Format
Sort by
Items per page

Send to

Choose Destination

Links from PubMed

Items: 1 to 20 of 196

1.

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.

2.

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
3.

Involvement of and interaction between WNT10A and EDA mutations in tooth agenesis cases in the Chinese population.

He H, Han D, Feng H, Qu H, Song S, Bai B, Zhang Z.

PLoS One. 2013 Nov 27;8(11):e80393. doi: 10.1371/journal.pone.0080393. eCollection 2013.

4.

WNT10A mutations account for ¼ of population-based isolated oligodontia and show phenotypic correlations.

Arzoo PS, Klar J, Bergendal B, Norderyd J, Dahl N.

Am J Med Genet A. 2014 Feb;164A(2):353-9. doi: 10.1002/ajmg.a.36243. Epub 2013 Nov 25.

PMID:
24449199
5.

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
6.

WNT10A variants are associated with non-syndromic tooth agenesis in the general population.

Song S, Zhao R, He H, Zhang J, Feng H, Lin L.

Hum Genet. 2014 Jan;133(1):117-24. doi: 10.1007/s00439-013-1360-x. Epub 2013 Sep 17.

PMID:
24043634
7.

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. doi: 10.3892/ijmm.2016.2742. Epub 2016 Sep 19.

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. doi: 10.1016/j.archoralbio.2016.03.015. Epub 2016 Mar 30.

PMID:
27054699
9.

Nucleotide variants of genes encoding components of the Wnt signalling pathway and the risk of non-syndromic tooth agenesis.

Mostowska A, Biedziak B, Zadurska M, Dunin-Wilczynska I, Lianeri M, Jagodzinski PP.

Clin Genet. 2013 Nov;84(5):429-40. doi: 10.1111/cge.12061. Epub 2012 Dec 7.

PMID:
23167694
10.

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 Nov-Dec;51(6):536-46. doi: 10.1016/j.ejmg.2008.06.002. Epub 2008 Jul 9.

PMID:
18657636
11.

Mutations in WNT10A are frequently involved in oligodontia associated with minor signs of ectodermal dysplasia.

Plaisancié J, Bailleul-Forestier I, Gaston V, Vaysse F, Lacombe D, Holder-Espinasse M, Abramowicz M, Coubes C, Plessis G, Faivre L, Demeer B, Vincent-Delorme C, Dollfus H, Sigaudy S, Guillén-Navarro E, Verloes A, Jonveaux P, Martin-Coignard D, Colin E, Bieth E, Calvas P, Chassaing N.

Am J Med Genet A. 2013 Apr;161A(4):671-8. doi: 10.1002/ajmg.a.35747. Epub 2013 Feb 7.

PMID:
23401279
12.

Only four genes (EDA1, EDAR, EDARADD, and WNT10A) account for 90% of hypohidrotic/anhidrotic ectodermal dysplasia cases.

Cluzeau C, Hadj-Rabia S, Jambou M, Mansour S, Guigue P, Masmoudi S, Bal E, Chassaing N, Vincent MC, Viot G, Clauss F, Manière MC, Toupenay S, Le Merrer M, Lyonnet S, Cormier-Daire V, Amiel J, Faivre L, de Prost Y, Munnich A, Bonnefont JP, Bodemer C, Smahi A.

Hum Mutat. 2011 Jan;32(1):70-2. doi: 10.1002/humu.21384.

PMID:
20979233
13.

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. doi: 10.1016/j.ejmg.2016.06.004. Epub 2016 Jun 27.

PMID:
27365112
14.

Oligodontia and curly hair occur with ectodysplasin-a mutations.

Lee KE, Ko J, Shin TJ, Hyun HK, Lee SH, Kim JW.

J Dent Res. 2014 Apr;93(4):371-5. doi: 10.1177/0022034514522059. Epub 2014 Jan 31.

PMID:
24487376
15.

A novel WNT10A mutation causes non-syndromic hypodontia in an Egyptian family.

Abdalla EM, Mostowska A, Jagodziński PP, Dwidar K, Ismail SR.

Arch Oral Biol. 2014 Jul;59(7):722-8. doi: 10.1016/j.archoralbio.2014.04.004. Epub 2014 Apr 19.

PMID:
24798981
16.

Non-syndromic tooth agenesis associated with a nonsense mutation in ectodysplasin-A (EDA).

Nikopensius T, Annilo T, Jagomägi T, Gilissen C, Kals M, Krjutškov K, Mägi R, Eelmets M, Gerst-Talas U, Remm M, Saag M, Hoischen A, Metspalu A.

J Dent Res. 2013 Jun;92(6):507-11. doi: 10.1177/0022034513487210. Epub 2013 Apr 19.

PMID:
23603338
17.

Genetic basis of tooth agenesis.

Nieminen P.

J Exp Zool B Mol Dev Evol. 2009 Jun 15;312B(4):320-42. doi: 10.1002/jez.b.21277.

PMID:
19219933
18.

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
19.

Identification of genetic risk factors for maxillary lateral incisor agenesis.

Alves-Ferreira M, Pinho T, Sousa A, Sequeiros J, Lemos C, Alonso I.

J Dent Res. 2014 May;93(5):452-8. doi: 10.1177/0022034514523986. Epub 2014 Feb 19.

PMID:
24554542
20.

Supplemental Content

Support Center