Authors:
Zhang, SQ
Fukase, K
Izumi, M
Fukase, Y
Kusumoto, S
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
Authors:
Fukase, Y
Zhang, SQ
Iseki, K
Oikawa, M
Fukase, K
Kusumoto, S
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
Authors:
Fukase, K
Kirikae, T
Kirikae, F
Liu, WC
Oikawa, M
Suda, Y
Kurosawa, M
Fukase, Y
Yoshizaki, H
Kusumoto, S
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:
Fukase, K
Oikawa, M
Suda, Y
Liu, WC
Fukase, Y
Shintaku, T
Sekljic, H
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
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
Authors:
Endo, M
Shinbori, N
Fukase, Y
Sawada, N
Ishikawa, T
Ishitsuka, H
Tanaka, Y
Citation: M. Endo et al., Induction of thymidine phosphorylase expression and enhancement of efficacy of capecitabine or 5 '-deoxy-5-fluorouridine by cyclophosphamide in mammary tumor models, INT J CANC, 83(1), 1999, pp. 127-134