210 related articles for article (PubMed ID: 33014315)
21. A review on non-syndromic tooth agenesis associated with
Fauzi NH; Ardini YD; Zainuddin Z; Lestari W
Jpn Dent Sci Rev; 2018 Feb; 54(1):30-36. PubMed ID: 29628999
[TBL] [Abstract][Full Text] [Related]
22. Genes affecting tooth morphogenesis.
Kapadia H; Mues G; D'Souza R
Orthod Craniofac Res; 2007 Aug; 10(3):105-13. PubMed ID: 17651126
[TBL] [Abstract][Full Text] [Related]
23. WNT10A variants in relation to nonsyndromic hypodontia in eastern Slovak population.
Grejtakova D; Gabrikova-Dojcakova D; Boronova I; Kyjovska L; Hubcejova J; Fecenkova M; Zigova M; Priganc M; Bernasovska J
J Genet; 2018 Dec; 97(5):1169-1177. PubMed ID: 30555066
[TBL] [Abstract][Full Text] [Related]
24. Novel EDA or EDAR Mutations Identified in Patients with X-Linked Hypohidrotic Ectodermal Dysplasia or Non-Syndromic Tooth Agenesis.
Zeng B; Zhao Q; Li S; Lu H; Lu J; Ma L; Zhao W; Yu D
Genes (Basel); 2017 Oct; 8(10):. PubMed ID: 28981473
[No Abstract] [Full Text] [Related]
25. Genes affecting tooth morphogenesis.
Kapadia H; Mues G; D'Souza R
Orthod Craniofac Res; 2007 Nov; 10(4):237-44. PubMed ID: 17973693
[TBL] [Abstract][Full Text] [Related]
26. 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. PubMed ID: 24043634
[TBL] [Abstract][Full Text] [Related]
27. Four Novel
Liu H; Liu H; Su L; Zheng J; Feng H; Liu Y; Yu M; Han D
Int J Mol Sci; 2022 Jul; 23(15):. PubMed ID: 35897718
[TBL] [Abstract][Full Text] [Related]
28. 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]
29. Exclusion of PAX9 and MSX1 mutation in six families affected by tooth agenesis. A genetic study and literature review.
Tallón-Walton V; Manzanares-Céspedes MC; Carvalho-Lobato P; Valdivia-Gandur I; Arte S; Nieminen P
Med Oral Patol Oral Cir Bucal; 2014 May; 19(3):e248-54. PubMed ID: 24316698
[TBL] [Abstract][Full Text] [Related]
30. Pathogenic mechanisms of tooth agenesis linked to paired domain mutations in human PAX9.
Wang Y; Groppe JC; Wu J; Ogawa T; Mues G; D'Souza RN; Kapadia H
Hum Mol Genet; 2009 Aug; 18(15):2863-74. PubMed ID: 19429910
[TBL] [Abstract][Full Text] [Related]
31. Novel PAX9 and COL1A2 missense mutations causing tooth agenesis and OI/DGI without skeletal abnormalities.
Wang SK; Chan HC; Makovey I; Simmer JP; Hu JC
PLoS One; 2012; 7(12):e51533. PubMed ID: 23227268
[TBL] [Abstract][Full Text] [Related]
32. Study of rs12532, rs8670 Polymorphism of Msh Homeobox 1 (MSX1), rs61754301, rs4904155 Polymorphism of Paired Box Gene 9 (PAX9), and rs2240308 Polymorphism of Axis Inhibitor Protein 2 (AXIN2) Genes in Nonsyndromic Hypodontia.
Mártha K; Kerekes Máthé B; Moldovan VG; Bănescu C
Biomed Res Int; 2019; 2019():2183720. PubMed ID: 31781599
[TBL] [Abstract][Full Text] [Related]
33. Functional analysis of a novel missense mutation in AXIN2 associated with non-syndromic tooth agenesis.
Yue H; Liang J; Yang K; Hua B; Bian Z
Eur J Oral Sci; 2016 Jun; 124(3):228-33. PubMed ID: 27090353
[TBL] [Abstract][Full Text] [Related]
34. 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]
35. Molecular basis of non-syndromic tooth agenesis: mutations of MSX1 and PAX9 reflect their role in patterning human dentition.
Mostowska A; Kobielak A; Trzeciak WH
Eur J Oral Sci; 2003 Oct; 111(5):365-70. PubMed ID: 12974677
[TBL] [Abstract][Full Text] [Related]
36. The phenotype and genotype of PAX9 mutations causing tooth agenesis.
Jiang C; Yu K; Shen Y; Wang F; Dai Q; Wu Y
Clin Oral Investig; 2023 Aug; 27(8):4369-4378. PubMed ID: 37184613
[TBL] [Abstract][Full Text] [Related]
37. Msx1 mutations: how do they cause tooth agenesis?
Wang Y; Kong H; Mues G; D'Souza R
J Dent Res; 2011 Mar; 90(3):311-6. PubMed ID: 21297014
[TBL] [Abstract][Full Text] [Related]
38. Novel PAX9 mutation associated with syndromic tooth agenesis.
Mostowska A; Zadurska M; Rakowska A; Lianeri M; Jagodziński PP
Eur J Oral Sci; 2013 Oct; 121(5):403-11. PubMed ID: 24028587
[TBL] [Abstract][Full Text] [Related]
39. Novel WNT10A variant in a Japanese case of nonsyndromic oligodontia.
Adachi J; Aoki Y; Izumi H; Nishiyama T; Nakayama A; Sana M; Morimoto K; Kaetsu A; Shirozu T; Osumi E; Matsuoka M; Hayakawa E; Maeda N; Machida J; Nagao T; Tokita Y
Hum Genome Var; 2023 Jan; 10(1):3. PubMed ID: 36702846
[TBL] [Abstract][Full Text] [Related]
40. WNT10A and RUNX2 mutations associated with non-syndromic tooth agenesis.
Živković M; Stefanović N; Glišić B; Brajović G; Miličić B; Kostić M; Popović B
Eur J Oral Sci; 2022 Dec; 130(6):e12896. PubMed ID: 36250548
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
