Search Results - SAIKAWA, Reiko

  • Showing 1 - 8 results of 8
Refine Results
  1. 1
    Selection of highly responsive T cell receptors by an analysis combining the expression of multiple markers

    Selection of highly responsive T cell receptors by an analysis combining the expression of multiple markers by Ha, My, Hamana, Hiroshi, Shitaoka, Kiyomi, Hayee, Abdul, Kobayashi, Eiji, Yoshikawa, Toshiaki, Nakatsura, Tetsuya, Saikawa, Reiko, Sato, Eri, Osawa, Mitsujiro, Hitoshi, Yasumichi, Dang, Tung, Ozawa, Tatsuhiko, Kishi, Hiroyuki

    Published in Cancer science
    Get full text
    Items that this one cites
    Article
    Save to List
    Saved in:
  2. 2
    Identification of 3,4-dihydro-2H-thiochromene 1,1-dioxide derivatives with a phenoxyethylamine group as highly potent and selective α1D adrenoceptor antagonists

    Identification of 3,4-dihydro-2H-thiochromene 1,1-dioxide derivatives with a phenoxyethylamine group as highly potent and selective α1D adrenoceptor antagonists by Sakauchi, Nobuki, Furukawa, Hideki, Shirai, Junya, Sato, Ayumu, Kuno, Haruhiko, Saikawa, Reiko, Yoshida, Masato

    Get full text
    Article
    Save to List
    Saved in:
  3. 3
    Identification of 3,4-dihydro-2 H -thiochromene 1,1-dioxide derivatives with a phenoxyethylamine group as highly potent and selective α 1D adrenoceptor antagonists

    Identification of 3,4-dihydro-2 H -thiochromene 1,1-dioxide derivatives with a phenoxyethylamine group as highly potent and selective α 1D adrenoceptor antagonists by Sakauchi, Nobuki, Furukawa, Hideki, Shirai, Junya, Sato, Ayumu, Kuno, Haruhiko, Saikawa, Reiko, Yoshida, Masato

    Get full text
    Items that this one cites
    Items that cite this one
    Article
    Save to List
    Saved in:
  4. 4
    Discovery of 5‑Chloro-1-(5-chloro-2-(methylsulfonyl)benzyl)-2-imino-1,2-dihydropyridine-3-carboxamide (TAK-259) as a Novel, Selective, and Orally Active α1D Adrenoceptor Antagonist with Antiurinary Frequency Effects: Reducing Human Ether-a-go-go-Related Gene (hERG) Liabilities

    Discovery of 5‑Chloro-1-(5-chloro-2-(methylsulfonyl)benzyl)-2-imino-1,2-dihydropyridine-3-carboxamide (TAK-259) as a Novel, Selective, and Orally Active α1D Adrenoceptor Antagonist... by Sakauchi, Nobuki, Kohara, Yasuhisa, Sato, Ayumu, Suzaki, Tomohiko, Imai, Yumi, Okabe, Yuichi, Imai, Shigemitsu, Saikawa, Reiko, Nagabukuro, Hiroshi, Kuno, Haruhiko, Fujita, Hisashi, Kamo, Izumi, Yoshida, Masato

    Get full text
    Article
    Save to List
    Saved in:
  5. 5
    Discovery of 5-Chloro-1-(5-chloro-2-(methylsulfonyl)benzyl)-2-imino-1,2-dihydropyridine-3-carboxamide (TAK-259) as a Novel, Selective, and Orally Active α 1D Adrenoceptor Antagonist with Antiurinary Frequency Effects: Reducing Human Ether-a-go-go-Related Gene (hERG) Liabilities

    Discovery of 5-Chloro-1-(5-chloro-2-(methylsulfonyl)benzyl)-2-imino-1,2-dihydropyridine-3-carboxamide (TAK-259) as a Novel, Selective, and Orally Active α 1D Adrenoceptor Antagonis... by Sakauchi, Nobuki, Kohara, Yasuhisa, Sato, Ayumu, Suzaki, Tomohiko, Imai, Yumi, Okabe, Yuichi, Imai, Shigemitsu, Saikawa, Reiko, Nagabukuro, Hiroshi, Kuno, Haruhiko, Fujita, Hisashi, Kamo, Izumi, Yoshida, Masato

    Get full text
    Items that this one cites
    Items that cite this one
    Article
    Save to List
    Saved in:
  6. 6
    Identification of 3,4-dihydro-2H-thiochromene 1,1-dioxide derivatives with a phenoxyethylamine group as highly potent and selective α 1D adrenoceptor antagonists

    Identification of 3,4-dihydro-2H-thiochromene 1,1-dioxide derivatives with a phenoxyethylamine group as highly potent and selective α 1D adrenoceptor antagonists by Sakauchi, Nobuki, Furukawa, Hideki, Shirai, Junya, Sato, Ayumu, Kuno, Haruhiko, Saikawa, Reiko, Yoshida, Masato

    Get full text
    Article
    Save to List
    Saved in:
  7. 7
    Novel acetylcholinesterase inhibitor as increasing agent on rhythmic bladder contractions: SAR of 8-{3-[1-(3-fluorobenzyl)piperidin-4-yl]propanoyl}-1,2,5,6-tetrahydro-4H-pyrrolo[ 3,2,1-ij]quinolin-4-one (TAK-802) and related compounds

    Novel acetylcholinesterase inhibitor as increasing agent on rhythmic bladder contractions: SAR of 8-{3-[1-(3-fluorobenzyl)piperidin-4-yl]propanoyl}-1,2,5,6-tetrahydro-4H-pyrrolo[ 3... by ISHICHI, Yuji, SASAKI, Mitsuru, ISHIHARA, Yuji, SETOH, Masaki, TSUKAMOTO, Tetsuya, MIWATASHI, Seiji, NAGABUKURO, Hiroshi, OKANISHI, Satoshi, IMAI, Shigemitsu, SAIKAWA, Reiko, DOI, Takayuki

    Get full text
    Items that this one cites
    Items that cite this one
    Article
    Save to List
    Saved in:
  8. 8
    Novel acetylcholinesterase inhibitor as increasing agent on rhythmic bladder contractions: SAR of 8-{3-[1-(3-fluorobenzyl)piperidin-4-yl]propanoyl}-1,2,5,6-tetrahydro-4 H-pyrrolo[3,2,1- ij]quinolin-4-one (TAK-802) and related compounds

    Novel acetylcholinesterase inhibitor as increasing agent on rhythmic bladder contractions: SAR of 8-{3-[1-(3-fluorobenzyl)piperidin-4-yl]propanoyl}-1,2,5,6-tetrahydro-4 H-pyrrolo[3... by Ishichi, Yuji, Sasaki, Mitsuru, Setoh, Masaki, Tsukamoto, Tetsuya, Miwatashi, Seiji, Nagabukuro, Hiroshi, Okanishi, Satoshi, Imai, Shigemitsu, Saikawa, Reiko, Doi, Takayuki, Ishihara, Yuji

    Get full text
    Article
    Save to List
    Saved in:

Search Tools: