125 related articles for article (PubMed ID: 38761453)
1. A novel mutation in GPR68 causes hypomaturation amelogenesis imperfecta.
Yu S; Liu D; Yan C; Yuan C; Zhang C; Zheng S
Arch Oral Biol; 2024 Aug; 164():105991. PubMed ID: 38761453
[TBL] [Abstract][Full Text] [Related]
2. Mutations in the pH-Sensing G-protein-Coupled Receptor GPR68 Cause Amelogenesis Imperfecta.
Parry DA; Smith CE; El-Sayed W; Poulter JA; Shore RC; Logan CV; Mogi C; Sato K; Okajima F; Harada A; Zhang H; Koruyucu M; Seymen F; Hu JC; Simmer JP; Ahmed M; Jafri H; Johnson CA; Inglehearn CF; Mighell AJ
Am J Hum Genet; 2016 Oct; 99(4):984-990. PubMed ID: 27693231
[TBL] [Abstract][Full Text] [Related]
3. A novel ENAM mutation causes hypoplastic amelogenesis imperfecta.
Yu S; Zhang C; Zhu C; Quan J; Liu D; Wang X; Zheng S
Oral Dis; 2022 Sep; 28(6):1610-1619. PubMed ID: 33864320
[TBL] [Abstract][Full Text] [Related]
4. Novel Mutations in
Seymen F; Zhang H; Kasimoglu Y; Koruyucu M; Simmer JP; Hu JC; Kim JW
J Pers Med; 2021 Dec; 12(1):. PubMed ID: 35055328
[TBL] [Abstract][Full Text] [Related]
5. Hypomaturation amelogenesis imperfecta due to WDR72 mutations: a novel mutation and ultrastructural analyses of deciduous teeth.
El-Sayed W; Shore RC; Parry DA; Inglehearn CF; Mighell AJ
Cells Tissues Organs; 2011; 194(1):60-6. PubMed ID: 21196691
[TBL] [Abstract][Full Text] [Related]
6. Enamel ultrastructure in pigmented hypomaturation amelogenesis imperfecta.
Wright JT; Lord V; Robinson C; Shore R
J Oral Pathol Med; 1992 Oct; 21(9):390-4. PubMed ID: 1432732
[TBL] [Abstract][Full Text] [Related]
7. Expanding the phenotype of hypomaturation amelogenesis imperfecta due to a novel SLC24A4 variant.
Lepperdinger U; Maurer E; Witsch-Baumgartner M; Stigler R; Zschocke J; Lussi A; Kapferer-Seebacher I
Clin Oral Investig; 2020 Oct; 24(10):3519-3525. PubMed ID: 32034543
[TBL] [Abstract][Full Text] [Related]
8.
Wang YL; Lin HC; Liang T; Lin JC; Simmer JP; Hu JC; Wang SK
J Dent Res; 2024 Jun; 103(6):662-671. PubMed ID: 38716742
[TBL] [Abstract][Full Text] [Related]
9. Inheritance pattern and elemental composition of enamel affected by hypomaturation amelogenesis imperfecta.
Shore RC; Bäckman B; Brookes SJ; Kirkham J; Wood SR; Robinson C
Connect Tissue Res; 2002; 43(2-3):466-71. PubMed ID: 12489199
[TBL] [Abstract][Full Text] [Related]
10. Whole exome sequencing identifies an AMBN missense mutation causing severe autosomal-dominant amelogenesis imperfecta and dentin disorders.
Lu T; Li M; Xu X; Xiong J; Huang C; Zhang X; Hu A; Peng L; Cai D; Zhang L; Wu B; Xiong F
Int J Oral Sci; 2018 Sep; 10(3):26. PubMed ID: 30174330
[TBL] [Abstract][Full Text] [Related]
11. Ultrastructural analyses of deciduous teeth affected by hypocalcified amelogenesis imperfecta from a family with a novel Y458X FAM83H nonsense mutation.
El-Sayed W; Shore RC; Parry DA; Inglehearn CF; Mighell AJ
Cells Tissues Organs; 2010; 191(3):235-9. PubMed ID: 20160442
[TBL] [Abstract][Full Text] [Related]
12. Alteration of Exon Definition Causes Amelogenesis Imperfecta.
Kim YJ; Kang J; Seymen F; Koruyucu M; Zhang H; Kasimoglu Y; Bayram M; Tuna-Ince EB; Bayrak S; Tuloglu N; Hu JC; Simmer JP; Kim JW
J Dent Res; 2020 Apr; 99(4):410-418. PubMed ID: 31999931
[TBL] [Abstract][Full Text] [Related]
13. A novel nonsense variant in SLC24A4 causing a rare form of amelogenesis imperfecta in a Pakistani family.
Khan SA; Khan MA; Muhammad N; Bashir H; Khan N; Muhammad N; Yilmaz R; Khan S; Wasif N
BMC Med Genet; 2020 May; 21(1):97. PubMed ID: 32380970
[TBL] [Abstract][Full Text] [Related]
14. Novel
Lee Y; Zhang H; Seymen F; Kim YJ; Kasimoglu Y; Koruyucu M; Simmer JP; Hu JC; Kim JW
J Pers Med; 2022 Jan; 12(2):. PubMed ID: 35207639
[TBL] [Abstract][Full Text] [Related]
15. Mutations in the beta propeller WDR72 cause autosomal-recessive hypomaturation amelogenesis imperfecta.
El-Sayed W; Parry DA; Shore RC; Ahmed M; Jafri H; Rashid Y; Al-Bahlani S; Al Harasi S; Kirkham J; Inglehearn CF; Mighell AJ
Am J Hum Genet; 2009 Nov; 85(5):699-705. PubMed ID: 19853237
[TBL] [Abstract][Full Text] [Related]
16.
Wang SK; Zhang H; Lin HC; Wang YL; Lin SC; Seymen F; Koruyucu M; Simmer JP; Hu JC
Int J Mol Sci; 2024 Jun; 25(11):. PubMed ID: 38892321
[No Abstract] [Full Text] [Related]
17. The mineral composition and enamel ultrastructure of hypocalcified amelogenesis imperfecta.
Wright JT; Duggal MS; Robinson C; Kirkham J; Shore R
J Craniofac Genet Dev Biol; 1993; 13(2):117-26. PubMed ID: 8325967
[TBL] [Abstract][Full Text] [Related]
18. Homozygous and compound heterozygous MMP20 mutations in amelogenesis imperfecta.
Gasse B; Karayigit E; Mathieu E; Jung S; Garret A; Huckert M; Morkmued S; Schneider C; Vidal L; Hemmerlé J; Sire JY; Bloch-Zupan A
J Dent Res; 2013 Jul; 92(7):598-603. PubMed ID: 23625376
[TBL] [Abstract][Full Text] [Related]
19. Hypomaturation amelogenesis imperfecta caused by a novel SLC24A4 mutation.
Herzog CR; Reid BM; Seymen F; Koruyucu M; Tuna EB; Simmer JP; Hu JC
Oral Surg Oral Med Oral Pathol Oral Radiol; 2015 Feb; 119(2):e77-81. PubMed ID: 25442250
[TBL] [Abstract][Full Text] [Related]
20. Ultrastructural analysis of the teeth affected by amelogenesis imperfecta resulting from FAM83H mutations and review of the literature.
Zhang C; Song Y; Bian Z
Oral Surg Oral Med Oral Pathol Oral Radiol; 2015 Feb; 119(2):e69-76. PubMed ID: 25487982
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]