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Citation: S. Akashi et al., Human MD-2 confers on mouse Toll-like receptor 4 species-specific lipopolysaccharide recognition, INT IMMUNOL, 13(12), 2001, pp. 1595-1599
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Zhang, SQ
Fukase, K
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Citation: Sq. Zhang et al., Synthesis based on affinity separation (SAS): Separation of products having barbituric acid tag from untagged compounds by using hydrogen bond interaction, SYNLETT, (5), 2001, pp. 590-596
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Citation: Y. Fukase et al., New efficient route for synthesis of lipid A by using affinity separations(Nov, pg 1693, 2001), SYNLETT, (12), 2001, pp. 2004-2004
Citation: S. Inamura et al., Synthetic study of peptidoglycan partial structures. Synthesis of tetrasaccharide and octasaccharide fragments, TETRAHEDR L, 42(43), 2001, pp. 7613-7616
Citation: K. Fukase et al., Chemoenzymatic synthesis of a trisaccharide-serine conjugate, Gal(beta 1-3)Gal(beta 1-4)Xyl(beta 1-O)-L-Ser, use of galactosyl fluoride as a donor for transglycosylation, B CHEM S J, 74(6), 2001, pp. 1123-1128
Authors:
Fukase, K
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Citation: K. Fukase et al., Synthesis of [H-3]-labeled bioactive lipid A analogs and their use for detection of lipid A-binding proteins on murine macrophages, B CHEM S J, 74(11), 2001, pp. 2189-2197
Authors:
Gutsmann, T
Schromm, AB
Koch, MHJ
Kusumoto, S
Fukase, K
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Brandenburg, K
Citation: T. Gutsmann et al., Lipopolysaccharide-binding protein-mediated interaction of lipid A from different origin with phospholipid membranes, PHYS CHEM P, 2(20), 2000, pp. 4521-4528
Citation: K. Egusa et al., Stereoselective glycosylation and oligosaccharide synthesis on solid support using a 4-azido-3-chiorobenzyl group for temporary protection, SYNLETT, (1), 2000, pp. 27-32
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Sakai, Y
Oikawa, M
Yoshizaki, H
Ogawa, T
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Citation: Y. Sakai et al., Synthesis of Helicobacter pylori lipid A and its analogue using p-(trifluoromethyl)benzyl protecting group, TETRAHEDR L, 41(35), 2000, pp. 6843-6847
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Fukase, K
Utsumi, H
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Citation: N. Iida-tanaka et al., Conformational studies on a unique bis-sulfated glycolipid using NMR spectroscopy and molecular dynamics simulations, EUR J BIOCH, 267(23), 2000, pp. 6790-6797
Authors:
Seydel, U
Oikawa, M
Fukase, K
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Citation: U. Seydel et al., Intrinsic conformation of lipid A is responsible for agonistic and antagonistic activity, EUR J BIOCH, 267(10), 2000, pp. 3032-3039
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Seydel, U
Citation: Ab. Schromm et al., A biophysical approach towards an understanding of endotoxin-induced signal transduction, J ENDOTOX R, 5(1-2), 1999, pp. 41-45
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Fukase, K
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Yoshizaki, H
Kusumoto, S
Citation: K. Fukase et al., New synthesis and conformational analysis of lipid A: biological activity and supramolecular assembly, J ENDOTOX R, 5(1-2), 1999, pp. 46-51
Authors:
Kirikae, T
Kirikae, F
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Qureshi, N
Fukase, K
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Nakano, M
Citation: T. Kirikae et al., LPS-dependent changes in the expression of 57 kDa and 53 kDa cell membraneproteins without participation of CD14, J ENDOTOX R, 5(1-2), 1999, pp. 62-65
Authors:
Fukase, K
Nakai, Y
Egusa, K
Porco, JA
Kusumoto, S
Citation: K. Fukase et al., A novel oxidatively removable linker and its application to alpha-selective solid-phase oligosaccharide synthesis on a macroporous polystyrene support, SYNLETT, (7), 1999, pp. 1074-1078
Authors:
Kawai, Y
Nakagawa, Y
Matuyama, T
Akagawa, K
Itagawa, K
Fukase, K
Kusumoto, S
Nishijima, M
Yano, I
Citation: Y. Kawai et al., A typical bacterial ornithine-containing lipid N-alpha-(D)-[3-(hexadecanoyloxy)hexadecanoyl]ornithine is a strong stimulant for macrophages and a useful adjuvant, FEMS IM MED, 23(1), 1999, pp. 67-73
Citation: Y. Fukase et al., Propargyloxycarbonyl and propargyl groups for novel protection of amino, hydroxy, and carboxy functions, TETRAHEDR L, 40(6), 1999, pp. 1169-1170