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Page 1
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.
Somatic mutation in RUNX1 underlies mucocutaneus inflammatory manifestations.
Okano T, Nishimura A, Inoue K, Naruto T, Tokoro S, Tomoda T, Kamiya T, Simbo A, Akutsu Y, Okamoto K, Yeh T, Isoda T, Yanagimachi M, Kajiwara M, Imai K, Kanegane H, Mori M, Morio T, Takagi M. Okano T, et al. Among authors: naruto t. Rheumatology (Oxford). 2021 Dec 1;60(12):e429-e431. doi: 10.1093/rheumatology/keab513. Rheumatology (Oxford). 2021. PMID: 34528076 No abstract available.
High-throughput analysis revealed the unique immunoglobulin gene rearrangements in plasmacytoma-like post-transplant lymphoproliferative disorder.
Hoshino A, Nishimura A, Naruto T, Okano T, Matsumoto K, Okamoto K, Shintaku H, Tokoro S, Okamoto H, Wada T, Takagi M, Imai K, Kanegane H, Morio T. Hoshino A, et al. Among authors: naruto t. Br J Haematol. 2020 May;189(4):e164-e168. doi: 10.1111/bjh.16583. Epub 2020 Mar 19. Br J Haematol. 2020. PMID: 32191347 Free article. No abstract available.
Genomics analysis of leukaemia predisposition in X-linked agammaglobulinaemia.
Nishimura A, Naruto T, Miyamoto S, Grigg A, Bosco JJ, Hoshino A, Amano K, Iwamoto S, Hirayama M, Migita M, Ohara O, Takagi M, Morio T, van Zelm MC, Kanegane H. Nishimura A, et al. Among authors: naruto t. Br J Haematol. 2021 Jun;193(6):1277-1281. doi: 10.1111/bjh.17459. Epub 2021 Apr 14. Br J Haematol. 2021. PMID: 33855700 No abstract available.
Influence of polymorphisms within the methotrexate pathway genes on the toxicity and efficacy of methotrexate in patients with juvenile idiopathic arthritis.
Yanagimachi M, Naruto T, Hara T, Kikuchi M, Hara R, Miyamae T, Imagawa T, Mori M, Kaneko T, Morita S, Goto H, Yokota S. Yanagimachi M, et al. Among authors: naruto t. Br J Clin Pharmacol. 2011 Feb;71(2):237-43. doi: 10.1111/j.1365-2125.2010.03814.x. Br J Clin Pharmacol. 2011. PMID: 21219404 Free PMC article.
Autosomal recessive complete STAT1 deficiency caused by compound heterozygous intronic mutations.
Sakata S, Tsumura M, Matsubayashi T, Karakawa S, Kimura S, Tamaura M, Okano T, Naruto T, Mizoguchi Y, Kagawa R, Nishimura S, Imai K, Le Voyer T, Casanova JL, Bustamante J, Morio T, Ohara O, Kobayashi M, Okada S. Sakata S, et al. Among authors: naruto t. Int Immunol. 2020 Sep 30;32(10):663-671. doi: 10.1093/intimm/dxaa043. Int Immunol. 2020. PMID: 32603428
119 results