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ENAM mutations and digenic inheritance.
Zhang H, Hu Y, Seymen F, Koruyucu M, Kasimoglu Y, Wang SK, Wright JT, Havel MW, Zhang C, Kim JW, Simmer JP, Hu JC. Zhang H, et al. Among authors: kim jw. Mol Genet Genomic Med. 2019 Oct;7(10):e00928. doi: 10.1002/mgg3.928. Epub 2019 Sep 2. Mol Genet Genomic Med. 2019. PMID: 31478359 Free PMC article.
Fam83h null mice support a neomorphic mechanism for human ADHCAI.
Wang SK, Hu Y, Yang J, Smith CE, Richardson AS, Yamakoshi Y, Lee YL, Seymen F, Koruyucu M, Gencay K, Lee M, Choi M, Kim JW, Hu JC, Simmer JP. Wang SK, et al. Among authors: kim jw. Mol Genet Genomic Med. 2015 Sep 21;4(1):46-67. doi: 10.1002/mgg3.178. eCollection 2016 Jan. Mol Genet Genomic Med. 2015. PMID: 26788537 Free PMC article.
A novel AMELX mutation causes hypoplastic amelogenesis imperfecta.
Kim YJ, Kim YJ, Kang J, Shin TJ, Hyun HK, Lee SH, Lee ZH, Kim JW. Kim YJ, et al. Among authors: kim jw. Arch Oral Biol. 2017 Apr;76:61-65. doi: 10.1016/j.archoralbio.2017.01.004. Epub 2017 Jan 12. Arch Oral Biol. 2017. PMID: 28130977
Mutations in RELT cause autosomal recessive amelogenesis imperfecta.
Kim JW, Zhang H, Seymen F, Koruyucu M, Hu Y, Kang J, Kim YJ, Ikeda A, Kasimoglu Y, Bayram M, Zhang C, Kawasaki K, Bartlett JD, Saunders TL, Simmer JP, Hu JC. Kim JW, et al. Among authors: kim yj. Clin Genet. 2019 Mar;95(3):375-383. doi: 10.1111/cge.13487. Epub 2018 Dec 21. Clin Genet. 2019. PMID: 30506946 Free PMC article.
The Enamel Phenotype in Homozygous Fam83h Truncation Mice.
Wang SK, Hu Y, Smith CE, Yang J, Zeng C, Kim JW, Hu JC, Simmer JP. Wang SK, et al. Among authors: kim jw. Mol Genet Genomic Med. 2019 Jun;7(6):e724. doi: 10.1002/mgg3.724. Epub 2019 May 6. Mol Genet Genomic Med. 2019. PMID: 31060110 Free PMC article.
WNT10A mutations causing oligodontia.
Park H, Song JS, Shin TJ, Hyun HK, Kim YJ, Kim JW. Park H, et al. Among authors: kim yj, kim jw. Arch Oral Biol. 2019 Jul;103:8-11. doi: 10.1016/j.archoralbio.2019.05.007. Epub 2019 May 9. Arch Oral Biol. 2019. PMID: 31103801
8,762 results