237 related articles for article (PubMed ID: 15615874)
1. 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. PubMed ID: 15615874
[TBL] [Abstract][Full Text] [Related]
2. A novel initiation codon mutation of PAX9 in a family with oligodontia.
Liang J; Qin C; Yue H; He H; Bian Z
Arch Oral Biol; 2016 Jan; 61():144-8. PubMed ID: 26571067
[TBL] [Abstract][Full Text] [Related]
3. Clinical, radiographic, and genetic evaluation of a novel form of autosomal-dominant oligodontia.
Goldenberg M; Das P; Messersmith M; Stockton DW; Patel PI; D'Souza RN
J Dent Res; 2000 Jul; 79(7):1469-75. PubMed ID: 11005730
[TBL] [Abstract][Full Text] [Related]
4. 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]
5. Novel mutation in the paired box sequence of PAX9 gene in a sporadic form of oligodontia.
Mostowska A; Kobielak A; Biedziak B; Trzeciak WH
Eur J Oral Sci; 2003 Jun; 111(3):272-6. PubMed ID: 12786960
[TBL] [Abstract][Full Text] [Related]
6. A novel missense mutation in the paired domain of PAX9 causes non-syndromic oligodontia.
Jumlongras D; Lin JY; Chapra A; Seidman CE; Seidman JG; Maas RL; Olsen BR
Hum Genet; 2004 Feb; 114(3):242-9. PubMed ID: 14689302
[TBL] [Abstract][Full Text] [Related]
7. Familial oligodontia and regional odontodysplasia associated with a PAX9 initiation codon mutation.
Koskinen S; Keski-Filppula R; Alapulli H; Nieminen P; Anttonen V
Clin Oral Investig; 2019 Nov; 23(11):4107-4111. PubMed ID: 30809714
[TBL] [Abstract][Full Text] [Related]
8. A novel mutation in human PAX9 causes molar oligodontia.
Frazier-Bowers SA; Guo DC; Cavender A; Xue L; Evans B; King T; Milewicz D; D'Souza RN
J Dent Res; 2002 Feb; 81(2):129-33. PubMed ID: 11827258
[TBL] [Abstract][Full Text] [Related]
9. Identification of a nonsense mutation in the PAX9 gene in molar oligodontia.
Nieminen P; Arte S; Tanner D; Paulin L; Alaluusua S; Thesleff I; Pirinen S
Eur J Hum Genet; 2001 Oct; 9(10):743-6. PubMed ID: 11781684
[TBL] [Abstract][Full Text] [Related]
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. PubMed ID: 18374898
[TBL] [Abstract][Full Text] [Related]
11. 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; 143A(21):2592-7. PubMed ID: 17910065
[TBL] [Abstract][Full Text] [Related]
12. 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]
13. Novel MSX1 frameshift causes autosomal-dominant oligodontia.
Kim JW; Simmer JP; Lin BP; Hu JC
J Dent Res; 2006 Mar; 85(3):267-71. PubMed ID: 16498076
[TBL] [Abstract][Full Text] [Related]
14. 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. PubMed ID: 23731659
[TBL] [Abstract][Full Text] [Related]
15. 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]
16. 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]
17. 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. PubMed ID: 21530942
[TBL] [Abstract][Full Text] [Related]
18. [Research advances in tooth agenesis].
Feng HL; Zhang XX; Wu H
Beijing Da Xue Xue Bao Yi Xue Ban; 2007 Feb; 39(1):13-7. PubMed ID: 17304318
[TBL] [Abstract][Full Text] [Related]
19. Nine Novel PAX9 Mutations and a Distinct Tooth Agenesis Genotype-Phenotype.
Wong SW; Han D; Zhang H; Liu Y; Zhang X; Miao MZ; Wang Y; Zhao N; Zeng L; Bai B; Wang YX; Liu H; Frazier-Bowers SA; Feng H
J Dent Res; 2018 Feb; 97(2):155-162. PubMed ID: 28910570
[TBL] [Abstract][Full Text] [Related]
20. 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]
[Next] [New Search]
