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1 o date about ion-pair dynamics in biological macromolecular systems.
2 -scale computations of many-atom and complex macromolecular systems.
3  underlying cooperative phenomena in diverse macromolecular systems.
4 nd temporal resolution for a wide variety of macromolecular systems.
5 tribution and anti-tumor effect of nano- and macromolecular systems.
6 ate products inhibit further reactions, this macromolecular system allows the product to be displaced
7 des and their precursors, the development of macromolecular systems (and their applications as drug/g
8 have been used to supply mechanical force to macromolecular systems, and highlight the advantages and
9                              The behavior of macromolecular systems at different temperatures is ofte
10 mic helical superstructures of molecular and macromolecular systems by external stimuli is a challeng
11     The Type VI secretion system (T6SS) is a macromolecular system distributed in Gram-negative bacte
12         The methodology is applicable to any macromolecular system for which a convenient phenotypic
13 stem is essential for the engineering of new macromolecular systems for in vivo applications.
14               Such functional nonequilibrium macromolecular systems hold great promise for on-demand
15                         The study of complex macromolecular systems, however, requires an extensive c
16 e Carlo simulations of conformationally rich macromolecular systems in an environment that efficientl
17  structures or structural ensembles of large macromolecular systems in solution poses a challenging p
18 ctrochemical approach that can be applied to macromolecular systems lacking essential disulfide bonds
19 roxy, from within the hydrophobic domains of macromolecular systems (log P > 1.9).
20           By adding ambient occlusion, large macromolecular systems look much more natural, and the p
21                This constitutionally dynamic macromolecular system offers the possibility of harnessi
22 s are important factors in nature's delicate macromolecular systems, our quantitative analysis of the
23 evel, and application of this methodology to macromolecular systems provides a means for extending su
24 s suggest that in general positively charged macromolecular systems should show inverse Hofmeister be
25                                  However, in macromolecular systems, the role that these clusters mig
26      Enteric bacteria use a limited array of macromolecular systems to implement diverse pathogenic s
27 valuation of the binding constant in complex macromolecular systems, to be introduced in a well defin
28 us molecular mechanics applications on large macromolecular systems undergoing large conformational c
29        Conformational heterogeneity in three macromolecular systems was analyzed with MESMER, demonst
30 o effects allow new design possibilities for macromolecular systems with enhanced catalytic OER/ORR a

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