WNT10A mutations account for ¼ of population‐based isolated oligodontia and show phenotypic correlations
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[1] P. Jagodziński,et al. Nucleotide variants of genes encoding components of the Wnt signalling pathway and the risk of non‐syndromic tooth agenesis , 2013, Clinical genetics.
[2] A. Torrelo,et al. Ectodermal dysplasias: a clinical and molecular review. , 2013, Actas dermo-sifiliograficas.
[3] P. Calvas,et al. Mutations in WNT10A are frequently involved in oligodontia associated with minor signs of ectodermal dysplasia , 2013, American journal of medical genetics. Part A.
[4] Jukka Jernvall,et al. Tooth shape formation and tooth renewal: evolving with the same signals , 2012, Development.
[5] D. Lindhout,et al. Mutations in WNT10A are present in more than half of isolated hypodontia cases , 2012, Journal of Medical Genetics.
[6] G. Petrof,et al. Schöpf–Schulz–Passarge syndrome resulting from a homozygous nonsense mutation, p.Cys107X, in WNT10A , 2011, The Australasian journal of dermatology.
[7] N. Dahl,et al. Isolated oligodontia associated with mutations in EDARADD, AXIN2, MSX1, and PAX9 genes , 2011, American journal of medical genetics. Part A.
[8] P. Kantaputra,et al. WNT10A and isolated hypodontia , 2011, American journal of medical genetics. Part A.
[9] J. McGrath,et al. Intra-familial variability of ectodermal defects associated with WNT10A mutations. , 2011, Acta dermato-venereologica.
[10] D. Murrell,et al. Phenotypic variability associated with WNT10A nonsense mutations , 2010, The British journal of dermatology.
[11] J. McGrath,et al. Schöpf-Schulz-Passarge syndrome resulting from a homozygous nonsense mutation in WNT10A. , 2010, Journal of dermatological science.
[12] S. Millar,et al. Wnt/β-catenin Signaling in Oral Tissue Development and Disease , 2010, Journal of dental research.
[13] I. Thesleff,et al. Patterns of Wnt pathway activity in the mouse incisor indicate absence of Wnt/β‐catenin signaling in the epithelial stem cells , 2009, Developmental dynamics : an official publication of the American Association of Anatomists.
[14] J. Helms,et al. Role of Wnt signaling in the biology of the periodontium , 2009, Developmental dynamics : an official publication of the American Association of Anatomists.
[15] J. Zonana,et al. Classifying ectodermal dysplasias: Incorporating the molecular basis and pathways (Workshop II) , 2009, American journal of medical genetics. Part A.
[16] S. Sel,et al. WNT10A mutations are a frequent cause of a broad spectrum of ectodermal dysplasias with sex-biased manifestation pattern in heterozygotes. , 2009, American journal of human genetics.
[17] P. Nieminen. Genetic basis of tooth agenesis. , 2009, Journal of experimental zoology. Part B, Molecular and developmental evolution.
[18] S. Baig,et al. WNT10A missense mutation associated with a complete Odonto-Onycho-Dermal Dysplasia syndrome , 2009, European Journal of Human Genetics.
[19] G. Fraser,et al. An Ancient Gene Network Is Co-opted for Teeth on Old and New Jaws , 2009, PLoS biology.
[20] R. Atit,et al. Wnt/β-catenin signaling directs multiple stages of tooth morphogenesis , 2008 .
[21] E. Chouery,et al. Mutation in WNT10A is associated with an autosomal recessive ectodermal dysplasia: the odonto-onycho-dermal dysplasia. , 2007, American journal of human genetics.
[22] T. Yamashiro,et al. Wnt10a regulates dentin sialophosphoprotein mRNA expression and possibly links odontoblast differentiation and tooth morphogenesis. , 2007, Differentiation; research in biological diversity.
[23] W. Birchmeier,et al. Continuous tooth generation in mouse is induced by activated epithelial Wnt/β-catenin signaling , 2006, Proceedings of the National Academy of Sciences.
[24] B. Bergendal,et al. Signs and symptoms from ectodermal organs in young Swedish individuals with oligodontia. , 2006, International journal of paediatric dentistry.
[25] A. Kuijpers-Jagtman,et al. A meta-analysis of the prevalence of dental agenesis of permanent teeth , 2004, Community dentistry and oral epidemiology.
[26] Rodrigo Lopez,et al. Multiple sequence alignment with the Clustal series of programs , 2003, Nucleic Acids Res..
[27] P. Bork,et al. Human non-synonymous SNPs: server and survey. , 2002, Nucleic acids research.
[28] Warren C. Lathe,et al. Prediction of deleterious human alleles. , 2001, Human molecular genetics.
[29] S. Poulsen,et al. Oligodontia in Danish schoolchildren , 2001, Acta odontologica Scandinavica.