Результати пошуку - Nao Yoshida

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  1. 1
    Tirabrutinib for CNS relapsed primary vitreoretinal lymphoma

    Tirabrutinib for CNS relapsed primary vitreoretinal lymphoma за авторством Nao Yoshida, Hiroshi Ureshino, Tomona Hiyama, Yosuke Harada, S. Nakatani, Ren Chishaki, Taro Edahiro, Tetsumi Yoshida, Takero Shindo, Tatsuo Ichinohe

    Опубліковано 2025
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    Carta
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  2. 2
    Predicting response to immunosuppressive therapy in childhood aplastic anemia

    Predicting response to immunosuppressive therapy in childhood aplastic anemia за авторством Nao Yoshida, Hiroshi Yagasaki, Asahito Hama, Yu Takahashi, Yoshiyuki Kosaka, R Kobayashi, Hiromasa Yabe, Takashi Kaneko, Masahiro Tsuchida, Akira Ohara, Tatsutoshi Nakahata, Seiji Kojima

    Опубліковано 2011
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    Artigo
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  3. 3
    Acute megakaryoblastic leukaemia (AMKL) in children: a comparison of AMKL with and without Down syndrome

    Acute megakaryoblastic leukaemia (AMKL) in children: a comparison of AMKL with and without Down syndrome за авторством Asahito Hama, Hiroshi Yagasaki, Yoshiyuki Takahashi, Nobuhiro Nishio, Hideki Muramatsu, Nao Yoshida, Makito Tanaka, Hirokazu Hidaka, Nobuhiro Watanabe, Ayami Yoshimi, Kimikazu Matsumoto, Kazuko Kudo, Koji Kato, Keizo Horibe, Seiji Kojima

    Опубліковано 2008
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    Artigo
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  4. 4
    First-line treatment for severe aplastic anemia in children: bone marrow transplantation from a matched family donor versus immunosuppressive therapy

    First-line treatment for severe aplastic anemia in children: bone marrow transplantation from a matched family donor versus immunosuppressive therapy за авторством Nao Yoshida, Ryōji Kobayashi, Hiromasa Yabe, Yoshiyuki Kosaka, Hiroshi Yagasaki, Kenichi Watanabe, Kazuko Kudo, Akira Morimoto, Shouichi Ohga, Hideki Muramatsu, Yoshiyuki Takahashi, Koji Kato, Ritsuro Suzuki, Akira Ohara, Seiji Kojima

    Опубліковано 2014
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    Artigo
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  5. 5
    Spectrum of molecular defects in juvenile myelomonocytic leukaemia includes <i>ASXL1</i> mutations

    Spectrum of molecular defects in juvenile myelomonocytic leukaemia includes <i>ASXL1</i> mutations за авторством Yuka Sugimoto, Hideki Muramatsu, Hideki Makishima, Courtney Prince, Anna Jankowska, Nao Yoshida, Yinyan Xu, Nobuhiro Nishio, Asahito Hama, Hiroshi Yagasaki, Yoshiyuki Takahashi, Koji Kato, Atsushi Manabe, Seiji Kojima, Jaroslaw P. Maciejewski

    Опубліковано 2010
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    Artigo
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  6. 6
    Mutations of an E3 ubiquitin ligase c-Cbl but not TET2 mutations are pathogenic in juvenile myelomonocytic leukemia

    Mutations of an E3 ubiquitin ligase c-Cbl but not TET2 mutations are pathogenic in juvenile myelomonocytic leukemia за авторством Hideki Muramatsu, Hideki Makishima, Anna Jankowska, Heather Cazzolli, Christine L. O’Keefe, Nao Yoshida, Yinyan Xu, Nobuhiro Nishio, Asahito Hama, Hiroshi Yagasaki, Yoshiyuki Takahashi, Koji Kato, Atsushi Manabe, Seiji Kojima, Jaroslaw P. Maciejewski

    Опубліковано 2009
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    Artigo
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  7. 7
    Activation of WNT/β-Catenin Signaling Enhances Pancreatic Cancer Development and the Malignant Potential Via Up-regulation of Cyr61

    Activation of WNT/β-Catenin Signaling Enhances Pancreatic Cancer Development and the Malignant Potential Via Up-regulation of Cyr61 за авторством Makoto Sano, David R. Driscoll, Wilfredo E De Jesús-Monge, Brian Quattrochi, Victoria A. Appleman, Jianhong Ou, Lihua Julie Zhu, Nao Yoshida, Shintaro Yamazaki, Tadatoshi Takayama, Masahiko Sugitani, Norimichi Nemoto, David S. Klimstra, Brian C. Lewis

    Опубліковано 2016
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    Artigo
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  8. 8
    Peripheral blood lymphocyte telomere length as a predictor of response to immunosuppressive therapy in childhood aplastic anemia

    Peripheral blood lymphocyte telomere length as a predictor of response to immunosuppressive therapy in childhood aplastic anemia за авторством Hiroshi Sakaguchi, Nobuhiko Nishio, Asahito Hama, Nozomu Kawashima, Xinan Wang, Atsushi Narita, Sayoko Doisaki, Yinyan Xu, Hideki Muramatsu, Nao Yoshida, Yoshiyuki Takahashi, Kazuko Kudo, Hiroshi Moritake, Kazumasa Nakamura, Ryōji Kobayashi, Etsuro Ito, Hayato Yabe, Shouichi Ohga, Akira Ohara, S Kojima

    Опубліковано 2014
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    Artigo
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  9. 9
    Correlation of Clinical Features With the Mutational Status of GM-CSF Signaling Pathway-Related Genes in Juvenile Myelomonocytic Leukemia

    Correlation of Clinical Features With the Mutational Status of GM-CSF Signaling Pathway-Related Genes in Juvenile Myelomonocytic Leukemia за авторством Nao Yoshida, Hiroshi Yagasaki, Yinyan Xu, Kazuyuki Matsuda, Ayami Yoshimi, Yoshiyuki Takahashi, Asahito Hama, Nobuhiro Nishio, Hideki Muramatsu, Nobuhiro Watanabe, Kimikazu Matsumoto, Koji Kato, Junichi Ueyama, Hiroko Inada, Hiroaki Goto, Miharu Yabe, Kazuko Kudo, J Mimaya, Akira Kikuchi, Atsushi Manabe, Kenichi Koike, Seiji Kojima

    Опубліковано 2009
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    Artigo
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  10. 10
    Spontaneous improvement of hematologic abnormalities in patients having juvenile myelomonocytic leukemia with specific RAS mutations

    Spontaneous improvement of hematologic abnormalities in patients having juvenile myelomonocytic leukemia with specific RAS mutations за авторством Kazuyuki Matsuda, Akira Shimada, Nao Yoshida, Atsushi Ogawa, Akihiro Watanabe, Shuhei Yajima, Susumu Iizuka, Kazutoshi Koike, Fumio Yanai, Keiichiro Kawasaki, Masakatsu Yanagimachi, Akira Kikuchi, Yoshitoshi Ohtsuka, Eiko Hidaka, Kazuyoshi Yamauchi, Miyuki Tanaka, Ryu Yanagisawa, Yozo Nakazawa, Masaaki Shiohara, Atsushi Manabe, Seiji Kojima, Kenichi Koike

    Опубліковано 2007
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    Artigo
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  11. 11
    Impact of graft-versus-host disease on relapse and survival after allogeneic stem cell transplantation for pediatric leukemia

    Impact of graft-versus-host disease on relapse and survival after allogeneic stem cell transplantation for pediatric leukemia за авторством Motohiro Kato, Mio Kurata, Junya Kanda, Koji Kato, Daisuke Tomizawa, Kazuko Kudo, Nao Yoshida, Kenichiro Watanabe, Hiroyuki Shimada, Jiro Inagaki, Katsuyoshi Koh, Hiroaki Goto, Keisuke Kato, Yuko Cho, Yuki Yuza, Atsushi Ogawa, Keiko Okada, Masami Inoue, Yoshiko Hashii, Takanori Teshima, Makoto Murata, Yoshiko Atsuta

    Опубліковано 2018
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    Artigo
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  12. 12
    Dominant-negative IKZF1 mutations cause a T, B, and myeloid cell combined immunodeficiency

    Dominant-negative IKZF1 mutations cause a T, B, and myeloid cell combined immunodeficiency за авторством David Boutboul, Hye Sun Kuehn, Zoé Van de Wyngaert, Julie E. Niemela, Isabelle Callebaut, Jennifer Stoddard, Christelle Lenoir, Vincent Barlogis, Catherine Farnarier, Frédéric Vely, Nao Yoshida, Seiji Kojima, Hirokazu Kanegane, Akihiro Hoshino, Fabian Hauck, Ludovic Lhermitte, Vahid Asnafi, Philip Roehrs, Shaoying Chen, James Verbsky, Katherine R. Calvo, Ammar Husami, Kejian Zhang, Joseph L. Roberts, David J. Amrol, John Sleaseman, Amy P. Hsu, Steven M. Holland, Rebecca Marsh, Alain Fischer, Thomas A. Fleisher, Capucine Pïcard, Sylvain Latour, Sergio D. Rosenzweig

    Опубліковано 2018
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    Artigo
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