368 related articles for article (PubMed ID: 27365112)
1. 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]
2. 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]
3. 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]
4. A screen of a large Czech cohort of oligodontia patients implicates a novel mutation in the PAX9 gene.
Šerý O; Bonczek O; Hloušková A; Černochová P; Vaněk J; Míšek I; Krejčí P; Izakovičová Hollá L
Eur J Oral Sci; 2015 Apr; 123(2):65-71. PubMed ID: 25683653
[TBL] [Abstract][Full Text] [Related]
5. 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]
6. 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]
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. 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]
9. 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]
10. 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]
11. 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]
12. 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]
13. 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]
14. 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]
15. Novel nonsense mutation in MSX1 in familial nonsyndromic oligodontia: subcellular localization and role of homeodomain/MH4.
Kimura M; Machida J; Yamaguchi S; Shibata A; Tatematsu T; Miyachi H; Jezewski PA; Nakayama A; Higashi Y; Shimozato K; Tokita Y
Eur J Oral Sci; 2014 Feb; 122(1):15-20. PubMed ID: 24329876
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. 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]
18. Mutational analysis of MSX1 and PAX9 genes in Portuguese families with maxillary lateral incisor agenesis.
Pinho T; Silva-Fernandes A; Bousbaa H; Maciel P
Eur J Orthod; 2010 Oct; 32(5):582-8. PubMed ID: 20660504
[TBL] [Abstract][Full Text] [Related]
19. 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]
20. A novel PAX9 mutation causing oligodontia.
Daw EM; Saliba C; Grech G; Camilleri S
Arch Oral Biol; 2017 Dec; 84():100-105. PubMed ID: 28965043
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
