UDΆΩνf}EX
jKNg[X]Ϊyf(GalT-IjΉ}EX
1) Asano, M., Furukawa, K., Kido, M., Matsumoto, S., Umesaki, Y., Kochibe, N. and Iwakura, Y. Growth retardation and early death of ΐ-1,4-galactosyltransferase knockout mice with augmented proliferation and abnormal differentiation of epithelial cells. EMBO J., 16,1850-1857 (1997).
2) Kido, M., Asano, M., Iwakura, Y., Ichinose, M., Miki, K., and Furukawa, K. Presence of polysialic acid and HNK-1 carbohydrate on brain glycoproteins from ΐ-1,4-galactosyltransferase-knockout mice. Biochem. Biophys. Res. Commun., 245, 860-864 (1998).
3) Kotani, N., Asano, M., Iwakura, Y., and Takasaki, S. Impaired b1, 4-galactosylation of core 2 O-glycans in erythrocytes of ΐ1, 4-galactosyl-transferase knockout mice. Biochem. Biophys. Res. Commun., 260, 94-98 (1999).
4) Kido, M., Asano, M., Iwakura, Y., Ichinose, M., Miki, K., and Furukawa, K. Normal levels of serum glycoproteins maintained in ΐ-1, 4-galactosyltransferase I-knockout mice. FEBS Letters, 464, 75-79 (1999).
5) Kido, M., Asano, M., Iwakura, Y., Ichinose, M., Miki, K., and Furukawa, K. Presence of a higher molecular weight ΐ-1, 4-galactosyltransferase in mouse liver. Acta Histochem. Cytochem., 33, 215-221 (2000).
6) Kotani, N., Asano, M., Iwakura, Y., and Takasaki, S. Knockout of mouse ΐ1,4-galactosyltransferase-1 gene results in a dramatic shift of outer chain moieties of N-glycans from type 2 to type 1 chains in hepatic membrane and plasma glycoproteins. Biochem J., 357, 827-834 (2001).
7) Asano, M., Nakae, S., Kotani, N., Shirafuji, N., Nambu, A., Hashimoto, N., Kawashima, H., Hirose, M., Miyasaka, M., Takasaki, S., and Iwakura, Y. Impaired selectin ligand biosynthesis and reduced inflammatory responses in ΐ-1,4-galactosyltransferase-I-deficient mice. Blood, 102, 1678-1685 (2003).
8) Kotani, N., Asano, M., Inoue, N., Iwakura, Y., and Takasaki, S. Polylactosamine synthesis and branch formation of N-glycans in ΐ1,4-galactosyltransferase-1-deficient mice. Arch. Biochem. Biophys., 426, 258-265 (2004).
jEph A2 Ή}EX
1) Naruse-Nakajima, C., Asano, M., and Iwakura, Y. Involvement of EphA2 in the formation of the tail notochord via interaction with ephrinA1. Mecha. Develop., 102, 95-105 (2001).
2) Irie, N., Takada, Y., Watanabe, Y., Matsuzaki, Y., Naruse, C., Asano, M., Iwakura, Y., Suda, T., and Matsuo, K. Bidirectional signaling through ephrinA2-EphA2 enhances osteoclastogenesis and suppresses osteoblastogenesis. J. Biol. Chem., 284, 14637-14644 (2009).
jSix-SΉ}EX
1) Ozaki, H., Watanabe, Y., Takahashi, K., Kitamura, K., Tanaka, A., Urase, K., Momoi., T., Sudo, K., Sakagami, J., Asano, M., Iwakura, Y., and Kawakami, K. Six-4, a putative myogenin gene regulator, is not essential for mouse embryonal development. Mol. Cell. Biol., 21, 3343-3350 (2001).
jMeltrinΏΉ}EX
1) Kurisaki, T., Masuda, A., Sudo, K., Sakagami, J., Higashiyama, S., Matsuda, Y., Nagabukuro, A., Nabeshima, Y., Asano, M., Iwakura, Y. and Sehara-Fujisawa, A. Phenotypic analysis of MeltrinΏ (ADAM12)-deficient mice: involvement of MeltrinΏ in adipogenesis and myogenesis. Mol. Cell. Biol., 23, 55-61 (2003).
jMeltrinΐΉ}EX
1) Kurohara, K., Komatsu, K., Kurisaki, T., Masuda, A., Irie, N., Asano, M., Sudo, K., Nabeshima, Y., Iwakura, Y., Sehara-Fujisawa, A. Essential roles of Meltrin ΐ (ADAM19) in heart development. Dev. Biol., 267, 14-28 (2004).
jFliceΉ}EX
1) Sakamaki, K., Inoue, T., Asano, M., Sudo, K., Kazama, H., Sakagami, J., Sakata, S., Ozaki, M., Nakamura, S., Toyokuni, S., Osumi, N., Iwakura, Y. and Yonehara, S. Ex vivo whole-embryo culture of caspase-8-deficient embryos normalize their aberrant phenotypes in the developing neural tube and heart. Cell Death Differ., 9, 1196-1206 (2002).
jSix-1Ή}EX
1) Ozaki, H., Nakamura, K., Funahashi, JI., Ikeda, K., Yamada, G., Tokano, H., Okamura, HO., Kitamura, K., Muto, S., Kotaki, H., Sudo, K., Horai, R., Iwakura, Y., and Kawakami, K. Six1 controls patterning of the mouse otic vesicle. Development, 131, 551-562 (2004).
jSix-1/Six-4Ή}EX
1) Konishi, Y., Ikeda, K., Iwakura, Y., and Kawakami, K. Six1 and Six4 promote survival of sensory neurons during early trigeminal gangliogenesis. Brain Res., 1116, 93-102 (2006).
jOvol2Ή}EX
1) Unezaki, S., Horai, R., Sudo, K., Iwakura, Y., and Ito, S. Ovol2/Movo, a homologue of Drosophila ovo, is required for angiogenesis, heart formation and placental development in mice. Genes Cells, 12, 773-785 (2007).
jcPGESΉ}EX
1) Nakatani, Y., Hokonohara, Y., Kakuta, S., Sudo, K., Iwakura, Y., and Kudo, I. Knockout mice lacking cPGES/p23, a constitutively expressed PGE2 synthetic enzyme, are peri-natally lethal. Biochem. Biophys. Res. Commun., 362, 387-392 (2007).
kjKidΉ}EX
1) Ohsugi, M., Adachi, K., Horai, R., Kakuta, S., Sudo, K., Kotaki, H., Tokai-Nishizumi, N., Sagara, H., Iwakuta, Y., and Yamamoto, T. Kid-Mediated Chromosome Compaction Ensures Proper Nuclear Envelope Formation. Cell, 132, 771-782 (2008).
ljGΐ1Ή}EX
1) Okae, H., and Iwakura, Y. Neural tube defects and impaired neural progenitor cell proliferation in Gΐ1-deficient mice. Dev. Dyn., 239, 1089-1101 (2010).