Lu Jie | Investigative Treatment Division National Cancer Center Research Institute East

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概要

• LU Jieの詳細を見る
• 同名の論文著者
• Investigative Treatment Division National Cancer Center Research Institute Eastの論文著者

関連著者

• Esumi Hiroyasu

  Investigative Treatment Division, National Cancer Center Research Institute East

• Lu Jie

  Investigative Treatment Division National Cancer Center Research Institute East

• Esumi Hiroyasu

  Invest. Treat. Div. Natl. Cancer Res. Inst.

• KAMINISHI Michio

  Department of Gastrointestinal Surgery, The University of Tokyo, Graduate School of Medicine

• Kondo S

  Institute Of Microbial Chemistry

• HANAOKA Tomoyuki

  Epidemiology and Prevention Division, Research Center for Cancer Prevention and Screening, National

• KUNIMOTO Setsuko

  Institute of Microbial Chemistry

• Yamazaki Yohko

  微生物化学研究会微生物化学研究センター沼津創薬医科学研究所

• KUNIMOTO Setsuko

  Numazu Bio-Medical Research Institute, Microbial Chemistry Research Center

• Hanaoka Tomoyuki

  Epidemiology And Biostatistics Division National Cancer Center Research Institute East

• Esumi Hiroyasu

  Investigative Treatment National Cancer Center Research Institute East

• Kaminishi Michio

  Department Of Breast And Endocrine Surgery Faculty Of Medicine The University Of Tokyo

• Kaminishi Michio

  Department Of Gastrointestinal Surgery University Of Tokyo

• Lu J

  National Cancer Center Res. Inst. East Chiba

• YAMAZAKI Yohko

  Institute of Microbial Chemistry

• KURASHIMA Yukiko

  Investigative Treatment Division, National Cancer Center Research Institute East

• Kunimoto S

  Numazu Bio-medical Research Institute Microbial Chemistry Research Center

• Kurashima Yukiko

  Investigative Treatment Division National Cancer Center Research Institute East

• 山嵜 行由

  School Of Pharmaceutical Sciences University Of Shizuoka

• KURASHIMA Yukiko

  Invest. Treat. Div., Natl. Cancer Res. Inst.

• Hanaoka Tomoyuki

  Epidemiology and Biostatistics Division, National Cancer Center Research Institute East

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著作論文

• Kigamicin D, a novel anticancer agent based on a new anti-austerity strategy targeting cancer cells' tolerance to nutrient starvation
• Antitumor activity of pyrvinium pamoate, 6-(dimethylamino)-2-[2-(2, 5-dimethyl-1-phenyl-1H-pyrrol-3-yl)ethenyl]-1-methyl-quinolinium pamoate salt, showing preferential cytotoxicity during glucose starvation

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