نتائج البحث - Shigeru Tsuchiya

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  1. 1
    Repetitive A epitope (type 3 chain A) defined by blood group A1-specific monoclonal antibody TH-1: chemical basis of qualitative A1 and A2 distinction.

    Repetitive A epitope (type 3 chain A) defined by blood group A1-specific monoclonal antibody TH-1: chemical basis of qualitative A1 and A2 distinction. حسب Henrik Clausen, Steven B. Levery, Edward Nudelman, Shigeru Tsuchiya, S Hakomori

    منشور في 1985
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  2. 2
    Morphological and Mechanical Characterization of the Acid-base Resistant Zone at the Adhesive-dentin Interface of Intact and Caries-affected Dentin

    Morphological and Mechanical Characterization of the Acid-base Resistant Zone at the Adhesive-dentin Interface of Intact and Caries-affected Dentin حسب Go Inoue, Shigeru Tsuchiya, Toru Nikaido, Richard M. FOXTON, Junji Tagami

    منشور في 2006
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  3. 3
    Cutting Edge: The Common γ-Chain Is an Indispensable Subunit of the IL-21 Receptor Complex

    Cutting Edge: The Common γ-Chain Is an Indispensable Subunit of the IL-21 Receptor Complex حسب Hironobu Asao, Chikara Okuyama, Satoru Kumaki, Naoto Ishii, Shigeru Tsuchiya, Don Foster, Kazuo Sugamura

    منشور في 2001
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  4. 4
    Differential Proliferation Rhythm of Neural Progenitor and Oligodendrocyte Precursor Cells in the Young Adult Hippocampus

    Differential Proliferation Rhythm of Neural Progenitor and Oligodendrocyte Precursor Cells in the Young Adult Hippocampus حسب Yōko Matsumoto, Yuji Tsunekawa, Tadashi Nomura, Fumikazu Suto, Miho Matsumata, Shigeru Tsuchiya, Noriko Osumi

    منشور في 2011
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  5. 5
    A homozygous mutation of voltage‐gated sodium channel β<sub>I</sub> gene <i>SCN1B</i> in a patient with Dravet syndrome

    A homozygous mutation of voltage‐gated sodium channel β<sub>I</sub> gene <i>SCN1B</i> in a patient with Dravet syndrome حسب Ikuo Ogiwara, Tojo Nakayama, Tetsushi Yamagata, Hideyuki Ohtani, Emi Mazaki, Shigeru Tsuchiya, Yushi Inoue, Kazuhiro Yamakawa

    منشور في 2012
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  6. 6
    Grf40, A Novel Grb2 Family Member, Is Involved in T Cell Signaling through Interaction with SLP-76 and LAT

    Grf40, A Novel Grb2 Family Member, Is Involved in T Cell Signaling through Interaction with SLP-76 and LAT حسب Hiroshi Asada, Naoto Ishii, Yoshiteru Sasaki, Kazuhiro Endo, Hirotake Kasai, Nobuyuki Tanaka, Toshikazu Takeshita, Shigeru Tsuchiya, Tasuke Konno, Kazuo Sugamura

    منشور في 1999
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  7. 7
    Transcription factor GATA-2 is expressed in erythroid, early myeloid, and CD34+ human leukemia-derived cell lines

    Transcription factor GATA-2 is expressed in erythroid, early myeloid, and CD34+ human leukemia-derived cell lines حسب Tadashi Nagai, Hideo Harigae, Hajime Ishihara, Hozumi Motohashi, Naoko Minegishi, Shigeru Tsuchiya, Norio Hayashi, L Gu, Belén de Andrés, JD Engel

    منشور في 1994
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  8. 8
    Molecular explanation for the contradiction between systemic Th17 defect and localized bacterial infection in hyper-IgE syndrome

    Molecular explanation for the contradiction between systemic Th17 defect and localized bacterial infection in hyper-IgE syndrome حسب Yoshiyuki Minegishi, Masako Saitō, Masayuki Nagasawa, Hidetoshi Takada, Toshiro Hara, Shigeru Tsuchiya, Kazunaga Agematsu, Masafumi Yamada, Nobuaki Kawamura, Tadashi Ariga, Ikuya Tsuge, Hajime Karasuyama

    منشور في 2009
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  9. 9
    The analysis of the functions of human B and T cells in humanized NOD/shi-scid/γcnull (NOG) mice (hu-HSC NOG mice)

    The analysis of the functions of human B and T cells in humanized NOD/shi-scid/γcnull (NOG) mice (hu-HSC NOG mice) حسب Y. Watanabe, Takeshi Takahashi, Akira Okajima, Miho Shiokawa, Naoto Ishii, Ikumi Katano, Ryoji Ito, Mamoru Ito, Masayoshi Minegishi, Naoko Minegishi, Shigeru Tsuchiya, Kazuo Sugamura

    منشور في 2009
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  10. 10
    All-trans Retinoic Acid Induces in Vitro Angiogenesis via Retinoic Acid Receptor: Possible Involvement of Paracrine Effects of Endogenous Vascular Endothelial Growth Factor Signaling

    All-trans Retinoic Acid Induces in Vitro Angiogenesis via Retinoic Acid Receptor: Possible Involvement of Paracrine Effects of Endogenous Vascular Endothelial Growth Factor Signali... حسب Akiko Saito, Akira Sugawara, Akira Uruno, Masataka Kudo, Hiroyuki Kagechika, Yasufumi Sato, Yuji Owada, Hisatake Kondo, Mayumi Sato, Masahiko Kurabayashi, Masue Imaizumi, Shigeru Tsuchiya, Sadayoshi Ito

    منشور في 2006
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  11. 11
    Outcome in patients with Wiskott–Aldrich syndrome following stem cell transplantation: an analysis of 57 patients in Japan

    Outcome in patients with Wiskott–Aldrich syndrome following stem cell transplantation: an analysis of 57 patients in Japan حسب Ryōji Kobayashi, Tadashi Ariga, Shigeaki Nonoyama, Hirokazu Kanegane, Shigeru Tsuchiya, Tomohiro Morio, Hiromasa Yabe, Yoshihisa Nagatoshi, Keisei Kawa, Ken Tabuchi, Masahiro Tsuchida, Toshio Miyawaki, Shunichi Kato

    منشور في 2006
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  12. 12
    Deletions of SCN1A 5′ genomic region with promoter activity in Dravet syndrome

    Deletions of SCN1A 5′ genomic region with promoter activity in Dravet syndrome حسب Tojo Nakayama, Ikuo Ogiwara, Koichi Ito, Makoto Kaneda, Emi Mazaki, Hitoshi Osaka, Hideyuki Ohtani, Yushi Inoue, Tateki Fujiwara, Mitsugu Uematsu, Kazuhiro Haginoya, Shigeru Tsuchiya, Kazuhiro Yamakawa

    منشور في 2010
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  13. 13
    Defective IL-10 signaling in hyper-IgE syndrome results in impaired generation of tolerogenic dendritic cells and induced regulatory T cells

    Defective IL-10 signaling in hyper-IgE syndrome results in impaired generation of tolerogenic dendritic cells and induced regulatory T cells حسب Masako Saitō, Masayuki Nagasawa, Hidetoshi Takada, Toshiro Hara, Shigeru Tsuchiya, Kazunaga Agematsu, Masafumi Yamada, Nobuaki Kawamura, Tadashi Ariga, Ikuya Tsuge, Shigeaki Nonoyama, Hajime Karasuyama, Yoshiyuki Minegishi

    منشور في 2011
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  14. 14
    Lentiviral Vector-Mediated Gene Transfer in T Cells from Wiskott–Aldrich Syndrome Patients Leads to Functional Correction

    Lentiviral Vector-Mediated Gene Transfer in T Cells from Wiskott–Aldrich Syndrome Patients Leads to Functional Correction حسب Loı̈c Dupré, Sara Trifari, Antonia Follenzi, Francesco Marangoni, Teresa Laı́n de Lera, António Bernad, Silvana Di Martino, Shigeru Tsuchiya, Claudio Bordignon, Luigi Naldini, Alessandro Aiuti, Maria‐Grazia Roncarolo

    منشور في 2004
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  15. 15
    Maternal Feeding Controls Fetal Biological Clock

    Maternal Feeding Controls Fetal Biological Clock حسب Hidenobu Ohta, Shanhai Xu, Takahiro Moriya, Masayuki Iigo, Tatsuya Watanabe, Norimichi Nakahata, Hiroshi Chisaka, Takushi Hanita, Tadashi Matsuda, Toshihiro Ohura, Yoshitaka Kimura, Nobuo Yaegashi, Shigeru Tsuchiya, Hajime Tei, Kunihiro Okamura

    منشور في 2008
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  16. 16
    Risk-Stratified Therapy and the Intensive Use of Cytarabine Improves the Outcome in Childhood Acute Myeloid Leukemia: The AML99 Trial From the Japanese Childhood AML Cooperative Study Group

    Risk-Stratified Therapy and the Intensive Use of Cytarabine Improves the Outcome in Childhood Acute Myeloid Leukemia: The AML99 Trial From the Japanese Childhood AML Cooperative St... حسب Ichiro Tsukimoto, Akio Tawa, Keizo Horibe, Ken Tabuchi, Hisato Kigasawa, Masahiro Tsuchida, Hiromasa Yabe, Hideki Nakayama, Kazuko Kudo, Ryōji Kobayashi, Kazuko Hamamoto, Masue Imaizumi, Akira Morimoto, Shigeru Tsuchiya, Ryoji Hanada

    منشور في 2009
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  17. 17
    Prognostic Factors for Chronic Active Epstein‐Barr Virus Infection

    Prognostic Factors for Chronic Active Epstein‐Barr Virus Infection حسب Hiroshi Kimura, Tsuneo Morishima, Hirokazu Kanegane, Shouichi Ohga, Yo Hoshino, Akihiko Maeda, Shosuke Imai, Motohiko Okano, Tomohiro Morio, Shumpei Yokota, Shigeru Tsuchiya, Akihiro Yachie, Shinsaku Imashuku, Keisei Kawa, Hiroshi Wakiguchi

    منشور في 2003
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  18. 18
    A genome-wide association study identifies RNF213 as the first Moyamoya disease gene

    A genome-wide association study identifies RNF213 as the first Moyamoya disease gene حسب Fumiaki Kamada, Yoko Aoki, Ayumi Narisawa, Yu Abe, Shoko Komatsuzaki, Atsuo Kikuchi, Junko Kanno, Tetsuya Niihori, Masao Ono, Naoto Ishii, Yuji Owada, Miki Fujimura, Yoichi Mashimo, Yoichi Suzuki, Akira Hata, Shigeru Tsuchiya, Teiji Tominaga, Yoichi Matsubara, Shigeo Kure

    منشور في 2010
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  19. 19
    Patients with Epstein–Fechtner syndromes owing to MYH9 R702 mutations develop progressive proteinuric renal disease

    Patients with Epstein–Fechtner syndromes owing to MYH9 R702 mutations develop progressive proteinuric renal disease حسب Takashi Sekine, Mutsuko Konno, Satoshi Sasaki, Suzuko Moritani, Takuma Miura, Wai-shan Wong, Hisanori Nishio, Toshihiro Nishiguchi, Miyako Yoshinari Ohuchi, Shigeru Tsuchiya, Takeshi Matsuyama, Hirokazu Kanegane, Komei Ida, Kenichiro Miura, Yutaka Harita, Motoshi Hattori, Shigeru Horita, Takashi Igarashi, Hidehiko Saito, Shinji Kunishima

    منشور في 2010
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  20. 20
    Mutation analysis of the SHOC2 gene in Noonan-like syndrome and in hematologic malignancies

    Mutation analysis of the SHOC2 gene in Noonan-like syndrome and in hematologic malignancies حسب Shoko Komatsuzaki, Yoko Aoki, Tetsuya Niihori, Nobuhiko Okamoto, Raoul C. M. Hennekam, Saskia Hopman, Hirofumi Ohashi, Seiji Mizuno, Yoriko Watanabe, Hotaka Kamasaki, Ikuko Kondo, Nobuko Moriyama, Kenji Kurosawa, Hiroshi Kawame, Ryuhei Okuyama, Masue Imaizumi, Takeshi Rikiishi, Shigeru Tsuchiya, Shigeo Kure, Yoichi Matsubara

    منشور في 2010
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