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Results: 1 to 20 of 159

1.

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. doi: 10.1002/ajmg.a.34045. Epub 2011 May 27.

PMID:
21626677
[PubMed - indexed for MEDLINE]
2.

Oligodontia ectodermal dysplasia--on signs, symptoms, genetics, and outcomes of dental treatment.

Bergendal B.

Swed Dent J Suppl. 2010;(205):13-78, 7-8.

PMID:
20626136
[PubMed - indexed for MEDLINE]
3.

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.

PMID:
16918677
[PubMed - indexed for MEDLINE]
4.

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. doi: 10.1016/j.archoralbio.2011.03.023. Epub 2011 Apr 29.

PMID:
21530942
[PubMed - indexed for MEDLINE]
5.

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. doi: 10.1136/jmedgenet-2012-100750.

PMID:
22581971
[PubMed - indexed for MEDLINE]
6.

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. doi: 10.1016/j.archoralbio.2013.04.007. Epub 2013 May 31.

PMID:
23731659
[PubMed - indexed for MEDLINE]
7.

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 10;12(4):4446-58. doi: 10.4238/2013.October.10.10.

PMID:
24222224
[PubMed - indexed for MEDLINE]
Free PMC Article
8.

Candidate gene analysis of tooth agenesis identifies novel mutations in six genes and suggests significant role for WNT and EDA signaling and allele combinations.

Arte S, Parmanen S, Pirinen S, Alaluusua S, Nieminen P.

PLoS One. 2013 Aug 22;8(8):e73705. doi: 10.1371/journal.pone.0073705. eCollection 2013.

PMID:
23991204
[PubMed - indexed for MEDLINE]
Free PMC Article
9.

Genetic background of nonsyndromic oligodontia: a systematic review and meta-analysis.

Ruf S, Klimas D, Hönemann M, Jabir S.

J Orofac Orthop. 2013 Jul;74(4):295-308. doi: 10.1007/s00056-013-0138-z. Epub 2013 Jul 5. Review.

PMID:
23828301
[PubMed - indexed for MEDLINE]
10.

Identification of a novel missense mutation of MSX1 gene in Chinese family with autosomal-dominant oligodontia.

Xuan K, Jin F, Liu YL, Yuan LT, Wen LY, Yang FS, Wang XJ, Wang GH, Jin Y.

Arch Oral Biol. 2008 Aug;53(8):773-9. doi: 10.1016/j.archoralbio.2008.02.012. Epub 2008 Mar 28.

PMID:
18374898
[PubMed - indexed for MEDLINE]
11.

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. doi: 10.1111/j.1601-6343.2008.00410.x.

PMID:
18199077
[PubMed - indexed for MEDLINE]
12.

Novel missense mutations in the AXIN2 gene associated with non-syndromic oligodontia.

Wong S, Liu H, Bai B, Chang H, Zhao H, Wang Y, Han D, Feng H.

Arch Oral Biol. 2014 Mar;59(3):349-53. doi: 10.1016/j.archoralbio.2013.12.009. Epub 2013 Dec 31.

PMID:
24581859
[PubMed - in process]
13.

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.

PMID:
17697174
[PubMed - indexed for MEDLINE]
14.

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. doi: 10.1177/0022034510390042. Epub 2010 Nov 22.

PMID:
21098475
[PubMed - indexed for MEDLINE]
15.

Novel mutation of the initiation codon of PAX9 causes oligodontia.

Klein ML, Nieminen P, Lammi L, Niebuhr E, Kreiborg S.

J Dent Res. 2005 Jan;84(1):43-7.

PMID:
15615874
[PubMed - indexed for MEDLINE]
16.

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. doi: 10.1590/1679-775720130079.

PMID:
23857653
[PubMed - indexed for MEDLINE]
Free PMC Article
17.

A novel missense mutation in the paired domain of human PAX9 causes oligodontia.

Zhao J, Hu Q, Chen Y, Luo S, Bao L, Xu Y.

Am J Med Genet A. 2007 Nov 1;143A(21):2592-7.

PMID:
17910065
[PubMed - indexed for MEDLINE]
18.

Familial human hypodontia--is it all in the genes?

Cobourne MT.

Br Dent J. 2007 Aug 25;203(4):203-8. Review.

PMID:
17721480
[PubMed - indexed for MEDLINE]
19.

A Mongolian patient with hypohidrotic ectodermal dysplasia with a novel P121S variant in EDARADD.

Suda N, Bazar A, Bold O, Jigjid B, Garidkhuu A, Ganburged G, Moriyama K.

Orthod Craniofac Res. 2010 May;13(2):114-7. doi: 10.1111/j.1601-6343.2010.01484.x.

PMID:
20477971
[PubMed - indexed for MEDLINE]
20.

A novel c.581C>T transition localized in a highly conserved homeobox sequence of MSX1: is it responsible for oligodontia?

Mostowska A, Biedziak B, Trzeciak WH.

J Appl Genet. 2006;47(2):159-64.

PMID:
16682758
[PubMed - indexed for MEDLINE]

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