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 physical models of complex porous structures were prepared using 3D printing technology.

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 )Zr-DFO-trastuzumab and (89)Zr-DFO-cetuximab were prepared using (89)ZrCl(4) The stability of each wa

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 The nanoemulsions are prepared using a low-energy process which offers an

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

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

18 Nanocomposite polymers are prepared using a new sustainable materials synthesis

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

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

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

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

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

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

25 bromide ((C(38)H(34)P(2))MnBr(4)), which can be prepared using a facile solution growth method at roo

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

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

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

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

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

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

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

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

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

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

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

37 talline films, structures and particles have been prepared using a variety of approaches.

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

39 The PCL Film is prepared using a combination of film casting and sacr

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

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

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

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

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

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

46 study, a biopolymer-based packaging material was prepared using a casting method, which consisted of

47 ructured electrochemical DNA-based biosensor was prepared using a commercial electrode assembly and t

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

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

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

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

52 (68)Ga-NeoBOMB1 was prepared using a kit procedure with a licensed (68)G

53 tiopure bis-helicenic 2,2'-bipyridine system was prepared using a Negishi coupling.

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

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

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

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

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

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

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

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

62 n orthogonally protected aristolactam, which was prepared using a Suzuki/aldol cascade to convert a d

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

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

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

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

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

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

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

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

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

72 Niosomes were prepared using a modified thin film hydration metho

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

74 Methods: OF-NB1 and MF-NB1 were prepared using a multistep synthesis, and their bin

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

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

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

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

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

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

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

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

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

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

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

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

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

88 alloy (Ti-6Al-2Sn-4Zr-6Mo, Ti6246, in wt.%) were prepared using a xenon-plasma FIB microscope equipp

89 Samples were prepared using accelerated solvent extraction prior

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

91 Six cellulase calibration standards were prepared using affinity digestion.

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

93 Sample was prepared using ammonium sulfate precipitation and su

94 Crosslinked micelles were prepared using amphiphilic PEG-b-poly(L-glutamic ac

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

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

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

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

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

100 nsive and efficient Mo(2)N nanobelt cathodes were prepared using an ethanol method with minimized cat

101 CPX and CPX-Zn nanosuspensions (NSs) were prepared using an evaporative nanoprecipitation-ult

102 (PBAT) nanocapsules loaded with linalool EO were prepared using an extrusion method with 1, 3, and 5

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

104 (lactide-co-glycolide) (PLGA) microparticles were prepared using an in-line homogenization method.

105 Libraries were prepared using an optimized semi-automated library

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

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

108 Subsequently, variants of CAGE are prepared using anions with structural similarity to

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

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

111 The copolymers were prepared using atom-transfer radical polymerization

112 5'-BAL-ODNs are prepared using automated DNA synthesis and an acetal

113 The oligomers were prepared using automated phosphoramidite chemistry

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

139 The epoxides were prepared using diastereoselective addition of a sul

140 s of arabinoxylan extracted from wheat chaff were prepared using different enzymatic treatments with

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

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

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

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

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

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

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

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

149 32Dcl3 and Ba/F3 cell cycle fractions were prepared using elutriation.

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

151 Microfluidic devices have historically been prepared using fabrication techniques that often in

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

153 ) and water vapour barrier coating films can be prepared using food safe liquid dispersions through a

154 Similar multilayer chip surface was prepared using functionalized lipoic acid AuNPs depo

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

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

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

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

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

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

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

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

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

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

165 covering the entire Ti-Ni-Cu ternary system were prepared using ion beam sputtering technique.

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

167 Wheat (Triticum aestivum L.) bread doughs were prepared using LAB strains belonging to different L

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

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

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

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

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

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

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

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

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

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

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

179 ucts of oxidation, when echium oil emulsions were prepared using negatively charged emulsifier under

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

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

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

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

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

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

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

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

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

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

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

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

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

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

194 The substrates were prepared using purified HS biosynthetic enzymes.

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

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

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

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

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

200 Uncooked and baked muffins were prepared using recipes from Mount Sinai and Imperia

201 (MR) antagonists, including dimeric ligands, were prepared using red-emitting cyanine dyes.

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

203 Two constructs were prepared using replication-deficient adenoviral vec

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

205 expeller-pressed (EP) corn germ oil oleogels were prepared using rice bran wax (RBX) at different con

206 ne (gDCC) mechanophores along their backbone were prepared using ring expansion metathesis polymeriza

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

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

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

210 carbon nanostructures (CNs=MWCNTs and RGO), are prepared using simple in-situ wet chemical method an

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

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

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

214 While lipovelutibol D was prepared using solid-phase peptide synthesis followe

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

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

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

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

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

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

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

222 The EC cell was prepared using standard semiconductor processing tec

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

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

225 These electrodes were prepared using standard templating or dealloying te

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

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

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

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

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

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

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

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

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

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

236 The polymers are prepared using the salen cobalt(III) complex catalyz

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

238 A new family of adj-dicarbaporphyrinoids has been prepared using the "2 + 2" MacDonald methodology.

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

240 An AlPO(4) zeotype has been prepared using the aromatic diamine 1,10-phenanthro

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

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

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

244 , methyl cinnamate (M), and linalool (L) has been prepared using the mixture design assay.

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

246 r 1,4-naphthyl; A for 9,10-anthracenyl) have been prepared using the same strategy, and [2]CPTN has b

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

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

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

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

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

252 125I-labeled-IGF-I was prepared using the chloramine T method.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

276 In the testing, groups of 1-20 swabs samples were prepared using the standard method (ISO, 18593:2018

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

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

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

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

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

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

283 aryl/heteroaryl pyrrolidines and piperidines were prepared using this method.

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

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

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

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

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

289 Total RNA was prepared using TRIzol reagent.

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

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

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

293 Samples were prepared using typical procedures from residue meth

294 Exosomes were prepared using ultracentrifugation.

295 The emulsions were prepared using ultrasonic processing.

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

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

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

299 Vaccines have typically been prepared using whole organisms.

300 Primary amine products have been prepared using zirconium-catalyzed hydroaminoalkyla