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The dentin phosphoprotein repeat region and inherited defects of dentin.
Yang J, Kawasaki K, Lee M, Reid BM, Nunez SM, Choi M, Seymen F, Koruyucu M, Kasimoglu Y, Estrella-Yuson N, Lin BP, Simmer JP, Hu JC. Yang J, et al. Among authors: lee m. Mol Genet Genomic Med. 2015 Sep 7;4(1):28-38. doi: 10.1002/mgg3.176. eCollection 2016 Jan. Mol Genet Genomic Med. 2015. PMID: 26788535 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: lee m, lee yl. 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.
LIN28A loss of function is associated with Parkinson's disease pathogenesis.
Chang MY, Oh B, Choi JE, Sulistio YA, Woo HJ, Jo A, Kim J, Kim EH, Kim SW, Hwang J, Park J, Song JJ, Kwon OC, Henry Kim H, Kim YH, Ko JY, Heo JY, Lee MJ, Lee M, Choi M, Chung SJ, Lee HS, Lee SH. Chang MY, et al. Among authors: lee sh, lee hs, lee mj, lee m. EMBO J. 2019 Dec 16;38(24):e101196. doi: 10.15252/embj.2018101196. Epub 2019 Nov 21. EMBO J. 2019. PMID: 31750563 Free PMC article.
Genomic profiling of 553 uncharacterized neurodevelopment patients reveals a high proportion of recessive pathogenic variant carriers in an outbred population.
Lee Y, Park S, Lee JS, Kim SY, Cho J, Yoo Y, Lee S, Yoo T, Lee M, Seo J, Lee J, Kneissl J, Lee J, Jeon H, Jeon EY, Hong SE, Kim E, Kim H, Kim WJ, Kim JS, Ko JM, Cho A, Lim BC, Kim WS, Choi M, Chae JH. Lee Y, et al. Among authors: lee js, lee j, lee m, lee s. Sci Rep. 2020 Jan 29;10(1):1413. doi: 10.1038/s41598-020-58101-8. Sci Rep. 2020. PMID: 31996704 Free PMC article.
Comprehensive molecular characterization of TFE3-rearranged renal cell carcinoma.
Lee CR, Suh J, Jang D, Jin BY, Cho J, Lee M, Sim H, Kang M, Lee J, Park JH, Lee KH, Hwang GS, Moon KC, Song C, Ku JH, Kwak C, Kim HH, Cho SY, Choi M, Jeong CW. Lee CR, et al. Among authors: lee j, lee m, lee kh. Exp Mol Med. 2024 Aug;56(8):1807-1815. doi: 10.1038/s12276-024-01291-2. Epub 2024 Aug 1. Exp Mol Med. 2024. PMID: 39085357 Free PMC article.
Root anomalies and dentin dysplasia in autosomal recessive hyperphosphatemic familial tumoral calcinosis (HFTC).
Vieira AR, Lee M, Vairo F, Loguercio Leite JC, Munerato MC, Visioli F, D'Ávila SR, Wang SK, Choi M, Simmer JP, Hu JC. Vieira AR, et al. Among authors: lee m. Oral Surg Oral Med Oral Pathol Oral Radiol. 2015 Dec;120(6):e235-9. doi: 10.1016/j.oooo.2015.05.006. Epub 2015 May 28. Oral Surg Oral Med Oral Pathol Oral Radiol. 2015. PMID: 26337219 Free PMC article.
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