169 related articles for article (PubMed ID: 34834569)
1. Synergistic Mutations of
Chu KY; Wang YL; Chou YR; Chen JT; Wang YP; Simmer JP; Hu JC; Wang SK
J Pers Med; 2021 Nov; 11(11):. PubMed ID: 34834569
[TBL] [Abstract][Full Text] [Related]
2. PAX9 mutations and genetic synergism in familial tooth agenesis.
Chu KY; Wang YL; Chen JT; Lin CH; Yao CJ; Chen YJ; Chen HW; Simmer JP; Hu JC; Wang SK
Ann N Y Acad Sci; 2023 Jun; 1524(1):87-96. PubMed ID: 37005710
[TBL] [Abstract][Full Text] [Related]
3. Loss-of-Function Mutations in the WNT Co-receptor LRP6 Cause Autosomal-Dominant Oligodontia.
Massink MP; Créton MA; Spanevello F; Fennis WM; Cune MS; Savelberg SM; Nijman IJ; Maurice MM; van den Boogaard MJ; van Haaften G
Am J Hum Genet; 2015 Oct; 97(4):621-6. PubMed ID: 26387593
[TBL] [Abstract][Full Text] [Related]
4. Whole-Exome Sequencing Identifies Novel Variants for Tooth Agenesis.
Dinckan N; Du R; Petty LE; Coban-Akdemir Z; Jhangiani SN; Paine I; Baugh EH; Erdem AP; Kayserili H; Doddapaneni H; Hu J; Muzny DM; Boerwinkle E; Gibbs RA; Lupski JR; Uyguner ZO; Below JE; Letra A
J Dent Res; 2018 Jan; 97(1):49-59. PubMed ID: 28813618
[TBL] [Abstract][Full Text] [Related]
5. 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]
6. Candidate gene analysis of tooth agenesis identifies novel mutations in six genes and suggests significant role for WNT and EDA signaling and allele combinations.
Arte S; Parmanen S; Pirinen S; Alaluusua S; Nieminen P
PLoS One; 2013; 8(8):e73705. PubMed ID: 23991204
[TBL] [Abstract][Full Text] [Related]
7. Genetic analysis: Wnt and other pathways in nonsyndromic tooth agenesis.
Yu M; Wong SW; Han D; Cai T
Oral Dis; 2019 Apr; 25(3):646-651. PubMed ID: 29969831
[TBL] [Abstract][Full Text] [Related]
8. 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]
9. Taurodontism, variations in tooth number, and misshapened crowns in Wnt10a null mice and human kindreds.
Yang J; Wang SK; Choi M; Reid BM; Hu Y; Lee YL; Herzog CR; Kim-Berman H; Lee M; Benke PJ; Lloyd KC; Simmer JP; Hu JC
Mol Genet Genomic Med; 2015 Jan; 3(1):40-58. PubMed ID: 25629078
[TBL] [Abstract][Full Text] [Related]
10. 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]
11. Targeted next-generation sequencing (NGS) analysis of mutations in nonsyndromic tooth agenesis candidate genes : Analysis of a Turkish cohort.
Keskin G; Karaer K; Uçar Gündoğar Z
J Orofac Orthop; 2022 Oct; 83(Suppl 1):65-74. PubMed ID: 33725141
[TBL] [Abstract][Full Text] [Related]
12. 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]
13.
Yu M; Fan Z; Wong SW; Sun K; Zhang L; Liu H; Feng H; Liu Y; Han D
J Dent Res; 2021 Apr; 100(4):415-422. PubMed ID: 33164649
[TBL] [Abstract][Full Text] [Related]
14. 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]
15. 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]
16. Mutation of KREMEN1, a modulator of Wnt signaling, is responsible for ectodermal dysplasia including oligodontia in Palestinian families.
Issa YA; Kamal L; Rayyan AA; Dweik D; Pierce S; Lee MK; King MC; Walsh T; Kanaan M
Eur J Hum Genet; 2016 Oct; 24(10):1430-5. PubMed ID: 27049303
[TBL] [Abstract][Full Text] [Related]
17. Tooth agenesis: What do we know and is there a connection to cancer?
Bonczek O; Krejci P; Izakovicova-Holla L; Cernochova P; Kiss I; Vojtesek B
Clin Genet; 2021 Apr; 99(4):493-502. PubMed ID: 33249565
[TBL] [Abstract][Full Text] [Related]
18. Phenotypic and Genotypic Features of Thai Patients With Nonsyndromic Tooth Agenesis and
Kanchanasevee C; Sriwattanapong K; Theerapanon T; Thaweesapphithak S; Chetruengchai W; Porntaveetus T; Shotelersuk V
Front Physiol; 2020; 11():573214. PubMed ID: 33329022
[TBL] [Abstract][Full Text] [Related]
19. Functional analysis of a novel missense mutation in AXIN2 associated with non-syndromic tooth agenesis.
Yue H; Liang J; Yang K; Hua B; Bian Z
Eur J Oral Sci; 2016 Jun; 124(3):228-33. PubMed ID: 27090353
[TBL] [Abstract][Full Text] [Related]
20. Analyses of oligodontia phenotypes and genetic etiologies.
Zhou M; Zhang H; Camhi H; Seymen F; Koruyucu M; Kasimoglu Y; Kim JW; Kim-Berman H; Yuson NMR; Benke PJ; Wu Y; Wang F; Zhu Y; Simmer JP; Hu JC
Int J Oral Sci; 2021 Sep; 13(1):32. PubMed ID: 34593752
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
