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2. WNT10B mutations associated with isolated dental anomalies. Kantaputra PN; Hutsadaloi A; Kaewgahya M; Intachai W; German R; Koparal M; Leethanakul C; Tolun A; Ketudat Cairns JR Clin Genet; 2018 May; 93(5):992-999. PubMed ID: 29364501 [TBL] [Abstract][Full Text] [Related]
3. Role of WNT10A in failure of tooth development in humans and zebrafish. Yuan Q; Zhao M; Tandon B; Maili L; Liu X; Zhang A; Baugh EH; Tran T; Silva RM; Hecht JT; Swindell EC; Wagner DS; Letra A Mol Genet Genomic Med; 2017 Nov; 5(6):730-741. PubMed ID: 29178643 [TBL] [Abstract][Full Text] [Related]
4. Functional Effects of Zeng Y; Baugh E; Akyalcin S; Letra A J Dent Res; 2021 Mar; 100(3):302-309. PubMed ID: 33034246 [TBL] [Abstract][Full Text] [Related]
5. Mutations in WNT10A are present in more than half of isolated hypodontia cases. van den Boogaard MJ; Créton M; Bronkhorst Y; van der Hout A; Hennekam E; Lindhout D; Cune M; Ploos van Amstel HK J Med Genet; 2012 May; 49(5):327-31. PubMed ID: 22581971 [TBL] [Abstract][Full Text] [Related]
6. Novel mutations identified in patients with tooth agenesis by whole-exome sequencing. Zhao K; Lian M; Zou D; Huang W; Zhou W; Shen Y; Wang F; Wu Y Oral Dis; 2019 Mar; 25(2):523-534. PubMed ID: 30417976 [TBL] [Abstract][Full Text] [Related]
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8. WNT10A variants are associated with non-syndromic tooth agenesis in the general population. Song S; Zhao R; He H; Zhang J; Feng H; Lin L Hum Genet; 2014 Jan; 133(1):117-24. PubMed ID: 24043634 [TBL] [Abstract][Full Text] [Related]
9. Mutations in LRP5 and BMP4 are associated with mesiodens, tooth agenesis, root malformation, and oral exostoses. Kantaputra PN; Guven Y; Tripuwabhrut K; Adisornkanj P; Hatsadaloi A; Kaewgahya M; Olsen B; Ngamphiw C; Jatooratthawichot P; Tongsima S; Ketudat Cairns JR Clin Genet; 2022 Oct; 102(4):333-338. PubMed ID: 35754005 [TBL] [Abstract][Full Text] [Related]
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11. A novel WNT10A mutation causes non-syndromic hypodontia in an Egyptian family. Abdalla EM; Mostowska A; Jagodziński PP; Dwidar K; Ismail SR Arch Oral Biol; 2014 Jul; 59(7):722-8. PubMed ID: 24798981 [TBL] [Abstract][Full Text] [Related]
13. Phenotypic characteristics of taurodontism and a novel WNT10A variant in non-syndromic oligodontia family. Zhao Y; Hou Y; Ren J; Gao X; Meng L; Liu Y; Xing C; Shen W Arch Oral Biol; 2023 Oct; 154():105759. PubMed ID: 37422997 [TBL] [Abstract][Full Text] [Related]
14. WNT10A mutations also associated with agenesis of the maxillary permanent canines, a separate entity. Kantaputra P; Kaewgahya M; Kantaputra W Am J Med Genet A; 2014 Feb; 164A(2):360-3. PubMed ID: 24311251 [TBL] [Abstract][Full Text] [Related]
15. Nucleotide variants of genes encoding components of the Wnt signalling pathway and the risk of non-syndromic tooth agenesis. Mostowska A; Biedziak B; Zadurska M; Dunin-Wilczynska I; Lianeri M; Jagodzinski PP Clin Genet; 2013 Nov; 84(5):429-40. PubMed ID: 23167694 [TBL] [Abstract][Full Text] [Related]
16. Involvement of and interaction between WNT10A and EDA mutations in tooth agenesis cases in the Chinese population. He H; Han D; Feng H; Qu H; Song S; Bai B; Zhang Z PLoS One; 2013; 8(11):e80393. PubMed ID: 24312213 [TBL] [Abstract][Full Text] [Related]
17. Compound heterozygous WNT10A missense variations exacerbated the tooth agenesis caused by hypohidrotic ectodermal dysplasia. Liu Y; Sun J; Zhang C; Wu Y; Ma S; Li X; Wu X; Gao Q BMC Oral Health; 2024 Jan; 24(1):136. PubMed ID: 38280992 [TBL] [Abstract][Full Text] [Related]
18. Deleterious Variants in Parveen A; Khan SA; Mirza MU; Bashir H; Arshad F; Iqbal M; Ahmad W; Wahab A; Fiaz A; Naz S; Ashraf F; Mobeen T; Aziz S; Ahmed SS; Muhammad N; Hassib NF; Mostafa MI; Gaboon NE; Gul R; Khan S; Froeyen M; Shoaib M; Wasif N Int J Mol Sci; 2019 Oct; 20(21):. PubMed ID: 31652981 [TBL] [Abstract][Full Text] [Related]
19. Mutation analysis by direct and whole exome sequencing in familial and sporadic tooth agenesis. Salvi A; Giacopuzzi E; Bardellini E; Amadori F; Ferrari L; De Petro G; Borsani G; Majorana A Int J Mol Med; 2016 Nov; 38(5):1338-1348. PubMed ID: 27665865 [TBL] [Abstract][Full Text] [Related]
20. The association between WNT10A variants and dental development in patients with isolated oligodontia. Dhamo B; Fennis W; Créton M; Vucic S; Cune M; Ploos van Amstel HK; Wolvius EB; van den Boogaard MJ; Ongkosuwito EM Eur J Hum Genet; 2016 Jan; 25(1):59-65. PubMed ID: 27650966 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]