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These statements have not been evaluated by the Food and Drug Administration
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With this caveat in mind, we assert that both the scaling exponent v and the intercept R^sub o^ calculated in the EV limit show statistically significant agreement with estimates from SAXS data (11)
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The first regime 0 ≤ q 0
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org--California Dairy Research Foundation site on bioactives and probioticsReferences:(1) Baer DJ, et al
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Apohorseradish peroxidase unfolding and refolding: intrinsic tryptophan fluorescence studies
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, changes in low-frequency modes leading to variations in MSDs below the sensitivity of our technique)
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In conclusion, residues with fast exchange can be identified from the combination of R^sub ex^ and ΔR^sub ex^ using either the fast exchange equations or the general fast/slow exchange equations derived by Ishima and Torchia (34)
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The CD data of the apoA-1-, apoA-2-, and apoC-1-containing disks recorded in a T-jump from 25 to 85°C indicate that the unfolding is slowest for apoA-1 and fastest for apoC-1 (Fig
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5 µm) and approximately three times more abundant (25 particles at 60°C versus 71 at 70°C particles per surface unit)
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The "diffusion-collision" approach, on the other hand, is supported by strong experimental evidence that folding rates are controlled by the rate of diffusion of pieces of the open coil in their search for favorable contacts, rather than a driven collapse along some continuous energy surface (Jacob et al
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Its yolk sac was small and the single oil globule was located on the anterior part of the yolk mass
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All ANCOVA analyses were conducted by using multiple linear regression with the function lm in S-PLUS 2000 (MathSoft, Inc
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The fluorescence emission was collected using the same objective, separated from the excitation light using a dichroic filter (540 DRLP, Omega Optical, Brattleboro, VT), spatially filtered using a 100-µ pinhole, and separated into donor and acceptor components using a second dichroic filter (630 DRLP, Omega Optical)
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The samples were analysed using a microplate fluorimeter (Fluoroskan Ascent, LabSystems, Oxford, UK), with excitation set at 360 nm and emission monitored at 460 nm
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