583 related articles for article (PubMed ID: 22581971)
1. 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]
2. 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]
3. 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]
4. 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]
5. 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]
6. 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]
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. Mutations in MSX1, PAX9 and MMP20 genes in Saudi Arabian patients with tooth agenesis.
Shahid M; Balto HA; Al-Hammad N; Joshi S; Khalil HS; Somily AM; Sinjilawi NA; Al-Ghamdi S; Faiyaz-Ul-Haque M; Dhillon VS
Eur J Med Genet; 2016 Aug; 59(8):377-85. PubMed ID: 27365112
[TBL] [Abstract][Full Text] [Related]
9. 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]
10. 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]
11. Dental agenesis: genetic and clinical perspectives.
De Coster PJ; Marks LA; Martens LC; Huysseune A
J Oral Pathol Med; 2009 Jan; 38(1):1-17. PubMed ID: 18771513
[TBL] [Abstract][Full Text] [Related]
12. WNT10A coding variants and maxillary lateral incisor agenesis with associated dental anomalies.
Mostowska A; Biedziak B; Zadurska M; Matuszewska-Trojan S; Jagodziński PP
Eur J Oral Sci; 2015 Feb; 123(1):1-8. PubMed ID: 25545742
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. 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]
15. 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]
16. Novel MSX1 mutation in a family with autosomal-dominant hypodontia of second premolars and third molars.
Mostowska A; Biedziak B; Jagodzinski PP
Arch Oral Biol; 2012 Jun; 57(6):790-5. PubMed ID: 22297032
[TBL] [Abstract][Full Text] [Related]
17. Novel PAX9 mutation associated with syndromic tooth agenesis.
Mostowska A; Zadurska M; Rakowska A; Lianeri M; Jagodziński PP
Eur J Oral Sci; 2013 Oct; 121(5):403-11. PubMed ID: 24028587
[TBL] [Abstract][Full Text] [Related]
18. Only four genes (EDA1, EDAR, EDARADD, and WNT10A) account for 90% of hypohidrotic/anhidrotic ectodermal dysplasia cases.
Cluzeau C; Hadj-Rabia S; Jambou M; Mansour S; Guigue P; Masmoudi S; Bal E; Chassaing N; Vincent MC; Viot G; Clauss F; Manière MC; Toupenay S; Le Merrer M; Lyonnet S; Cormier-Daire V; Amiel J; Faivre L; de Prost Y; Munnich A; Bonnefont JP; Bodemer C; Smahi A
Hum Mutat; 2011 Jan; 32(1):70-2. PubMed ID: 20979233
[TBL] [Abstract][Full Text] [Related]
19. A novel initiation codon mutation of PAX9 in a family with oligodontia.
Liang J; Qin C; Yue H; He H; Bian Z
Arch Oral Biol; 2016 Jan; 61():144-8. PubMed ID: 26571067
[TBL] [Abstract][Full Text] [Related]
20. Characterization of a novel mutation in PAX9 gene in a family with non-syndromic dental agenesis.
Haddaji Mastouri M; De Coster P; Zaghabani A; Trabelsi S; May Y; Saad A; Coucke P; H'mida Ben Brahim D
Arch Oral Biol; 2016 Nov; 71():110-116. PubMed ID: 27491081
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
