ライフサイエンスコーパス: TPP

1 TPP is homologous to Escherichia coli type I signal pept

2 TPP likely is a major contributor to these biological ac

3 TPP might also be a promising platform for tumor-specifi

4 r (CP), 3, prepared from S = 1/2 Co(TPP), 1 (TPP = 5,10,15,20-tetraphenylporphyrin dianion), and S =

5 ic-structure analysis of [Fe(V)(N)(TPP)] (1, TPP(2-) = tetraphenylporphyrinato), and [Fe(V)(N)(cyclam

6 otal structural determination of Ag29(BDT)12(TPP)4, an atomically precise tetravalent nanocluster (NC

7 A TPP unit is appended for targeting mitochondria, as demo

8 es indicate that many fungal species carry a TPP riboswitch with similar intron architecture, and the

9 undant theoretical metabolite database for a TPP of any topology (e.g., branched, multicyclic, etc.).

10 esponding host-guest surface inclusions in a TPP matrix.

11 es cerevisiae) showed that all encode active TPP enzymes with an essential role for some conserved re

12 tive trait loci (QTLs) responsible for adult TPP mortality and fecundity in several RILs carrying ins

13 resence of Lso is required to increase adult TPP mortality.

14 acterization of a specific and high-affinity TPP uptake system in human colonocytes.

15 and previously uncharacterised low-affinity TPP binding-site was also observed, and hence indicated

16 sPbI(3) NCs, the stability of the LSCs after TPP treatments has been greatly improved, even after lon

17 This class includes [Ag18H16(TPP)10]2+, [Ag25H22(DPPE)8]3+, and [Ag26H22(TFPP)13]2+.

18 n at saturating concentrations of Mg(2+) and TPP, the P1 helix, as well as distal regions surrounding

19 s no correlation between uncorrected DPP and TPP measured in house dust (r(S) < 0.1).

20 ntioxidant, while the BODIPY fluorophore and TPP ensure partitioning within the inner mitochondrial m

21 FM550 and TPP diverted osteogenic differentiation toward adipogene

22 in the absence and presence of magnesium and TPP.

23 oryl substituent is absent (e.g., Zn-TPP and TPP).

24 ed the three-way junction of the Arabidopsis TPP riboswitch as an elaborated k-turn.

25 tween photorespiration and the TCA cycle, as TPP riboswitch mutants accumulate less photorespiratory

26 irect interaction between substrates such as TPP(+) and the essential residue E14 in transmembrane he

27 xymethylpyrimidine pyrophosphate, as well as TPP, but with an identical alternative splicing mechanis

28 lone-pair electrons on the phosphorus atom, TPP is also used as a photoinitiator, with higher effici

29 nalogue Mito-Met10, synthesized by attaching TPP(+) to Met via a 10-carbon aliphatic side chain, was

30 eposition of atomic silicon onto a free-base TPP layer on a Ag(100) surface under ultrahigh vacuum (U

31 t nanocluster (NC) (BDT, 1,3-benzenedithiol; TPP, triphenylphosphine).

32 e been trapped: the covalent adducts between TPP and oxalate and between TPP and CO2.

33 adducts between TPP and oxalate and between TPP and CO2.

34 d intermolecular electronic coupling between TPP(+) cations in TPP(2) ZnCl(4) than in the pristine or

35 nsor that exhibits fluorescence upon binding TPP.

36 This TPP Spinach riboswitch binds TPP with affinity and selectivity similar to that of the

37 Thus, catalyses by TPP that are so important in modern biochemistry in the

38 ing desirable reactions that are mediated by TPP on a large scale.

39 d binding appeared to be driven primarily by TPP.

40 hs containing a triphenylphosphonium cation (TPP(+)).

41 orophore, and a triphenylphosphonium cation (TPP).

42 released and 80% remained absorbed to the CH:TPP carriers.

43 PP)2 has been synthesized and characterized (TPP=tetraphenylporphyrin).

44 ve the protein retention ability of chitosan-TPP beads in a simulated gastric environment.

45 on polymer (CP), 3, prepared from S = 1/2 Co(TPP), 1 (TPP = 5,10,15,20-tetraphenylporphyrin dianion),

46 amagnetic five-coordinate S-bound adduct, Co(TPP)(S-py-DTDA), 3a.

47 ce hybrid repeat unit best formulated as [Co(TPP)](0.5+) hemication (Co(2.5+)) bound to a dithiadiazo

48 he isolated 2-methylimidazole Cobalt(II) [Co(TPP)(2-MeHIm)] and [Co(TTP)(2-MeHIm)], and the correspon

49 upramolecular cage Co-PB-1(6) bearing six Co-TPP subunits connected through twenty-four imine bonds.

50 We utilized cobalt tetraphenylporphyrin (Co-TPP), an oxygen reduction reaction (ORR) catalyst with h

51 atalysis in neutral pH water, whereas the Co-TPP monomer gives a 50 % mixture of H(2) O(2) and H(2) O

52 The Escherichia coli TPP riboswitch contains a related k-junction, and analys

53 the molecular identification of the colonic TPP uptake system as the product of the SLC44A4 gene.

54 The better compound (TPP(+)C10) contained 10 carbon atoms within the linker c

55 family of smaller proteins with a conserved TPP domain.

56 ts into the molecular mechanisms controlling TPP formation and transport to the cell surface, enablin

57 CS-TPP-dsRNA nanoparticles were prepared by ionic gelation

58 copy revealed the distribution of the fed CS-TPP-dsRNA nanoparticles in midgut, fat body and epidermi

59 also showed knockdown of a target gene in CS-TPP-dsRNA nanoparticle fed larvae.

60 ults showed that at a 5:1 weight ratio of CS-TPP to dsRNA, nanoparticles of less than 200 nm mean dia

61 ortality and gene knockdown efficiency of CS-TPP-dsRNA nanoparticles were determined.

62 ed significant mortality of larvae fed on CS-TPP-dsRNA nanoparticles.

63 These data suggest that CS-TPP nanoparticles may be used for delivery of dsRNA to m

64 s with tris(o-phenylene)cyclotriphosphazene (TPP) was synthesized.

65 l tris(o-phenylenedioxy)cyclotriphosphazene (TPP) has been designed and synthesized.

66 tris( o-phenylenedioxy)cyclotriphosphazene (TPP) host.

67 l tris(o-phenylenedioxy)cyclotriphosphazene (TPP) is used as ahost for organizing dipolar molecular r

68 f tris(o-phenylenedioxy)cyclotriphosphazene (TPP) nanocrystals, was synthesized.

69 , tris(o-phenylenedioxy)cyclotriphosphazene (TPP).

70 , tris(o-phenylenedioxy)cyclotriphosphazine (TPP, 1), using differential scanning calorimetry, solid-

71 ated for the most likely application of each TPP.

72 ng ribosome binding, whereas most eukaryotic TPP riboswitches are predicted to regulate gene expressi

73 en the widespread distribution of eukaryotic TPP riboswitches and the diversity of their locations in

74 ) catalyzed by iron tetraphenylporphyrin (Fe(TPP)) in N, N'-dimethylformamide using decamethylferroce

75 Complex 1 readily reacts with [Fe(TPP)Cl] or Ph3P to afford the {FeNO}(7) porphyrin or Ph3

76 iron meso-tetraphenylporphyrin chloride (Fe[TPP]Cl) complex in 1,1,1,3,3,3-hexafluoropropan-2-ol (HF

77 ustworthiness is payoff-maximizing will find TPP to be less net costly (for example, because mechanis

78 the WWTP ranged from 0.02 mg/day/person for TPP to 28.7 mg/day/person for TBOEP, whereas the emissio

79 re, we screened 11 wild tomato relatives for TPP resistance as potential resources for tomato (Solanu

80 eptide and that this process is required for TPP biosynthesis, indicating that the last step of TPP f

81 0.17 +/- 0.064 muM; and highly specific for TPP and not affected by free thiamine, thiamine monophos

82 regulated carrier-mediated uptake system for TPP in human colonocytes.

83 O over P-C bond cleavage to selectively form TPP over other byproducts.

84 of phleic acids onto diacyltrehalose to form TPP, and an MmpL transporter promotes the export of TPP

85 alternative splicing regulation by a fungal TPP riboswitch from Neurospora crassa, which is mostly l

86 d that combining BH3 mimetics and gamitrinib-TPP blunted cellular proliferation in a synergistic mann

87 ndrial matrix chaperone inhibitor gamitrinib-TPP.

88 etics and enhanced the effects of gamitrinib-TPP.

89 stic investigations revealed that gamitrinib-TPP activated a PERK-dependent integrated stress respons

90 lementary experiments yielding Si-TPP and Ge-TPP on Ag(111) highlight the applicability to different

91 n experiment, revealing the desorption of Ge-TPP.

92 the hypothesis that the microbiota-generated TPP is absorbable and could contribute toward host thiam

93 icant (p < 0.01, >5-fold) induction in [(3)H]TPP uptake.

94 e hybrids containing distinct metal halides, TPP(2) MX(n) (MX(n) =SbCl(5) , MnCl(4) , ZnCl(4) , ZnCl(

95 gnitude lower than the previously known high TPP-affinity and high-activity form, TK(high), in the pr

96 ll confocal imaging studies showed the human TPP transporter protein to be expressed at the apical me

97 Expression of the human TPP transporter was found to be high in the colon and ne

98 II)TPP --> Fe(II)TPP, and Fe(II)TPP --> Fe(I)TPP) both occur in <200 fs.

99 n steps (Fe(III)TPP --> Fe(II)TPP, and Fe(II)TPP --> Fe(I)TPP) both occur in <200 fs.

100 wo sensitization steps (Fe(III)TPP --> Fe(II)TPP, and Fe(II)TPP --> Fe(I)TPP) both occur in <200 fs.

101 )](+)(,) forms the ferrous porphyrin, Fe(II)(TPP), which binds O(2) reversibly to form the ferric-sup

102 or the first two sensitization steps (Fe(III)TPP --> Fe(II)TPP, and Fe(II)TPP --> Fe(I)TPP) both occu

103 gnetic six-coordinate purple N-bound Co(III)(TPP)(N-py-DTDA(-))(O horizontal lineSMe2) complex (lambd

104 ane affords bright green diamagnetic Co(III)(TPP)(N-py-DTDA(-)), 3b, with multiple MLCT bands in the

105 ygen reduction is the protonation of Fe(III)(TPP)(O(2)(*-)) by pTsOH, which proceeds with a substanti

106 ferric-superoxide porphyrin complex, Fe(III)(TPP)(O(2)(*-)).

107 reduction of the ferric porphyrin, [Fe(III)(TPP)](+)(,) forms the ferrous porphyrin, Fe(II)(TPP), wh

108 Moreover, the afterglow in TPP(2) ZnX(4) can be tuned by controlling the halide com

109 lectronic coupling between TPP(+) cations in TPP(2) ZnCl(4) than in the pristine organic ionic compou

110 ly, many of these changes are not present in TPP riboswitch mutant plants, demonstrating their lack o

111 Increasing TPP concentration or the BSA concentration loaded, led t

112 450 inhibitor PBO, or the esterase inhibitor TPP resulted in markedly increased mortality (to ~80%),

113 diagnose active TB for treatment initiation (TPP#1) and for a community-based triage or referral test

114 ant triglyceride reduction for i.v.-injected TPP-HDL-apoA-I-QD NPs in rats.

115 lphavbeta3-integrin antagonist IntegriSense, TPP exhibits a significantly higher tumor-to-background

116 Moreover, in contrast with IntegriSense, TPP reliably differentiates between tumor cells and cell

117 tors with transversely dipolar rotators into TPP channels is followed by solid-state nuclear magnetic

118 Resonant electron transfer into TPP molecules occurs at <+1 V in the presence of mobile

119 tosan (1-2.5%w/w) and BSA (0.25-10%w/w) into TPP solutions ranging in concentration from 0.1 to 10%w/

120 imaging of dynamic changes in intracellular TPP concentrations in individual cells.

121 Direct interaction between (13)C-labeled TPP(+) and key residues within the EmrE dimer has been p

122 ate of membrane Hsp70, fluorescently labeled TPP is continuously internalized into syngeneic, spontan

123 A new BiLi porphyrin sandwich compound, LiBi(TPP)2 has been synthesized and characterized (TPP=tetrap

124 The unique molecular structure of LiBi(TPP)2 is such that the Bi sits between the porphyrins an

125 Beads produced at a low TPP concentration of 0.4% w/w had the highest BSA entrap

126 ate that plastidic SPI 1 (Plsp1) is the main TPP in Arabidopsis thaliana (Arabidopsis) although bioch

127 ributions within PDAC leads to microregional TPP values that vary on the hundred micron distance scal

128 Solvent mapping was used to model TPP in the PPARgamma binding site.

129 Moreover, TPP(+)C10 significantly inhibited the growth of TA3/Ha t

130 d electronic-structure analysis of [Fe(V)(N)(TPP)] (1, TPP(2-) = tetraphenylporphyrinato), and [Fe(V)

131 mportant source of exposure to TDCPP but not TPP.

132 nts provide a formal reputational account of TPP, and demonstrate how the costs of punishing may be r

133 negligible concentration of the C-2 anion of TPP, but of course not with an enzyme in modern biology.

134 understanding in intracellular behaviors of TPP in the course of targeting mitochondria due to the d

135 Concentrations of TPP and the EPC0 were significantly higher downstream of

136 t the utilization of lower concentrations of TPP is a good approach to improve the protein retention

137 ake rate and intracellular concentrations of TPP.

138 dissociation constants and cooperativity of TPP binding and provide the first comprehensive study ov

139 d an MmpL transporter promotes the export of TPP or its precursor across the plasma membrane.

140 to protonophores; saturable as a function of TPP concentration, with an apparent Km of 0.17 +/- 0.064

141 To utilize the powerful functionality of TPP without the need for manual intervention to launch e

142 Here, we investigated the functions of TPP in the regulation of the metabolic networks during p

143 the provision of both of the heterocycles of TPP appears to be an important requirement.

144 We present a game theoretic model of TPP as a costly signal of trustworthiness.

145 1(PPh3)8Cl2]Cl, differ only in the number of TPP ligands bound to the core.

146 l with the key pharmacokinetic parameters of TPP inside the live cells.

147 t photosynthetic and metabolic phenotypes of TPP riboswitch mutants are photoperiod dependent.

148 tection ability and therapeutic potential of TPP-HDL-apoA-I-QD NPs.

149 The afterglow properties of TPP(+) cations could be suspended for the hybrids contai

150 real-time visualization and quantitation of TPP dynamics within live cells at the subcellular level.

151 nzyme has been well documented, the roles of TPP in plant metabolism are still not fully understood.

152 s, the antineoplastic activity and safety of TPP(+)C10 warrant further comprehensive evaluation.

153 80% specificity, the HR6 model fell short of TPP#1 but reached TPP#2 performance criteria.

154 bcellular localization of the final stage of TPP biosynthesis and the chemical nature of the substrat

155 osynthesis, indicating that the last step of TPP formation occurs in the outer layers of the mycobact

156 Three phase partitioning (TPP), a bioseparation technique, based on partitioning o

157 ated with blended NPs composed of PLGA-b-PEG-TPP and a triblock copolymer containing a fluorescent qu

158 onsidering efficacy, the targeted PLGA-b-PEG-TPP NP provides a remarkable improvement in the drug the

159 ase called thylakoidal processing peptidase (TPP).

160 Triphenyl phosphate (TPP), a component of FM550, has a structure similar to t

161 ) phosphate (TDCPP) and triphenyl phosphate (TPP), respectively.

162 phate FRs that included triphenyl phosphate (TPP), tris(4-butylphenyl) phosphate (TBPP), and a mix of

163 etween 4.14 ng/g dw for tripropyl phosphate (TPP) and 7290 ng/g dw for TBOEP; for ash, they were betw

164 Total particulate phosphorus (TPP) and particulate phosphorus forms (nonapatite inorga

165 omains of TPS and trehalose-6-phosphorylase (TPP) in tandem as a fused gene product of Escherichia co

166 Trans-Proteomic Pipeline (TPP) provides a wide range of useful tools through its w

167 study investigated their total polyphenols (TPP), catechins, caffeine, gallic acid and theanine.

168 Trehalose polyphleates (TPP) are high-molecular-weight, surface-exposed glycolip

169 ters in themselves do not suffice to predict TPP channel entry.

170 tumor cell-penetrating peptide-based probe (TPP) recognizes an epitope of Hsp70 that is exclusively

171 alog, and in complex with a pair of products TPP and adenosine diphosphate.

172 h Organization (WHO) target product profile (TPP) criteria for a detection test and triage test to ev

173 f the high-priority target product profiles (TPP) published by the World Health Organization (WHO), t

174 applied MS-based thermal proteome profiling (TPP) to investigate the proteome-wide effects of missens

175 e application of thermal proteome profiling (TPP), a cellular thermal shift assay with an unbiased pr

176 ubunits based on thermal proteome profiling (TPP).

177 rank test p = 0.11); treatment per-protocol (TPP) 78.1% (95% CI: 0.65 to 0.86) and 53.5% (95% CI: 0.3

178 The tomato-potato psyllid (TPP), Bactericera cockerelli, is a vector for the phloem

179 Third-party punishment (TPP), in which unaffected observers punish selfishness,

180 n the case of the thiamine 5'-pyrophosphate (TPP) riboswitch from the Escherichia coli thiM gene enco

181 Thiamin pyrophosphate (TPP) is the active form of vitamin B(1) and works as an

182 Thiamin pyrophosphate (TPP) riboswitches are found in organisms from all three

183 final active coenzyme thiamin pyrophosphate (TPP).

184 r this control is via thiamin-pyrophosphate (TPP) riboswitches, regions of the mRNA to which TPP can

185 the cooperativity of thiamine pyrophosphate (TPP) binding into the two active sites, in the presence

186 The thiamine pyrophosphate (TPP) riboswitch is a cis-regulatory element in mRNA that

187 zes the last step of thiamine pyrophosphate (TPP) synthesis, the ATP-dependent phosphorylation of thi

188 o binds the cofactor thiamine pyrophosphate (TPP) with an affinity up to two-orders of magnitude lowe

189 Thiamine pyrophosphate (TPP)-dependent oxalate oxidoreductase (OOR) metabolizes

190 Thiamine pyrophosphate (TPP)-sensitive mRNA domains are the most prevalent ribos

191 amine in the form of thiamine pyrophosphate (TPP).

192 its modern catalyst, thiamine pyrophosphate (TPP).

193 he HR6 model fell short of TPP#1 but reached TPP#2 performance criteria.

194 By contrast, the reduced TPP oviposition trait in LA3952 is independent of Lso.

195 s work, we report Total Polyphenols results (TPP) obtained by these two techniques from a set of nine

196 We analyze a sample TPP riboswitch, and apply our algorithm to the class of

197 ays covering the large facets of disc-shaped TPP nanocrystals.

198 in, namely, silicon tetraphenylporphyrin (Si-TPP), by the deposition of atomic silicon onto a free-ba

199 The Si-TPP complex presents a saddle-shaped conformation that i

200 Complementary experiments yielding Si-TPP and Ge-TPP on Ag(111) highlight the applicability to

201 ockdown and overexpression lines of a single TPP, AtTPPG, points to unique properties of individual T

202 Six accessions with strong TPP resistance (survival <10%) were identified within S.

203 ly, our data show that neither the substrate TPP nor protonation induces large-scale conformational c

204 ve probed the specific binding of substrates TPP(+) and MTP(+) to EmrE reconstituted into 1,2-dimyris

205 r a community-based triage or referral test (TPP#2) have been published by the WHO.

206 rted for a series of tetraphenylphosphonium (TPP) metal halide hybrids containing distinct metal hali

207 ster relative to the tetraphenylphosphonium (TPP(+)) substrate-bound form of the protein.

208 yrins 1(P1) (P1 = meso-tetraphenylporphyrin (TPP)) and 1(P2) (P2 = 3,5-Di(t)Bu-ChenPhyrin) with organ

209 para positions of the tetraphenylporphyrin (TPP) phenyls results in an important positive deviation

210 in a large-area carbon/tetraphenylporphyrin(TPP)/LiF/carbon junction, where the LiF layer provides m

211 merized with diluents (tetraphenylporphyrin, TPP), followed by pyrolysis to N-doped porous carbon sup

212 Given that TPP is ubiquitous in house dust, further studies are war

213 Solvent mapping revealed that TPP interacted with binding hot spots within the PPARgam

214 spectral SRS microscopy imaging reveals that TPP can maintain stable affinity to mitochondria during

215 Here, we show that TPP aptamer folding can be decomposed into ligand-indepe

216 We show that TPP is indeed a signal of trustworthiness: third-party p

217 y to a long-day photoperiod, suggesting that TPP also plays a role in metabolic acclimation to the ph

218 s study demonstrates for the first time that TPP enables organ-specific drug target engagement and id

219 The TPP cation leads to the accumulation of MitoA inside mit

220 (VIA 71.3% vs. BMS 36.8%; p = 0.01) and the TPP analysis (VIA 73.3% vs. BMS 33.3%; p = 0.004).

221 result of increased planning or because the TPP promotes well-organized regulatory dialog.

222 lesions >/=20 cm and for all lesions in the TPP analysis.

223 ion and concomitant folding processes in the TPP riboswitch that culminate in the regulation of gene

224 as revealed new tertiary interactions in the TPP riboswitch.

225 evidence that the rate-limiting step in the TPP(+) transport cycle is not the outward-inward conform

226 lecules were not inserted as deeply into the TPP channels as the other half.

227 or tests that have the potential to meet the TPP specifications, we hope to support harmonized eviden

228 ondingly, we posit that such features of the TPP aptamer domain contribute directly to the mechanism

229 maging to probe the folding landscape of the TPP aptamer domain in the absence and presence of magnes

230 abling us to propose an updated model of the TPP biosynthetic pathway.

231 rotation potentials within a channel of the TPP host.

232 s likely to facilitate entry and exit of the TPP ligand.

233 rdinates with all four nitrogen atoms of the TPP macrocycle and interacts with a silver atom of the s

234 vides insights into the self-assembly of the TPP molecules before and after Si insertion.

235 are introduced at the ortho positions of the TPP phenyls.

236 also installed in the para positions of the TPP phenyls.

237 Injection of holes, i.e. formation of the TPP radical cation, inside the junction was monitored by

238 discovery of agonists and antagonists of the TPP riboswitch using simple fluorescence readouts.

239 ach instance, conformational dynamics of the TPP riboswitch were influenced by ligand binding.

240 structural mechanism similar to that of the TPP riboswitch, including the guanine and adenine ribosw

241 provides insight into the plasticity of the TPP riboswitches but also shows that their maintenance i

242 Furthermore, expression of the TPP Spinach riboswitch in Escherichia coli enables live

243 This difference, that can reach 50% of the TPP value, was related to the presence of total sulphur

244 as 2 degrees C broader in the absence of the TPP(+) substrate versus its presence, which suggested th

245 Specifically, a portion of the TPP-binding aptamer can form a base-paired structure wit

246 a linear dependence of the SRS signal on the TPP concentration, we successfully establish a quantitat

247 x, as well as distal regions surrounding the TPP-binding site, exhibit an unexpected degree of residu

248 These results suggest that the TPP genes function in the regulation of T6P levels, with

249 s without further labeling, we find that the TPP uptake causes little cytotoxicity to the host cells.

250 rstanding molecular mechanism throughout the TPP riboswitch family.

251 dichlorophenyl rotator contained within the TPP channel.

252 Therefore, TPP provides a useful tool for multimodal imaging of tum

253 This TPP Spinach riboswitch binds TPP with affinity and selec

254 Thus, TPP-PEG-PE can serve as a targeting ligand to prepare no

255 At the same time, TPP-PEG-L demonstrated efficient mitochondrial targeting

256 the weaker binding state is able to bind to TPP, but is unable to form a tertiary docking interactio

257 1:1, for unloaded ChNPs and 1:1:1 for Ch to TPP to CEO, for CEO-loaded ChNPs (CEO-ChNPs), were selec

258 We estimated exposure of children to TPP using a screening-level indoor exposure model and ho

259 s the major route of exposure of children to TPP.

260 Compared to TPP(H)A, reactive concordance of rp17 was 93.7%, while r

261 ma) ligands and estimated indoor exposure to TPP.

262 that modifies gene expression in response to TPP concentration.

263 ogy for the single-step reduction of TPPO to TPP using an aluminum anode in combination with a suppor

264 TPE-TPP exhibits a distinctive spectral shift in the presenc

265 Importantly, TPE-TPP can detect the presence of prefibrillar species form

266 An increase in TPE-TPP fluorescence intensity is observed only with ordered

267 e demonstrate the broad applicability of TPE-TPP to monitor amyloid fibril aggregation, including und

268 triphenylphosphonium) tetraphenylethene (TPE-TPP)) with aggregation-induced emission characteristics

269 tandard treponemal laboratory (TPPA or TPHA [TPP(H)A]) and quantitative RPR test data.

270 ith phos-phines, such as triphenylphosphine (TPP), 1,2-bis(diphenylphosphino)ethane [DPPE], and tris(

271 f the smallest clusters, triphenylphosphine (TPP)-stabilized undecagold, there are conflicting report

272 A novel triphenylphosphine (TPP) treatment strategy was developed to prepare the nea

273 tic organic reactions-to triphenylphosphine (TPP) remains an unmet challenge that would dramatically

274 Triphenylphosphonium (TPP) is a commonly used mitochondria-targeting agent for

275 comprises a lipophilic triphenylphosphonium (TPP) cation coupled to an aryl azide.

276 that is decorated with triphenylphosphonium (TPP) cations for detection of mitochondrial membrane pot

277 prepared via complexation with triphosphate (TPP) anions and were successively coated with hyaluronic

278 albumin (BSA) in chitosan-tripolyphosphate (TPP) hydrogel beads.

279 was cross-linked to sodium tripolyphosphate (TPP) to produce nano-sized polyelectrolyte complexes wit

280 ionic gelation with sodium tripolyphosphate (TPP), further encapsulated in ZN microparticles, were fo

281 ratios of chitosan (Ch) to tripolyphosphate (TPP), 1:1, for unloaded ChNPs and 1:1:1 for Ch to TPP to

282 ipids produced by Mycobacterium tuberculosis TPP production starts in the cytosol with the formation

283 1 showed processing activity against various TPP substrates at a level comparable to that of LepB.

284 o that matched those observed previously via TPP binding to each variant.

285 reate benefits for deterring selfishness via TPP).

286 nide was actually a better catalyst than was TPP in simple solution, where there is a negligible conc

287 Of 589 specimens, 241 were TPP(H)A(+)/RPR(+), 88 were TPP(H)A(+)/RPR(-), 6 were TPP

288 +)/RPR(+), 88 were TPP(H)A(+)/RPR(-), 6 were TPP(H)A(-)/RPR(+), and 254 were negative for both tests.

289 ecimens, 241 were TPP(H)A(+)/RPR(+), 88 were TPP(H)A(+)/RPR(-), 6 were TPP(H)A(-)/RPR(+), and 254 wer

290 is a strong and highly used signal even when TPP is also possible.

291 ) riboswitches, regions of the mRNA to which TPP can bind directly, thus facilitating fine-tuning to

292 multiantigen set performance approached WHO TPP criteria for clinical utility among HIV-uninfected a

293 Two gene signatures achieved the minimal WHO TPP for a non-sputum-based triage test.

294 It seamlessly integrates with TPP and other external command-line programs, supporting

295 Using TT with TPP characteristics (unit cost of US$1-2) followed by Xp

296 primitive enzymes were present to work with TPP, or most likely its primitive precursors.

297 en the boryl substituent is absent (e.g., Zn-TPP and TPP).

298 The practical utility of DA-ZP1-TPP is demonstrated by experiments revealing that, in co

299 DA-ZP1-TPP is insensitive to intracellular esterases over a 2-h

300 phenylphosphonium Zinpyr-1 diacetate (DA-ZP1-TPP), is essentially nonfluorescent in the metal-free st