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One-Shot Multiple Borylation toward BN-Doped Nanographenes.
Matsui K, Oda S, Yoshiura K, Nakajima K, Yasuda N, Hatakeyama T. Matsui K, et al. Among authors: yoshiura k. J Am Chem Soc. 2018 Jan 31;140(4):1195-1198. doi: 10.1021/jacs.7b10578. Epub 2017 Nov 9. J Am Chem Soc. 2018. PMID: 29120174
Characteristic phenotypes of ADH5/ALDH2 deficiency during childhood.
Matsumoto M, Oyake M, Itonaga T, Maeda M, Suenobu S, Sato D, Sasahara Y, Mishima H, Yoshiura KI, Ihara K. Matsumoto M, et al. Among authors: yoshiura ki. Eur J Med Genet. 2024 Apr 15;69:104939. doi: 10.1016/j.ejmg.2024.104939. Online ahead of print. Eur J Med Genet. 2024. PMID: 38614309 Free article.
Correction: 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: yoshiura ki. J Hum Genet. 2024 May;69(5):223. doi: 10.1038/s10038-024-01238-5. J Hum Genet. 2024. PMID: 38459226 No abstract available.
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: yoshiura ki. 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.
457 results