ライフサイエンスコーパス: nonionic

1 he electrode where the reaction moieties are nonionic.

2 Comprising the nonionic 1-decanoyl-rac-glycerol and the zwitterionic la

3 ons (8.0%) was higher with ionic (9.9%) than nonionic (2.9%) contrast material (relative risk = 3.4).

4 However, the nonionic additive carriers IPA and sucrose show quality

5 trast agents decreased impedance and that of nonionic agents increased impedance.

6 ilage compared to that of similar anionic or nonionic agents, and CA4+ uptake follows Donnan equilibr

7 photeric (cocamidopropylbetaine, CAPB) and a nonionic (alcohol polyethoxylate, AE) surfactant were ch

8 In contrast, a nonionic alkyl sugar detergent resisted micelle inversio

9 At pH 4.0 (nonionic), all diastereomers have a critical micelle con

10 ) in the presence of zinc powder, aided by a nonionic amphiphile, to give the alkylated aromatic.

11 re/area isotherms of insoluble monolayers of nonionic analogues of the amphiphiles.

12 Monodisperse nonionic and cationic nanogels were produced with contro

13 One family, Series-A, is nonionic and has amide groups separating the long chains

14 -amphiphilic CPE (propylene glycol) and both nonionic and ionic amphiphilic CPEs (octyl glucoside and

15 The time-resolved uptake of 17 nonionic and ionic polar compounds (logD </= 2) with a d

16 Cross-optimization of all parameters (nonionic and ionic surfactant, chelating agent, bromate,

17 at adhesin-ligand interactions are primarily nonionic and occur through the non-heparin-binding regio

18 lization of cell bound 125I-DBP with various nonionic and zwitterionic detergents demonstrated that D

19 o the inhibitory effect on MGAT2 activities, nonionic and zwitterionic detergents led to a striking a

20 From a retrosynthetic point of view, the nonionic, anionic, cationic, and zwitterionic micelles w

21 For that purpose, we have used ionic and nonionic APols and as model proteins (i) the transmembra

22 ther, the data suggest that RNA may tolerate nonionic backbone modifications better than DNA.

23 nthesis of the commercially available strong nonionic base 1, a precursor to the title polymer-bound

24 ide prepared from the commercially available nonionic base P[MeNCH(2)CH(2)](3)N, reacts with aldehyde

25 f desilylations of silyl ethers catalyzed by nonionic bases.

26 oligocholate stayed folded in the micelle of nonionic Brij 30, in the presence or absence of NaCl.

27 Nonionic, cationic, anionic, and steroid-based detergent

28 owed NIP4;1 and NIP4;2 function as water and nonionic channels.

29 itu chemical derivatization of the otherwise nonionic cholesterol.

30 ir critical micelle concentrations, from the nonionic class (Triton X-100, Tween 20) or from the zwit

31 embrane ranged from 0.02 to 24 h(-1) for the nonionic compounds and were slower for ionic compounds (

32 y to adjust stationary-phase selectivity for nonionic compounds.

33 tivity of 350 S cm(-1), the highest reported nonionic conductivity among films made from dopant-polym

34 de, a neutral hydrophobic agent to probe for nonionic contacts, we observed that at -2, -4, and -17 t

35 after intravenous injection of gadoteridol (nonionic contrast agent; n = 6) or gadopentetate dimeglu

36 reactions to intravenous administration of a nonionic contrast material (ioversol) are rare in childr

37 subjects underwent intravenous injection of nonionic contrast material at 4 mL/sec.

38 Use of nonionic contrast material resulted in less patient moti

39 Nonionic contrast material was injected to confirm the i

40 venous bolus administration of 150-180 mL of nonionic contrast material.

41 Scan quality was better with nonionic contrast material.

42 he two gadolinium-based contrast agents: The nonionic contrast medium is better suited for evaluating

43 Average age and use of ionic versus nonionic contrast medium were identical in patients with

44 Seventeen patients had extravasation of nonionic contrast medium; seven of these had extravasati

45 Cytotoxicity was the result of ionic and nonionic Cu fractions.

46 ere readily dissociable upon the addition of nonionic detergent (0.1% Triton X-100).

47 s (bilayer interfacial area), inclusion of a nonionic detergent (C(12)E(8)), and the presence of chol

48 cause a fraction of DAH remains insoluble to nonionic detergent along with actin.

49 measured by resistance to solubilization in nonionic detergent and by copatching with a raft-residen

50 be induced to deflagellate by treatment with nonionic detergent and Ca2+.

51 etermined crystal structure solubilized by a nonionic detergent and complexed with an antibody fragme

52 The enzyme requires a nonionic detergent and divalent metal ions for activity.

53 scopic scale measured as lower solubility in nonionic detergent and in the microscopic scale evident

54 d was partially released by treatment with a nonionic detergent and reducing agent, consistent with a

55 ion of mature virions after treatment with a nonionic detergent and reducing agent.

56 fied virions occurred after treatment with a nonionic detergent and reducing agent.

57 hese differences, each mutant was soluble in nonionic detergent but unable to assemble into homomeric

58 ion of the Ca-ATPase into monomers using the nonionic detergent C(12)E(8) gave a pattern of phosphory

59 ich dissociates and loses kinase activity in nonionic detergent conditions.

60 of mannose 6-phosphate or octyl glucoside, a nonionic detergent containing a sugar group, to cocultur

61 Examination of virions after treatment with nonionic detergent demonstrated that: (i) in extracellul

62 In addition, we establish with both the nonionic detergent dodecylmaltoside and the anionic dete

63 The nonionic detergent dodecylmaltoside solubilized function

64 The receptors are resistant to extraction by nonionic detergent even after latrunculin A treatment.

65 brain, it was immunoaffinity-purified from a nonionic detergent extract of washed mouse brain membran

66 Lipid rafts were isolated after cold, nonionic detergent extraction of cells and gradient cent

67 Nonionic detergent extraction of cultured epithelial cel

68 urified virions and was largely resistant to nonionic detergent extraction, suggesting a location wit

69 supported monolayers and remains bound after nonionic detergent extraction.

70 In nonionic detergent extracts from MDCK II cells, the tigh

71 gh the extraction of the outer membrane with nonionic detergent followed by ion-exchange chromatograp

72 e-exposure to 4-nonylphenol (4-NP), a common nonionic detergent found in sewage sludge amended soils.

73 e chain oxidation is observed for TBP when a nonionic detergent is present.

74 s stimulated to a much greater extent by the nonionic detergent lauryldimethylamine oxide (LDAO) than

75 r to the fidelity when using IN derived from nonionic detergent lysates of HIV-1 virions.

76 ganic dyes that uses a reagent composed of a nonionic detergent mixed with an alcohol is described.

77 ively modulating TATA box binding by TBP and nonionic detergent modulating the interdomain interactio

78 The nonionic detergent n-dodecyl-beta-D-maltopyranoside is c

79 etergent sodium dodecyl sulfate (SDS) or the nonionic detergent n-octyl-beta-D-glucopyranoside (betaO

80 ted membranes and membranes treated with the nonionic detergent n-octyl-beta-d-glucopyranoside, sugge

81 protein was monodisperse and dimeric in the nonionic detergent n-octyl-beta-D-glucopyranoside.

82 Treatment of intact organisms with the nonionic detergent NP-40 resulted in dissolution of the

83 It was extracted from the membrane by the nonionic detergent NP-40, together with glycerophospholi

84 Escherichia coli polar lipid extract and the nonionic detergent octyl-beta-d-glucopyranoside.

85 and extracted in buffer without or with the nonionic detergent polidocanol.

86 ane-associated Type I ROPs display increased nonionic detergent solubility in pan1 mutants, suggestin

87 Addition of a nonionic detergent to CVM caused the average pore size t

88 subfraction of particulate PIKfyve resisted nonionic detergent treatment, implying association with

89 of the membrane by low concentrations of the nonionic detergent Triton X-100 (0.3%) or the mild ionic

90 omplex was not altered by treatment with the nonionic detergent Triton X-100, suggesting a lack of as

91 tion of M. tuberculosis H37Ra lysates by the nonionic detergent Triton X-114 revealed the Eis protein

92 strategy based on micelle formation with the nonionic detergent Triton X-114.

93 ins extracted from the viral membrane with a nonionic detergent were shown to conserve the a-determin

94 , Duffy, XK, and Kell readily extractable by nonionic detergent with no effect on the retention of ba

95 y pure systems that contain a bile salt or a nonionic detergent, a phosphatidylcholine or a fatty aci

96 luble molecule to one that aggregated, bound nonionic detergent, and bound to lipid vesicles, propert

97 ne tag was overexpressed, solubilized with a nonionic detergent, and purified by nickel affinity chro

98 When fresh erythrocytes are solubilized by nonionic detergent, CR1 partitions to the cytoskeleton f

99 column eluate after displacement of SDS with nonionic detergent, demonstrated by gel filtration and c

100 The nonionic detergent, digitonin, and the anionic detergent

101 oli and solubilized from cell lysates in the nonionic detergent, dodecyl maltoside.

102 nant by treating the stock suspension with a nonionic detergent, Igepal CA-630.

103 d purified using ionic detergent, LDS-P5, or nonionic detergent, OG-P5.

104 purified virions and could be extracted with nonionic detergent, suggesting membrane insertion.

105 The presence of a nonionic detergent, Triton X-100, was found essential to

106 s, we analyzed whether they partitioned into nonionic detergent-insoluble glycolipid-enriched membran

107 a in two distinct intracellular pools (i.e., nonionic detergent-soluble and detergent-insoluble pools

108 d with immature HIV-1 particles treated with nonionic detergent.

109 viral cores from particles treated with mild nonionic detergent; cores were isolated by sedimentation

110 ells and was extracted from the membranes by nonionic detergents (Triton X-100, dodecyl maltoside).

111 rmined biochemically using solubilization in nonionic detergents and by confocal microscopy.

112 ter-soluble organic dyes are also soluble in nonionic detergents and can be extracted by adding salt,

113 p235 PI 5-kinase include high sensitivity to nonionic detergents and relative resistance to wortmanni

114 ive to the presence of contaminants, such as nonionic detergents commonly found in biological samples

115 ssed in Sf9 insect cells and stabilized with nonionic detergents during purification.

116 A detailed list of compatible nonionic detergents is included, along with a protocol f

117 The effect of nonionic detergents of the n-alkyl-beta-D-glucopyranosid

118 The effects of the ionic and nonionic detergents on catalytic activity of endometase

119 Cell extraction with cold nonionic detergents or alkaline carbonate prepares an in

120 f bands around 27 kDa, and extractions using nonionic detergents or high pH conditions demonstrate th

121 hrome c oxidase (CcO), solubilized by either nonionic detergents or phospholipids, completely dimeriz

122 ing a multiwell detergent screening assay, 4 nonionic detergents out of 80 tested were found to dispe

123 On the other hand, nonionic detergents readily induced homodimers and heter

124 s are characterized by their insolubility in nonionic detergents such as Triton X-100 at 4 degrees C.

125 the critical micelle concentration (CMC) of nonionic detergents tested.

126 within certain temperature ranges, or other nonionic detergents than bilayers in the fluid phase.

127 The nonionic detergents that are typically used to achieve s

128 The nonionic detergents Triton X-100, Nonidet P-40, Brij, Tw

129 We have also found that mixing nonionic detergents with alcohols markedly reduces their

130 e outer membrane complex by a combination of nonionic detergents with reducing agents but not by the

131 nd resistance of E-cadherin to extraction by nonionic detergents, a measure for the association of th

132 Treatment of the extracts with nonionic detergents, a membrane-altering inhibitor of fa

133 embrane vesicles, it can be solubilized with nonionic detergents, and it shifts from 220 to 200 kDa u

134 In the absence of nonionic detergents, gp140 of the KNH1144 genotype, term

135 ents or heat but are relatively resistant to nonionic detergents, high salt concentrations, or exposu

136 he SC-TR assay is compatible with the use of nonionic detergents, making it more versatile than other

137 ntrolled manner with various combinations of nonionic detergents, reducing agents, and proteolytic en

138 uantify the effects that a popular series of nonionic detergents, the n-alkyl-beta-D-glucopyranosides

139 DeltaE-torsin A were readily solubilized by nonionic detergents, were similarly accessible to protea

140 ucrose gradients nor decreased solubility in nonionic detergents-hence it does not promote lipid raft

141 urea or sodium dodecyl sulfate (SDS) but not nonionic detergents.

142 C-MMOH complex is perturbed by salts but not nonionic detergents.

143 ngth but is nearly unaffected by addition of nonionic detergents.

144 ions of Triton X100, Nonidet P40 and Brij-58 nonionic detergents.

145 n Stat5bA630P in cell extracts prepared with nonionic detergents.

146 egions that are resistant to extraction with nonionic detergents.

147 ies of straight chain anionic, cationic, and nonionic detergents.

148 ains can be extracted differentially by cold nonionic detergents.

149 sucrose density gradients and are stable in nonionic detergents.

150 drated aluminum cations in the presence of a nonionic diblock or triblock poly(ethylene oxide) surfac

151 ia reduction of the pyridinium moiety to the nonionic dihydropyridine.

152 The objective was to compare the isosmolar nonionic dimer iodixanol (n=405) with the low osmolar io

153 The cohort receiving the nonionic dimer iodixanol experienced a 45% reduction in

154 Peptide nucleic acids (PNAs) are nonionic DNA/RNA mimics that can recognize complementary

155 ion of energetic contributions revealed that nonionic forces contribute nearly 87% of binding energy

156 In contrast, the contribution of nonionic forces is miniscule, resulting in an interactio

157 tigated model mixed micelles consisting of a nonionic glucosylated alkane surfactant from the maltosi

158 ved an average of 0.44 mm per section in the nonionic group and 0.71 mm per section in the ionic grou

159 n 98 patients (47 in the ionic and 51 in the nonionic group).

160 isooctane and the surfactant Igepal CO 520 (nonionic head group) in 50/50 wt % cyclohexane/hexane ar

161 gths, combined with ionic, zwitterionic, and nonionic headgroups.

162 ane rejection was observed for all ionic and nonionic hydrophilic TOrCs and lower rejection was obser

163 c TOrCs and lower rejection was observed for nonionic hydrophobic TOrCs.

164 The contacts are both ionic and nonionic (hydrophobic).

165 trione (1) was designed and synthesized as a nonionic inhibitor for the donor binding site of human b

166 raction ( approximately 30%) and the loss of nonionic interactions ( approximately 70%).

167 predominantly ionic but at certain positions nonionic interactions also existed.

168 f the medium at pH 6.0 and 7.4 suggests that nonionic interactions contribute a major proportion ( ap

169 ates in the ionic interaction and that other nonionic interactions may be involved in forming a compl

170 uption of a cooperative network of ionic and nonionic interactions.

171 or salt concentrations, suggesting primarily nonionic interactions.

172 Next, 135-150 mL of nonionic iodinated (300 mg/mL) contrast material was inj

173 an unenhanced abdominal scan, iobitridol, a nonionic iodinated contrast agent containing 350 mg of i

174 Nonionic iodinated contrast agents can be divided into m

175 Group 3 (n = 22) ingested nonionic iodinated contrast material (iohexol) with a co

176 Group 2 (n = 21) ingested 10-mL aliquots of nonionic iodinated contrast material (iopromide) with a

177 Nonionic iodinated contrast material in conjunction with

178 For 69,657 intravenous injections of nonionic iodinated contrast medium for computed tomograp

179 Extravasation of nonionic iodinated contrast medium results only rarely i

180 of extravasations of intravenously injected nonionic iodinated contrast medium.

181 There were 57 adverse events related to nonionic iodinated intravenous contrast material in 12,4

182 o differentiate between gadolinium-based and nonionic iodine-based contrast material in a colon phant

183 A custom-made colon phantom was filled with nonionic iodine-based contrast material, and a gadoliniu

184 ed to a range of concentrations of ionic and nonionic linear and macrocyclic contrast agents over 4 d

185 The nonionic linear chelate gadodiamide had the lowest rate

186 iate allergic adverse events with use of the nonionic linear GBCA gadodiamide in comparison with thos

187 resence of n-octyl beta-d-glucopyranoside, a nonionic lipid mimicking detergent, above its critical m

188 n GC x GC, focusing on the application of 30 nonionic liquid and 111 ionic liquid (IL) stationary pha

189 The specific toxic effect of monomeric nonionic low-osmolar iodinated contrast medium in ICU pa

190 al drugs specifically interact with HEMA and nonionic MAA (at pH2) moieties.

191 9, 0.36]; P < .00001) and less than that for nonionic macrocyclic GBCAs at 16 (95% CI: 14, 19) per 10

192 in comparison with those of ionic linear or nonionic macrocyclic GBCAs.

193 creased sensitivity to both ionic (NaCl) and nonionic (mannitol) osmotic stress in a root-bending ass

194 c medium for biological samples, and for two nonionic materials common in bioparticle analysis: isopr

195 are the differences between zwitterionic and nonionic materials?

196 Surrounding the GTG sequence with nonionic methylphosphonate linkages inhibited or elimina

197 as sensitive to the nonideal mixing of ionic/nonionic micelles and to the unconventional aggregation

198 We demonstrate that the use of wormlike nonionic micelles as drag-tags in end-labeled free-solut

199 attached PNA amphiphiles (PNAA) partition to nonionic micelles in the running buffer (Triton X-100),

200 roscopy in homogeneous solution, anionic and nonionic micelles, and lipid bilayers.

201 sistent with the monomer exchange process in nonionic micelles.

202 ives with higher densities than their parent nonionic molecules and (2) to achieve a fine balance bet

203 mido)-2-methylpropanesulfonate (AMPS), and a nonionic monomer, acrylamide (AAM).

204 e surface contents of the two monomer units: nonionic N-(2-hydroxypropyl) methacrylamide (HPMAA) and

205 Ionic (n = 4,851) or nonionic (n = 1,809) contrast material was injected at 0

206 the most rapid approach for the anionic and nonionic nanoparticles, although the cationic and zwitte

207 In an attempt to combine the nonionic nature and high nuclease stability of the P-C b

208 anges in the reaction kinetics and the ionic/nonionic nature of the TS with the ionizing ability of t

209 transport occurs almost exclusively through nonionic NH(3) diffusion and NH(4)(+) trapping has given

210 The presence of certain nonionic or zwitterionic detergent was sufficient to est

211 gnificant difference between the protonated (nonionic) or deprotonated (anionic) states.

212 This work compares the sorption of four nonionic organic pollutants of different polarities (nap

213 which up to 90% of the salt was replaced by nonionic osmolytes such as sucrose.

214 high temperature, pH stress, and presence of nonionic osmolytes.

215 artially independent of signals that mediate nonionic osmotic responses.

216 In this system, a gadolinium-based nonionic paramagnetic agent is used in conjunction with

217 In both crops, the nonionic PCs (carbamazepine, caffeine, and lamotrigine)

218 Nonionic PCs were taken up and accumulated at higher lev

219 MORFs support the nitrogenous bases by nonionic phosphorodiamidate linkages and, besides being

220 We have introduced a series of nonionic photoacid generators (PAGs) for carboxylic and

221 We explore how two nonionic polar groups (primary amine and primary amide)

222 ct experiment systems indicate that proximal nonionic polar groups have pronounced effects on hydroph

223 The sorption isotherms of the nonionic pollutants were highly linear, while paraquat s

224 ts [anionic sodium dodecyl sulfate (SDS) and nonionic poly(ethylene glycol)-poly(propylene glycol)-po

225 ed the biodegradability of three widely used nonionic polyglycol ether surfactants (alkyl ethoxylates

226 hese results suggest that the influence of a nonionic polymer or plasma protein on RBC aggregation is

227 The effects of nonionic polymers on human red blood cell (RBC) aggregat

228 inical surfactants in vitro; addition of the nonionic polymers polyethylene glycol, dextran, or hyalu

229 Nonionic polymers reverse inactivation of surfactant by

230 Addition of nonionic polymers such as polyethylene glycol (PEG) and

231 erent coagulant aids (anionic, cationic, and nonionic polymers) on membrane surface properties and fo

232 surfactant could be prevented or reduced by nonionic polymers, we added dextrans, polyethylene glyco

233 th novel alternative mechanisms that involve nonionic rearrangement processes.

234 nanoparticles (L-MNPs) by the combination of nonionic reverse micelle method and Fe3O4 nanoparticles.

235 to follow signaling traffic, sense ionic and nonionic second messengers, and report various kinase ac

236 f the NMDAR requirement is consistent with a nonionic signaling mechanism.

237 e (5-tetramethyl-rhodamine-maleimide), and a nonionic, smaller probe (N-ethyl-maleimide) reveals the

238 lfonate (CHAPS, zwitterionic), Triton X-100 (nonionic), sodium dodecyl sulfate (SDS, anionic), and do

239 ong-term hyperosmotic challenge by ionic and nonionic solutes without exhibiting the normal change in

240 unctions have low permeability for ionic and nonionic solutes, and are slightly cation-selective.

241 nce of high concentrations of ionic (but not nonionic) solutes, and these filamented cells drasticall

242 m the Kolyma River basin with a use of three nonionic sorbents: Amberlite XAD-8 resin, PPL- and C18 -

243 nhanced germination on both ionic (NaCl) and nonionic (sorbitol) hyperosmotic media.

244 Diffusion of ionic and nonionic species in multilayered tissues plays an import

245 y an order of magnitude higher than in their nonionic states, whereas the (R,S) diastereomer exhibits

246 in the presence of catalytic amounts of the nonionic strong bases P(RNCH(2)CH(2))(3)N (R = Me, i-Pr,

247 an be combined in the design of highly basic nonionic superbases of pincer type.

248 e membrane were subsequently removed using a nonionic surfactant before the final measurement was car

249 We present here a sponge phase consisting of nonionic surfactant bilayers.

250 The effects of nonionic surfactant chain length on the properties of tr

251 Polysorbate 20 is a nonionic surfactant commonly used in the formulation of

252 In this mixed surfactant system, the nonionic surfactant DDM functions as a surface blocking

253 taminants including metal complexing agents, nonionic surfactant degradates, personal care products,

254 Measurements are made and analyzed for large nonionic surfactant Igepal CO-520reverse micelles (water

255 sity are observed as the chain length of the nonionic surfactant increases.

256 The nonionic surfactant insoluble fraction enriched for cyto

257 1) lyotropic liquid crystalline phase of the nonionic surfactant octaethyleneglycol monohexadecyl eth

258 rmaldehyde in water, formaldehyde-water with nonionic surfactant Tergitol NP-9, and formaldehyde-wate

259 The effects of the nonionic surfactant Triton X-100 (poly(ethylene glycol)

260 e dispersed in 20 mM KCl solution containing nonionic surfactant Triton X-100 and their translocation

261 lipid membrane can be removed effectively by nonionic surfactant Triton X-100.

262 onomer glycidyl methacrylate combined with a nonionic surfactant Triton X-100.

263 50-fold) are observed in the presence of the nonionic surfactant Triton X-100.

264 enhance nanoparticle stability (Tween 80, a nonionic surfactant), and residual contaminants resultin

265 ty (IM) separation to characterize a complex nonionic surfactant, consisting of a methylated glucose

266 The nonionic surfactant, n-alkyl poly(ethylene oxide), and w

267 Trace amounts of Triton X100, a nonionic surfactant, release the trapped cells from thes

268 We utilize purified Triton-X 100, a nonionic surfactant, to make soap bubbles.

269 icellar electrokinetic chromatography with a nonionic surfactant, Triton X-100.

270 d by the presence of Triton X-100 (TX100), a nonionic surfactant, were studied by scanning electroche

271 d enzyme immobilization in the presence of a nonionic surfactant.

272 A total of five nonionic surfactants (Brij 30, Span 20, Ecosurf EH-3, po

273 reatest for the zwitterionic (i.e., APS) and nonionic surfactants (i.e., POE).

274 inner space of reverse micelles formed from nonionic surfactants (isotropic phase).

275 eractions between proteins and AS as well as nonionic surfactants (NIS) are of both basic and applied

276 In aqueous solution of nonionic surfactants (Triton X-100 and Tween 20) arrays

277 ithin; 3:1) to replace some concentration of nonionic surfactants (Tween 80) with natural surfactant

278 Ru(bpy)3(2+) in the presence of a series of nonionic surfactants are reported (Triton X-100, 114, 16

279 CEC-ESI-MS analysis of these very long chain nonionic surfactants for the first time.

280 Poloxamers and poloxamine nonionic surfactants have diverse applications in variou

281 ide variety of soluble polymeric, ionic, and nonionic surfactants of high- and low-foaming character.

282 series are alkylphenol polyethoxylates -type nonionic surfactants of varying numbers of ethylene oxid

283 pyridyl) were studied in the presence of the nonionic surfactants Triton X-100, Thesit, and Nonidet P

284 iety of anionic, cationic, zwitterionic, and nonionic surfactants were evaluated for their ability to

285 onolithic C-18 column and mixed (anionic and nonionic surfactants) micellar eluent for determination

286 Subsequently, the ocular toxicities of six nonionic surfactants, Brij 700, -58, -56, -78, -97, and

287 generalized to other surfactants, including nonionic surfactants, by making use of fluorophore-surfa

288 ght mass spectrometry (UPLC-QTOFMS) revealed nonionic surfactants, including alcohol polyethoxylates

289 Aqueous solutions of monomeric nonionic surfactants, n-alkyl polyoxyethylene ethers (C1

290 g formulated in lipid vesicles prepared from nonionic surfactants, we describe a novel mechanism infl

291 long-chain length (e.g., n = 1-16) TX-series nonionic surfactants.

292 protein and purified using over 50 different nonionic surfactants.

293 egradation of the polycarbonate plastics and nonionic surfactants.

294 used to make alkylphenol ethoxylates, common nonionic surfactants.

295 ic interactions between Ru(bpy)3(2+) and the nonionic surfactants.

296 y of the tight junctions were assessed using nonionic tracers and electrophysiology.

297 pressed and stretched polyacrylamide gels, a nonionic type of lipid bilayer disk or bicelle, and a li

298 Our finding that the nonionic urea stabilizes the aldimine of L-serine in the

299 Thus, nonionic VDeltaC signaling is vital to the function of C

300 At pH2, MAA chains are nonionic, whereas at pH7.4, MAA chains are anionic (pKa