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

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

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

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

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

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

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

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

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

16 7.6 for 2,4-DBA and from 18 to 94 for 2,4,6-TBA, indicating net volatilization.

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

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

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

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

21 rsible photohydration of trenbolone acetate (TBA) metabolites.

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

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

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

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

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

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

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

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

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

31 ,2':5',2''-terthiophene-3' (p-benzoic acid) (TBA) nanocomposite film.

32 ted varied transmission-blocking activities (TBA).

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

57 ant contradictory results were found between TBA and SBA.

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

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

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

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

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

63 l chairlike G-quadruplex structure formed by TBA.

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

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

66 .0 microM crystallographically characterized TBA x Eu(DO2A)(DPA)) were titrated with EuCl3 (1.0 nM-1.

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

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

69 nt and their mixture significantly decreased TBA values.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

90 0(-4) mol dm(-3) tetrabutylammonium nitrate (TBA(+)NO3(-)), which induces rapid self-assembly of the

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

92 also react to produce structural analogs of TBA metabolites.

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

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

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

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

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

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

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

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

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

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

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

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

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

106 t least two distinct binding orientations of TBA.

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

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

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

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

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

112 ithm to simulate the measured decay rates of TBA.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

146 The TBA-thrombin complex formation was monitored by differen

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

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

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

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

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

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

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

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

155 of resulting G-quadruplexes with respect to TBA.

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

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

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

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

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

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

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

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

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

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

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

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

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

169 (2+) can form a long-lived G-quadruplex with TBA.

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