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1 lectivity sequence of Cl(-) > I(-) > Br(-) > gluconate(-).
2 n is severely limited by large anions (i.e., gluconate).
3 complex combinations thereof (l-arabinose, d-gluconate).
4 ility sequence: SCN- > I- > Br- > Cl- > F- > gluconate-.
5 al Na(+) with NMDG and by internal F(-) with gluconate.
6 ronate but grows normally on glucuronate and gluconate.
7 a hypertonic solution in which the anion was gluconate.
8 aspartate increased quantal size similar to gluconate.
9 ng cells was SCN(-) > I(-) > Br(-) > Cl(-) > gluconate.
10 paracellular pathway is limited by the anion gluconate.
11 e activity, but there was less activity with gluconate.
12 that were still able to oxidize glucose into gluconate.
13 SO42- were similar and about half of that in gluconate.
14 with a measured apparent Km of 6 microM for gluconate.
15 arge intestine is defined by the presence of gluconate.
16 skin cleansing protocol using chlorhexidine gluconate.
17 calcium lactate pentahydrate instead of zinc gluconate.
18 hydrolysed by TM0413 (IolN) to form 5-keto-l-gluconate.
19 ntly 6 hours after administration of calcium gluconate.
20 loz1Delta cells accumulate higher levels of gluconate.
22 y assigned to no iron (control) or to ferric gluconate 125 mg intravenously with eight consecutive he
24 e randomly assigned to receive either ferric gluconate 187.5 mg intravenously (IV) every 3 weeks, ora
25 nt stereo-specific reduction of 2,5-diketo-d-gluconate (2,5-DKG) to 2-keto-l-gulonate, a precursor in
27 dextran was 3.6 (95% CI, 2.4-5.4); for iron gluconate, 2.0 (95% CI 1.2, 3.5); and for ferumoxytol, 2
28 /mL, respectively; and with 2% chlorhexidine gluconate, 2.1 (2.0-2.3), 1.8 (1.5-2.0), and 1.7 (1.5-1.
31 nate, modestly induced by very low levels of gluconate (4 microM), and partially catabolite repressed
33 hat includes 118 mL of aqueous chlorhexidine gluconate, 4%, per shower; a minimum of 2 sequential sho
34 g the preadmission shower with chlorhexidine gluconate, 4%, resulting in maximal, persistent skin ant
35 olunteers were randomized to 2 chlorhexidine gluconate, 4%, showering groups (2 vs 3 showers), contai
37 ing a precise dose (volume) of chlorhexidine gluconate, 4%; duration (number of showers); and timing
39 The L-idonate 5-dehydrogenase and 5-keto-D-gluconate 5-reductase reactions were characterized both
40 encodes L-idonate 5-dehydrogenase, 5-keto-D-gluconate 5-reductase, an L-idonate transporter, and an
41 ive pentose phosphate pathway, gnd (encoding gluconate 6-phosphate [6-P] dehydrogenase) or zwf (encod
42 e complexed with the competitive inhibitor D-gluconate 6-phosphate by X-ray crystallography at 2.5 A
45 zation was the redistribution of 6-phospho-D-gluconate (6-PG) between the Entner-Doudoroff pathway an
46 nd showed that the Crc-regulated edd mutant (gluconate-6-phosphate dehydratase) had similar gluconate
47 ternal solutions containing CH(3)SO(3)(-) or gluconate, a replacement of the Ca(2+) with Mg(2+) reduc
48 Patients rinsed with 0.12% chlorhexidine gluconate after debridement, and twice daily, for 2 week
50 al mouthrinses containing 0.2% chlorhexidine gluconate, an herbal mouthwash, and water in reducing th
51 ng of GntR to the operators is eliminated by gluconate and also by 6-phosphogluconate at a 10-fold-hi
52 , calcium chloride, calcium lactate, calcium gluconate and calcium lactobionate, on the physico-chemi
53 eads to the induction of genes involved with gluconate and formate metabolism and represses genes req
56 ive, while expression of gntKU is induced by gluconate and is subject to fourfold glucose catabolite
65 r the substrate analogue 6-phospho-2-deoxy-D-gluconate and suggest targets for anti-parasite drug des
66 , these results implicate the utilization of gluconate and the Entner-Doudoroff pathway as important
67 f antifungal agents (cinnamon bark oil, zinc gluconate and trans-ferulic acid) in oil-in-water emulsi
70 ran IV iron products combined (iron sucrose, gluconate, and ferumoxytol) (95% CI, 20.0-29.5 per 100,0
73 athing all patients daily with chlorhexidine gluconate; and healthcare-worker education and adherence
77 > SO4(2-) approximately HCO3- approximately gluconate- approximately aspartate- approximately cyclam
78 e in the ED pathway grows poorly not only on gluconate as a sole carbon source but on a number of oth
79 n defined media with d-gluconate or 2-keto-d-gluconate as a sole carbon source, revealing that glucon
80 suggest that the ability of C. jejuni to use gluconate as an electron donor via GADH activity is an i
84 ] and French fries (40 mEq K) with potassium gluconate at the same doses when added to a basal diet t
86 and personnel cohorting; daily chlorhexidine gluconate baths; dedicating equipment to be used solely
87 enase, catalyzes the oxidation of glucose to gluconate, but has been shown to have activity with a br
90 ot CF, epithelia, replacing mucosal Cl- with gluconate caused intracellular pH (pHi) to increase, and
91 intraperitoneal injections of chlorhexidine gluconate (CG) in mice with type I pro-collagen promoter
92 oneal MCs to myofibroblasts in chlorhexidine gluconate (CG)-induced fibrosis compared with that of ph
93 d tested for susceptibility to chlorhexidine gluconate (CHG) by microtiter dilution; mupirocin suscep
94 ssess whether daily bathing in chlorhexidine gluconate (CHG) compared with standard bathing practices
95 5 days and to bathe daily with chlorhexidine-gluconate (CHG) for up to 5 days before their operations
96 pecies oral biofilms following chlorhexidine gluconate (CHX) and CHX with surface modifiers (CHX-Plus
98 ed with discontinuation of the chlorhexidine gluconate-containing dressings, local wound care, and al
99 tage-clamp recordings with KCl- or potassium gluconate-containing electrodes, bath-applied NA increas
102 nt with cardiac glycosides in the hypertonic gluconate-containing solutions hitherto reported to emph
103 ume and in vitro concentrations of GM within gluconate-containing solutions of infused Plasma-Lyte.
104 hibian skeletal muscle fibres studied in the gluconate-containing solutions previously reported to em
105 bian muscle fibres studied in the hypertonic gluconate-containing solutions that were hitherto report
106 tant for colonization, including L-fucose, D-gluconate, D-glucuronate, N-acetyl-D-glucosamine, D-mann
107 mutants, and the activity of the Fe-S enzyme gluconate dehydratase is diminished in the suf mutant du
108 the presence of Mg2+ and the 2-keto-3-keto-d-gluconate dehydration product; the structure of the cata
109 proteins, Cj0414 and Cj0415, orthologous to gluconate dehydrogenase (GADH) from Pectobacterium cypri
111 f deuterium 3 relative to deuterium 2 in the gluconate derivative as quantitated by (2)H NMR was show
113 that replacement of extracellular Cl(-) with gluconate(-) diminishes the inward tail current (Cl(-) e
114 th either soap and water or 2% chlorhexidine gluconate eliminated 1.5 to 2.0 log10 CFUs/mL of B atrop
116 90% of the consumed sugar was converted into gluconate, entering central carbon metabolism as 6-phosp
119 d >98% by treatment in vitro with 50 mM zinc gluconate for 2 h and nine were inactivated >97% by trea
121 sed the safety and efficacy of chlorhexidine gluconate for cutaneous antisepsis and silver alginate-i
122 mportant for growth on low concentrations of gluconate, for entry into the logarithmic phase, and for
123 sodium gluconate-containing solution but not gluconate-free Plasma-Lyte resulted in positive serum GM
125 w that Eda synthesis is induced by growth on gluconate, glucuronate, or methyl-beta-D-glucuronide; ph
126 In the presence of the impermeant anion gluconate, glutamate pulses activated smaller currents p
127 zinc may be an effective treatment, and zinc gluconate glycine (ZGG) lozenges have been shown to redu
128 nal mutation resulted in the partial loss of gluconate (gnt) and xylose (xyl) operon catabolite repre
129 more serious adverse events than the ferric gluconate group (incidence rate ratio = 1.73, P = 0.041)
130 e end of observation, patients in the ferric gluconate group required significantly less epoetin than
131 erritin levels remained higher in the ferric gluconate group than in the control group (P = 0.062, P
132 esponding metabolic lesions on colonization: gluconate > N-acetylglucosamine > N-acetylneuraminic aci
134 tion of Cl- by the larger (impermeant) anion gluconate had no effect on the reversal potential of SV
137 patients each to receive 0.2% chlorhexidine gluconate, herbal mouthwash, and water, respectively, as
138 cts of three test agents, 0.2% chlorhexidine gluconate, honey mouthwash, and saline, against six oral
139 sible reduction of 5-ketogluconate to form D-gluconate; IdnK catalyzes an ATP-dependent phosphorylati
142 ange of this adverse effect of chlorhexidine gluconate-impregnated dressings in critically ill patien
144 oup), a standard catheter plus chlorhexidine-gluconate-impregnated sponge (chlorhexidine-gluconate-im
145 ence was observed between the chlorhexidine- gluconate-impregnated sponge group and the standard grou
146 -gluconate-impregnated sponge (chlorhexidine-gluconate-impregnated sponge group), or an Oligon cathet
147 the standard-group, 150 in the chlorhexidine-gluconate-impregnated sponge group, and 159 in the Oligo
148 ard catheters, 21 (14%) in the chlorhexidine-gluconate-impregnated sponge group, and 25 (15.7%) in th
149 ard catheters, six (4%) in the chlorhexidine-gluconate-impregnated sponge group, and seven (4.4%) in
152 external Ba2+ or by replacement of potassium gluconate in the electrode solution with caesium acetate
155 tropic anion thiocyanate was substituted for gluconate in the whole-cell recording pipette, consisten
156 supply of a readily metabolized sugar, i.e., gluconate, in the animal's drinking water, the competiti
157 ences in the regulatory regions of all known gluconate-inducible genes, and these seven putative gnt
159 -100 mV due to the lowered outward current (gluconate(-) influx) at membrane potential of 100 mV.
160 can be inhibited by zinc, we found that zinc gluconate inhibited potassium efflux from RBC exposed to
169 ranscript (kdgK1) levels of 2-keto-3-deoxy-D-gluconate kinase (KDGK), a key enzyme of haloarchaeal gl
170 In this shunt glucose dehydrogenase and gluconate kinase catalyze the two-step conversion of glu
172 gntU, which code for a regulatory protein, a gluconate kinase, and a gluconate transporter, respectiv
173 y: the idnK gene, encoding a thermosensitive gluconate kinase, is monocistronic and transcribed diver
178 f recombinant Gcd1 in vitro and by measuring gluconate levels in strains lacking enzymes of the gluco
179 .009 and 0.011 vs. 0.006 mM, P = 0.036), and gluconate levels were also significantly different betwe
180 es accumulated and secreted large amounts of gluconate, likely derived from labile 6-phosphogluconola
185 (EGTA) and the potassium salts of aspartate, gluconate, methylsulfate and monobasic phosphate increas
186 that gntT is maximally induced by 500 microM gluconate, modestly induced by very low levels of glucon
190 nalysis of GntU indicates an apparent Km for gluconate of 212 microM, indicating that this is a low-a
191 ther the possible beneficial effects of zinc gluconate on cold symptoms outweigh the possible adverse
192 ospitals must maintain intravenous quinidine gluconate on formulary because it is the only drug avail
194 Neither strain grew in defined media with d-gluconate or 2-keto-d-gluconate as a sole carbon source,
195 x mutants were found to be unable to oxidize gluconate or 2-ketogluconate, resulting in an inability
196 'impermeant' anion, such as SO42-, CH3SO3-, gluconate or glutamate, greatly reduced the calcium-depe
199 nge of 6.1 to 7.6 since inactivation by zinc gluconate or zinc lactate in that pH range was 99.7 to 1
200 3 ml of sterile saline, 0.12% chlorhexidine gluconate, or 0.1% phosphate-buffered chlorine dioxide m
201 ashing with soap and water, 2% chlorhexidine gluconate, or chlorine-containing towels reduced the amo
204 urrent when the external Cl- was replaced by gluconate (permeability ratio P(gluconate)/PCl = 0.17).
208 were randomly assigned to Ca/Mg (1g calcium gluconate plus 1g magnesium sulfate pre- and post-oxalip
209 aining 61% ethyl alcohol, a 2% chlorhexidine gluconate preparation, and an antibacterial microfiber t
210 ages, substitution of extracellular Cl- with gluconate produced a 10-fold increase in the rate and ex
211 ol intermediate to yield the 2-keto-3-keto-d-gluconate product with the observed retention of configu
212 phic DNA (RAPD) type-specific differences in gluconate production, which were associated significantl
214 acid dehydrogenase) and b0207 (2,5-diketo-D-gluconate reductase B), is assigned to 15 of those react
217 on-gamma (IFN-gamma; n = 9), sodium antimony gluconate (SAG; n = 8), or amphotericin B lipid complex
219 ate levels in strains lacking enzymes of the gluconate shunt we demonstrate that Gcd1 encodes a novel
221 The safety and efficacy of chlorhexidine gluconate, silver alginate, and antibiotic-coated cathet
222 effect by measuring responses to NaCl and Na-gluconate (small and large anion sodium salts, respectiv
223 hird larger than those in a CH(3)SO(3)(-) or gluconate solution, whereas the values in the CH(3)SO(3)
224 whereas the values in the CH(3)SO(3)(-) and gluconate solutions had no statistically significant dif
225 0.50, 1.00 and 1.50)molkg(-1) aqueous sodium gluconate solutions over a temperature range of (288.15-
227 , 40, and 60 mEq K/d consumed as a potassium gluconate supplement or as unfried potato or 40 mEq K fr
229 microg/cm2) concentrations of chlorhexidine gluconate that are sufficient to inhibit or kill gram-po
230 activity, converting d-gluconate to 2-keto-d-gluconate, that was higher at 42 degrees C than at 37 de
231 eletion strains are grown in the presence of gluconate, there is a twofold decrease in gntT expressio
232 176 demonstrated GADH activity, converting d-gluconate to 2-keto-d-gluconate, that was higher at 42 d
235 In patients with CAA, addition of IV ferric gluconate to darbepoetin failed to provide additional be
236 alyzes an ATP-dependent phosphorylation of D-gluconate to form 6-phosphogluconate, which is metaboliz
237 onstrated the efficacy of intravenous ferric gluconate to improve hemoglobin levels in anemic hemodia
238 ented mutant E. coli strains with defects in gluconate transport and directed the formation of a high
239 sence of two systems in Escherichia coli for gluconate transport and phosphorylation is puzzling.
240 rm that gntK and gntU, together with another gluconate transport gene, gntT, constitute the GntI syst
241 nd directed the formation of a high-affinity gluconate transporter with a measured apparent Km of 6 m
242 egulatory protein, a gluconate kinase, and a gluconate transporter, respectively, were cloned from Es
245 u kinetic studies reveal that the rates of 6-gluconate turnover are indistinguishable in samples from
247 e oxidase that generates the 2-amino-2-deoxy-gluconate unit from a glucosamine-containing precursor i
248 t gene, gntT, constitute the GntI system for gluconate utilization, under control of the gntR gene pr
253 ted with hypertonic solution in which sodium gluconate was the major constituent, which substantially
254 nate as a sole carbon source, revealing that gluconate was used as an electron donor rather than as a
255 -glucamine (NMDG) and of Cl- with sulfate or gluconate was used to evaluate the contribution that the
256 tion of 1% sodium alginate plus 0.3% calcium gluconate, was administered by selective injection throu
257 decontamination protocol using chlorhexidine gluconate washcloths and intranasal antiseptic ointment
259 Skin surface concentrations of chlorhexidine gluconate were analyzed using colorimetric assay at 5 se
260 e to utilize glucuronate, galacturonate, and gluconate) were constructed by insertional mutagenesis.
262 lasma glucose was enzymatically converted to gluconate, which displays fully resolved deuterium 2 and
263 is initiated by the oxidation of glucose to gluconate, which is followed by further oxidation of glu
264 s-enediol(ate) intermediate than 6-phospho-D-gluconate, which was used in a previously reported cryst
265 n) treatments of selected isolates with zinc gluconate, zinc lactate, zinc acetate, or zinc sulfate y
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