112 related articles for article (PubMed ID: 18452891)
1. Evidence of linkage disequilibrium between polymorphisms at the IRF6 locus and isolate tooth agenesis, in a Turkish population.
Vieira AR; Seymen F; Patir A; Menezes R
Arch Oral Biol; 2008 Aug; 53(8):780-4. PubMed ID: 18452891
[TBL] [Abstract][Full Text] [Related]
2. Transforming growth factor-alfa gene (TGFA), human tooth agenesis, and evidence of segmental uniparental isodisomy.
Callahan N; Modesto A; Deeley K; Meira R; Vieira AR
Eur J Oral Sci; 2009 Feb; 117(1):20-6. PubMed ID: 19196314
[TBL] [Abstract][Full Text] [Related]
3. Interferon regulatory factor 6 (IRF6) and fibroblast growth factor receptor 1 (FGFR1) contribute to human tooth agenesis.
Vieira AR; Modesto A; Meira R; Barbosa AR; Lidral AC; Murray JC
Am J Med Genet A; 2007 Mar; 143A(6):538-45. PubMed ID: 17318851
[TBL] [Abstract][Full Text] [Related]
4. Familial non-syndromic cleft lip and palate--analysis of the IRF6 gene and clinical phenotypes.
Pegelow M; Peyrard-Janvid M; Zucchelli M; Fransson I; Larson O; Kere J; Larsson C; Karsten A
Eur J Orthod; 2008 Apr; 30(2):169-75. PubMed ID: 18209213
[TBL] [Abstract][Full Text] [Related]
5. Interferon regulatory factor-6: a gene predisposing to isolated cleft lip with or without cleft palate in the Belgian population.
Ghassibé M; Bayet B; Revencu N; Verellen-Dumoulin C; Gillerot Y; Vanwijck R; Vikkula M
Eur J Hum Genet; 2005 Nov; 13(11):1239-42. PubMed ID: 16132054
[TBL] [Abstract][Full Text] [Related]
6. Studies of palatine rugae and interferon regulatory factor 6 variations in a group of families with sporadic hypodontia.
Murdoch AM; Patir A; Seymen F; Vieira AR
J Oral Sci; 2009 Dec; 51(4):521-6. PubMed ID: 20032603
[TBL] [Abstract][Full Text] [Related]
7. Orofacial clefting: update on the role of genetics.
Ghassibe M; Bayet B; Revencu N; Desmyter L; Verellen-Dumoulin C; Gillerot Y; Deggouj N; Vanwijck R; Vikkula M;
B-ENT; 2006; 2 Suppl 4():20-4. PubMed ID: 17366841
[TBL] [Abstract][Full Text] [Related]
8. PAX9 polymorphisms and susceptibility to sporadic tooth agenesis: a case-control study in southeast China.
Pan Y; Wang L; Ma J; Zhang W; Wang M; Zhong W; Huang Y
Eur J Oral Sci; 2008 Apr; 116(2):98-103. PubMed ID: 18353002
[TBL] [Abstract][Full Text] [Related]
9. Van Der Woude syndrome: variable penetrance of a novel mutation (p.Arg 84Gly) of the IRF6 gene in a Turkish family.
Item CB; Turhani D; Thurnher D; Yerit K; Sinko K; Wittwer G; Adeyemo WL; Frei K; Erginel-Unaltuna N; Watzinger F; Ewers R
Int J Mol Med; 2005 Feb; 15(2):247-51. PubMed ID: 15647839
[TBL] [Abstract][Full Text] [Related]
10. [Msh homebox-1 polymorphisms and susceptibility to 198 sporadic tooth agenesis: a case-control study].
Wang H; Wang L; Pan YC; Ma JQ; Zhang WB
Zhonghua Kou Qiang Yi Xue Za Zhi; 2010 Mar; 45(3):135-40. PubMed ID: 20450679
[TBL] [Abstract][Full Text] [Related]
11. IRF6 AP-2a binding site promoter polymorphism is associated with oral clefts in Latvia.
Krasone K; Lāce B; Akota I; Care R; Deeley K; Küchler EC; Vieira AR
Stomatologija; 2014; 16(4):132-6. PubMed ID: 25896037
[TBL] [Abstract][Full Text] [Related]
12. Axis inhibition protein 2 (AXIN2) polymorphisms and tooth agenesis.
Callahan N; Modesto A; Meira R; Seymen F; Patir A; Vieira AR
Arch Oral Biol; 2009 Jan; 54(1):45-9. PubMed ID: 18790474
[TBL] [Abstract][Full Text] [Related]
13. Identification of IRF6 gene variants in three families with Van der Woude syndrome.
Tan EC; Lim EC; Yap SH; Lee ST; Cheng J; Por YC; Yeow V
Int J Mol Med; 2008 Jun; 21(6):747-51. PubMed ID: 18506368
[TBL] [Abstract][Full Text] [Related]
14. Novel and de novo mutations of the IRF6 gene detected in patients with Van der Woude or popliteal pterygium syndrome.
Peyrard-Janvid M; Pegelow M; Koillinen H; Larsson C; Fransson I; Rautio J; Hukki J; Larson O; Karsten AL; Kere J
Eur J Hum Genet; 2005 Dec; 13(12):1261-7. PubMed ID: 16160700
[TBL] [Abstract][Full Text] [Related]
15. Tooth agenesis association with self-reported family history of cancer.
Küchler EC; Lips A; Tannure PN; Ho B; Costa MC; Granjeiro JM; Vieira AR
J Dent Res; 2013 Feb; 92(2):149-55. PubMed ID: 23169889
[TBL] [Abstract][Full Text] [Related]
16. A novel IRF6 nonsense mutation (Y67X) in a German family with Van der Woude syndrome.
Brosch S; Baur M; Blin N; Reinert S; Pfister M
Int J Mol Med; 2007 Jul; 20(1):85-9. PubMed ID: 17549393
[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. Maxillary canine anomalies and tooth agenesis.
Camilleri S
Eur J Orthod; 2005 Oct; 27(5):450-6. PubMed ID: 16093260
[TBL] [Abstract][Full Text] [Related]
19. Genetic Variants of BMP2 and Their Association with the Risk of Non-Syndromic Tooth Agenesis.
Lu Y; Qian Y; Zhang J; Gong M; Wang Y; Gu N; Ma L; Xu M; Ma J; Zhang W; Pan Y; Wang L
PLoS One; 2016; 11(6):e0158273. PubMed ID: 27362534
[TBL] [Abstract][Full Text] [Related]
20. Association of genetic polymorphisms in vitamin D receptor gene and susceptibility to sporadic prostate cancer.
Onen IH; Ekmekci A; Eroglu M; Konac E; Yesil S; Biri H
Exp Biol Med (Maywood); 2008 Dec; 233(12):1608-14. PubMed ID: 18849534
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]