151 related articles for article (PubMed ID: 36374296)
1. An in vitro and computational validation of a novel loss-of-functional mutation in PAX9 associated with non-syndromic tooth agenesis.
Sarkar T; Ranjan P; Kanathur S; Gupta A; Das P
Mol Genet Genomics; 2023 Jan; 298(1):183-199. PubMed ID: 36374296
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. 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]
4. Characterization of PAX9 variant P20L identified in a Japanese family with tooth agenesis.
Murakami A; Yasuhira S; Mayama H; Miura H; Maesawa C; Satoh K
PLoS One; 2017; 12(10):e0186260. PubMed ID: 29023497
[TBL] [Abstract][Full Text] [Related]
5. Characterization of a novel mutation in PAX9 gene in a family with non-syndromic dental agenesis.
Haddaji Mastouri M; De Coster P; Zaghabani A; Trabelsi S; May Y; Saad A; Coucke P; H'mida Ben Brahim D
Arch Oral Biol; 2016 Nov; 71():110-116. PubMed ID: 27491081
[TBL] [Abstract][Full Text] [Related]
6. Novel PAX9 mutations cause non-syndromic tooth agenesis.
Mitsui SN; Yasue A; Masuda K; Watanabe K; Horiuchi S; Imoto I; Tanaka E
J Dent Res; 2014 Mar; 93(3):245-9. PubMed ID: 24436340
[TBL] [Abstract][Full Text] [Related]
7. Genetic study of non-syndromic tooth agenesis through the screening of paired box 9, msh homeobox 1, axin 2, and Wnt family member 10A genes: a case-series.
Haddaji Mastouri M; De Coster P; Zaghabani A; Jammali F; Raouahi N; Ben Salem A; Saad A; Coucke P; H'mida Ben Brahim D
Eur J Oral Sci; 2018 Feb; 126(1):24-32. PubMed ID: 29114927
[TBL] [Abstract][Full Text] [Related]
8. Functional analysis of a mutation in PAX9 associated with familial tooth agenesis in humans.
Mensah JK; Ogawa T; Kapadia H; Cavender AC; D'Souza RN
J Biol Chem; 2004 Feb; 279(7):5924-33. PubMed ID: 14607846
[TBL] [Abstract][Full Text] [Related]
9. 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]
10. Novel PAX9 gene polymorphisms and mutations and susceptibility to tooth agenesis in the Czech population.
Hlousková A; Bonczek O; Izakovicová-Hollá L; Lochman J; Soukalová J; Stembírek J; Mísek I; Cernochová P; Krejcí P; Vanek J; Šerý O
Neuro Endocrinol Lett; 2015; 36(5):452-7. PubMed ID: 26707046
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. 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]
13. 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]
14. 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. PubMed ID: 23857653
[TBL] [Abstract][Full Text] [Related]
15. 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]
16. 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]
17. Screening
Safari S; Ebadifar A; Najmabadi H; Kamali K; Abedini SS
Avicenna J Med Biotechnol; 2020; 12(4):236-240. PubMed ID: 33014315
[TBL] [Abstract][Full Text] [Related]
18. 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]
19. PAX9 and MSX1 transcription factor genes in non-syndromic dental agenesis.
Paixão-Côrtes VR; Braga T; Salzano FM; Mundstock K; Mundstock CA; Bortolini MC
Arch Oral Biol; 2011 Apr; 56(4):337-44. PubMed ID: 21111400
[TBL] [Abstract][Full Text] [Related]
20. 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]
[Next] [New Search]
