ライフサイエンスコーパス: be prepared using

1 Artificially ventilated rats were prepared using 1.2-1.5% isoflurane anesthesia for f

2 Vesicles were prepared using 10,12-pentacosadienoic acid (PCDA)/1

3 (165)Ho-MSNs were prepared using (165)Ho-acetylacetonate and MCM-41 s

4 (89)Zr-labeled liposomes were prepared using 2 different approaches: click labeli

5 oxy-2'-fluoro-beta-D-ribofuranosyl compounds were prepared using 2'-deoxy-2'-fluorouridine, N-deoxyri

6 A cDNA library was prepared using 21 different pools of maize (Zea mays

7 nine, thymine and cytosine PNA monomers have been prepared using 3-amino-1,2-propanediol as a startin

8 The polymer was prepared using 4-vinylpiridine (VIPY) and methacryla

9 The requisite five-carbon skeletons were prepared using 4 + 1, 3 + 2, 2 + 2 + 1, and 2 + 1 +

10 A homogeneously labeled insulin sample was prepared using 6-aminoquinolyl-N-hydroxysuccinimidyl

11 The primary cultures were prepared using 6- to 9-day-old Sprague-Dawley rats.

12 Low-fat patties with 0.5-3% MCC/CMC were prepared using 90% of beef and 10% of an aqueous fi

13 nd a LiFePO4 cathode with 80% stretchability are prepared using a 3D interconnected porous polydimeth

14 ticles with an option of nitrogen (N) doping are prepared using a cost-effective method.

15 These novel fluorophores are prepared using a microwave-assisted dehydrogenative

16 MoS2(1-x) Se2x single-layer films are prepared using a mixture of organic selenium and sul

17 Nanocomposite polymers are prepared using a new sustainable materials synthesis

18 Functionalized diazatetracenes are prepared using a new two-step sequence.

19 of enzymatically active hybrid nanoclusters are prepared using a novel approach based on electrostat

20 Polyelectrolyte complex microcapsules are prepared using a novel template- and surfactant-free

21 brid, mesostructured SBA-15 silica materials are prepared using a postsynthetic grafting procedure th

22 These cylindrical-shaped nanochannels are prepared using a simple laser-assisted mechanical pu

23 ntiomerically enriched heterocycles can also be prepared using a Cinchona alkaloid-derived bifunction

24 f the phosphodiester backbone of RNA and can be prepared using a relatively straightforward peptide c

25 f the phosphodiester backbone of RNA and can be prepared using a relatively straightforward peptide c

26 roach is scalable, and thousands of DIBs can be prepared using a robot in one hour; therefore, it is

27 The bicyclic core of octosyl acid A has been prepared using a diastereoselective acetylide addit

28 cyclic isophthalamide polyether ligands have been prepared using a general anion templation procedure

29 guanosine and cytidine at the end groups has been prepared using a modular one-pot azide-alkyne cyclo

30 wever, until now, single MFI nanosheets have been prepared using a multi-step approach based on the e

31 tags, with distinct encoding patterns, have been prepared using a one-step templated electrodepositi

32 A dyad assembly has been prepared using a pyrazine-based linker to join a ph

33 c aromatic hydrocarbons (PAHs) as donors has been prepared using a solventless technique.

34 ymer of intrinsic microporosity (PIM-1) have been prepared using a spin-coating technique.

35 (CAAC = cyclic (alkyl) (amino)carbene), has been prepared using a transfer reaction from the linear

36 These nanoparticles have been prepared using a water-in-oil (W/O) microemulsion m

37 and dry-air-stable glass 0.4LiI-0.6Li4 SnS4 is prepared using a homogeneous methanol solution.

38 scribe a diiron sulfide hydride complex that is prepared using a mild method involving C-S cleavage o

39 e, we present a graphene-based membrane that is prepared using a simple and environmentally friendly

40 r demonstration purposes, duplex CIT reagent is prepared using a single isotope-coded precursor, ally

41 ynthetic, fault-free gmelinite (GME) zeolite is prepared using a specific organic structure-directing

42 This compound, which was prepared using a [(18)F]fluoroethyl prosthetic group

43 diate 4-[(18)F]fluoro-m-tyramine ([(18)F]16) was prepared using a diaryliodonium salt precursor for n

44 The contact site fraction was prepared using a discontinuous sucrose gradient from

45 the shell of polyvinylidene fluoride (PVdF) was prepared using a facile one-pot electrospinning tech

46 (R)-Sarkomycin was prepared using a five-step total synthesis.

47 Pyrene-labeled P4-P6 was prepared using a new phosphoramidite that allows hig

48 The more exhaustive series was prepared using a nitrated isoquinoline ring that has

49 -coordinate Pd(0)-hydroquinone complex (4-H) was prepared using a one-pot metalation with Pd(II) foll

50 rotein isolate solution as outer water phase was prepared using a rotor stator system.

51 The library (8000 compounds) was prepared using a solution-phase synthetic protocol e

52 The library was prepared using a solution-phase synthetic protocol w

53 (64)Cu-TP3805 was prepared using a sterile kit containing 20 mug of TP

54 ermed metal-organic framework-901 (MOF-901), was prepared using a strategy that combines the chemistr

55 In this study, in which posterior lamellae were prepared using a 300-mum head microkeratome, adjust

56 The compounds were prepared using a 4-5-step process, involving as a k

57 cosamine derivatives of sialyl Lewis X (1-3) were prepared using a combined chemical enzymatic approa

58 vesicles with an exposed cytoplasmic surface were prepared using a French pressure cell.

59 -bridged cycloparaphenylene dimers (1 and 2) were prepared using a functionalized precursor, bromo-su

60 displaying 5035 unique binding environments were prepared using a library of 19 small molecule build

61 ants (E302D, S478A, S478T, H480K, and H480Q) were prepared using a mammalian cell expression system.

62 In an effort to increase sensitivity, smears were prepared using a minimum sputum volume of 5.0 ml.

63 The cubic Pb(2-x)Sn(x)S(2) nanocrystals were prepared using a modified hot injection colloidal s

64 The two key intermediates were prepared using a modified Strecker reaction for the

65 Niosomes were prepared using a modified thin film hydration metho

66 Trimer and 7-mer monodendrons were prepared using a monomer with 3, 3-diethyltriazene

67 onodisperse fluoreneborane oligomers (n=1-6) were prepared using a new iterative synthetic procedure

68 Left-handed gold nanoparticle double helices were prepared using a new method that allows simultaneou

69 eries of substituted angular benzophenazines were prepared using a new synthetic route via a novel re

70 to give "staggered" interstrand cross-links were prepared using a novel N(4)C-ethyl-N(4)C phosphoram

71 Peptide-coated CdSe/ZnS quantum dots were prepared using a one-step ligand exchange process i

72 Compounds such as 20 were prepared using a palladium-catalyzed Ullmann cross-

73 changes accessible only by total synthesis, were prepared using a powerful intramolecular [4 + 2]/[3

74 olatile organic compounds (VOCs) in nitrogen were prepared using a procedure previously developed to

75 ximal promoter activity, deletion constructs were prepared using a pSEAP vector system and transfecte

76 ne (at C-2 and C-3 of the quinolizin-4-one), were prepared using a sequence of seven synthetic transf

77 dium bimetallic heterogeneous nanostructures were prepared using a sequential synthetic method, in wh

78 ing of a BODIPY donor and a cyanine acceptor were prepared using a simple synthetic route, and their

79 The meat samples were prepared using a treatment that allowed the product

80 a His26 to Gln or His33 to Asn substitution were prepared using a yeast expression system.

81 Samples were prepared using accelerated solvent extraction prior

82 Successful cultures were prepared using adult mouse basal cells selected for

83 Six cellulase calibration standards were prepared using affinity digestion.

84 In the present work, lectin arrays were prepared using aldehyde-terminated self-assembled m

85 tags, with distinct encoding patterns, have been prepared using an apoferritin template.

86 hylpyrrolidin-2-ylmethyl)-4-hydoxyindole, 3, were prepared using an asymmetric synthesis that employe

87 Enantiopure TpMo(CO)2(pyridinyl) complexes were prepared using an efficient and scalable enzymatic

88 ium channels, several novel beta-amino acids were prepared using an efficient nitroalkane-mediated cy

89 FVIII-polyethylene glycol (PEG) conjugates were prepared using an enzymatic process coupling PEG (r

90 contulakin-G and its nonglycosylated analog were prepared using an Fmoc (9-fluorenylmethoxycarbonyl)

91 Libraries were prepared using an optimized semi-automated library

92 ot tandem process, a series of cyclic dienes were prepared using an Overman rearrangement under therm

93 ce and presence of alpha-tocopherol (4 wt.%) were prepared using an ultradisperser (10,000 rpm for 10

94 In the current study, proteoliposomes were prepared using AquaporinZ from Escherichia coli cel

95 Two synthetic hosts were prepared, using as templates 5,10,15,20-tetrakis(4-

96 The copolymers were prepared using atom-transfer radical polymerization

97 5'-BAL-ODNs are prepared using automated DNA synthesis and an acetal

98 The oligomers were prepared using automated phosphoramidite chemistry

99 Low bandgap polymers (bandgap = 1.4-1.5 eV) were prepared using BDTT, BDTP, FDPP, and DPP units via

100 The nanomeshes are prepared using block copolymer lithography and can h

101 However, when a substrate is prepared using both Nafion and a hydrophilic, high-mo

102 y-4-fluoro-N-acetylgalactosamine (4FGalNAc), were prepared using both chemical and chemoenzymatic syn

103 A total of 28 variants were prepared using both naturally occurring and non-nat

104 ors and biofuel cells, the enzyme electrodes were prepared using CA, EC, and EPC samples.

105 ation of industrial potato fruit juice (PFJ) was prepared, using Canadian variety of potatoes, and wa

106 Patients were prepared using carmustine, etoposide, cytarabine, a

107 s differing in these hydrophobic amino acids was prepared using cassette mutagenesis, then displayed

108 Carbon-fiber reinforced composites are prepared using catalyst-free malleable polyimine net

109 g enantiomer) and (+)-11-epi-terpestacin (2) were prepared using catalyst-controlled, stereoselective

110 in an average flake size and zeta-potential were prepared using centrifugation and consequently empl

111 The CdS was prepared using chemical bath deposition in a solutio

112 oup B meningococcal (GBM) conjugate vaccines were prepared using chemically modified N-propionylated

113 The Fp subcomplex was prepared using chromatography and contained the 51 a

114 A focused library of these compounds was prepared using click chemistry and the selectivity c

115 One tripeptide arm was prepared using combinatorial chemistry to generate t

116 ix- and seven-membered cyclic enaminones can be prepared using common, environmentally benign reagent

117 ss, it is suitable for many applications and is prepared using conventional equipment without the use

118 ubstituted pyrrole, furan, or thiophene ring were prepared using conventional methods, and these were

119 SiNc solutions were prepared using Cremophor EL in water and evaluated

120 The beta-alanine component was prepared using Davies' asymmetric 1,4-addition metho

121 pproach to catalysis, a Zn(II) metalloenzyme was prepared using de novo design.

122 latinum nanoparticles between 0.8 and 5.0 nm were prepared using dendrimer and polymer capping agents

123 Thiol monolayer-protected Au clusters (MPCs) were prepared using dendrimer templates, deposited onto

124 ydroxy-substituted homopipecolic acids, have been prepared using diastereoselective olefinic oxidatio

125 The epoxides were prepared using diastereoselective addition of a sul

126 In this study, microelectrode biosensors were prepared using different enzyme immobilization meth

127 heres with different release characteristics were prepared using different manufacturing processes.

128 many promising self-assembled materials have been prepared using disordered or liquid coacervate poly

129 rials with unusual mechanical properties can be prepared using DNA as a building block.

130 ion of elements was increased when infusions were prepared using dripper or Turkish coffee preparatio

131 Immunoliposome nanoparticles (ILs) were prepared using EGFR scFv with a 280-fold range of a

132 atic differentiated thyroid cancer (DTC) may be prepared using either thyroid-stimulating hormone wit

133 joins the two C residues of a -CNG- sequence were prepared using either a phosphoramidite or converti

134 32Dcl3 and Ba/F3 cell cycle fractions were prepared using elutriation.

135 Whey protein isolate (WPI) nanoparticles were prepared using ethanol desolvation, and their capac

136 0 putative transcript clones from the region was prepared using exon amplification and pituitary cDNA

137 d phase extraction (SPE) of florfenicol (FF) was prepared using FF as template and 4-vinyl pyridine (

138 x environments, model extracellular matrices were prepared using gelatin, Hanks' solution, Bodipy-BSA

139 Nanoporous silicon films were prepared using glancing angle deposition (GLAD) thi

140 chiroptical activity and strong luminescence are prepared using gold nanorods and upconversion nanopa

141 hyde-substituted distyrylbenzene derivatives were prepared using Heck or Horner methodologies.

142 sults were confirmed via EM using cells that were prepared using high-pressure freezing.

143 of Crotalus adamanteus L-amino acid oxidase was prepared using hydrophobic interaction chromatograph

144 s of retinal astrocytes, microglia, and RGCs were prepared using immunomagnetic separation.

145 turally occurring aminoglycoside tobramycin, was prepared using improved synthetic procedures that al

146 ART was prepared using indinavir (IDV) nanoparticles (NP, na

147 In addition, six CSPs were prepared using individual selectors from the librar

148 The teas were prepared using infusion times of 3, 6, and 10min at

149 Sequence-defined non-natural polyphosphates were prepared using iterative phosphoramidite protocols

150 lipids at air-water and air-solid interfaces were prepared using Langmuir and Langmuir-Blodgett (LB)

151 A single-material battery is prepared using Li10GeP2S12 as the electrolyte, anode,

152 r the 3,5-positions of the meso phenyl rings were prepared using Lindsey conditions.

153 methylthiolane and (-)-2,5-dimethylsulfolane were prepared using literature procedures and investigat

154 as 500 nm, surrounded by hydrophobic regions were prepared using lithography and self assembled monol

155 Hydroxyl-terminated polymeric precursors were prepared using living anionic polymerization and su

156 l predictions and that effective sensors can be prepared using low plate number columns.

157 Binary systems comprising CNTs and HemNPs were prepared using low ionic strength solutions to mini

158 substrates with a long duplex region (50 bp) were prepared using M13mp19 ssDNA and synthetic oligonuc

159 A CMAC(alpha4beta2 nAChR) column was prepared using membrane fragments from a SH-EP1-pCEP

160 o-2-substituted-5,6-norbornene skeleton, can be prepared using Mo(N-2,6-Me2C6H3)(CHCMe2Ph)(OHMT)(pyrr

161 osed of approximately 200 nm diameter fibers were prepared using needleless electrospinning.

162 calibration source currently on the market, were prepared using NIST-calibrated solutions of (68)GeC

163 The optically pure arylsilylcarbinols were prepared using Noyori's transfer hydrogenation cata

164 Nitric oxide (NO.) sensors were prepared using o-phenylenediamine (o-PD) and Nafion

165 sites, nanoflowers, nanotubes and nanofibers were prepared using optimized value of f.

166 library of substituted benzamide derivatives was prepared using parallel synthesis on solid support.

167 Both C-glycosides were prepared using Pd-mediated coupling of iodinated ba

168 The copolymer is prepared using pNIPAM, which governs the thermal prop

169 NPS were prepared using poly(lactic-co-glycolic acid) (PLGA)

170 m-ring and macrocyclic nitrogen heterocycles were prepared using polyene and polyenyne metathesis cas

171 Macroporous TaON (mac-TaON) is prepared using polymer sphere templating and controll

172 Six samples each of mephedrone were prepared using precursor chemicals from two differe

173 liposomes containing calcein or doxorubicin were prepared using pteroyl-gamma-glutamate-cysteine-PEG

174 printed electrode (NiONPs/Nafion-MWCNTs/SPE) were prepared using pulsed electrodeposition of NiONPs o

175 The standards were prepared using pure CO2 obtained from different sou

176 topology, BINAP-MOF (I) or BINAP-dMOF (II), were prepared using purely BINAP-derived dicarboxylate l

177 Peptide-decorated fibrin was prepared using purified fibrinogen as the starting m

178 The substrates were prepared using purified HS biosynthetic enzymes.

179 The ring C precursor was prepared using pyridine substitution and directed li

180 CD19+, and CD3+ cell subsets; DNA templates were prepared using quantitative polymerase chain reacti

181 mulsions containing alpha-tocopherol acetate were prepared using quillaja saponin as a natural surfac

182 ally and pharmaceutically relevant alkaloids were prepared using (R)-TRIP as the chiral catalyst: (R)

183 Heterocylcles 9a-j were prepared using readily available starting materials

184 dditional stereoisomers of lobatamide C have been prepared using related synthetic routes.

185 Two constructs were prepared using replication-deficient adenoviral vec

186 s in the sequence of PAA-PC5MA-PEO-PC5MA-PAA were prepared using reversible addition-fragmentation ch

187 ivity of 22 +/- 1 mS cm(-1) at 22 degrees C) were prepared using ring-opening metathesis polymerizati

188 en PBLs were activated in vitro, and lysates were prepared using RIPA buffer which contains 1% Nonide

189 Replicate cultures were prepared using RPE cell sheets isolated with Dispas

190 able activity and sustained biocidal release were prepared using sequential chemical grafting of nano

191 variations (mutations and/or polymorphisms) were prepared using site-directed mutagenesis from the w

192 f aligned single-walled carbon nanotubes can be prepared using slow vacuum filtration.

193 ol-gel coated fused-silica capillary columns were prepared using sol-gel-active PEG derivatives.

194 These peptides were prepared using solid-phase peptide synthesis with F

195 LLP2A-DOTA and LLP2A-CB-TE2A were prepared using solid-phase synthesis; LLP2A-DOTA-PE

196 A large number of analogues were prepared using solution-phase parallel synthesis.

197 o diverse superstructures of nanoscopic CdSe were prepared using solvothermal conversion of the same

198 xane/divinylbenzene (PDMS/DVB) TFME samplers were prepared using spin coating and glass wool fabric m

199 ermeable polymer with enhanced selectivities is prepared using spirobifluorene as the main structural

200 ) were positive before treatment when smears were prepared using sputum of any volume, and significan

201 The EC cell was prepared using standard semiconductor processing tec

202 Two orthogonal channels were prepared using standard PDMS techniques with pressu

203 and Rh + Pt monometallic nanoparticles (NPs) were prepared using standard polyol reduction chemistry

204 These electrodes were prepared using standard templating or dealloying te

205 t work it is shown that "liquid marbles" can be prepared using sterically stabilized polystyrene late

206 However, alpha-stannyl benzoates need to be prepared using stoichiometric amounts of the (+)- or

207 ith 100-microns optical fiber but could also be prepared using submicrometer fiber tips.

208 nriched detergent-resistant membrane domains were prepared using sucrose gradient ultracentrifugation

209 ange order and semiconducting properties can be prepared using suitable molecular building blocks, li

210 Six treatments were prepared using sunflower oil to prepare the primary

211 RNA sequences, each with a biotin tag, have been prepared using T7 RNA polymerase-catalyzed transcri

212 When isogenic toxin null mutants were prepared using TargeTron technology, even a double

213 aquat-p-phenylene) (CBPQT(4+)) ring has also been prepared using template-directed protocols.

214 Zn and Co homochiral CPs (1P, 1M and 2P, 2M) are prepared using the achiral precursors.

215 ions allowing gold nanoparticles (AuNPs) to be prepared using the ONPs as templates.

216 macrocycles, containing a furan moiety, have been prepared using the all-in-solution approach of dyna

217 harge-differentiated platinum complexes have been prepared using the bidentate phosphine ligands [Ph(

218 R spectra of the dodecylated SWNTs that have been prepared using the different alkali metals and may

219 Complexes of hLL2 that had been prepared using the DTPA-type chelates lost 3%-4% of

220 A new aluminosilicate zeolite, ITQ-27, has been prepared using the phosphorus-containing structure-

221 production of chiral separation media, have been prepared using the staged templated suspension poly

222 The mixed-metal linear array was prepared using the "synthesis at metal" approach, an

223 The anti-inflammatory Oxaprozin was prepared using the alpha-sulfonyl carbanion strategy

224 oupling protocol, whereas the (1-->4)-mannan was prepared using the analogous thioglycoside/sulfinami

225 Recombinant CYP2J2 protein was prepared using the baculovirus expression system and

226 oaded membrane with high extraction capacity was prepared using the bar coating method.

227 125I-labeled-IGF-I was prepared using the chloramine T method.

228 (18)F-AFETP was prepared using the click reaction.

229 Indoprofen itself was prepared using the conventional VNS reaction in four

230 ntary target, containing 156 mer nucleotide, was prepared using the fresh blood from patients with al

231 One apheresis product from each patient was prepared using the Isolex 300 Magnetic Cell Separati

232 op-2 x antihapten bispecific antibody, TF12, was prepared using the modular dock-and-lock method.

233 paste electrode that is sensitive to glucose was prepared using the nanoparticles modified (4-Formyl-

234 An affinity column was prepared using the recombinant fragment.

235 richloro-(1-beta-D-ribofuranosyl)indole (19) was prepared using the same synthetic route with 2,5,6-t

236 mology model of a putative YaaD-YaaE complex was prepared using the structure of HisH-F as a model.

237 ecyl ethers (X-POEs, where X = H, Cl, Br, I) was prepared using the Williamson ether synthesis and ch

238 tudy, S. cerevisiae crude membrane fractions were prepared using the acid-labile detergent RapiGest f

239 The alpha-aminomethylacrylates (2a-c) were prepared using the Baylis-Hillman reaction of an ap

240 le PLGA Flt23k loaded or blank nanoparticles were prepared using the emulsion solvent evaporation MET

241 ructures with good stereochemical parameters were prepared using the EXDIS/DIAMOD/FANTOM program suit

242 Regular prismatic KPR crystals were prepared using the hanging drop technique.

243 Several chiral sulfonyl compounds were prepared using the iridium catalyzed asymmetric hyd

244 nation of LPV/ritonavir (RTV) ISNP granules, were prepared using the ISNP nanotechnology, which spont

245 r mass 2400 Da and low polydispersity (1.09) were prepared using the Langmuir-Blodgett technique to i

246 Asymmetric PSLBs were prepared using the Langmuir-Blodgett/Langmuir-Schae

247 hree isomeric adj-dinaphthoporphyrin systems were prepared using the MacDonald "2 + 2" condensation o

248 of structural isomers [(SnSe)1.05]m(MoSe2)n were prepared using the modulated elemental reactant met

249 Initial adducts were prepared using the peptide sequence valine-citrulli

250 Two forms of double-stranded DNA fragments were prepared using the polymerase chain reaction: one w

251 nstituent stereoisomers (69-72) of the BI 60 were prepared using the S- and R-isomers of bromide 17.

252 All of the hybrids were prepared using the same 81-base RNA template.

253 e loaded nanostructured lipid carriers (NLC) were prepared using the solvent diffusion method.

254 Cyclic peptides and peptoids were prepared using the thiol-ene Michael-type reaction.

255 After 5-8 wk, the same patients were prepared using the THW method and imaged as before.

256 nduction in mice dosed orally with VLPs that were prepared using the VEE-NV1 replicon construct, a re

257 ty of C-5 substituted N-aryl 1,2,3-triazoles were prepared using these conditions with yields in the

258 mplex multifunctional protein assemblies can be prepared using this facile triorthogonal approach.

259 Large batches of samples can be prepared using this technique with high recoveries (

260 Several new and previously reported ligands were prepared using this procedure.

261 zed enantiopure carbocycles and heterocycles were prepared using this strategy.

262 tions and standards of small drug molecules) were prepared using three deposition methods (electrospr

263 series of NDs containing GM1 and cholesterol were prepared using three different phospholipids (1,2-d

264 Milk sample slurries were prepared using Triton X-100 and nitric acid for dir

265 Total RNA was prepared using TRIzol reagent.

266 some-bound nascent chains of defined lengths was prepared using truncated mRNAs.

267 Lutein nanodispersions were prepared using Tween 80, sodium dodecyl sulfate (SD

268 The tetrahydronaphthyridine component was prepared using two different methods, both of which

269 Samples were prepared using typical procedures from residue meth

270 Exosomes were prepared using ultracentrifugation.

271 The emulsions were prepared using ultrasonic processing.

272 ers supported onto 4.0 x 3.3 cm glass plates were prepared using UV-initiated polymerization in a sim

273 ured and subsequently monitored when samples are prepared using VCFD, removing a barrier that has pre

274 ame, bone and skin (FBSH) of threadfin bream was prepared using Virgibacillus sp. SK33 proteinase and

275 Vaccines have typically been prepared using whole organisms.