188 related articles for article (PubMed ID: 22813217)
21. Novel human mutation and CRISPR/Cas genome-edited mice reveal the importance of C-terminal domain of MSX1 in tooth and palate development.
Mitsui SN; Yasue A; Masuda K; Naruto T; Minegishi Y; Oyadomari S; Noji S; Imoto I; Tanaka E
Sci Rep; 2016 Dec; 6():38398. PubMed ID: 27917906
[TBL] [Abstract][Full Text] [Related]
22. Msx1 mutations: how do they cause tooth agenesis?
Wang Y; Kong H; Mues G; D'Souza R
J Dent Res; 2011 Mar; 90(3):311-6. PubMed ID: 21297014
[TBL] [Abstract][Full Text] [Related]
23. 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]
24. A novel nonsense mutation in PAX9 is associated with marked variability in number of missing teeth.
Hansen L; Kreiborg S; Jarlov H; Niebuhr E; Eiberg H
Eur J Oral Sci; 2007 Aug; 115(4):330-3. PubMed ID: 17697174
[TBL] [Abstract][Full Text] [Related]
25. Genes affecting tooth morphogenesis.
Kapadia H; Mues G; D'Souza R
Orthod Craniofac Res; 2007 Aug; 10(3):105-13. PubMed ID: 17651126
[TBL] [Abstract][Full Text] [Related]
26. [Correlation between the phenotype and genotype of tooth agenesis patients by tooth agenesis code].
Gong Y; Feng HL; He HY; Ge YJ
Zhongguo Yi Xue Ke Xue Yuan Xue Bao; 2010 Jun; 32(3):254-9. PubMed ID: 20602873
[TBL] [Abstract][Full Text] [Related]
27. 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]
28. 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]
29. 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]
30. Genes affecting tooth morphogenesis.
Kapadia H; Mues G; D'Souza R
Orthod Craniofac Res; 2007 Nov; 10(4):237-44. PubMed ID: 17973693
[TBL] [Abstract][Full Text] [Related]
31. 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]
32. MSX1 and PAX9 investigation in monozygotic twins with variable expression of tooth agenesis.
Lopez SI; Mundstock KS; Paixão-Côrtes VR; Schüler-Faccini L; Mundstock CA; Bortolini MC; Salzano FM
Twin Res Hum Genet; 2013 Dec; 16(6):1112-6. PubMed ID: 24103583
[TBL] [Abstract][Full Text] [Related]
33. Non-syndromic oligodontia with a novel mutation of PAX9.
Suda N; Ogawa T; Kojima T; Saito C; Moriyama K
J Dent Res; 2011 Mar; 90(3):382-6. PubMed ID: 21098475
[TBL] [Abstract][Full Text] [Related]
34. Pathogenic mechanisms of tooth agenesis linked to paired domain mutations in human PAX9.
Wang Y; Groppe JC; Wu J; Ogawa T; Mues G; D'Souza RN; Kapadia H
Hum Mol Genet; 2009 Aug; 18(15):2863-74. PubMed ID: 19429910
[TBL] [Abstract][Full Text] [Related]
35. Two novel mutations in MSX1 causing oligodontia.
Yang L; Liang J; Yue H; Bian Z
PLoS One; 2020; 15(1):e0227287. PubMed ID: 31914153
[TBL] [Abstract][Full Text] [Related]
36. 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]
37. 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]
38. Investigating the etiology of multiple tooth agenesis in three sisters with severe oligodontia.
Swinnen S; Bailleul-Forestier I; Arte S; Nieminen P; Devriendt K; Carels C
Orthod Craniofac Res; 2008 Feb; 11(1):24-31. PubMed ID: 18199077
[TBL] [Abstract][Full Text] [Related]
39. 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]
40. 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]
[Previous] [Next] [New Search]
