149 related articles for article (PubMed ID: 28683132)
1. Evolutionary analysis of FAM83H in vertebrates.
Huang W; Yang M; Wang C; Song Y
PLoS One; 2017; 12(7):e0180360. PubMed ID: 28683132
[TBL] [Abstract][Full Text] [Related]
2. Evolutionary analysis of selective constraints identifies ameloblastin (AMBN) as a potential candidate for amelogenesis imperfecta.
Delsuc F; Gasse B; Sire JY
BMC Evol Biol; 2015 Jul; 15():148. PubMed ID: 26223266
[TBL] [Abstract][Full Text] [Related]
3. Identification of a novel FAM83H mutation and microhardness of an affected molar in autosomal dominant hypocalcified amelogenesis imperfecta.
Hyun HK; Lee SK; Lee KE; Kang HY; Kim EJ; Choung PH; Kim JW
Int Endod J; 2009 Nov; 42(11):1039-43. PubMed ID: 19825039
[TBL] [Abstract][Full Text] [Related]
4. Limited phenotypic variation of hypocalcified amelogenesis imperfecta in a Danish five-generation family with a novel FAM83H nonsense mutation.
Haubek D; Gjørup H; Jensen LG; Juncker I; Nyegaard M; Børglum AD; Poulsen S; Hertz JM
Int J Paediatr Dent; 2011 Nov; 21(6):407-12. PubMed ID: 21702852
[TBL] [Abstract][Full Text] [Related]
5. The Enamel Phenotype in Homozygous Fam83h Truncation Mice.
Wang SK; Hu Y; Smith CE; Yang J; Zeng C; Kim JW; Hu JC; Simmer JP
Mol Genet Genomic Med; 2019 Jun; 7(6):e724. PubMed ID: 31060110
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. Inactivation of C4orf26 in toothless placental mammals.
Springer MS; Starrett J; Morin PA; Lanzetti A; Hayashi C; Gatesy J
Mol Phylogenet Evol; 2016 Feb; 95():34-45. PubMed ID: 26596502
[TBL] [Abstract][Full Text] [Related]
8. FAM83H mutations in families with autosomal-dominant hypocalcified amelogenesis imperfecta.
Kim JW; Lee SK; Lee ZH; Park JC; Lee KE; Lee MH; Park JT; Seo BM; Hu JC; Simmer JP
Am J Hum Genet; 2008 Feb; 82(2):489-94. PubMed ID: 18252228
[TBL] [Abstract][Full Text] [Related]
9. Molecular characterization of amelogenesis imperfecta in Chinese patients.
Song YL; Wang CN; Zhang CZ; Yang K; Bian Z
Cells Tissues Organs; 2012; 196(3):271-9. PubMed ID: 22414746
[TBL] [Abstract][Full Text] [Related]
10. Evolutionary analysis suggests that AMTN is enamel-specific and a candidate for AI.
Gasse B; Silvent J; Sire JY
J Dent Res; 2012 Nov; 91(11):1085-9. PubMed ID: 22968158
[TBL] [Abstract][Full Text] [Related]
11. Effects of Fam83h truncation mutation on enamel developmental defects in male C57/BL6J mice.
Zheng X; Huang W; He Z; Li Y; Li S; Song Y
Bone; 2023 Jan; 166():116595. PubMed ID: 36272714
[TBL] [Abstract][Full Text] [Related]
12. Phenotypic variation in FAM83H-associated amelogenesis imperfecta.
Wright JT; Frazier-Bowers S; Simmons D; Alexander K; Crawford P; Han ST; Hart PS; Hart TC
J Dent Res; 2009 Apr; 88(4):356-60. PubMed ID: 19407157
[TBL] [Abstract][Full Text] [Related]
13. Novel FAM83H mutations in patients with amelogenesis imperfecta.
Xin W; Wenjun W; Man Q; Yuming Z
Sci Rep; 2017 Jul; 7(1):6075. PubMed ID: 28729668
[TBL] [Abstract][Full Text] [Related]
14. 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]
15. Characterisation of the biochemical and cellular roles of native and pathogenic amelogenesis imperfecta mutants of FAM83H.
Tachie-Menson T; Gázquez-Gutiérrez A; Fulcher LJ; Macartney TJ; Wood NT; Varghese J; Gourlay R; Soares RF; Sapkota GP
Cell Signal; 2020 Aug; 72():109632. PubMed ID: 32289446
[TBL] [Abstract][Full Text] [Related]
16. Amelogenesis imperfecta: A novel FAM83H mutation and characteristics of periodontal ligament cells.
Nowwarote N; Theerapanon T; Osathanon T; Pavasant P; Porntaveetus T; Shotelersuk V
Oral Dis; 2018 Nov; 24(8):1522-1531. PubMed ID: 29949226
[TBL] [Abstract][Full Text] [Related]
17. FAM83H mutations cause ADHCAI and alter intracellular protein localization.
Lee SK; Lee KE; Jeong TS; Hwang YH; Kim S; Hu JC; Simmer JP; Kim JW
J Dent Res; 2011 Mar; 90(3):377-81. PubMed ID: 21118793
[TBL] [Abstract][Full Text] [Related]
18.
Wang SK; Zhang H; Hu CY; Liu JF; Chadha S; Kim JW; Simmer JP; Hu JCC
J Dent Res; 2021 Mar; 100(3):293-301. PubMed ID: 33034243
[TBL] [Abstract][Full Text] [Related]
19. [Analysis of amelogenesis imperfecta with abnormal tooth eruption caused by FAM83H mutation].
Mao SY; Duan XH
Zhonghua Kou Qiang Yi Xue Za Zhi; 2023 Sep; 58(9):933-937. PubMed ID: 37659852
[No Abstract] [Full Text] [Related]
20. Defining a new candidate gene for amelogenesis imperfecta: from molecular genetics to biochemistry.
Urzúa B; Ortega-Pinto A; Morales-Bozo I; Rojas-Alcayaga G; Cifuentes V
Biochem Genet; 2011 Feb; 49(1-2):104-21. PubMed ID: 21127961
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
