Search Results - "Arai, Harumi"

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  1. 1

    M-Phase Kinases Induce Phospho-Dependent Ubiquitination of Somatic Wee1 by SCFβ - TrCP by Watanabe, Nobumoto, Arai, Harumi, Nishihara, Yoshifumi, Taniguchi, Makoto, Watanabe, Naoko, Hunter, Tony, Osada, Hiroyuki, Ruderman, Joan V.

    “…Wee1, the Cdc2 inhibitory kinase, needs to be down-regulated at the onset of mitosis to ensure rapid activation of Cdc2. Previously, we have shown that human…”
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    Journal Article
  2. 2

    Cyclin-Dependent Kinase (CDK) Phosphorylation Destabilizes Somatic Wee1 via Multiple Pathways by Watanabe, Nobumoto, Arai, Harumi, Iwasaki, Jun-ichi, Shiina, Masaaki, Ogata, Kazuhiro, Hunter, Tony, Osada, Hiroyuki, Ruderman, Joan V.

    “…At the onset of M phase, the activity of somatic Wee1 (Wee1A), the inhibitory kinase for cyclin-dependent kinase (CDK), is down-regulated primarily through…”
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  3. 3
  4. 4

    Effect of adsorbents on the absorption of lansoprazole with surfactant by Ito, Yukako, Arai, Harumi, Uchino, Kaori, Iwasaki, Kouji, Shibata, Nobuhito, Takada, Kanji

    Published in International journal of pharmaceutics (31-01-2005)
    “…Lansoprazole (LPZ) is a representative drug that shows a high inter-subject variation of bioavailability (BA). Solid preparation composed of surfactant,…”
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  5. 5

    WE-NET: Japanese hydrogen program by Mitsugi, Chiba, Harumi, Arai, Kenzo, Fukuda

    Published in International journal of hydrogen energy (01-03-1998)
    “…The Agency of Industrial Science and Technology (AIST), in the Ministry of International Trade and Industry (MITI), started the New Sunshine Program in 1993 by…”
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  6. 6

    M-phase kinases induce phospho-dependent ubiquitination of somatic Wee1 by SCFbeta-TrCP by Watanabe, Nobumoto, Arai, Harumi, Nishihara, Yoshifumi, Taniguchi, Makoto, Watanabe, Naoko, Hunter, Tony, Osada, Hiroyuki

    “…Wee1, the Cdc2 inhibitory kinase, needs to be down-regulated at the onset of mitosis to ensure rapid activation of Cdc2. Previously, we have shown that human…”
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    Journal Article
  7. 7

    Modulation of the immune response to tumors by a novel synthetic compound, (4R)-3-benzoyl-N-[(1R)-1-phenylethyl]-4-thiazolidinecarboxamide (RS-0481) by KURAKATA, S, TOMATSU, M, ARAI, M, ARAI, H, HISHINUMA, A, KOHNO, H, KITAMURA, K, KOBAYASHI, T, NOMOTO, K

    Published in Cancer Immunology Immunotherapy (01-03-1991)
    “…RS-0481, (4R)-3-benzoyl-N-[(1R)-phenylethyl]-4-thiazolidinecarboxamide, is a compound that can re-establish the function of certain lymphoid cell populations…”
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  8. 8

    A new method for the synthesis of novel 6-quinoxalinylpyrazolo[5,1-c][1,2,4]triazines by Kurasawa, Yoshihisa, Satoh, Atsushi, Ninomiya, Satoyuki, Arai, Harumi, Arai, Kiyoko, Okamoto, Yoshihisa, Takada, Atsushi

    Published in Journal of heterocyclic chemistry (01-07-1987)
    “…The reaction of the quinoxaline 1 with 4‐ethoxycarbonyl‐1H‐pyrazole‐5‐diazonium chloride 7 at room temperature gave…”
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  9. 9

    A convenient synthesis of novel pyridazino[3,4-b]quinoxalines by Kurasawa, Yoshihisa, Arai, Harumi, Arai, Kiyoko, Satoh, Atsushi, Ninomiya, Satoyuki, Okamoto, Yoshihisa, Takada, Atsushi

    Published in Journal of heterocyclic chemistry (01-07-1987)
    “…Novel 4‐chlorophenylhydrazono‐3‐oxo‐1,2,3,4‐tetrahydropyridazino[3,4‐b]quinoxalines 10a‐c were synthesized by the cyclization of the α‐hydrazonohydrazides…”
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