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1 l and basic pH and Asn(16)-Gly(17) rather at basic pH.
2 exchange in residues other than histidine at basic pH.
3  stable, particularly at a neutral to a more basic pH.
4 fluorimetric techniques in physiological and basic pH.
5 dation of hydroquinone to quinone by O(2) at basic pH.
6  = 7 and decreases sharply at more acidic or basic pH.
7 within a matter of hours, even at neutral to basic pH.
8 een generated in water at neutral and mildly basic pH.
9 ows the current to activate at slightly more basic pH.
10 ionality, and optimal DNA cleavage occurs at basic pH.
11  aggregation-prone in vitro, particularly at basic pH.
12 e in aqueous medium, which becomes faster at basic pH.
13 t acidic pH or by fluid phase endocytosis at basic pH.
14 ees C at acidic pH and 32 to 37 degrees C at basic pH.
15  increased beta-sheet content at neutral and basic pH.
16  was also found to be extremely sensitive to basic pH.
17  decreases by 4 kcal/mol between neutral and basic pH.
18 as increased by illumination, Zn2+ ions, and basic pH.
19  water-exchangeable proton on the protein at basic pHs.
20  (hydro)peroxo ligand of the intermediate at basic pHs.
21 nd 4.58, respectively) and under "acidic and basic" pH (2.8 and 8.0) conditions.
22 mol Blue distinguished samples with slightly basic pH (8.0) from samples with slightly acidic pH (6.5
23 4 M urea or 2 M guanidine hydrochloride) and basic pH (8.0), reduced mPrP(23-231) refolds to the nati
24      Mucilage activity was greater in weakly basic (pH 9) and weakly acidic (pH 5.5) pH.
25                                  At slightly basic pH, 9.0, scrambling of the Cys5-Cys22 disulfide bo
26  Strand invasion was efficient at neutral to basic pH, a wide range of temperatures (0-65 degrees C),
27 ignificant decreases in Cerenkov emission at basic pH and allowed the estimation of absolute pH in vi
28 deamidated spontaneously at near-neutral and basic pH and Asn(16)-Gly(17) rather at basic pH.
29  improved in shorter chain lipids, with more basic pH and low ionic strength; it is hindered by unsat
30 age activity is greatly stimulated at mildly basic pH and requires divalent cations.
31 s conditions of high ionic strength, neutral/basic pH, and low temperatures (26 degrees C) and is sti
32 d with the uptake of approximately 2 H(+) at basic pH, and this value increases with decreasing pH.
33 ediate, which is sensitive to hydroxylamine, basic pH, and treatments with ATP or ADP.
34 tion constant) of the potentiation to a more basic pH as compared with P2X(2) and revealed a substant
35                 While exposure to acidic and basic pHs, as well as iron-free medium, had no significa
36 ral pseudostationary phase in neutral pH and basic pH background electrolytes.
37 ng the sensitivity of a vma-1 null mutant to basic pH but did not correct the morphological defects.
38  with diffusion-limited complex formation at basic pH but rapid dissociation under acidic conditions.
39 eptide can form a triple helix at acidic and basic pH, but is insoluble around neutral pH.
40    Both acute barrier disruption and topical basic pH challenges accelerate reacidification of SKH2/J
41                                           At basic pH cis-12-OH-TBOH decayed quickly via hydroxide/wa
42 h with monoclonal antibodies incubated under basic pH conditions and on antibodies isolated from huma
43 generated by thermolysis of persulfate under basic pH conditions and perfluoroalkyl acid (PFAA) precu
44 cemic compounds at very acidic, neutral, and basic pH conditions in micellar electrokinetic chromatog
45                                        Under basic pH conditions, the heavy chain 220-light chain 214
46 nnulus, making it more fragile under neutral/basic pH conditions.
47 (VI) is effective under acidic, neutral, and basic pH conditions.
48 was 2-fold higher at pH 6.5-7 than at a more basic pH, consistent with the formation and transport of
49                                At neutral to basic pH, deamidation proceeds by the initial formation
50                 At 20 degrees C and slightly basic pH, derivatives 4 and 5 undergo amide cleavage wit
51 ne complexes and facilitate their release at basic pH for subsequent quantification.
52 , was increased in the presence of an inward basic pH gradient.
53                    Our results indicate that basic pH (&gt;/=8.5), low NaCl concentrations (</=50 mm), a
54                                At acidic and basic pH, however, we again observed the trimer conforma
55                                           At basic pH increasing the salt concentration reduced the T
56 lipophilic, electrically charged, and highly basic pH indicator, which is used for the readout in abs
57  unfractionated protein digest is infused at basic pH into an electrospray mass spectrometer at a flo
58 s IgG in acidic endosomes and releases it at basic pH into blood.
59 rs a strong competitive fitness advantage at basic pH, it confers a reduced advantage under neutral c
60 due to the stimulation of efflux, whereas at basic pH, it is due to the inhibition of influx.
61  reduced with increasing lipid chain length, basic pH, low salt, the incorporation of negatively char
62 le to promote water oxidation under neutral, basic (pH &lt; 13), and acidic conditions (pH > 1).
63 g and endocytosis occurred at acidic but not basic pH, mimicking pH-dependent uptake of IgG by FcRn.
64                               Conversely, at basic pH, NO3- uptake by NO3- and NO2(-)-induced and uni
65 endosomes and ligand release at the slightly basic pH of blood.
66 idic pH of endosomes and releases IgG at the basic pH of blood.
67 esicles (pH </= 6.5) and releases IgG at the basic pH of the bloodstream (pH approximately 7.4).
68 sicles and releases IgG upon exposure to the basic pH of the bloodstream.
69 inding events, respectively, at the slightly basic pH of the cell surface (pH 7.4), but undetectable
70 that soluble TfR and HFE bind tightly at the basic pH of the cell surface, but not at the acidic pH o
71   The action of A22 and MP265 is enhanced by basic pH of the culture medium.
72 e gE-gI, which binds Fcgamma at the slightly basic pH of the extracellular milieu but not at the acid
73 cs of imino proton exchange as a function of basic pH or added ammonia catalyst are used to measure t
74 ns (30 microg/ml) was rapidly inactivated at basic pH or in the presence of formate under anaerobic c
75                                      At very basic pH, PL quenching was observed independent of surfa
76 Fe(VI)) were investigated over the acidic to basic pH range.
77 The molecular dynamic study of MD3 at mildly basic pH reveals that reactive ground state conformers (
78 nalysis of peptides fractionated off-line by basic pH reversed-phase (bRP) chromatography.
79 vior is especially observable at neutral and basic pH's in water and in organic solvents like dimethy
80  not strictly associated with freezing while basic pH shifts in the core more consistently followed b
81                              From neutral to basic pH, TAML activators with H2O2 efficiently degrade
82 s found to be much higher at near neutral or basic pH than at acidic pH.
83  pH but undergoes a conformational change at basic pH that disrupts the site.
84                                      At more basic pH values (>or=9.6), however, adsorbed PDDA molecu
85  killing P. aeruginosa and S. epidermidis at basic pH values (pH = 9) compared to acidic pH values (p
86 cs was slow at low Cu(2+) concentrations and basic pH values (up to several hours), while the unquenc
87 showed increased activity rate at relatively basic pH values of 7.9 and 8.5.
88  were almost completely unquenched, while at basic pH values significant quenching (85-90%) was obser
89 on was carried out in solutions of different basic pH values to study the effect of hydrogen ion conc
90 ady-state desensitization is induced at more basic pH values, and Big Dynorphin sensitivity is enhanc
91                  At both acidic and slightly basic pH values, PfAPP efficiently hydrolyzed the amino-
92 etention of chitinase activity at acidic and basic pH values.
93 ing a homogeneous negative charge density at basic pH were initially coated with a two-domain recombi
94 The reducing capacity of FeS was greatest at basic pH where surface-mediated FeS oxidation dominated.
95 in water, at room temperature, and at mildly basic pH, which makes them a suitable platform for furth
96 ores predominantly to multimer or monomer at basic pH with or without Ca2+, respectively.

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