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2 of the surface of the antigens.
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(d) Matsui, J.; Kaneko, A.; Miyoshi, Y.; Yokoyama, K.; Tamiya, E.; Takeuchi, T. Anal. Lett. 1996, 29, 2071.
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0026250885
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In solid, cholesterol forms 1:3 complex with β-CyD: Claudy, P.; Letoffe, J. M.; Germain, P.; Bastide, J. P.; Bayol, A.; Blasquez, S.; Rao, R. C.; Gonzalez, B. J. Therm. Anal. 1991, 37, 2497.
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Other steroid receptors: (a) Wallimann, P.; Marti, T.; Furer, A.; Diederich, F. Chem. Rev. 1997, 97, 1567.
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Murakami, Y.1
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25
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0032480502
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After our preliminary communication (ref 1) was published, β-CyD carrying acrylic residues was polymerized in the presence of cholesterol, and the cholesterol binding by the polymer was reported (Sreenivasan, K. J. Appl. Polym. Sci. 1998, 70, 15). However, this study is entirely different from ours in that the polymerization was carried out in chloroform where CyD inclusion complexes are not formed (see ref 4).
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Sreenivasan, K.1
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27
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0032212210
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The polymers, prepared by molecular-imprinting technique, have been widely used for column separation: Haupt, K.; Mosbach, K. Trends Biotechnol. 1998, 16, 468 and references therein.
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Haupt, K.1
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28
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0345684542
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note
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The present arguments never rule out the possibility that other β-CyD residues in the polymers make subsidiary roles in the molecular recognition. Connection of these two β-CyDs by two (or more) TDI molecules is also plausible.
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29
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0000709062
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Cooperative binding of peptides by dimeric CyDs was reported: (a) Breslow, R.; Yang, Z.; Ching, R.; Trojandt, G.; Odobel, F. J. Am. Chem. Soc. 1998, 120, 3536.
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Breslow, R.1
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0029782398
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Maletic, M.1
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31
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0344389981
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note
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The hydrogen bonding of the urethane linkages, derived from the diisocyanates, does not play a significant role in the guest binding. Thus, the dextran cross-linked by hexamethylene diisocyanate showed no guest-binding activity.
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32
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0001767982
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Oakenfull, D. G.; Pearce, R. J.; Sidhu, G. S. Aust. J. Diary Technol. 1991, 46, 110.
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