551 related articles for article (PubMed ID: 29969831)
1. 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]
2. 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]
3. Nonsyndromic oligodontia : Does the Tooth Agenesis Code (TAC) enable prediction of the causative mutation?
Bock NC; Lenz S; Ruiz-Heiland G; Ruf S
J Orofac Orthop; 2017 Mar; 78(2):112-120. PubMed ID: 28204848
[TBL] [Abstract][Full Text] [Related]
4. Isolated oligodontia associated with mutations in EDARADD, AXIN2, MSX1, and PAX9 genes.
Bergendal B; Klar J; Stecksén-Blicks C; Norderyd J; Dahl N
Am J Med Genet A; 2011 Jul; 155A(7):1616-22. PubMed ID: 21626677
[TBL] [Abstract][Full Text] [Related]
5. De novo EDA mutations: Variable expression in two Egyptian families.
Gaczkowska A; Abdalla EM; Dowidar KM; Elhady GM; Jagodzinski PP; Mostowska A
Arch Oral Biol; 2016 Aug; 68():21-8. PubMed ID: 27054699
[TBL] [Abstract][Full Text] [Related]
6. 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.
Haddaji Mastouri M; De Coster P; Zaghabani A; Jammali F; Raouahi N; Ben Salem A; Saad A; Coucke P; H'mida Ben Brahim D
Eur J Oral Sci; 2018 Feb; 126(1):24-32. PubMed ID: 29114927
[TBL] [Abstract][Full Text] [Related]
7. 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]
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. 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]
10. Identification of genetic risk factors for maxillary lateral incisor agenesis.
Alves-Ferreira M; Pinho T; Sousa A; Sequeiros J; Lemos C; Alonso I
J Dent Res; 2014 May; 93(5):452-8. PubMed ID: 24554542
[TBL] [Abstract][Full Text] [Related]
11. EDA, EDAR, EDARADD and WNT10A allelic variants in patients with ectodermal derivative impairment in the Spanish population.
Martínez-Romero MC; Ballesta-Martínez MJ; López-González V; Sánchez-Soler MJ; Serrano-Antón AT; Barreda-Sánchez M; Rodriguez-Peña L; Martínez-Menchon MT; Frías-Iniesta J; Sánchez-Pedreño P; Carbonell-Meseguer P; Glover-López G; Guillén-Navarro E;
Orphanet J Rare Dis; 2019 Dec; 14(1):281. PubMed ID: 31796081
[TBL] [Abstract][Full Text] [Related]
12. 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]
13. GREMLIN 2 Mutations and Dental Anomalies.
Kantaputra PN; Kaewgahya M; Hatsadaloi A; Vogel P; Kawasaki K; Ohazama A; Ketudat Cairns JR
J Dent Res; 2015 Dec; 94(12):1646-52. PubMed ID: 26416033
[TBL] [Abstract][Full Text] [Related]
14. PAX9 polymorphism and susceptibility to sporadic non-syndromic severe anodontia: a case-control study in southwest China.
Wang J; Xu Y; Chen J; Wang F; Huang R; Wu S; Shu L; Qiu J; Yang Z; Xue J; Wang R; Zhao J; Lai W
J Appl Oral Sci; 2013; 21(3):256-64. PubMed ID: 23857653
[TBL] [Abstract][Full Text] [Related]
15. Functional Study of Ectodysplasin-A Mutations Causing Non-Syndromic Tooth Agenesis.
Shen W; Wang Y; Liu Y; Liu H; Zhao H; Zhang G; Snead ML; Han D; Feng H
PLoS One; 2016; 11(5):e0154884. PubMed ID: 27144394
[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. 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]
18. Gene Mutations of the Three Ectodysplasin Pathway Key Players (
Ahmed HA; El-Kamah GY; Rabie E; Mostafa MI; Abouzaid MR; Hassib NF; Mehrez MI; Abdel-Kader MA; Mohsen YH; Zada SK; Amr KS; Sayed ISM
Genes (Basel); 2021 Sep; 12(9):. PubMed ID: 34573371
[TBL] [Abstract][Full Text] [Related]
19. 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]
20. 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]
[Next] [New Search]