European Journal of Medical Genetics

Genetic study of non-syndromic tooth agenesis through the screening of paired box 9, msh homeobox 1, axin 2, and Wnt family member 10A genes: a case-series

(2017) Marwa Haddaji Mastouri et al.   EUROPEAN JOURNAL OF ORAL SCIENCES

A novel mutation of adenomatous polyposis coli (APC) gene results in the formation of supernumerary teeth

(2017) Fang Yu et al.   JOURNAL OF CELLULAR AND MOLECULAR MEDICINE

Whole-Exome Sequencing Identifies Novel Variants for Tooth Agenesis

(2017) N. Dinckan et al.   JOURNAL OF DENTAL RESEARCH

Case report of Schöpf-Schulz-Passarge syndrome resulting from a missense mutation, p.Arg104Cys, in WNT10A

(2017) Tzu-Chien Hsu et al.   JOURNAL OF DERMATOLOGY

DVL3 Alleles Resulting in a −1 Frameshift of the Last Exon Mediate Autosomal-Dominant Robinow Syndrome

(2016) Janson J. White et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Mutations in WNT10B Are Identified in Individuals with Oligodontia

(2016) Ping Yu et al.   AMERICAN JOURNAL OF HUMAN GENETICS

The Wnt signaling pathway in cancer

(2016) Yann Duchartre et al.   CRITICAL REVIEWS IN ONCOLOGY HEMATOLOGY

Mutation of KREMEN1, a modulator of Wnt signaling, is responsible for ectodermal dysplasia including oligodontia in Palestinian families

(2016) Yasmin A Issa et al.   EUROPEAN JOURNAL OF HUMAN GENETICS

Novel mutations in LRP6 highlight the role of WNT signaling in tooth agenesis

(2016) Charlotte W. Ockeloen et al.   GENETICS IN MEDICINE

Osteogenesis imperfecta

(2016) Antonella Forlino et al.   LANCET

A recurrent de novo CTBP1 mutation is associated with developmental delay, hypotonia, ataxia, and tooth enamel defects

(2016) David B. Beck et al.   NEUROGENETICS

Wnt/β-Catenin Signaling Determines the Vasculogenic Fate of Postnatal Mesenchymal Stem Cells

(2016) Zhaocheng Zhang et al.   STEM CELLS

Notum deacylates Wnt proteins to suppress signalling activity

(2015) Satoshi Kakugawa et al.   NATURE

Wnts talking with the TGF-β superfamily: WISPers about modulation of osteoarthritis

(2015) Martijn H. van den Bosch et al.   RHEUMATOLOGY

Clinical features andWNT10Amutations in seven unrelated cases of Schöpf-Schulz-Passarge syndrome

(2014) C. Tziotzios et al.   BRITISH JOURNAL OF DERMATOLOGY

De novo WNT5A-associated autosomal dominant Robinow syndrome suggests specificity of genotype and phenotype

(2014) M. Roifman et al.   CLINICAL GENETICS

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

WNT10A variants are associated with non-syndromic tooth agenesis in the general population

(2013) Shujuan Song et al.   HUMAN GENETICS

Heterogeneity of mutational mechanisms and modes of inheritance in auriculocondylar syndrome

(2013) Christopher T Gordon et al.   JOURNAL OF MEDICAL GENETICS

LHX2 regulates the neural differentiation of human embryonic stem cells via transcriptional modulation of PAX6 and CER1

(2013) Pei-Shan Hou et al.   NUCLEIC ACIDS 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

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

(2012) A Mostowska et al.   CLINICAL GENETICS

Identification of signal peptide domain SOST mutations in autosomal dominant craniodiaphyseal dysplasia

(2011) Su Jin Kim et al.   HUMAN GENETICS

Post-natal Effect of Overexpressed DKK1 on Mandibular Molar Formation

(2011) X.L. Han et al.   JOURNAL OF DENTAL RESEARCH

Frizzled-10 promotes sensory neuron development in Xenopus embryos

(2009) Carla Garcia-Morales et al.   DEVELOPMENTAL BIOLOGY

WNT5Amutations in patients with autosomal dominant Robinow syndrome

(2009) Anthony D. Person et al.   DEVELOPMENTAL DYNAMICS