246 related articles for article (PubMed ID: 23857653)
1. 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]
2. Sequence analysis of PAX9, MSX1 and AXIN2 genes in a Chinese oligodontia family.
Wang J; Jian F; Chen J; Wang H; Lin Y; Yang Z; Pan X; Lai W
Arch Oral Biol; 2011 Oct; 56(10):1027-34. PubMed ID: 21530942
[TBL] [Abstract][Full Text] [Related]
3. Mutational analysis of AXIN2, MSX1, and PAX9 in two Mexican oligodontia families.
Mu YD; Xu Z; Contreras CI; McDaniel JS; Donly KJ; Chen S
Genet Mol Res; 2013 Oct; 12(4):4446-58. PubMed ID: 24222224
[TBL] [Abstract][Full Text] [Related]
4. Clinical and genetic evaluation of a Chinese family with isolated oligodontia.
Qin H; Xu HZ; Xuan K
Arch Oral Biol; 2013 Sep; 58(9):1180-6. PubMed ID: 23731659
[TBL] [Abstract][Full Text] [Related]
5. Study of rs12532, rs8670 Polymorphism of Msh Homeobox 1 (MSX1), rs61754301, rs4904155 Polymorphism of Paired Box Gene 9 (PAX9), and rs2240308 Polymorphism of Axis Inhibitor Protein 2 (AXIN2) Genes in Nonsyndromic Hypodontia.
Mártha K; Kerekes Máthé B; Moldovan VG; Bănescu C
Biomed Res Int; 2019; 2019():2183720. PubMed ID: 31781599
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. 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]
8. Exclusion of coding region mutations in MSX1, PAX9 and AXIN2 in eight patients with severe oligodontia phenotype.
Gerits A; Nieminen P; De Muynck S; Carels C
Orthod Craniofac Res; 2006 Aug; 9(3):129-36. PubMed ID: 16918677
[TBL] [Abstract][Full Text] [Related]
9. 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]
10. 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]
11. 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]
12. 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]
13. 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]
14. 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]
15. Nine Novel PAX9 Mutations and a Distinct Tooth Agenesis Genotype-Phenotype.
Wong SW; Han D; Zhang H; Liu Y; Zhang X; Miao MZ; Wang Y; Zhao N; Zeng L; Bai B; Wang YX; Liu H; Frazier-Bowers SA; Feng H
J Dent Res; 2018 Feb; 97(2):155-162. PubMed ID: 28910570
[TBL] [Abstract][Full Text] [Related]
16. Novel nonsense mutation in MSX1 causes tooth agenesis with cleft lip in a Chinese family.
Liang J; Zhu L; Meng L; Chen D; Bian Z
Eur J Oral Sci; 2012 Aug; 120(4):278-82. PubMed ID: 22813217
[TBL] [Abstract][Full Text] [Related]
17. 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]
18. PAX9 and MSX1 transcription factor genes in non-syndromic dental agenesis.
Paixão-Côrtes VR; Braga T; Salzano FM; Mundstock K; Mundstock CA; Bortolini MC
Arch Oral Biol; 2011 Apr; 56(4):337-44. PubMed ID: 21111400
[TBL] [Abstract][Full Text] [Related]
19. Novel PAX9 gene polymorphisms and mutations and susceptibility to tooth agenesis in the Czech population.
Hlousková A; Bonczek O; Izakovicová-Hollá L; Lochman J; Soukalová J; Stembírek J; Mísek I; Cernochová P; Krejcí P; Vanek J; Šerý O
Neuro Endocrinol Lett; 2015; 36(5):452-7. PubMed ID: 26707046
[TBL] [Abstract][Full Text] [Related]
20. Effects of PAX9 and MSX1 gene variants to hypodontia, tooth size and the type of congenitally missing teeth.
Kirac D; Eraydin F; Avcilar T; Ulucan K; Özdemir F; Guney AI; Kaspar EÇ; Keshi E; Isbir T
Cell Mol Biol (Noisy-le-grand); 2016 Nov; 62(13):78-84. PubMed ID: 28040065
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]