ライフサイエンスコーパス: TBA

1 TBA achieved was IgG concentration dependent.

2 TBA and TBAL transcripts and promoter activities were de

3 TBA is designed to be appropriate for aligning many, but

4 TBA proteins are secreted to the mucilage pocket during

5 In Model 2 TBA levels were significantly lower in U74389G treated a

6 ing aptamer, d(G(2)T(2)G(2)TGTG(2)T(2)G(2)) (TBA), in the presence of Pb(2+) ions.

7 1) was prepared from [TBA][P(SiCl(3))(2)] ([TBA]2, TBA = tetra-n-butylammonium) and triflic acid in

8 egion between the two quartets in the Pb(2+)-TBA complex, coordinated to the eight surrounding guanin

9 asured by EXAFS for the Pb(2+)-G1 and Pb(2+)-TBA complexes.

10 prepared from [TBA][P(SiCl(3))(2)] ([TBA]2, TBA = tetra-n-butylammonium) and triflic acid in 36% yie

11 nitriledithiolate (MNT) in (TBA)2[Cu(MNT)2] (TBA= tetra-n-butylammonium).

12 etalate (POM) (nBu4N)6[{(mu-MeO)ZrW5O18}2], (TBA)61, has been synthesized by stoichiometric hydrolysi

13 for TBA dehydration to isobutylene, and (3) TBA also reacts to break node-linker bonds to form ester

14 rence device containing [Ru(Htctpy)(NCS)(3)][TBA](3) (N749), where H(3)tctpy and TBA are 4,4',4"-tric

15 ncluding a new hybrid of the sequence (CG)(4)TBA, where TBA stands for tetrakis(p-hydroxybiphenyl)ada

16 Concentrations of 2,4-DBA and 2,4,6-TBA in September were higher in the southern than in the

17 also decreased in the following order: 2,4,6-TBA>2,4-DBA.

18 ollowing order: 2,4,6-tribromoanisole (2,4,6-TBA)>2,4-dibromoanisole (2,4-DBA)>>2,6-dibromoanisole (2

19 7.6 for 2,4-DBA and from 18 to 94 for 2,4,6-TBA, indicating net volatilization.

20 occurrence and fates of trenbolone acetate (TBA) and metabolites 17a-trenbolone (17a-TBOH), 17B-TBOH

21 of the anabolic androgen trenbolone acetate (TBA) in animal agriculture, evidence demonstrating the o

22 Trenbolone acetate (TBA) is a high-value steroidal growth promoter often adm

23 valuate the transport of trenbolone acetate (TBA) metabolites from beef cattle CAFOs, rainfall simula

24 e occurrence and fate of trenbolone acetate (TBA) metabolites in soil and water.

25 Photolysis of trenbolone acetate (TBA) metabolites in the presence of various nitrogen-, s

26 rsible photohydration of trenbolone acetate (TBA) metabolites.

27 nt reversion pathway for trenbolone acetate (TBA) metabolites.

28 tive ecological risks of trenbolone acetate (TBA) use in agro-ecosystems, we evaluated the spatiotemp

29 characterized by increased total bile acid (TBA) levels, which are regulated by farnesoid X receptor

30 (TCA), reaction with 2-thiobarbituric acid (TBA) and quantification with ultraperformance liquid chr

31 basic-nitrogen (TVB-N), thiobarbituric acid (TBA) as well as free amino acid (FAA).

32 snap frozen tissue for thiobarbituric acid (TBA) concentrations (nmol/g tissue weight).

33 onate relationship with thiobarbituric acid (TBA) number, an indicator of lipid peroxidation responsi

34 sic nitrogen (TVBN) and thiobarbituric acid (TBA) of the dried milkfish samples prepared with the sam

35 e specification number, thiobarbituric acid (TBA) value and colour of pistachio oil extracted from sa

36 oxidase value (POV) and thiobarbituric acid (TBA) values during storage period.

37 ng to peroxide (PV) and thiobarbituric acid (TBA) values.

38 Addition of tribromoacetic acid (TBA) as a chemical fuel perturbs this equilibrium to res

39 ve oxygen species (ROS; thiobarbituric acid [TBA]-reacting material, and dichlorofluorescein [DCF]),

40 ,2':5',2''-terthiophene-3' (p-benzoic acid) (TBA) nanocomposite film.

41 transport of taurine-conjugated bile acids (TBA) facilitates TBA chemical chaperone function and all

42 t of 119 C57Bl/6J mice for total bile acids (TBA) in plasma, identified 11 animals (9.2%) with high T

43 ted varied transmission-blocking activities (TBA).

44 Theta band activity (TBA) in distributed brain networks is likely essential t

45 squitoes (% transmission blocking activity, %TBA).

46 eactions cannot be examined simply by adding TBA: the effects of secondary ROO(*) must also be consid

47 ue (ASAT)) relative to total body adiposity (TBA) differentially relate to WML volume or whether thes

48 Cattle were administered TBA, MGA, or RAC, and their residues were measured in fr

49 Across age, TBA appears to serve distinct functions during sensorimo

50 rification reaction with tert-butyl alcohol (TBA) is proposed.

51 hyl sulfoxide (PMSO) and tert-butyl alcohol (TBA) revealed Fe(IV) as the major reactive species in al

52 catalytic dehydration of tert-butyl alcohol (TBA) used to probe the activities of OH groups of Zr(6)O

53 cific scavenger, such as tert-butyl alcohol (TBA), is usually added to eliminate (*)OH effects.

54 Although TBA is commonly assumed to transform (*)OH into oxidativ

55 s analogous to those of tetrabutyl ammonium (TBA), and kinetics slow enough to be reliably measured.

56 cally varied between treatments (P<0.05) and TBA that ranged between approximately 0.15 and 0.30 mg M

57 bulin isotypes--the alpha-tubulins TBA-6 and TBA-9 and the beta-tubulin TBB-4--are specifically expre

58 constants for HIM monomers with TBA(Cl) and TBA(Br) are calculated and show a correlation with the s

59 n of 80% and 72% in lipid hydroperoxides and TBA-RS formation after digestion, respectively.

60 opies of the resulting aptamers, TBA-T7b and TBA-T12b, showed their ability to fold into the typical

61 ide (TPA), whereas guanines of free TBA- and TBA-conjugated 6-FAM immobilized on the surface of graph

62 NCS)(3)][TBA](3) (N749), where H(3)tctpy and TBA are 4,4',4"-tricarboxy-2,2':6',2"-terpyridine and te

63 Patients with TGA and TBA were offered ASO irrespective of patient size and as

64 e was achieved in 32 and 672 days in THF and TBA hydro-organic media, respectively.

65 had better quality in term of lower TVBN and TBA values than those of samples prepared with other dry

66 Contrary, peroxide value and TBA-reactive substances in herring- and cod-derived prod

67 canalization therapy for vertebrobasilar and TBA occlusion deserves further attention.

68 For comparison, Cu(II) isocorrole and [TBA][Cu(CF3)4] were studied as authentic Cu(II) and Cu(I

69 ies for anions, including the sulfate anion (TBA(+) salts), in organic media (CD2Cl2).

70 eat arteries (TGA) and Taussig-Bing anomaly (TBA).

71 VSD, n = 37, 30%), and Taussig Bing Anomaly (TBA, n = 9, 7%).

72 ionally, fat-soluble vitamins, antioxidants, TBA, and FRAP were measured at 0, 24, 48, 72, 96, and 12

73 ture (CVAMA) into topology-based approaches (TBA) and statistics-based approaches (SBA).

74 rallel fold of the thrombin binding aptamer (TBA) by this approach.

75 ions of the 15-mer thrombin-binding aptamer (TBA) immobilized on porous silica surfaces.

76 x structure of the thrombin binding aptamer (TBA) is disrupted at 37 degrees C by a short PNA probe.

77 specific receptor, thrombin binding aptamer (TBA) modified on Au nanorods (AuNRs), causes a measurabl

78 lar anchoring of a thrombin-binding aptamer (TBA) onto polymethacrylate monolith pore surface, and th

79 r (DBA) or the tyrosinamide binding aptamer (TBA), for the catalyzed oxidation of dopamine to aminoch

80 GTGGTTGG, known as thrombin-binding aptamer (TBA).

81 structures of the thrombin binding aptamer (TBA).

82 ene oxide (GO) and thrombin binding aptamer (TBA).

83 plex formed by the thrombin-binding aptamer (TBA, GGTTGGTGTGGTTGG).

84 by intercalating hemin into the TB aptamer (TBA) and glucose oxidase (GOx).

85 serum was developed using thrombin aptamer (TBA), one of the G-quadruplex DNA aptamers, without expe

86 CD spectroscopies of the resulting aptamers, TBA-T7b and TBA-T12b, showed their ability to fold into

87 A raster map of total tree basal area (TBA) for the conterminous United States was compared wit

88 nduced bone loss (BL), trabecular bone area (TBA), and postextraction bone healing (BH).

89 atients with isolated tip of basilar artery (TBA) occlusion had significantly more BP excursion of 20

90 Formation of green trihydroxy benzacridine (TBA) derivatives when chlorogenic acid (CGA) quinones an

91 ant contradictory results were found between TBA and SBA.

92 devised using the rapid interaction between TBA-conjugated 6-FAM and thrombin quantified trace level

93 PO(4)) or tetra- n-butylammonium bisulfate ([TBA][HSO(4)]) with trichlorosilane leads to the formatio

94 BL, TBA, the positive cells for tartrate-resistant acid phos

95 transforms of the Pb(2+) complexes with both TBA and G1 show a first-shell interaction at about 2.6 A

96 nol (EtOH), isopropanol (IPA), tert-butanol (TBA) and tetrahydrofuran (THF)) and a combination thereo

97 rent: The reaction of tri-tert-butylaniline (TBA) with AgSbF6 in CH2 Cl2 produces a green-colored int

98 form cyclooctene (COE) and tert-butylethane (TBA).

99 l chairlike G-quadruplex structure formed by TBA.

100 A new computer program called TBA (for "threaded blockset aligner") builds a threaded

101 In the absence of the cobound cation (TBA(+) salts) receptor 1 preferably binds nitrate and ni

102 .0 microM crystallographically characterized TBA x Eu(DO2A)(DPA)) were titrated with EuCl3 (1.0 nM-1.

103 Copper(II) aryl complexes [TBA][LCu(II)-Ar(R)] were synthesized via the treatment o

104 O(5) consisting of very small crystallites (TBA-V(2) O(5) ).

105 Circulating levels of cytokines, TBA, DCF, PAI-1, FFAs, cortisol, and GH on admission wer

106 affeine and/or estrogen deficiency decreased TBA in the unligated teeth and reduced BH after tooth ex

107 nt and their mixture significantly decreased TBA values.

108 rine-conjugated bile acids (TBA) facilitates TBA chemical chaperone function and alleviates endoplasm

109 acancies act as Bronsted bases, facilitating TBA dehydration via a carbocation intermediate in an E1

110 ) these OH groups act as catalytic sites for TBA dehydration to isobutylene, and (3) TBA also reacts

111 um hydroxide (TPA), whereas guanines of free TBA- and TBA-conjugated 6-FAM immobilized on the surface

112 laccase air-breathing cathodes prepared from TBA(+) modified Aquivion ionomers were able to reach max

113 EFCs constructed with cathodes prepared from TBA(+) modified Nafion.

114 Anion 1 was also prepared from [TBA][H(2)PO(4)] and isolated in 62% yield on a gram scal

115 phine (HP(SiCl(3))(2), 1) was prepared from [TBA][P(SiCl(3))(2)] ([TBA]2, TBA = tetra-n-butylammonium

116 Adolescents rely on frontal TBA signaling surprise and prediction error, with no inp

117 -dots or sets of structurally functionalized TBA-modified Cu(2+) ion-functionalized C-dots are introd

118 the different parameters was observed (e.g. TBA value correlated with the peroxide value: r=0.466 fo

119 Green TBA formation was promoted at higher pH and inhibited as

120 asma, identified 11 animals (9.2%) with high TBA (>11 um; 171.1 +/- 76.8 um), and confirmed PSS prese

121 more favorable to mass transport and higher TBA(+) concentrations.

122 gers (P < 0.05), while GS burgers had higher TBA and gamma-tocopherol (P < 0.05).

123 The control group presented higher TBA and BH than the other groups (P <0.05).

124 in TBA(+) suggest that the large hydrophobic TBA(+) ions are preferentially excluded from the vicinit

125 mediates with tetrabutylammonium hydroxide ([TBA][OH]) yields adenosine and uridine tetraphosphates (

126 The increased mobilities observed in TBA(+) suggest that the large hydrophobic TBA(+) ions ar

127 grated faster than the reference oligomer in TBA(+) and slower than the reference in Li(+).

128 se mechanism, whereas the release profile in TBA was deemed suitable following model fitting.

129 mulation of TBA into HSPCs, which results in TBA-mediated alleviation of ER stress and erythroid apop

130 lene ligand maleonitriledithiolate (MNT) in (TBA)2[Cu(MNT)2] (TBA= tetra-n-butylammonium).

131 a key role in liver damage and DR, including TBA regulation through alteration of intestinal and bili

132 ) mice injected with MCs displayed increased TBA content, biliary FXR/FGF15, and intestinal inflammat

133 elegans, we show that alpha-tubulin isotype TBA-6 sculpts 18 A- and B-tubule singlets from nine cili

134 n, we report a crystal structure of the KcsA-TBA complex at 2.9 A resolution, with TBA bound inside t

135 to promoting Mn(2+)(aq) oxidation kinetics, TBA can also affect the crystalline phases, oxidation st

136 Slc29a3(-/-) HSPCs accumulate less TBA despite elevated levels of TBA in Slc29a3(-/-) mouse

137 The off-flavour determining parameters like TBA value, carbonyl value and lipid hydroperoxides (LHPO

138 y (MALDI-TOF-MS) using the same ionic liquid TBA-CHCA as MALDI matrix, that was found to be very suit

139 indow of o-dichlorobenzene containing 0.1 M (TBA)ClO(4) are observed.

140 In o-dichlorobenzene, 0.1 M (TBA)ClO(4), the synthesized zincporphyrin-fullerene dyad

141 Across each of four regions, median TBA was significantly higher within forest areas defolia

142 e use of confocal Raman microscopy, membrane TBA(+) ion content was predicted in calibration studies

143 ial from manure excreted by implanted (40 mg TBA, 8 mg 17beta-estradiol) beef cattle.

144 thin a pasture, TBA-implanted heifers (40 mg TBA, 8 mg estradiol) were briefly penned (24 h) at high

145 A3; a less abundant fourth homolog was named TBA-LIKE (TBAL).

146 0(-4) mol dm(-3) tetrabutylammonium nitrate (TBA(+)NO3(-)), which induces rapid self-assembly of the

147 1 and 2 quickly react with TBAOH.30 H(2)O ([TBA](+) = [(n)Bu(4)N](+)) to form the corresponding hydr

148 a proper error range, rather than observed %TBA both in SMFA and DMFA.

149 transfer kinetics parameters, a and k(0), of TBA(+) at the NPOE/water nanoITIES by fitting theoretica

150 ated a lower Variation Ratio (VR) (8.10%) of TBA at 6 simulated levels.

151 he small pores of UiO-66 limit the access of TBA and the reaction with the formate/acetate ligands bo

152 of ENT3 allows for increased accumulation of TBA into HSPCs, which results in TBA-mediated alleviatio

153 also react to produce structural analogs of TBA metabolites.

154 rse substitutions in the all-RNA analogue of TBA result in a parallel to antiparallel change in topol

155 crystallite size and higher surface area of TBA-V(2) O(5) allow faster lithium insertion and superio

156 Our results demonstrate that binding of TBA or TBSb causes no significant change in the KcsA str

157 Binding of TBA to KcsA was very slow, whereas binding of Dauda was

158 nic liquid resulting from the combination of TBA (tributylamine) and CHCA (alpha-Cyano-4-hydroxycinna

159 that ecologically relevant concentrations of TBA metabolites can be mobilized from CAFO surfaces in s

160 ion of CBC 5, with subsequent consumption of TBA via decarboxylation driving the system back to the s

161 roles in dimerization and crystallization of TBA, but they are changeable for Pb(2+)-binding.

162 ng ability to GO, leads to the desorption of TBA-thrombin complex from electrode surface and signific

163 ilitate transport and help mask detection of TBA metabolites in surface waters and treatment systems.

164 we evaluated the spatiotemporal dynamics of TBA metabolite transport during irrigation and rainfall

165 sformation experiments to assess the fate of TBA metabolites and their photoproducts.

166 formed from the reaction between guanines of TBA and TMPG in the presence of TPA, transfers energy to

167 but this change appears to be independent of TBA or TBSb blockade.

168 cumulate less TBA despite elevated levels of TBA in Slc29a3(-/-) mouse plasma and have elevated basal

169 tructure unraveled that the T7G8T9 linker of TBA is also variable.

170 Loss of TBA-7 led to the formation of hyperstable MTs and the ge

171 onformational sampling of an atomic model of TBA bound in the central cavity of KcsA, using the Hamil

172 re, evidence demonstrating the occurrence of TBA metabolites such as 17beta-trenbolone (17beta-TBOH),

173 t least two distinct binding orientations of TBA.

174 The output of TBA can be projected onto any genome chosen as a referen

175 we observed that the rapid photohydration of TBA metabolites is reversible under conditions represent

176 , we investigated the phototransformation of TBA metabolites and associated ecological implications b

177 rest is the observation that the presence of TBA has a negligible effect on the channel structure and

178 titrimetric method across the full range of TBA(+): SO3(-) ratios of practical interest (0.1 to 1.7)

179 ithm to simulate the measured decay rates of TBA.

180 UiO-66 become accessible for the reaction of TBA, with the activity depending on the density of defec

181 rnal cycling and substantial regeneration of TBA metabolites at rates that are strongly temperature-

182 her, these results reveal the active role of TBA residues T7 and T12 and the relevance of some amino

183 anced Guanine 4 (G4) structural stability of TBA upon interaction with thrombin in an ionic environme

184 th modified sequences was lower than that of TBA using human enzyme, whereas the potency trend was ag

185 -4 orders of magnitude greater than those of TBA and MGA.

186 rombin, the conformational transformation of TBA after incubating with the thrombin solution and form

187 In addition, the use of TBA as thrombin recognition units makes the biosensor re

188 Oxidation of [TBA][LCu(II)-Ar(R)] produces formal copper(III) aryl com

189 Trichlorosilane reduction of [TBA](2)[Si(P(3)O(9))(2)] also provided anion 1.

190 Treatment of [TBA]1 with an excess of benzyl chloride leads to the for

191 ased specification number, with no effect on TBA value.

192 s for polyamination and polyglutamination on TBA-7 may be responsible for this destabilization.

193 ct of this rinsing on peroxide value (PV) or TBA-reactive substances (TBARS) development was limited.

194 decline correlated with increased oxidation (TBA) in both burger types.

195 only condition where its reversion to parent TBA metabolite occurred.

196 Within a pasture, TBA-implanted heifers (40 mg TBA, 8 mg estradiol) were b

197 al and thermodynamic stabilities for the PNA-TBA hybrid.

198 BOH), and trendione (TBO), the three primary TBA metabolites, occur in soils and runoff.

199 of DLK-1 signaling in ben-1 mutants promotes TBA-2 transcription and protects axon and synapse morpho

200 We report a single fusion protein (TBA(225)) consisting of the toxoid versions of TSST-1, S

201 G-quadruplex TBA aptasensor devised using the rapid interaction betwe

202 nd + 3 x standard deviation) of G-quadruplex TBA aptasensor with good linear calibration curve, accur

203 uenched due to the formation of G-quadruplex TBA-conjugated 6-FAM bound with thrombin in a sample.

204 Guanines of G-quadruplex TBA-conjugated carboxyfluorescein (6-FAM) bound with thr

205 version of phosphates into P(V)-X reagents, [TBA][PO(2)X(2)] (X = Cl, F), via a redox-neutral halogen

206 nthesis, a tributylammonium cefadroxil salt (TBA-CFD) was used as template with methacrylic acid and

207 Thus, even under intense grazing scenarios, TBA-metabolite transport potential is expected to be low

208 e to provide bis(trimetaphosphate)silicate, [TBA](2)[Si(P(3)O(9))(2)], characterized by NMR spectrosc

209 form the dynamic-programming alignment step, TBA runs a stand-alone program called MULTIZ, which can

210 as estimated by the TBA reactive substances (TBA-RS) measurement.

211 Terbuthylazine (TBA) is a widely used herbicide, and its heterogeneous r

212 e reference; lithium and tetrabutylammonium (TBA(+)) ions were used as the probe ions.

213 csA potassium channel by tetrabutylammonium (TBA) is investigated through functional, structural and

214 9 V versus the E(1/2) of tetrabutylammonium (TBA(+)).

215 ding via the addition of tetrabutylammonium (TBA) salts or removal of the anion by the addition of si

216 KcsA-bound Dauda by the tetrabutylammonium (TBA) ion confirmed that the Dauda binding site was in th

217 trapropylammonium (TPA), tetrabutylammonium (TBA), tetraethylphosphonium (TEP), tetrabutylphosphonium

218 (+)) ions beginning with tetrabutylammonium (TBA(+)) reduced KCl junctional currents disproportionate

219 channel in complex with tetrabutylammonium (TBA) and tetrabutylantimony (TBSb) under various ionic c

220 salts (tetrabutylammonium-tetrabutylborate (TBA-TBB) and Potassium tetrakis(4-chlorphenyl)borate (KT

221 ith higher affinity and faster kinetics than TBA(+) or TPeA(+), indicative of a hydrophobic site with

222 it resulted that TBA-T7b is more potent than TBA in prolonging clotting time.

223 apacity and superior capacity retention than TBA-V(2) O(5) .

224 change in genomic sequences, indicates that TBA is more accurate than earlier programs.

225 hen valued in PT assay, and it resulted that TBA-T7b is more potent than TBA in prolonging clotting t

226 gh-resolution crystal structures showed that TBA forms intramolecular G-quadruplex and Pb(2+) is boun

227 s binding of Dauda was fast, suggesting that TBA can enter the cavity only through an open channel wh

228 The TBA is of interest because its binding of alpha-thrombin

229 The TBA of the Zsummary value had a higher Validation Succes

230 The TBA salt of trimetaphosphate ([TBA](3)[P(3)O(9)].2H(2)O)

231 The TBA-thrombin complex formation was monitored by differen

232 rings together several novel algorithms: the TBA multi-aligner program for rapid identification of lo

233 ed the levels of residual PLs as well as the TBA number.

234 s a contact ion pair complex, where both the TBA(+) and SO4(2-) groups are pseudoencapsulated in the

235 MS) and lipid oxidation was estimated by the TBA reactive substances (TBA-RS) measurement.

236 iet was the most effective in decreasing the TBA-RS value after intestinal digestion (23.3 % decrease

237 and a mass balance approach to estimate the TBA metabolite leaching potential from manure excreted b

238 Balanced equations for the formation of the TBA salts of anions 1 and 2 were formulated based on the

239 anding of the conformational response of the TBA, we utilize Raman spectroscopy to quantify the effec

240 Molecular dynamics (MD) simulations of the TBA-thrombin binding indicated enhanced Guanine 4 (G4) s

241 uadruplex versus unfolded populations of the TBA.

242 ed to identify a function for TBAs/TBAL, the TBA promoters are highly expressed and cell type specifi

243 In Li(+) solutions, however, where the TBA is unfolded prior to alpha-thrombin association, pro

244 ives Li(+)/H(+) photointercalation into the (TBA)(+)(NbWO(6))(-) photoanode, leading to small polaron

245 Therefore, TBA may serve as a regional-scale indicator of forest he

246 ion of the electron density corresponding to TBA suggests that the ligand may adopt more than one con

247 ble uncertainty still exists with respect to TBA risk in agro-ecosystems because limited data are ava

248 of resulting G-quadruplexes with respect to TBA.

249 h the permeability ratios K+:NMDG+:TEA+:TPA+:TBA+:Gluc- = 1:0.45:0.35:0.2:0.2:0.2.

250 In the case of TPA, TBA, and TBP, the ITC data could not be fit to a 1:1 bin

251 Transplanting TBA-preconditioned HSPCs expressing ENT3 into Slc29a3(-/

252 The TBA salt of trimetaphosphate ([TBA](3)[P(3)O(9)].2H(2)O), also a precursor to anion 1,

253 We also discovered an alpha-tubulin (TBA-7) that appears to destabilize MTs.

254 ntified amino acid residues in alpha-tubulin/TBA-2 that are necessary for formation of BEN-1 islands.

255 t three tubulin isotypes--the alpha-tubulins TBA-6 and TBA-9 and the beta-tubulin TBB-4--are specific

256 e two-dimensional layered niobium tungstate (TBA)(+)(NbWO(6))(-) for on-demand hydrogen evolution and

257 h represents data never before reached using TBA as reactant.

258 ucts, this study demonstrates that utilizing TBA as an (*)OH scavenger generates the secondary peroxy

259 6 log CFU/g), pH, thiobarbituric acid value (TBA), and total volatile nitrogen (TVN) compared with th

260 evaluated in soybean oil by peroxide value, TBA value and rancimat thermal stability test and was co

261 rated using a new visualization tool to view TBA-generated alignments of vertebrate Hox clusters from

262 in was lower than that without thrombin when TBA-conjugated 6-FAM was added in two samples and incuba

263 or 532 nm light excitation of TBAI(3), where TBA is tetrabutyl ammonium, in CH(3)CN at room temperatu

264 new hybrid of the sequence (CG)(4)TBA, where TBA stands for tetrakis(p-hydroxybiphenyl)adamantane tha

265 ays and then decreased dramatically, whereas TBA and Totox values began to increase after this time.

266 espectively, and of r=0.767 and r=0.498 with TBA value for back-fat and ham fat, respectively).

267 with PPN[HCO3]; and (iii) free cryptand with TBA[OH] and atmospheric CO2.

268 association constants for HIM monomers with TBA(Cl) and TBA(Br) are calculated and show a correlatio

269 (2+) can form a long-lived G-quadruplex with TBA.

270 ds present initially on the nodes react with TBA to form esters, (2) these OH groups act as catalytic

271 e KcsA-TBA complex at 2.9 A resolution, with TBA bound inside the large hydrophobic cavity located at

272 cid) can react via thermal substitution with TBA metabolite photohydrates, although this reaction wit

273 Ring opening of these ultraphosphates with [TBA][OH] yields p(5)A and p(5)U in 58% and 70% yield fro