228 related articles for article (PubMed ID: 26030286)
1. An aberrant splice acceptor site due to a novel intronic nucleotide substitution in MSX1 gene is the cause of congenital tooth agenesis in a Japanese family.
Tatematsu T; Kimura M; Nakashima M; Machida J; Yamaguchi S; Shibata A; Goto H; Nakayama A; Higashi Y; Miyachi H; Shimozato K; Matsumoto N; Tokita Y
PLoS One; 2015; 10(6):e0128227. PubMed ID: 26030286
[TBL] [Abstract][Full Text] [Related]
2. Characterization of novel MSX1 mutations identified in Japanese patients with nonsyndromic tooth agenesis.
Yamaguchi S; Machida J; Kamamoto M; Kimura M; Shibata A; Tatematsu T; Miyachi H; Higashi Y; Jezewski P; Nakayama A; Shimozato K; Tokita Y
PLoS One; 2014; 9(8):e102944. PubMed ID: 25101640
[TBL] [Abstract][Full Text] [Related]
3. Novel nonsense mutation in MSX1 in familial nonsyndromic oligodontia: subcellular localization and role of homeodomain/MH4.
Kimura M; Machida J; Yamaguchi S; Shibata A; Tatematsu T; Miyachi H; Jezewski PA; Nakayama A; Higashi Y; Shimozato K; Tokita Y
Eur J Oral Sci; 2014 Feb; 122(1):15-20. PubMed ID: 24329876
[TBL] [Abstract][Full Text] [Related]
4. A novel MSX1 intronic mutation associated with autosomal dominant non-syndromic oligodontia in a large Chinese family pedigree.
Xue J; Gao Q; Huang Y; Zhang X; Yang P; Cram DS; Liang D; Wu L
Clin Chim Acta; 2016 Oct; 461():135-40. PubMed ID: 27485761
[TBL] [Abstract][Full Text] [Related]
5. Novel nonsense mutation in MSX1 causes tooth agenesis with cleft lip in a Chinese family.
Liang J; Zhu L; Meng L; Chen D; Bian Z
Eur J Oral Sci; 2012 Aug; 120(4):278-82. PubMed ID: 22813217
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. 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]
8. 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]
9. A screen of a large Czech cohort of oligodontia patients implicates a novel mutation in the PAX9 gene.
Šerý O; Bonczek O; Hloušková A; Černochová P; Vaněk J; Míšek I; Krejčí P; Izakovičová Hollá L
Eur J Oral Sci; 2015 Apr; 123(2):65-71. PubMed ID: 25683653
[TBL] [Abstract][Full Text] [Related]
10. Next generation sequencing reveals a novel nonsense mutation in MSX1 gene related to oligodontia.
Bonczek O; Bielik P; Krejčí P; Zeman T; Izakovičová-Hollá L; Šoukalová J; Vaněk J; Gerguri T; Balcar VJ; Šerý O
PLoS One; 2018; 13(9):e0202989. PubMed ID: 30192788
[TBL] [Abstract][Full Text] [Related]
11. 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. PubMed ID: 16682758
[TBL] [Abstract][Full Text] [Related]
12. Two novel mutations in MSX1 causing oligodontia.
Yang L; Liang J; Yue H; Bian Z
PLoS One; 2020; 15(1):e0227287. PubMed ID: 31914153
[TBL] [Abstract][Full Text] [Related]
13. Mutations in the human homeobox MSX1 gene in the congenital lack of permanent teeth.
Pawlowska E; Janik-Papis K; Wisniewska-Jarosinska M; Szczepanska J; Blasiak J
Tohoku J Exp Med; 2009 Apr; 217(4):307-12. PubMed ID: 19346736
[TBL] [Abstract][Full Text] [Related]
14. 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; 12(4):4446-58. PubMed ID: 24222224
[TBL] [Abstract][Full Text] [Related]
15. 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]
16. 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]
17. 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]
18. A novel mutation of MSX1 in oligodontia inhibits odontogenesis of dental pulp stem cells via the ERK pathway.
Xin T; Zhang T; Li Q; Yu T; Zhu Y; Yang R; Zhou Y
Stem Cell Res Ther; 2018 Aug; 9(1):221. PubMed ID: 30134957
[TBL] [Abstract][Full Text] [Related]
19. Associations between the risk of tooth agenesis and single-nucleotide polymorphisms of MSX1 and PAX9 genes in nonsyndromic cleft patients.
Seo YJ; Park JW; Kim YH; Baek SH
Angle Orthod; 2013 Nov; 83(6):1036-42. PubMed ID: 23718693
[TBL] [Abstract][Full Text] [Related]
20. The role of MSX1 in human tooth agenesis.
Lidral AC; Reising BC
J Dent Res; 2002 Apr; 81(4):274-8. PubMed ID: 12097313
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
