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  1. Ryoji Ito currently works at the Immunology Laboratory, Central Institute for Experimental Animals. Ryoji does research in Immunology and Xenobiology.

  2. Nov 2, 2018 · Although mouse models have provided insight into the mechanisms by which type-2 cytokines induce asthmatic airway inflammation, differences between the rodent and human immune systems hamper efforts to improve understanding of human allergic diseases.

    • Ryoji Ito, Shuichiro Maruoka, Kaori Soda, Ikumi Katano, Kenji Kawai, Mika Yagoto, Asami Hanazawa, Ta...
    • 2018
  3. en.wikipedia.org › wiki › Ryuji_ItoRyuji Ito - Wikipedia

    Ryuji Ito (伊東 竜二, Itō Ryūji) (born April 8, 1976) [1] is a Japanese professional wrestler currently competing in Big Japan Pro Wrestling in the Deathmatch division. Career. Big Japan Pro Wrestling (1999–present)

  4. Nov 2, 2018 · Or to: Ryoji Ito, Central Institute for Experimental Animals, 3-25-12 Tonomachi, Kawasaki-ku, Kawasaki, Kanagawa 210-0821, Japan. Phone: 81.44.201.8537; Email: rito@ciea.or.jp. Authorship note: RI and SM contributed equally to this work. Find articles by Ito, M. in: JCI | PubMed | Google Scholar

    • Ryoji Ito, Shuichiro Maruoka, Kaori Soda, Ikumi Katano, Kenji Kawai, Mika Yagoto, Asami Hanazawa, Ta...
    • 2018
  5. Ryoji Ito 1 , Takeshi Takahashi , Ikumi Katano , Mamoru Ito. Affiliation. 1 Central Institute for Experimental Animals, Kawasaki, Japan. PMID: 22327211. PMCID: PMC4012844. DOI: 10.1038/cmi.2012.2. Abstract. Humanized mouse models that have received human cells or tissue transplants are extremely useful in basic and applied human disease research.

    • Ryoji Ito, Takeshi Takahashi, Ikumi Katano, Mamoru Ito
    • 2012
  6. Ryoji Ito currently works at the Immunology Laboratory, Central Institute for Experimental Animals. Ryoji does research in Immunology and Xenobiology.

  7. Sep 15, 2013 · In this study, we developed a novel transgenic (Tg) strain, NOD/Shi-scid-IL2rγ (null) (NOG), bearing human IL-3 and GM-CSF genes (NOG IL-3/GM-Tg). In this strain, a large number of human myeloid cells of various lineages developed after transplantation of human CD34⁺ hematopoietic stem cells.