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Louis, MO, 99%) was dissolved in 20 ml of distilled water (Milli-Q purification, Millipore, Bedford, MA)
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Protein stability in mixed solvents: A balance of contact interactions and excluded volume
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Direct demonstration of structural similarity between native and denatured eglin C
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We have undertaken an extensive description of the structures and conformational stabilities of the PTS proteins of S
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The three cubes in the image indicate the actual position and width selected for the recording of localized spectra from isotropic voxels of (180 µm)^sup 3^ in each compartment
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6 ms and δ = 450 µs is significantly above zero
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5) or 40 mM Na-acetate (pH 3
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5 A, we present results showing that the affinity between CPM-PLCβ and Gβγ at atmospheric pressure on lipid membranes is strong and matches the K^sub d^(app) (i
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semifasciata has a quadrangulate anterior end and a margin almost straight, whereas the margin of the dentary in P
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These findings strongly suggest that the method developed in this study is useful for identifying P
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) Unknown May '97 japonicaTable 3Reactivity of monoclonal antibodies to fish eggs
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Identification of eggs and hatched larvae
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[FIGURES 1-2 OMITTED]On examination in our clinic, the patient indicated that she had mild bifrontal headache and nasal congestion
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Connect Tissue Res 1982:9:247-8
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Pharmacy gears up for Medicaid budget battleJames FrederickALEXANDRIA, Va
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"Author Carlson of Fotodynamics thanks the following for their assistance with this article: LTCOL Keith Danel; CDRs Jeff Danielson, John Fleming, John Treutler; LCDRs John Gallegro, Colin Smith; MAJs Tony Archer, Victor Argobright, John Selby; Mr
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.Thus, the effective size of the monocation in compact DNA is expected to be closer to the size of free ion without hydration shell, where the sequence of the monocation radius is Li+ CONCLUSIONOur investigation highlights the inverse relation between DNA compaction potentials of monovalent cations in a crowded environment and the previously reported DNA binding properties of different alkali ions
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., ≤1 kbar), we find that the volume change of PLCβ-Gβγ association is reduced
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.To confirm that our labeled ribozyme constructs are active in cleavage, we performed activity assays using a cleavable all-RNA substrate strand, as described in the Materials and Methods section
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