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 e, we present an in-depth analysis of the 10 TPP genes and gene products in Arabidopsis (TPPA-TPPJ).

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

7 ) and pyrimidine (Pyr) binding domains of 17 TPP-dependent enzymes.

8 ment of GeCl2(dioxane) with Li2(TPP)(OEt2)2 (TPP = tetraphenylporphyrin) in THF yields Ge(TPP), the f

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

10 expression of this operon is regulated by a TPP-binding riboswitch via a feedback inhibition mechani

11 ulated by exogenous TPP and is mediated by a TPP-sensing riboswitch (Td(thi-)(box)).

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

13 we identified a gene cluster that encodes a TPP ABC transporter which consists of a TPP-binding prot

14 n, the structure shows that the protein is a TPP-binding protein, opening up many avenues for future

15 es a TPP ABC transporter which consists of a TPP-binding protein (TDE0143), a transmembrane permease

16 We have established that a TPP-sensing riboswitch is present in the 3' untranslated

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

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

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

20 , whose evolutionary histories extend to all TPP-dependent enzymes.

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

22 o with the products of the reaction, ADP and TPP.

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

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

25 FM550 and TPP diverted osteogenic differentiation toward adipogene

26 and the density maps of the ligand-free and TPP+-bound forms of EmrE, we identify regions within the

27 in the absence and presence of magnesium and TPP.

28 gether, our studies suggest that thiamin and TPP function as important stress-response molecules that

29 xidative treatments, accumulated thiamin and TPP.

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

31 11 genes encode proteins with both TPS- and TPP-like domains but only one of these (AtTPS1) appears

32 e site models (TPP)FeII(ImH)2 (FeIIImH) and (TPP)Fe(Im)(ImH) (FeIIIIm) have been examined in acetonit

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

34 ind at the same pocket within the protein as TPP+.

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

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

37 of Kir2.6 are associated with SPP as well as TPP.

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

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

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

41 adducts between TPP and oxalate and between TPP and CO2.

42 boswitch employs modular domains for binding TPP to form a platform for gene expression regulation.

43 nsor that exhibits fluorescence upon binding TPP.

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

45 attached to the distal end of the PEG block (TPP-PEG-PE).

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

47 d binding appeared to be driven primarily by TPP.

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

49 orophore, and a triphenylphosphonium cation (TPP).

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

51 es were investigated as a function of the CH:TPP molar ratio (2.0:1.0-5.0:1.0).

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

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

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

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

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

57 bsence of olefin substrates, reaction of [Co(TPP)] with ethyl styryldiazoacetate was found to generat

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

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

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

61 family of smaller proteins with a conserved TPP domain.

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

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

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

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

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

67 ated for the most likely application of each TPP.

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

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

70 operon is negatively regulated by exogenous TPP and is mediated by a TPP-sensing riboswitch (Td(thi-

71 TPP biosynthesis pathway and needs exogenous TPP for growth, suggesting that it may obtain exogenous

72 wth, suggesting that it may obtain exogenous TPP via a thiamine transporter.

73 that is required for the uptake of exogenous TPP and that the expression of this operon is regulated

74 d a decreased ability to transport exogenous TPP, and the mutant failed to grow when exogenous TPP wa

75 and the mutant failed to grow when exogenous TPP was insufficient.

76 The corresponding model complex, [Fe(TPP)(MI)(NO)](BF4) (MI = 1-methylimidazole), is studied

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

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

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

80 lternative 3' end processing is critical for TPP-dependent feedback control of THIC expression.

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

82 0.17 +/- 0.064 muM; and highly specific for TPP and not affected by free thiamine, thiamine monophos

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

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

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

86 ndrial matrix chaperone inhibitor gamitrinib-TPP.

87 etics and enhanced the effects of gamitrinib-TPP.

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

89 ine dissociates from Ge(TPP)(py)2 to form Ge(TPP).

90 s reversed, and pyridine dissociates from Ge(TPP)(py)2 to form Ge(TPP).

91 constant of the reaction Ge(TPP) + 2 py = Ge(TPP)(py)2 in C6D6 is 22 M-2.

92 In pyridine Ge(TPP) is converted to Ge(TPP)(py)2, an antiaromatic Ge(IV

93 The equilibrium constant of the reaction Ge(TPP) + 2 py = Ge(TPP)(py)2 in C6D6 is 22 M-2.

94 In pyridine Ge(TPP) is converted to Ge(TPP)(py)2, an antiaromatic Ge(IV) complex, whereas in be

95 TPP = tetraphenylporphyrin) in THF yields Ge(TPP), the first free Ge(II) porphyrin complex.

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

97 The order of reactivity was OEP > TPP > TMP.

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

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

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

101 ted with triphenylphosphonium hydroethidine (TPP-HE), which forms the superoxide specific reporter hy

102 Tripeptidyl peptidase I (TPP I) is the first mammalian representative of a family

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

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

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

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

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

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

109 mRNAs, which code for a protein involved in TPP metabolism.

110 Naturally occurring mutations in TPP I underlie a neurodegenerative disorder of childhood

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

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

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

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

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

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

117 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/

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

119 The 64Cu-labeled TPP/TPA cations are very selective radiotracers that are

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

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

122 Treatment of GeCl2(dioxane) with Li2(TPP)(OEt2)2 (TPP = tetraphenylporphyrin) in THF yields G

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 These TPP-PEG-PE-modified liposomes (TPP-PEG-L), surface grafted with as high as 8 mol% of th

126 PTX-loaded TPP-PEG-L demonstrated enhanced PTX-induced cytotoxicity

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

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

129 Generation of mature TPP I is associated with removal of a long prosegment of

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

131 transfer catalyst and manganese porphyrin Mn(TPP)Cl 1, reaction of sodium hypochlorite with different

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

133 is(histidine) cytochrome active site models (TPP)FeII(ImH)2 (FeIIImH) and (TPP)Fe(Im)(ImH) (FeIIIIm)

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

135 mportant source of exposure to TDCPP but not TPP.

136 It lacks a de novo TPP biosynthesis pathway and needs exogenous TPP for gro

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

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

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

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

141 vealed the double mutant is nearly devoid of TPP and instead accumulates the precursor of the TPK rea

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

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

144 n glioma xenografts to explore the impact of TPP moieties, linkers, bifunctional chelators (BFCs), an

145 ) are suitable BFCs for the 64Cu-labeling of TPP cations; (3) NOTA-Bn ( S-2-(4-thioureidobenzyl)-1,4,

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

147 1(PPh3)8Cl2]Cl, differ only in the number of TPP ligands bound to the core.

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

149 we investigated the inhibitory properties of TPP I prosegment expressed and isolated from Escherichia

150 Interestingly, the inhibitory properties of TPP I prosegment with the introduced classic late infant

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

152 80% specificity, the HR6 model fell short of TPP#1 but reached TPP#2 performance criteria.

153 ter hydroxytriphenylphosphonium ethidium (OH-TPP-E(+)).

154 ing mainly of thyrotoxic periodic paralysis (TPP) and sporadic periodic paralysis (SPP), is largely u

155 Thyrotoxic hypokalemic periodic paralysis (TPP) is characterized by acute attacks of weakness, hypo

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

157 dentified threonine phosphorylation pathway (TPP) share the property of secretory ATPase recruitment

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

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

160 iphenylphosphonium (TPP) polymer (PLGA-b-PEG-TPP) with either nontargeted PLGA-b-PEG-OH or PLGA-COOH.

161 ase called thylakoidal processing peptidase (TPP).

162 ide trehalose (catalyzed by T6P phosphatase [TPP]).

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

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

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

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

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

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

169 nalyzed according to the IL28B polymorphism, TPP SVR rates did not reach statistically significant di

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

171 Temperature pulse potentiometry (TPP) gives convenient peak-shaped analytical signals and

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

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

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

175 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

176 t when calculated on a treated-per-protocol (TPP) basis.

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

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

179 Thiamin and thiamin pyrophosphate (TPP) are well known for their important roles in human n

180 Thiamin pyrophosphate (TPP) is an essential enzyme cofactor required for the vi

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

182 osphate (TMP) to form thiamin pyrophosphate (TPP), the active form of vitamin B 1.

183 tamin B(1) derivative thiamin pyrophosphate (TPP).

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

185 The structure shows thiamine pyrophosphate (TPP) and two calcium ions are bound to Cypl and give the

186 ucture of the native thiamine pyrophosphate (TPP) riboswitch aptamer domain and identified large chan

187 The thiamine pyrophosphate (TPP) riboswitch employs modular domains for binding TPP

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

189 latory mechanisms of thiamine pyrophosphate (TPP) riboswitches and has not been fully characterized.

190 Thiamine pyrophosphate (TPP), a biologically active form of thiamine (vitamin B(

191 onds to the coenzyme thiamine pyrophosphate (TPP), which is a derivative of vitamin B1.

192 relationships of the thiamine pyrophosphate (TPP)-dependent family of enzymes was investigated by gen

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

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

195 its modern catalyst, thiamine pyrophosphate (TPP).

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

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

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

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

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

201 have been examined in acetonitrile solvent (TPP = tetraphenylporphyrin, ImH = 4-methylimidazole).

202 g K(+) channel Kir2.6, were reported in some TPP patients.

203 Specifically, TPP binding triggers a conformational switch in the RNA

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

205 Microorganisms either synthesize TPP via de novo biosynthesis pathways or uptake exogenou

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

207 tionic drugs such as tetraphenylphosphonium (TPP+), ethidium, propidium and dequalinium.

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

209 tudied were 5,10,15,20-tetraphenylporphyrin (TPP), 5,10,15,20-tetramesitylporphyrin (TMP), and 2,3,7,

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

211 lective bromination of tetraphenylporphyrin (TPP) by NBS.

212 In 10% MeOH/H(2)O, the tetraphenylporphyrin (TPP) and 1,4,5,8-naphthalenetetracarboxylic acid diimide

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

214 better mitochondrion-targeting molecule than TPP and 3mTPP (tris(2,4,6-trimethoxyphenyl)phosphonium);

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

216 ty of these conditions, we hypothesized that TPP might also be a channelopathy.

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

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

219 We show that TPP binding proceeds in two steps, from a weakly to a st

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

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

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

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

224 MeOH, assembly is driven exclusively by the TPP ring, leading to the formation of nonspecific, unstr

225 resentative values of rate constants for the TPP derivative were k = 8.6 x 10(5) M(-1) s(-1) for styr

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

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

228 as revealed new tertiary interactions in the TPP riboswitch.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

245 We show that the TPP I prosegment is a potent, slow-binding inhibitor of

246 ctivates the H1-T6SS exclusively through the TPP.

247 rstanding molecular mechanism throughout the TPP riboswitch family.

248 The phylogeny is most parsimonious with the TPP enzymes having arisen from a homotetramer which subs

249 idylethanolamine (PEG-PE) conjugate with the TPP group attached to the distal end of the PEG block (T

250 dichlorophenyl rotator contained within the TPP channel.

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

252 These TPP-PEG-PE-modified liposomes (TPP-PEG-L), surface graft

253 The THIC TPP riboswitch controls the formation of transcripts wit

254 This TPP Spinach riboswitch binds TPP with affinity and selec

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

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

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

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 TPE-TPP exhibits a distinctive spectral shift in the presenc

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

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

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

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

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

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

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

271 on of the 64Cu-labeled triphenylphosphonium (TPP) cations as new radiotracers for imaging tumors by p

272 f six new 64Cu-labeled triphenylphosphonium (TPP) cations.

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

274 ethylene glycol) (PEG)-triphenylphosphonium (TPP) polymer (PLGA-b-PEG-TPP) with either nontargeted PL

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

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

277 Chitosan (CH)-tripolyphosphate (TPP) submicron particles were formed as carriers of entr

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

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

280 erved heterozygous mutation in KCNJ18 in two TPP patients and two separate heterozygous mutations in

281 s were present in up to 33% of the unrelated TPP patients in our collection.

282 1 showed processing activity against various TPP substrates at a level comparable to that of LepB.

283 reate benefits for deterring selfishness via TPP).

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

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

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

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

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

289 that are different to those that occur when TPP+ binds.

290 le during transcription elongation and where TPP's binding shifts the preference to one form.

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

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

295 uptake and tumor/liver ratios, 64Cu(DO2A-xy-TPP)+ is the best candidate for more extensive evaluatio

296 c finger protein 36 C3H type-like 1 (ZFP36L1/TPP).

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