FTY720 induces the sequestration of circulating lymphocytes into the bone marrow in alymphoplasia mice
スポンサーリンク
概要
- 論文の詳細を見る
- 日本炎症・再生医学会の論文
- 2010-05-25
著者
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Sugahara Kunio
Pharmacology Research Laboratories I Research Division Mitsubishi Tanabe Pharma Corporation
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Chiba Kenji
Pharmacology Research Laboratories I Research Division Mitsubishi Tanabe Pharma Corporation
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Maeda Yasuhiro
Pharmacology Research Laboratories I Research Division Mitsubishi Tanabe Pharma Corporation
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KATAOKA Hirotoshi
Pharmacology Research Laboratories I, Research Division, Mitsubishi Tanabe Pharma Corporation
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SEKI Noriyasu
Pharmacology Research Laboratories I, Research Division, Mitsubishi Tanabe Pharma Corporation
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KOYAMA Mamoru
Advanced Medical Research Laboratories, Research Division, Mitsubishi Tanabe Pharma Corporation
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KAKIMOTO Tetsuhiro
Advanced Medical Research Laboratories, Research Division, Mitsubishi Tanabe Pharma Corporation
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FUKUNARI Atsushi
Advanced Medical Research Laboratories, Research Division, Mitsubishi Tanabe Pharma Corporation
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Seki Noriyasu
Pharmacology Research Laboratories I Research Division Mitsubishi Tanabe Pharma Corporation
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Koyama Mamoru
Advanced Medical Research Laboratories Research Division Mitsubishi Tanabe Pharma Corporation
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Kakimoto Tetsuhiro
Advanced Medical Research Laboratories Research Division Mitsubishi Tanabe Pharma Corporation
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Fukunari Atsushi
Advanced Medical Research Laboratories Research Division Mitsubishi Tanabe Pharma Corporation
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Kataoka Hirotoshi
Pharmacology Research Laboratories I Research Division Mitsubishi Tanabe Pharma Corporation
関連論文
- FTY720 induces the sequestration of circulating lymphocytes into the bone marrow in alymphoplasia mice
- Fingolimod (FTY720) ameliorates experimental autoimmune encephalomyelitis (EAE) (2) FTY720 decreases infiltration of Th17 and Th1 cells into the central nervous system in EAE
- Sphingosine 1-phosphate receptor modulator, fingolimod (FTY720), provides a new therapeutic approach for autoimmune diseases
- Sphingosine 1-phosphate receptor type 1 as a novel target for the therapy of autoimmune diseases
- Fingolimod (FTY720) ameliorates experimental autoimmune encephalomyelitis (EAE) : II. FTY720 decreases infiltration of Th17 and Th1 cells into the central nervous system in EAE
- Fingolimod (FTY720) ameliorates experimental autoimmune encephalomyelitis (EAE) : I. Oral administration of FTY720 effectively inhibits relapse of EAE
- Sphingosine 1-phosphate receptor modulator, fingolimod (FTY720), provides a new therapeutic approach for autoimmune diseases
- Sphingosine 1-phosphate receptor type 1 regulates egress of mature T cells from mouse bone marrow