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Exome-wide benchmark of difficult-to-sequence regions using short-read next-generation DNA sequencing.
Hijikata A, Suyama M, Kikugawa S, Matoba R, Naruto T, Enomoto Y, Kurosawa K, Harada N, Yanagi K, Kaname T, Miyako K, Takazawa M, Sasai H, Hosokawa J, Itoga S, Yamaguchi T, Kosho T, Matsubara K, Kuroki Y, Fukami M, Adachi K, Nanba E, Tsuchida N, Uchiyama Y, Matsumoto N, Nishimura K, Ohara O. Hijikata A, et al. Among authors: naruto t. Nucleic Acids Res. 2024 Jan 11;52(1):114-124. doi: 10.1093/nar/gkad1140. Nucleic Acids Res. 2024. PMID: 38015437 Free PMC article.
Myeloid/natural killer (NK) cell precursor acute leukemia as a distinct leukemia type.
Nishimura A, Yokoyama K, Naruto T, Yamagishi C, Imamura T, Nakazono H, Kimura S, Ito M, Sagisaka M, Tanaka Y, Piao J, Namikawa Y, Yanagimachi M, Isoda T, Kanai A, Matsui H, Isobe T, Sato-Otsubo A, Higuchi N, Takada A, Okuno H, Saito S, Karakawa S, Kobayashi S, Hasegawa D, Fujisaki H, Hasegawa D, Koike K, Koike T, Rai S, Umeda K, Sano H, Sekinaka Y, Ogawa A, Kinoshita A, Shiba N, Miki M, Kimura F, Nakayama H, Nakazawa Y, Taga T, Taki T, Adachi S, Manabe A, Koh K, Ishida Y, Takita J, Ishikawa F, Goto H, Morio T, Mizutani S, Tojo A, Takagi M. Nishimura A, et al. Among authors: naruto t. Sci Adv. 2023 Dec 15;9(50):eadj4407. doi: 10.1126/sciadv.adj4407. Epub 2023 Dec 13. Sci Adv. 2023. PMID: 38091391 Free PMC article.
A novel PTCH1 mutation in a patient with Gorlin syndrome.
Okamoto N, Naruto T, Kohmoto T, Komori T, Imoto I. Okamoto N, et al. Among authors: naruto t. Hum Genome Var. 2014 Nov 13;1:14022. doi: 10.1038/hgv.2014.22. eCollection 2014. Hum Genome Var. 2014. PMID: 27081512 Free PMC article.
A FRMD7 variant in a Japanese family causes congenital nystagmus.
Kohmoto T, Okamoto N, Satomura S, Naruto T, Komori T, Hashimoto T, Imoto I. Kohmoto T, et al. Among authors: naruto t. Hum Genome Var. 2015 Feb 12;2:15002. doi: 10.1038/hgv.2015.2. eCollection 2015. Hum Genome Var. 2015. PMID: 27081518 Free PMC article.
125 results