Associated Papers
WNT10A, dermatology and dentistry.
Doolan BJ et al.
The British Journal of Dermatology, 2021
MicroRNA-374a, -4680, and -133b suppress cell proliferation through the regulation of genes associated with human cleft palate in cultured human palate cells.
Suzuki A et al.
Bmc Medical Genomics, 2019
MicroRNA-655-3p and microRNA-497-5p inhibit cell proliferation in cultured human lip cells through the regulation of genes related to human cleft lip.
Gajera M et al.
Bmc Medical Genomics, 2019
Distinct impacts of bi-allelic WNT10A mutations on the permanent and primary dentitions in odonto-onycho-dermal dysplasia.
Yu M et al.
American Journal of Medical Genetics. Part A, 2019
Association of single nucleotide polymorphisms in WNT genes with the risk of nonsyndromic cleft lip with or without cleft palate.
Rafighdoost H et al.
Congenital Anomalies, 2018
Variations in WNT3 gene are associated with incidence of non-syndromic cleft lip with or without cleft palate in a northeast Chinese population.
Lu YP et al.
Genetics and Molecular Research : Gmr, 2015
Taurodontism, variations in tooth number, and misshapened crowns in Wnt10a null mice and human kindreds.
Yang J et al.
Molecular Genetics & Genomic Medicine, 2015
Variability in dentofacial phenotypes in four families with WNT10A mutations.
Vink CP et al.
European Journal of Human Genetics : Ejhg, 2014
Mutations in WNT10A are frequently involved in oligodontia associated with minor signs of ectodermal dysplasia.
Plaisancié J et al.
American Journal of Medical Genetics. Part A, 2013
Schöpf-Schulz-Passarge syndrome resulting from a homozygous nonsense mutation, p.Cys107X, in WNT10A.
Petrof G et al.
The Australasian Journal of Dermatology, 2011
Two families confirm Schöpf-Schulz-Passarge syndrome as a discrete entity within the WNT10A phenotypic spectrum.
Castori M et al.
Clinical Genetics, 2011
Schöpf-Schulz-Passarge syndrome resulting from a homozygous nonsense mutation in WNT10A.
Nagy N et al.
Journal of Dermatological Science, 2010
WNT10A missense mutation associated with a complete odonto-onycho-dermal dysplasia syndrome.
Nawaz S et al.
European Journal of Human Genetics : Ejhg, 2009
Association of the WNT3 Variations and the Risk of Non-Syndromic Cleft Lip and Palate in a Population of Iranian Infants.
Farrokhi Karibozorg H et al.
Avicenna Journal of Medical Biotechnology, 0