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Novel calmodulin mutations associated with congenital arrhythmia susceptibility.
Makita N, Yagihara N, Crotti L, Johnson CN, Beckmann BM, Roh MS, Shigemizu D, Lichtner P, Ishikawa T, Aiba T, Homfray T, Behr ER, Klug D, Denjoy I, Mastantuono E, Theisen D, Tsunoda T, Satake W, Toda T, Nakagawa H, Tsuji Y, Tsuchiya T, Yamamoto H, Miyamoto Y, Endo N, Kimura A, Ozaki K, Motomura H, Suda K, Tanaka T, Schwartz PJ, Meitinger T, Kääb S, Guicheney P, Shimizu W, Bhuiyan ZA, Watanabe H, Chazin WJ, George AL Jr. Makita N, et al. Among authors: suda k. Circ Cardiovasc Genet. 2014 Aug;7(4):466-74. doi: 10.1161/CIRCGENETICS.113.000459. Epub 2014 Jun 10. Circ Cardiovasc Genet. 2014. PMID: 24917665 Free PMC article.
The c.1617del variant of TMEM260 is identified as the most frequent single gene determinant for Japanese patients with a specific type of congenital heart disease.
Inoue T, Takase R, Uchida K, Kodo K, Suda K, Watanabe Y, Yoshiura KI, Kunimatsu M, Ishizaki R, Azuma K, Inai K, Muneuchi J, Furutani Y, Akagawa H, Yamagishi H. Inoue T, et al. Among authors: suda k. J Hum Genet. 2024 May;69(5):215-222. doi: 10.1038/s10038-024-01225-w. Epub 2024 Feb 26. J Hum Genet. 2024. PMID: 38409496 Free PMC article.
Unimolecular Chemiexcited Oxygenation of Pathogenic Amyloids.
Umeda H, Suda K, Yokogawa D, Azumaya Y, Kitada N, Maki SA, Kawashima SA, Mitsunuma H, Yamanashi Y, Kanai M. Umeda H, et al. Among authors: suda k. Angew Chem Int Ed Engl. 2024 May 17:e202405605. doi: 10.1002/anie.202405605. Online ahead of print. Angew Chem Int Ed Engl. 2024. PMID: 38757875
Drug Shortages Prior to and During the COVID-19 Pandemic.
Callaway Kim K, Rothenberger SD, Tadrous M, Hernandez I, Gellad WF, Devine JW, Hershey TB, Maillart LM, Suda KJ. Callaway Kim K, et al. Among authors: suda kj. JAMA Netw Open. 2024 Apr 1;7(4):e244246. doi: 10.1001/jamanetworkopen.2024.4246. JAMA Netw Open. 2024. PMID: 38578641 Free PMC article.
1,468 results