These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
93 related articles for article (PubMed ID: 29745815)
1. Physicochemical analysis of human pulpal mineralization secondary to FAM20A mutations. Berès F; Lignon G; Rouzière S; Mauprivez C; Simon S; Berdal A; Dessombz A Connect Tissue Res; 2018 Dec; 59(sup1):46-51. PubMed ID: 29745815 [No Abstract] [Full Text] [Related]
2. Nephrocalcinosis in Amelogenesis Imperfecta Caused by the FAM20A Mutation. Koruyucu M; Seymen F; Gencay G; Gencay K; Tuna EB; Shin TJ; Hyun HK; Kim YJ; Kim JW Nephron; 2018; 139(2):189-196. PubMed ID: 29439260 [TBL] [Abstract][Full Text] [Related]
3. Enamel-renal-gingival syndrome and FAM20A mutations. Kantaputra PN; Kaewgahya M; Khemaleelakul U; Dejkhamron P; Sutthimethakorn S; Thongboonkerd V; Iamaroon A Am J Med Genet A; 2014 Jan; 164A(1):1-9. PubMed ID: 24259279 [TBL] [Abstract][Full Text] [Related]
4. Four novel mutations of FAM20A in amelogenesis imperfecta type IG and review of literature for its genotype and phenotype spectra. Nitayavardhana I; Theerapanon T; Srichomthong C; Piwluang S; Wichadakul D; Porntaveetus T; Shotelersuk V Mol Genet Genomics; 2020 Jul; 295(4):923-931. PubMed ID: 32246227 [TBL] [Abstract][Full Text] [Related]
5. Two new families with enamel renal syndrome: A novel FAM20A gene mutation and review of literature. Hassib NF; Shoeib MA; ElSadek HA; Wali ME; Mostafa MI; Abdel-Hamid MS Eur J Med Genet; 2020 Nov; 63(11):104045. PubMed ID: 32835847 [TBL] [Abstract][Full Text] [Related]
6. FAM20A mutations can cause enamel-renal syndrome (ERS). Wang SK; Aref P; Hu Y; Milkovich RN; Simmer JP; El-Khateeb M; Daggag H; Baqain ZH; Hu JC PLoS Genet; 2013; 9(2):e1003302. PubMed ID: 23468644 [TBL] [Abstract][Full Text] [Related]
7. Enamel-Renal-Gingival syndrome, hypodontia, and a novel FAM20A mutation. Kantaputra PN; Bongkochwilawan C; Kaewgahya M; Ohazama A; Kayserili H; Erdem AP; Aktoren O; Guven Y Am J Med Genet A; 2014 Aug; 164A(8):2124-8. PubMed ID: 24756937 [No Abstract] [Full Text] [Related]
9. Enamel renal syndrome: A novel homozygous FAM20A founder mutation in 5 new Brazilian families. Dourado MR; Dos Santos CRR; Dumitriu S; Iancu D; Albanyan S; Kleta R; Coletta RD; Marques Mesquita AT Eur J Med Genet; 2019 Nov; 62(11):103561. PubMed ID: 30394349 [TBL] [Abstract][Full Text] [Related]
10. FAM20A is essential for amelogenesis, but is dispensable for dentinogenesis. Li L; Saiyin W; Zhang H; Wang S; Xu Q; Qin C; Lu Y J Mol Histol; 2019 Dec; 50(6):581-591. PubMed ID: 31667691 [TBL] [Abstract][Full Text] [Related]
12. Hypoplastic amelogenesis imperfecta, bilateral nephrolithiasis and FGF-23-mediated hypophosphataemia: a triad of FAM20A-related enamel renal syndrome. Agrawal N; Awasthi A; Chakraborty PP; Maiti A BMJ Case Rep; 2022 Nov; 15(11):. PubMed ID: 36351670 [TBL] [Abstract][Full Text] [Related]
13. Pathognomonic oral profile of Enamel Renal Syndrome (ERS) caused by recessive FAM20A mutations. de la Dure-Molla M; Quentric M; Yamaguti PM; Acevedo AC; Mighell AJ; Vikkula M; Huckert M; Berdal A; Bloch-Zupan A Orphanet J Rare Dis; 2014 Jun; 9():84. PubMed ID: 24927635 [TBL] [Abstract][Full Text] [Related]
14. Pathogenesis of Enamel-Renal Syndrome Associated Gingival Fibromatosis: A Proteomic Approach. Simancas Escorcia V; Guillou C; Abbad L; Derrien L; Rodrigues Rezende Costa C; Cannaya V; Benassarou M; Chatziantoniou C; Berdal A; Acevedo AC; Cases O; Cosette P; Kozyraki R Front Endocrinol (Lausanne); 2021; 12():752568. PubMed ID: 34777248 [TBL] [Abstract][Full Text] [Related]
15. Loss of epithelial FAM20A in mice causes amelogenesis imperfecta, tooth eruption delay and gingival overgrowth. Li LL; Liu PH; Xie XH; Ma S; Liu C; Chen L; Qin CL Int J Oral Sci; 2016 Jun; 8(2):98-109. PubMed ID: 27281036 [TBL] [Abstract][Full Text] [Related]
16. Enamel formation and amelogenesis imperfecta. Hu JC; Chun YH; Al Hazzazzi T; Simmer JP Cells Tissues Organs; 2007; 186(1):78-85. PubMed ID: 17627121 [TBL] [Abstract][Full Text] [Related]
17. Amelogenesis imperfecta, nephrocalcinosis, and hypocalciuria syndrome in two siblings from a large family with consanguineous parents. Dellow EL; Harley KE; Unwin RJ; Wrong O; Winter GB; Parkins BJ Nephrol Dial Transplant; 1998 Dec; 13(12):3193-6. PubMed ID: 9870488 [No Abstract] [Full Text] [Related]
18. Further evidence for causal FAM20A mutations and first case of amelogenesis imperfecta and gingival hyperplasia syndrome in Morocco: a case report. Cherkaoui Jaouad I; El Alloussi M; Chafai El Alaoui S; Laarabi FZ; Lyahyai J; Sefiani A BMC Oral Health; 2015 Jan; 15():14. PubMed ID: 25636655 [TBL] [Abstract][Full Text] [Related]
19. Amelogenesis imperfecta and other biomineralization defects in Fam20a and Fam20c null mice. Vogel P; Hansen GM; Read RW; Vance RB; Thiel M; Liu J; Wronski TJ; Smith DD; Jeter-Jones S; Brommage R Vet Pathol; 2012 Nov; 49(6):998-1017. PubMed ID: 22732358 [TBL] [Abstract][Full Text] [Related]
20. Transcriptome analysis of gingival tissues of enamel-renal syndrome. Wang YP; Lin HY; Zhong WL; Simmer JP; Wang SK J Periodontal Res; 2019 Dec; 54(6):653-661. PubMed ID: 31131889 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]