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521 results

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Page 1
Genetic and transcriptional landscape of plasma cells in POEMS syndrome.
Nagao Y, Mimura N, Takeda J, Yoshida K, Shiozawa Y, Oshima M, Aoyama K, Saraya A, Koide S, Rizq O, Hasegawa Y, Shiraishi Y, Chiba K, Tanaka H, Nishijima D, Isshiki Y, Kayamori K, Kawajiri-Manako C, Oshima-Hasegawa N, Tsukamoto S, Mitsukawa S, Takeda Y, Ohwada C, Takeuchi M, Iseki T, Misawa S, Miyano S, Ohara O, Yokote K, Sakaida E, Kuwabara S, Sanada M, Iwama A, Ogawa S, Nakaseko C. Nagao Y, et al. Among authors: ohara o. Leukemia. 2019 Jul;33(7):1723-1735. doi: 10.1038/s41375-018-0348-x. Epub 2019 Jan 11. Leukemia. 2019. PMID: 30635632
Expression profile of mRNAs from human pancreatic islet tumors.
Jin L, Wang H, Narita T, Kikuno R, Ohara O, Shihara N, Nishigori T, Horikawa Y, Takeda J. Jin L, et al. Among authors: ohara o. J Mol Endocrinol. 2003 Dec;31(3):519-28. doi: 10.1677/jme.0.0310519. J Mol Endocrinol. 2003. PMID: 14664712
Phosphatase and tensin homolog (PTEN) mutation can cause activated phosphatidylinositol 3-kinase δ syndrome-like immunodeficiency.
Tsujita Y, Mitsui-Sekinaka K, Imai K, Yeh TW, Mitsuiki N, Asano T, Ohnishi H, Kato Z, Sekinaka Y, Zaha K, Kato T, Okano T, Takashima T, Kobayashi K, Kimura M, Kunitsu T, Maruo Y, Kanegane H, Takagi M, Yoshida K, Okuno Y, Muramatsu H, Shiraishi Y, Chiba K, Tanaka H, Miyano S, Kojima S, Ogawa S, Ohara O, Okada S, Kobayashi M, Morio T, Nonoyama S. Tsujita Y, et al. Among authors: ohara o. J Allergy Clin Immunol. 2016 Dec;138(6):1672-1680.e10. doi: 10.1016/j.jaci.2016.03.055. Epub 2016 Jul 14. J Allergy Clin Immunol. 2016. PMID: 27426521
Common Variable Immunodeficiency Caused by FANC Mutations.
Sekinaka Y, Mitsuiki N, Imai K, Yabe M, Yabe H, Mitsui-Sekinaka K, Honma K, Takagi M, Arai A, Yoshida K, Okuno Y, Shiraishi Y, Chiba K, Tanaka H, Miyano S, Muramatsu H, Kojima S, Hira A, Takata M, Ohara O, Ogawa S, Morio T, Nonoyama S. Sekinaka Y, et al. Among authors: ohara o. J Clin Immunol. 2017 Jul;37(5):434-444. doi: 10.1007/s10875-017-0396-4. Epub 2017 May 11. J Clin Immunol. 2017. PMID: 28493158
Detection of MYD88 L265P mutation by next-generation deep sequencing in peripheral blood mononuclear cells of Waldenström's macroglobulinemia and IgM monoclonal gammopathy of undetermined significance.
Nakamura A, Ohwada C, Takeuchi M, Takeda Y, Tsukamoto S, Mimura N, Nagisa OH, Sugita Y, Tanaka H, Wakita H, Aotsuka N, Matsue K, Yokote K, Ohara O, Nakaseko C, Sakaida E. Nakamura A, et al. Among authors: ohara o. PLoS One. 2019 Sep 4;14(9):e0221941. doi: 10.1371/journal.pone.0221941. eCollection 2019. PLoS One. 2019. PMID: 31483817 Free PMC article.
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: ohara o. 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
Genetic subtype classification using a simplified algorithm and mutational characteristics of diffuse large B-cell lymphoma in a Japanese cohort.
Mishina T, Oshima-Hasegawa N, Tsukamoto S, Fukuyo M, Kageyama H, Muto T, Mimura N, Rahmutulla B, Nagai Y, Kayamori K, Hino Y, Mitsukawa S, Takeda Y, Ohwada C, Takeuchi M, Tsujimura H, Iseki T, Nakaseko C, Ikeda JI, Itami M, Yokote K, Ohara O, Kaneda A, Sakaida E. Mishina T, et al. Among authors: ohara o. Br J Haematol. 2021 Dec;195(5):731-742. doi: 10.1111/bjh.17765. Epub 2021 Aug 10. Br J Haematol. 2021. PMID: 34378195
521 results