243 related articles for article (PubMed ID: 21911943)
1. The genetic basis of tooth agenesis: basic concepts and genes involved.
Pani SC
J Indian Soc Pedod Prev Dent; 2011; 29(2):84-9. PubMed ID: 21911943
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. 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]
4. 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]
5. 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]
6. [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]
7. 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]
8. 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]
9. 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]
10. 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]
11. 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]
12. 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]
13. Familial human hypodontia--is it all in the genes?
Cobourne MT
Br Dent J; 2007 Aug; 203(4):203-8. PubMed ID: 17721480
[TBL] [Abstract][Full Text] [Related]
14. Concomitant occurrence of canine malposition and tooth agenesis: evidence of orofacial genetic fields.
Peck S; Peck L; Kataja M
Am J Orthod Dentofacial Orthop; 2002 Dec; 122(6):657-60. PubMed ID: 12490878
[TBL] [Abstract][Full Text] [Related]
15. Genes underlying familial hypodontia: a review and discussion of the role of dental hygienists in future research.
Nino-Rosales ML; Patel PI
J Dent Hyg; 2005; 79(3):10. PubMed ID: 16197775
[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 EDA mutation resulting in X-linked non-syndromic hypodontia and the pattern of EDA-associated isolated tooth agenesis.
Han D; Gong Y; Wu H; Zhang X; Yan M; Wang X; Qu H; Feng H; Song S
Eur J Med Genet; 2008; 51(6):536-46. PubMed ID: 18657636
[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. Molecular basis of non-syndromic tooth agenesis: mutations of MSX1 and PAX9 reflect their role in patterning human dentition.
Mostowska A; Kobielak A; Trzeciak WH
Eur J Oral Sci; 2003 Oct; 111(5):365-70. PubMed ID: 12974677
[TBL] [Abstract][Full Text] [Related]
20. Exclusion of PAX9 and MSX1 mutation in six families affected by tooth agenesis. A genetic study and literature review.
Tallón-Walton V; Manzanares-Céspedes MC; Carvalho-Lobato P; Valdivia-Gandur I; Arte S; Nieminen P
Med Oral Patol Oral Cir Bucal; 2014 May; 19(3):e248-54. PubMed ID: 24316698
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]