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Journal Abstract Search

148 related items for PubMed ID: 35055328

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  • 2. Novel KLK4 Mutations Cause Hypomaturation Amelogenesis Imperfecta.
    Lee Y, Zhang H, Seymen F, Kim YJ, Kasimoglu Y, Koruyucu M, Simmer JP, Hu JC, Kim JW.
    J Pers Med; 2022 Jan 24; 12(2):. PubMed ID: 35207639
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  • 3. 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 07; 21(1):97. PubMed ID: 32380970
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  • 5. 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 07; 24(10):3519-3525. PubMed ID: 32034543
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  • 6. Novel WDR72 Mutations Causing Hypomaturation Amelogenesis Imperfecta.
    Kim YJ, Zhang H, Lee Y, Seymen F, Koruyucu M, Kasimoglu Y, Simmer JP, Hu JC, Kim JW.
    J Pers Med; 2023 Feb 14; 13(2):. PubMed ID: 36836560
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  • 7. Analyses of MMP20 Missense Mutations in Two Families with Hypomaturation Amelogenesis Imperfecta.
    Kim YJ, Kang J, Seymen F, Koruyucu M, Gencay K, Shin TJ, Hyun HK, Lee ZH, Hu JC, Simmer JP, Kim JW.
    Front Physiol; 2017 Feb 14; 8():229. PubMed ID: 28473773
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  • 12. 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 14; 119(2):e77-81. PubMed ID: 25442250
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  • 15. 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 06; 99(4):984-990. PubMed ID: 27693231
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  • 16. Identification of mutations in SLC24A4, encoding a potassium-dependent sodium/calcium exchanger, as a cause of amelogenesis imperfecta.
    Parry DA, Poulter JA, Logan CV, Brookes SJ, Jafri H, Ferguson CH, Anwari BM, Rashid Y, Zhao H, Johnson CA, Inglehearn CF, Mighell AJ.
    Am J Hum Genet; 2013 Feb 07; 92(2):307-12. PubMed ID: 23375655
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  • 17. A novel ODAPH mutation causing amelogenesis imperfecta and its expression in human dental tissues.
    Wang SK, Lee ZH, Aref P, Chu KY.
    J Dent Sci; 2024 Jan 07; 19(1):524-531. PubMed ID: 38303846
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  • 18. Novel MMP20 and KLK4 Mutations in Amelogenesis Imperfecta.
    Seymen F, Park JC, Lee KE, Lee HK, Lee DS, Koruyucu M, Gencay K, Bayram M, Tuna EB, Lee ZH, Kim YJ, Kim JW.
    J Dent Res; 2015 Aug 07; 94(8):1063-9. PubMed ID: 26124219
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  • 19. 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 Aug 07; 194(1):60-6. PubMed ID: 21196691
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  • 20. Enamel ultrastructure in pigmented hypomaturation amelogenesis imperfecta.
    Wright JT, Lord V, Robinson C, Shore R.
    J Oral Pathol Med; 1992 Oct 07; 21(9):390-4. PubMed ID: 1432732
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