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1 ses, and unaffected by oxidation with sodium periodate.
2 ished by treatment of the glycopeptides with periodate.
3 ith hydrogen peroxide, air oxygen, or dilute periodate.
4  to o-aminophenols in the presence of sodium periodate.
5 s secondary alcohols, at specified levels of periodate.
6 hloride and subsequent oxidation with sodium periodate.
7 were subjected to oxidation by tyrosinase or periodate.
8 atment of T. vaginalis with metronidazole or periodate abolished the adhesion of parasites to cell mo
9 of binding to MAb 1B5 whereas treatment with periodate abolished this binding, suggesting the presenc
10 oelectric point of 4.2-4.6, and was shown by periodate acid Schiff's staining to be glycosylated.
11                                Additionally, periodate activation of CPS often gives rise to heteroge
12 as highly selective fluorescence sensors for periodate amongst a set of different anions.
13 elective interaction of peanut proteins with periodate amongst chloride, sulphate, iodide, phosphate,
14 s abolished by pretreatment of sections with periodate and in the presence of excess sialic acid or l
15 etected by oxidization of carbohydrates with periodate and labeling with hydrazide-conjugated digoxig
16 face area, depending on the concentration of periodate and length of the reaction time.
17 chment of terminal glycerol for oxidation by periodate and reaction of the resulting aldehyde with am
18 reated Arabidopsis thaliana RNA samples with periodate and then performed tRNA-seq to distinguish bet
19 harides were isolated, oxidized using sodium periodate, and conjugated to CRM197 by reductive aminati
20 mmediately fixed in paraformaldehyde, sodium periodate, and lysine (PLP); (2) some were stored at 4 d
21                                      HA with periodate- and neuraminidase-treated RBCs indicated that
22 hlorite, hydrogen peroxide, ozone and sodium periodate, are described in this review.
23 e couplings with anilines in the presence of periodate as oxidant.
24 M 3 binding when specimens were treated with periodate at high pH, which specifically destroys NeuPSA
25                                            A periodate based oxidation was performed for an AHB-based
26 urface-displayed mannan by acid treatment of periodate-borohydride cells exposes glucan.
27 nnan-dependent resistance can be overcome by periodate-borohydride conversion of mannose polysacchari
28 charides to polyalcohols; cells treated with periodate-borohydride initiate the alternative pathway w
29                   Pretreatment of mucin with periodate but not with pronase reduced adherence.
30 posure of C. pneumoniae elementary bodies to periodate, but not elevated temperatures, inhibited chol
31 d be demonstrated that iodate is oxidized to periodate by a CuO-activated hypohalous acid, which is a
32 amine oxidized with one equivalent of sodium periodate causes a concentration-dependent inactivation
33 groups was prepared using sub-stoichiometric periodate/cis-diol molar ratios.
34 oretic methods and by controlled cleavage at periodate-cleavable moieties incorporated during synthes
35 oretic methods and by controlled cleavage at periodate-cleavable moieties incorporated during synthes
36  D(3) by comigration on two HPLC systems and periodate cleavage reaction.
37             Comigration on two HPLC systems, periodate cleavage reactions, and NaBH4 reduction establ
38                  We found that low levels of periodate, commonly used to oxidize specifically termina
39                                           No periodate could be measured in filtered solutions becaus
40 oprotein P by N-glycosidase assay and by the periodate-dansylhydrazine test, which indicated no detec
41                          We term this method periodate-dependent analysis of queuosine and sulfur mod
42 , oxidation of the mucin glycans in pLL with periodate did not abrogate the effects on cells.
43 d oxidation with hydrogen peroxide or sodium periodate (i.e., the phenylselenocysteine side chain is
44                   Treatment with sodium meta-periodate impaired this immunostimulatory activity, indi
45 roduct 4 was oxidatively cleaved with sodium periodate in the presence of methylamine.
46 bilizes developing charge on both sulfur and periodate in the transition state via cation-pi and elec
47               It is sensitive to pronase and periodate, indicating that it is likely a glycoprotein.
48 ut were susceptible to treatment with sodium periodate, indicating that the antigen inducing opsonic
49  Using mildly basic reaction conditions, the periodate-induced diol cleavage of meso-tetraphenyl-2,3-
50                 Second, we demonstrated that periodate-induced DOPA-protein cross-linking could be ca
51                                  The protein periodate interactions have also resulted in a simultane
52 ylazo dienophiles with tetra-n-butylammonium periodate is reported.
53 ced by 3,4-dihydroxyphenylalanine (DOPA) for periodate-mediated chemical cross-linking, and biotin wa
54               Erosion of the inner shell via periodate-mediated cleavage of the 1,2-diol bond in DHEA
55 oupled receptor (GPCR), has been analyzed by periodate-mediated cross-linking.
56                      The method involves the periodate-mediated reaction of phenylene diamine substit
57  in various concentrations of aqueous sodium periodate (NaIO(4)) for varying lengths of time.
58 s employed for this derivatization is sodium periodate (NaIO(4)) oxidation of vicinal diols found wit
59 as determined using a murine model of sodium periodate (NaIO(4))-induced peritonitis.
60 otocol that can greatly reduce the amount of periodate necessary for effective coupling.
61 xyfunctionalization of steroidal ethers with periodate or bromate as terminal oxidants in phosphate b
62  chains of cell surface Sia residues by mild periodate oxidation (known to abrogate Sia recognition b
63 ion with ethylthioacetyl chloride and sodium periodate oxidation afforded a E/Z mixture of alpha-sulf
64 two novel procedures: triethylamine-assisted periodate oxidation and acetolysis.
65                     Leveraging RNA-optimized periodate oxidation and aldehyde ligation (rPAL) and seq
66 ribe a technique termed GLIB (glucosylation, periodate oxidation and biotinylation), which combines s
67 emical modification of a standard heparin by periodate oxidation and borohydride reduction enhanced i
68 ivatives of digoxin have been synthesized by periodate oxidation and reductive amination using a vari
69 ide (2AB) labeling derivatization, including periodate oxidation and reductive amination, took only ~
70 after modification of the GalNAc residues by periodate oxidation and sodium borohydride reduction, in
71 ides were monitored for activation by sodium periodate oxidation and subsequent analysis by gas chrom
72 bstituted, peptide-linked GalNAc residues by periodate oxidation and subsequent trimming of the remai
73                                              Periodate oxidation indicates that it is the carbohydrat
74                   The lesion is released via periodate oxidation of a triol containing a vicinal diol
75 etal-dependent hydroxyquinone formation from periodate oxidation of catechol 1, suggested a rate-limi
76 yde monomer, AGEO5MA, is prepared by aqueous periodate oxidation of GEO5MA at 22 C.
77            Polyaldehyde kefiran, produced by periodate oxidation of kefiran, showed an aldehyde conte
78                                          The periodate oxidation of paralytic shellfish toxins (PSTs)
79                                         Mild periodate oxidation of sialic acids to their correspondi
80 try, frequent use is made of formaldehyde by periodate oxidation of terminal vicinal diols.
81 lboronate was achieved in part by controlled periodate oxidation of the 9,21-diol to the 21-nor-9-oxo
82 ily the exoplasmic leaflet as detected using periodate oxidation of the cell surface.
83 3) of triacylglycerol was measured following periodate oxidation of the glycerol isolated from hydrol
84                                         Mild periodate oxidation of the L-selectin ligand CD34, or L-
85 advance for assessing specificity using mild periodate oxidation of the sialic acid chain.
86                   Under the same conditions, periodate oxidation of the simple catechol 4-tert-butylc
87                                      Aqueous periodate oxidation of the terminal cis-diol units on PG
88                                  The in situ periodate oxidation of the unstable N-hydroxyphosphorami
89                                              Periodate oxidation of this lactam led directly to an al
90                        The strategy includes periodate oxidation of tryptic digests, solid-phase enri
91 pald reagent, especially in conjunction with periodate oxidation reactions.
92 l nucleic acid ribosides, such as ATP, using periodate oxidation simplifies the chromatogram and mini
93                               The results of periodate oxidation studies suggested that the product f
94 ethylated and 2'-hydroxylated nucleosides to periodate oxidation to develop Nm-seq, a sensitive metho
95                         The method uses mild periodate oxidation to generate an aldehyde on sialic ac
96 lly obtained as bench stable compounds after periodate oxidation with yields of 60-81%.
97  by labeling with biotin hydrazide following periodate oxidation, a specific and well established met
98  first approach, termed GLIB (glucosylation, periodate oxidation, biotinylation) uses a combination o
99        Here, a novel workflow combining mild periodate oxidation, hydrazide chemistry, copper-catalyz
100 l N-BocGlu, further Boc N-protection, OsO(4)-periodate oxidation, O-Me oxime formation, and RaNi-cata
101 four monokines were found to be sensitive to periodate oxidation, the TNF-alpha-stimulating activity
102 on of FT-IR, methylation and GC-MS analysis, periodate oxidation-Smith degradation, partial acid hydr
103 used as substrates for galactose oxidase and periodate oxidation.
104 nd rapidly converted to the aldehyde form by periodate oxidation.
105 (DOPA) as a protein cross-linking agent upon periodate oxidation.
106 ins, and reactivity with hydrazide following periodate oxidation.
107 ylsulfeny)acetyl chloride followed by sodium periodate oxidation.
108      Antigenicity was abolished by chemical (periodate) oxidation of gTSSA-I glycosylation but retain
109                                      Limited periodate oxidations suggested that the +258-Da modifica
110 ed tetrahydro-beta-carbolines undergo sodium periodate oxidative ring expansion in the presence of fo
111 blocked by P2X7RS-specific concentrations of periodate oxidised ATP (OxATP: 100 microM) and brilliant
112 ophages with a P2Z/P2X7 receptor antagonist, periodate oxidized adenosine 5'-triphosphate (o-ATP), su
113  receptor antagonists, including suramin and periodate oxidized ATP (oATP), resulted in a significant
114 -2',4'-disulphonic acid, Brilliant Blue G or periodate oxidized ATP dialdehyde to the site of ATP rel
115 ct of the cross-linking reaction between the periodate-oxidized AMP moiety of the tRNA and Lys207 is
116 etween aldehyde groups on the Fc moieties of periodate-oxidized antibodies and hydrazide groups on fu
117 tropic nucleotide (P2X) receptors, including periodate-oxidized ATP (oATP), attenuate a subset of end
118    In vivo short-term P2X7R targeting (using periodate-oxidized ATP [oATP]) delays islet allograft re
119 y the P2X(7) purinergic receptor antagonists periodate-oxidized ATP and pyridoxal-phosphate-6-azophen
120 ular ATP/P2X purinergic signaling pathway by periodate-oxidized ATP delayed the progression of the dy
121              Short-term P2X7R targeting with periodate-oxidized ATP promotes long-term cardiac transp
122 ed by the P2 receptor antagonists XAMR 0721, periodate-oxidized ATP, and suramin.
123 sion of IL-6 were revealed in the muscles of periodate-oxidized ATP-treated mdx mice.
124 nnective tissue growth factor, in muscles of periodate-oxidized ATP-treated mdx mice.
125 the P2X(7) receptor and that is inhibited by periodate-oxidized ATP.
126 proved humoral response over the traditional periodate-oxidized group.
127            This reagent reacted rapidly with periodate-oxidized N-terminal Ser or Thr peptides and wi
128 ted enhanced macrophage and mast cell death; periodate-oxidized-ATP (oATP)-treated macrophage and mas
129                                              Periodate oxidizes the Q-base, which results in specific
130  vivo perfusion with paraformaldehyde-lysine-periodate (PLP) and processed for light and electron mic
131                                 Furthermore, periodate reactivity of the final product signifies acqu
132 n good agreement with those from the current periodate-resorcinol method (P>0.05) thus indicating tha
133 iol (1) to Cu(II) and subsequent addition of periodate resulted in rapid formation of the TPQ-like co
134 dation but rather were obtained using sodium periodate, resulting in variable NDA yields (13-51%) fro
135                                          The periodate salts may garner widespread use in military an
136                                              Periodate sensing using different synthesized organic mo
137 ng a battery of monoclonal antibodies (MAbs) periodate-sensitive epitopes were identified on Tf190, s
138 of pneumococci with pronase E but not sodium periodate significantly reduced C1q binding.
139 ody that was serovar specific for Oag and by periodate-silver staining.
140 Using both thin-layer chromatography and the periodate-thiobarbituric acid reaction, we found that th
141                    When a 2:1 molar ratio of periodate to alditol is used, the core mannitol is cleav
142 f the sulfide derivatives were oxidized with periodate to give their corresponding sulfones.
143 ting can be miniaturized by treating it with periodate to produce higher-resolution, high-fidelity mi
144 )glycero-d-manno-heptose of LPS molecules by periodate to release formaldehyde.
145 could be generated in situ by oxidation with periodate (to avoid generation of H(2)O(2)).
146                                              Periodate-treated ehrlichiae did not induce production o
147                                              Periodate-treated parasites showed no adherence to host
148  hand, lymphocytes from mice sensitized with periodate-treated SEA did not produce any of these same
149                         Mice sensitized with periodate-treated SEA displayed a significant decrease i
150      Furthermore, sensitization of mice with periodate-treated SEA significantly reduced levels of Ag
151 ice sensitized with native SEA, but not with periodate-treated SEA, produced IL-4, IL-5, and IL-10 wh
152                            Metronidazole- or periodate-treated T. foetus showed no damage to BVEC mon
153 those containing a cP, are cleaved through a periodate treatment after phosphatase treatment; hence,
154 ective cleavage at the core mannitol by mild periodate treatment and analysis of the reaction product
155 region, which were missing from the mutants; periodate treatment and carbohydrate staining confirmed
156 s sensitive to proteinase K and resistant to periodate treatment and glycoprotein staining.
157 t treatment of E. chaffeensis had no effect, periodate treatment completely abolished the ability of
158 ees C for acid hydrolysis of PS precedes the periodate treatment in the purpald assay.
159       Heat or proteinase K treatment but not periodate treatment of E. chaffeensis abrogated the inhi
160                                              Periodate treatment of lysates of the clone confirmed th
161                                              Periodate treatment of MG2 did not affect the interactio
162   Binding of MAb 4A4-2 was inhibited by mild periodate treatment of N. caninum antigen, demonstrating
163                                              Periodate treatment of recombinant gp36 reduced the anti
164 the synthetic (nonglycosylated) peptide, and periodate treatment of the recombinant glycopeptide epit
165 nsitive to proteinase K treatment but not to periodate treatment, indicating that the cognate epitope
166 rformance liquid chromatography analysis and periodate treatment.
167 ost with proteinase K treatment but not with periodate treatment.
168                  Unexpectedly, we found that periodate-treatment also enables the detection of severa
169                          Here, we describe a periodate-treatment method that enables single base reso
170 e Man alpha(1-3)Man branch was oxidized with periodate under controlled conditions.
171                                 The adsorbed periodate was identified by scanning electron microscopy
172                            In this approach, periodate was used under mild conditions to oxidize the
173 eness of modification of sialic acid by mild periodate was verified with monoclonal antibody to sialy
174        The interactions of the proteins with periodate were also confirmed by other spectral methods
175                      However, treatment with periodate, which degrades polysaccharides, significantly
176              Further, treatment of R36A with periodate, which selectively destroys PC residues, had n

 
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