Titlebook: Chemical Relaxation in Molecular Biology; Israel Pecht,Rudolf Rigler Book 1977 Springer-Verlag Berlin · Heidelberg 1977 Molekularbiologie.

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Structural Dynamics of tRNA A Fluorescence Relaxation Study of tRNA yeast Phe,nd UHLENBECK, 197 3) and the anticodon-loop (UHLENBECK, 1972; EISINGER and SPAHR, 1973) which are not accessible in the crystal lattice. Studies of the solution structure of tRNA applying spectroscopic techniques such as low-angle X-ray diffraction (KRIGBAUM and GOODWIN, 1966; CONNORS et al., 1969;

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Kinetics of Antibody-Hapten Interactions,ed heterogeneity found in their primary structure. This heterogeneity is confined, however, to the first 110 N-terminal residues of the two chains (variable region) and expresses the diversity of the antigen combining site. Certain stretches in the variable region were found to exhibit higher variab

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Book 1977t which ions can interact and form structures differing in volume from the non interacting species. The step from this experimental observation and its correct, non­ trivial explanation to the discovery that all fast chemical pro­ cesses must reveal themselves quantitatively in the relaxation rate o

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Basic MIP and Fixed Cost Flow Modelstion have been extensively discussed in literature. It is the aim of this chapter to summarize the theoretical approach and to provide a computer program for the simulation of relaxation kinetic progress curves.

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Mixed Integer Programming Algorithms-ing, as it were, excessively modest: their lack of suitable spec-tral and magnetic properties has made it necessary to resort to such techniques as atomic absorption spectroscopy to detect them at all and no reliable method has yet been found for character-ising their immediate environment when the

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0077-0221 ion and its correct, non­ trivial explanation to the discovery that all fast chemical pro­ cesses must reveal themselves quantitatively in the relaxation rate o978-3-642-81119-7978-3-642-81117-3Series ISSN 0077-0221

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https://doi.org/10.1007/0-387-33477-7Proton transfer reactions in principle belong to the simplest possible chemical processes, since only a naked proton is exchanged between the two molecules concerned.