主要論文
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Koga S, Hozumi K, Hirano KI, Yazawa M3, Terooatea T, Minoda A, Nagasawa T, Koyasu S, Moro K. Peripheral PDGFRα+gp38+ mesenchymal cells support the differentiation of fetal liver-derived ILC2. J. Exp. Med. 215: 1609-1626, 2018.
[PUB MED]
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Hirano K, Negishi N, Yazawa M, Yagita H, Habu S and Hozumi K*. Delta-like 4-mediated Notch signaling is required for early T cell development in a three-dimensional thymic structure. Eur J Immunol. 45: 2252-2262, 2015. (*corresponding)
[PUB MED]
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Nakano Y, Negishi N, Gocho S, Mine T, Sakurai Y, Yazawa M, Abe K, Yagita H, Habu S, Kageyama R, Kawaguchi Y* and Hozumi K*. Disappearance of centroacinar cells in the Notch ligand-deficient pancreas. Genes Cells. 20: 500-511, 2015.
[PUB MED]
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Abe N, Hozumi K*, Hirano K, Yagita H and Habu S. Notch ligands transduce different magnitudes of signaling critical for determination of T-cell fate. Eur. J. Immunol. 40: 2608-2617, 2010.
[PUB MED]
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Hozumi K*, Mailhos C, Negishi N, Hirano K, Yahata T, Ando K, Zuklys S, Holländer GA, Shima DT and Habu S. Delta-like 4 is indispensable in thymic environment specific for T cell development. J. Exp. Med. 205: 2507-2513, 2008.
[PUB MED]
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Hozumi K*, Negishi N, Tsuchiya I, Abe N, Hirano K, Suzuki D, Yamamoto M, Engel JD and Habu S. Notch signaling is necessary for GATA3 function in the initiation of T cell development. Eur. J. Immunol. 38:977-985, 2008.
[PUB MED]
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Hozumi K, Negishi N, Suzuki D, Abe N, Sotomaru Y, Tamaoki N, Mailhos C, Ish-Horowicz D, Habu S and Owen M.J. Delta-like 1 is necessary for the generation of marginal zone B cells but not T cells in vivo. Nat. Immunol. 5: 638-644, 2004.
[PUB MED]
-
Hozumi K, Abe N, Chiba S, Hirai H and Habu S. Active form of Notch members can enforce T lymphopoiesis on lymphoid progenitors in the monolayer culture specific for B cell development. J. Immunol. 170: 4973-4979, 2003.
[PUB MED]
Koga S, Hozumi K, Hirano KI, Yazawa M3, Terooatea T, Minoda A, Nagasawa T, Koyasu S, Moro K. Peripheral PDGFRα+gp38+ mesenchymal cells support the differentiation of fetal liver-derived ILC2. J. Exp. Med. 215: 1609-1626, 2018. [PUB MED]
Hirano K, Negishi N, Yazawa M, Yagita H, Habu S and Hozumi K*. Delta-like 4-mediated Notch signaling is required for early T cell development in a three-dimensional thymic structure. Eur J Immunol. 45: 2252-2262, 2015. (*corresponding) [PUB MED]
Nakano Y, Negishi N, Gocho S, Mine T, Sakurai Y, Yazawa M, Abe K, Yagita H, Habu S, Kageyama R, Kawaguchi Y* and Hozumi K*. Disappearance of centroacinar cells in the Notch ligand-deficient pancreas. Genes Cells. 20: 500-511, 2015. [PUB MED]
Abe N, Hozumi K*, Hirano K, Yagita H and Habu S. Notch ligands transduce different magnitudes of signaling critical for determination of T-cell fate. Eur. J. Immunol. 40: 2608-2617, 2010.
[PUB MED]
Hozumi K*, Mailhos C, Negishi N, Hirano K, Yahata T, Ando K, Zuklys S, Holländer GA, Shima DT and Habu S. Delta-like 4 is indispensable in thymic environment specific for T cell development. J. Exp. Med. 205: 2507-2513, 2008. [PUB MED]
Hozumi K*, Negishi N, Tsuchiya I, Abe N, Hirano K, Suzuki D, Yamamoto M, Engel JD and Habu S. Notch signaling is necessary for GATA3 function in the initiation of T cell development. Eur. J. Immunol. 38:977-985, 2008. [PUB MED]
Hozumi K, Negishi N, Suzuki D, Abe N, Sotomaru Y, Tamaoki N, Mailhos C, Ish-Horowicz D, Habu S and Owen M.J. Delta-like 1 is necessary for the generation of marginal zone B cells but not T cells in vivo. Nat. Immunol. 5: 638-644, 2004. [PUB MED]
Hozumi K, Abe N, Chiba S, Hirai H and Habu S. Active form of Notch members can enforce T lymphopoiesis on lymphoid progenitors in the monolayer culture specific for B cell development. J. Immunol. 170: 4973-4979, 2003. [PUB MED]