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Whole-Exome Sequencing-Based Approach for Germline Mutations in Patients with Inborn Errors of Immunity.
Okano T, Imai K, Naruto T, Okada S, Yamashita M, Yeh TW, Ono S, Tanaka K, Okamoto K, Tanita K, Matsumoto K, Toyofuku E, Kumaki-Matsumoto E, Okamura M, Ueno H, Ogawa S, Ohara O, Takagi M, Kanegane H, Morio T. Okano T, et al. Among authors: naruto t. J Clin Immunol. 2020 Jul;40(5):729-740. doi: 10.1007/s10875-020-00798-3. Epub 2020 Jun 6. J Clin Immunol. 2020. PMID: 32506361
Status of KRAS in iPSCs Impacts upon Self-Renewal and Differentiation Propensity.
Kubara K, Yamazaki K, Ishihara Y, Naruto T, Lin HT, Nishimura K, Ohtaka M, Nakanishi M, Ito M, Tsukahara K, Morio T, Takagi M, Otsu M. Kubara K, et al. Among authors: naruto t. Stem Cell Reports. 2018 Aug 14;11(2):380-394. doi: 10.1016/j.stemcr.2018.06.008. Epub 2018 Jul 5. Stem Cell Reports. 2018. PMID: 29983389 Free PMC article.
A deep intronic mutation of c.1166-285 T > G in SLC46A1 is shared by four unrelated Japanese patients with hereditary folate malabsorption (HFM).
Tozawa Y, Abdrabou SSMA, Nogawa-Chida N, Nishiuchi R, Ishida T, Suzuki Y, Sano H, Kobayashi R, Kishimoto K, Ohara O, Imai K, Naruto T, Kobayashi K, Ariga T, Yamada M. Tozawa Y, et al. Among authors: naruto t. Clin Immunol. 2019 Nov;208:108256. doi: 10.1016/j.clim.2019.108256. Epub 2019 Sep 5. Clin Immunol. 2019. PMID: 31494288
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.
APRIL-dependent lifelong plasmacyte maintenance and immunoglobulin production in humans.
Yeh TW, Okano T, Naruto T, Yamashita M, Okamura M, Tanita K, Du L, Pan-Hammarström Q, Mitsuiki N, Okada S, Kanegane H, Imai K, Morio T. Yeh TW, et al. Among authors: naruto t. J Allergy Clin Immunol. 2020 Nov;146(5):1109-1120.e4. doi: 10.1016/j.jaci.2020.03.025. Epub 2020 Apr 13. J Allergy Clin Immunol. 2020. PMID: 32298700
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
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