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Journal Abstract Search

177 related items for PubMed ID: 37159186

  • 1. FAM20A mutations and transcriptome analyses of dental pulp tissues of enamel renal syndrome.
    Wang SK, Zhang H, Wang YL, Lin HY, Seymen F, Koruyucu M, Wright JT, Kim JW, Simmer JP, Hu JC.
    Int Endod J; 2023 Aug; 56(8):943-954. PubMed ID: 37159186
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  • 2. 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 Aug; 9(2):e1003302. PubMed ID: 23468644
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  • 3. FAM20A mutations associated with enamel renal syndrome.
    Wang SK, Reid BM, Dugan SL, Roggenbuck JA, Read L, Aref P, Taheri AP, Yeganeh MZ, Simmer JP, Hu JC.
    J Dent Res; 2014 Jan; 93(1):42-8. PubMed ID: 24196488
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  • 5. In-depth investigation of FAM20A insufficiency effects on deciduous dental pulp cells: Altered behaviours, osteogenic differentiation, and inflammatory gene expression.
    Sriwattanapong K, Theerapanon T, Khamwachirapitak C, Sae-Ear P, Sa-Ard-Iam N, Shotelersuk V, Porntaveetus T.
    Int Endod J; 2024 Jun; 57(6):745-758. PubMed ID: 38477421
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  • 7. 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
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  • 8. 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
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  • 9. 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 Nov; 12():752568. PubMed ID: 34777248
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  • 10. 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
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  • 11. 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 08; 15(11):. PubMed ID: 36351670
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  • 12. 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 Nov 08; 139(2):189-196. PubMed ID: 29439260
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