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1 a phase coupling, indicating a role in motor preparation.
2 ideo revealed sterility breaches in contrast preparation.
3 and without the digestion step in the sample preparation.
4 ed on MinION after applying a custom library preparation.
5 n cultured cells and in an acute brain slice preparation.
6 ly, to those of the cocoa beans used for its preparation.
7 ts low cost and fast speed of contrast agent preparation.
8 c and vagal nerves in the perfused brainstem preparation.
9  quick, less expensive, and less variable in preparation.
10 e not added promptly into SVOCs solutions on preparation.
11 hetic chemistry have allowed their efficient preparation.
12 ) during both stimulus encoding and response preparation.
13 in the normal time scale of MALDI MSI sample preparation.
14 purees can be obtained with a limited sample preparation.
15  background and requires little to no sample preparation.
16 ated hearts were studied using a Langendorff preparation.
17 rylation is the most common method for their preparation.
18 attractive though elusive strategy for their preparation.
19 ental data in buffer solution with no sample preparation.
20 s in soft beverages and powders for gelatine preparation.
21 neous calcium transients in a chronic window preparation.
22 thmic, mexiletine, using the rat Langendorff preparation.
23 ing platform was utilized for one-pot sample preparation.
24 erate enough ChIP DNA for sequencing library preparation.
25 LA)-ICPMS or coupled to a destructive sample preparation.
26 d, efficient, and highly reproducible sample preparation.
27 nto a PCR solution using our DM-based sample preparation.
28 ime and human resources necessary for sample preparation.
29 uced endotoxins by up to 10(6)-fold in phage preparations.
30 Many synthetic ligands are in use as racemic preparations.
31 ducing dietary supplements or pharmaceutical preparations.
32 or the best sequencing platforms and library preparations.
33  and proliferated in response to human islet preparations.
34 lity and methylation from single DNA library preparations.
35 tial presence of FE producing bacteria in FE preparations.
36 m to investigate neural coding in biological preparations.
37 rization (variable timing), proteomic sample preparation (5-7 d), mass spectrometric data acquisition
38 l cleanliness when compared to larger volume preparation, although we cannot overreach any definitive
39 this bottleneck, we combine automated sample preparation, an ultra-fast 84-second LC-MS method, and b
40  h of preparation time, 1/2 d for sequencing preparation and 2-4 h for data analysis.
41 ic characteristics, past diagnoses, and drug preparation and administration practices.
42 ating the ability to completely finish bowel preparation and adverse effects (unpleasant taste, nause
43 his technique eliminates the need for sample preparation and allows the construction of customized se
44 ntered food matrices which can affect sample preparation and analysis.
45                                          The preparation and characterisation of the reported sorbent
46                                              Preparation and characterization of novel encapsulation
47 extra procedures may be needed during sample preparation and clean-up to address the issue of matrix
48 r resumption of elective procedures, patient preparation and communication, prioritization of procedu
49 arryover, ion suppression, as well as sample preparation and consumption.
50 oling, coherent operations and quantum state preparation and detection of Sr(+) qubits.
51 or this purpose, honed a protocol for sample preparation and developed custom software that analyzes
52  research of FCDI in terms of flow-electrode preparation and device configuration optimization.
53 dministration, and standardised the parasite preparation and dose.
54                                              Preparation and electrochemical interrogation of a novel
55 tion to the motor cortex, to assess movement preparation and execution.
56 ability to handle large variations in sample preparation and image collection.
57                                    Identical preparation and imaging protocols (except administration
58 ontent of cholesterol were used for liposome preparation and it was demonstrated, that an increase in
59 nstrate that this method can be used for the preparation and late-stage functionalization of pharmace
60    The entire procedure including the sample preparation and LC-MS/MS takes less than 55 min, enablin
61  techniques but require sophisticated sample preparation and long incubation time.
62 l as they utilized entirely different sample preparation and MS analysis workflows, targeted differen
63 tential difficulty (e.g., MACOCHA score); 2) preparation and optimization of the patient and team for
64 other common approaches by minimizing sample preparation and preserving endogenous modifications.
65 iology workflow employing plate-based sample preparation and rapid, single-run, data-independent mass
66 nabling integration of SPE with other sample preparation and separation methods.
67 le accounting for effects from input library preparation and sequencing depth.
68               This interaction between motor preparation and the error-driven learning system may fac
69 facts generated in PCR-based RNA-Seq library preparation and the lack of normal RNA-Seq data, present
70                                  When sample preparation and throughput capabilities are integrated w
71             Main outcome measures were graft preparation and unfolding times, best spectacle-correcte
72                In this work, we describe the preparation and use of a thin metal film modified Indium
73 native plant materials of varied origins and preparations and could be applied to other inorganic-org
74     Our method avoids high-cost system state preparations and expensive running procedures and measur
75                    It is widely used in food preparations and industrial products like candies, chewi
76  they also feature prominently in veterinary preparations and processed foodstuffs.
77 se peptides to an efficient multistep sample preparation, and a micro-LC chromatography.
78 of reference spectra, difficulties in sample preparation, and an absence of two-dimensional (2D) NMR
79 g transfected HEK293T cells, rodent neuronal preparations, and behavioural and electrophysiological a
80 by using computer simulations, ex vivo heart preparations, and dogs.
81                      Finally, we construct a preparation-and-postselection procedure that yields an a
82 rrently available methods for peptide sample preparation are mostly suitable for ex situ analysis via
83 find that most GPMVs isolated using standard preparations are passively permeable to various hydrophi
84          We conclude that nacreous walls are preparation artefacts rather than structural features of
85 pe, limited training sample size, and sample preparation artifacts.
86             Patients who received low-volume preparation averaged a higher mean total BBPS (7.4, SD 1
87 tems; however, protein solubility and sample preparation before MS remain a bottleneck preventing hig
88 ntraction arrested ex vivo Langendorff heart preparations before and during simulated ischemia.
89                  The fully automated library preparation by centrifugal microfluidics thus offers att
90 e and straightforward strategy for electrode preparation by silver nanoparticles may provide an alter
91 Recent studies have demonstrated that sample preparation can decrease (13) C and (15) N enrichment in
92 ient instructions, mechanical and oral bowel preparation, chlorhexidine washes, and carbohydrate drin
93                 This highly efficient enzyme preparation combines enzyme immobilization (enhanced sta
94 dy assesses the effects of varying substrate preparation conditions and growth and prebake temperatur
95                                         IVIG preparations consisting of pooled IgG are increasingly u
96 ng measurements showed that the polydisperse preparation contains significant amounts of aggregates,
97 s analysis largely relies on detergent-based preparations devoid of endogenous ligands.
98 igned metrics of UNGD activity by phase (pad preparation, drilling, stimulation, and production) 30 d
99    The method comprised four steps: solution preparation, droplet creation, image capture and image a
100 e olfactory nerve in an in vitro whole-brain preparation elicited synaptic responses in reticulospina
101                                         This preparation enables us to use an imaging approach to ide
102 f the respiratory pattern persist in in situ preparations even after minimizing pulmonary and chemo-a
103                                    In DM-PSI preparations excited at 740 nm, the excitation remained
104            We found that volitional movement preparation, execution and inhibition (proactive and rea
105 ent component analysis demonstrated that all preparations exhibited rLFPs with a similar temporal str
106 t included continuous water sampling, sample preparation (extraction), and analysis for the determina
107                    The low cost, easy sample preparation, fast response and high reproducibility (RSD
108                         Methods: Radiotracer preparation followed the manufacturer's indications.
109 trates the essential concepts, strategies of preparation following the two general approaches, bottom
110 selectively enriches for rereplicated DNA in preparation for analysis by DNA sequencing that can be a
111 mory-guided attention is supported by neural preparation for anticipated attentional states.
112 gn process of the biosensor and enhances our preparation for any future outbreaks.
113  which the genome undergoes reprogramming in preparation for embryogenesis.
114 croscopy images, including optimizing sample preparation for fixed and live cells, choosing the most
115 nal M1 within gamma frequencies during motor preparation for hand opening.
116               The Affect of Low-Volume Bowel Preparation for Hospitalized Patients Colonoscopies.
117  contact materials, the importance of sample preparation for nontarget screening should be addressed.
118 Reliable forecasts of ILI can support better preparation for patient surges in healthcare systems.
119 ws, volumes, and access must be optimized in preparation for the expected surges in the number of pat
120 ere, we discuss the steps involved in tissue preparation for three-dimensional volumetric imaging and
121 B should focus on resuscitation, triage, and preparation for upper endoscopy.
122                          However, the sample preparations for such imaging are often onerous, and the
123 idates, such as the use of systemic hormonal preparations for the treatment of respiratory illnesses.
124 n to the rRNA-depletion protocol for library preparation from blood RNA effectively reduces highly ab
125 isingly, the fictive patterns of the in situ preparations from ALI pups retained these characteristic
126                                   In ex vivo preparations from mice of both sexes, we measured MC and
127 taryl and adipoyl phosphonates on the enzyme preparations from tissues with varied DHTKD1 expression
128 ide both qualitative and quantitative sample preparation guidelines that increase the chances of obta
129                                       Sample preparation has been the critical step that should provi
130 gle-particle analysis workflow (e.g., sample preparation, image acquisition and processing, and struc
131  disruption in a mouse brainstem-spinal cord preparation impedes the amplitude augmentation of the ce
132 ed benefits and challenges of hospital Ebola preparation in developed countries.
133 sultation service, tumor board, and specific preparations in advance of therapy and day-of-therapy pr
134  for 96 hours and longer to combine multiple preparations in order to reach the desired beta-cell dos
135  information, and another that encodes motor preparation information.
136 ted metabolomics protocols, including sample preparation, instrumentation, data processing, etc., is
137 ture, from aquaculture, without prior sample preparation is demonstrated.
138 ant amounts of aggregates, whereas the other preparation is essentially monodisperse.
139 utting-edge tools for DNA-origami design and preparation, it remains challenging to separate structur
140                              Improper sample preparation leads to detrimental cascades, resulting in
141                         This two-step sample preparation led to excellent extraction efficiency and m
142 strumentation that requires extensive sample preparation, long run times, and is destructive to the s
143 s pilot study we found that low-volume colon preparation may be preferred in the inpatient setting du
144 plied in microplastic research during sample preparation, may also be mistaken for PE.
145                                 The proposed preparation method ensures safe handling of the tissue s
146 , isothermal assays with a simplified sample preparation method independent of nucleic acid extractio
147              For this purpose, a bulk sample-preparation method was developed, allowing a high-throug
148 erein, the emerging sulfide electrolytes and preparation methods are reviewed.
149 n traditionally lost in standard NGS library preparation methods.
150  cortex using poly(A)+ and Ribo-Zero library preparation methods.
151 d nature of quaternary carbons hinders their preparation, most notably when stereocontrol is required
152  perfused donor heart left ventricular wedge preparations (n=12), and adapted for sequentially acquir
153 ions because of its low cost, minimal sample preparation, non-destructive nature and substantially ac
154                                          The preparation of (15)N-labeled NaHMDS has been improved.
155 di-O-isopropylidene-myo-inositol allowed the preparation of 11.
156             The method is exemplified by the preparation of 2,3,6,7-anthracenetetracarbonitrile and e
157        A versatile one-pot procedure for the preparation of 2-alkyl-substituted N-arylindoles is desc
158                   We also describe the first preparation of 3-aryloxazolidin-2-ones bearing new funct
159              The first global method for the preparation of 3-phosphorylated-pyrroles, -furans, -thio
160                 However, to date, the direct preparation of [(18)F]-aryl fluorides from aryl halides
161 TBE) is reported, and its application in the preparation of [4+0]-tetraarylethenes (TAEs) is elucidat
162 rated a facile approach for the simultaneous preparation of a bi-functional PEDOT interface with a tu
163           Formal genetic counseling includes preparation of a family pedigree; a discussion about pot
164                            These include the preparation of a few glycosyl triazoles and aryl triazol
165  tyrosinase inhibitors, based on (a) one-pot preparation of a library of thiosemicarbazide compounds,
166                        An application to the preparation of a potential chiral phosphorus organocatal
167 ility of the reaction is demonstrated by the preparation of a potential drug candidate containing a t
168                      Furthermore, we propose preparation of a shaped single photons with an efficienc
169 changes in beta frequency are related to the preparation of adapted movements in human, and whether s
170 synthetic strategy allowed for the efficient preparation of alpha-aminophosphonic acid derivatives an
171                            Concurrently, the preparation of AMPP* ligands with a P-chirogenic phosphi
172                                 The in vitro preparation of amyloid fibrils that exhibit structural a
173 r groups could be achieved, providing facile preparation of an indolizidine framework commonly found
174 pirocyclic intermediates, we exemplified the preparation of an undescribed class of carbocyclic nucle
175 alyzed borylation has been developed for the preparation of aryl boronate esters.
176  processes and is expected to facilitate the preparation of bioactive organic molecules.
177 , which are valuable building blocks for the preparation of biologically relevant molecules.
178 ective, we discuss a design approach for the preparation of biologically relevant small-molecule libr
179 controlled method has been developed for the preparation of chiral 3,4-dihydro-2H-naphtho[1,2-b][1,4]
180                                      A novel preparation of clean-surfaced, faceted gold nanocrystals
181 resented that address key challenges for the preparation of coordination cages that are soluble and s
182             This method allows for a one-pot preparation of diarylalkylamine bearing different aryl g
183 and applicability of this methodology in the preparation of different kinds of amines, which are of c
184 novo synthesis creates opportunities for the preparation of diversity libraries and will support effo
185 cesses for abiotic synthesis might allow the preparation of engineered hybrid living systems.
186                          Here, we report the preparation of five nanomaterials and a study of their a
187 ions of the secondary alkylboronate, and the preparation of free boronic acids and hemiboronic hetero
188                        However, the rational preparation of heterostructures with highly active heter
189 s a considerable amount of template DNA, the preparation of high-quality DNA "parts" in large quantit
190 por deposition, show broader promise for the preparation of high-quality molecular frameworks, and ma
191 d precursor designs, enabling the systematic preparation of high-quality QD of any sizes and material
192 tic Pd(II) and a Cu(II) additive enables the preparation of KATs in high yields and with good functio
193                                          The preparation of large, low-entropy, highly coherent ensem
194 p based on Pauli spin blockade (PSB) for the preparation of large-scale W states of electrons in a do
195 r substrates has the potential to enable the preparation of low-dimensional materials with prescribed
196  a suitable bioisostere may well require the preparation of many candidates, in our case, 32 compound
197                                  The precise preparation of monodisperse nanomaterials is among the m
198 93F amino acid labelling kit is suitable for preparation of multi-milligram quantities of high qualit
199  Synthetic utility of the title azide in the preparation of N-tetrafluoroethylated and N-difluorometh
200                   The main methodologies for preparation of NHCs-based SAMs either requires inert atm
201 er our conditions (i) in the first 2 s after preparation of oversaturated calcium phosphate solutions
202                                 However, the preparation of oxide membranes, especially those with in
203 e derivatives, amines, and aldehydes for the preparation of phosphorus and fluorine substituted gamma
204 oach paves the way for large-scale synthetic preparation of pocket-modified vancomycin analogues that
205 unctionality metal-organic materials via the preparation of porous salts.
206 s, may be useful intermediates for the rapid preparation of potential lead compounds with biological
207                                          The preparation of pure samples of these reactive compounds
208       The experimental procedure details the preparation of pyrogen-free NANPs, isolation of PBMCs fr
209                           Here we report the preparation of rare sugar isomers directly from biomass
210                          Here, we report the preparation of representative classes of 3D-inorganic na
211                            The importance of preparation of representative samples of enantioenriched
212                                      Yet the preparation of robust and ultraclean graphene EM grids r
213 ns, and includes (i) experimental design and preparation of samples, (ii) data recording, (iii) softw
214                                Moreover, the preparation of smooth surfaces is crucial for vertically
215              This combination is driving the preparation of sophisticated 2D, 3D, and 4D materials at
216 eness (c.a. 1 euro /Kg), and easiness in the preparation of stable dispersions.
217                         Here we describe the preparation of stereoselectively deuterated building blo
218 interest in medicinal chemistry, wherein the preparation of structural variants of known pharmacophor
219  investigations of membrane proteins and for preparation of suitable platforms for drug testing or bi
220 proteins, with special emphasis given to the preparation of suitable samples and their characterizati
221                                              Preparation of supported metal catalysts with uniform pa
222                     The approach permits the preparation of target compounds in high yields using rea
223 he synthetic method is demonstrated with the preparation of ten new hangman chlorins bearing a xanthe
224   For the first time, we report a gram-scale preparation of the common carbon framework of the baulam
225 ategy in the near-infrared range through the preparation of the first restrained heptamethine indocya
226                                   During the preparation of the food models (i.e. the extracts and em
227                          We report the first preparation of the s-cis,s-cis conformer of dihydroxycar
228 -made marmoset chair, head-cap implantation, preparation of the sharp electrode and guide tube, neuro
229 vice, we demonstrate spin selectivity in the preparation of the spin-valley state of localized single
230  of all developed methods for the gram-scale preparation of the title chromones was also demonstrated
231  the synthetic methods that have enabled the preparation of these materials and the manifold properti
232 nal reagents and chemical procedures for the preparation of ureas.
233 igand, which was successfully applied in the preparation of various alkylated arene products with goo
234                This strategy streamlines the preparation of vicinal diamines from multistep sequences
235 for the precisely controlled high-throughput preparation of well-defined interfaces containing polyat
236 ow that both standard and exosome-associated preparations of AAV8 vectors can effectively transduce a
237 ed studies comparing the effect of different preparations of CHG and PVI on the dichotomous outcome o
238 man serum (HS) and five different commercial preparations of IVIg were tested for IgM and IgG binding
239        Here, we investigate microcrystalline preparations of two differently metalated forms of SOD,
240 imized proteoliposome isolation, cryo-sample preparation on graphene grids, and an efficient particle
241                                    No sample preparation or internal standards were needed for calibr
242 tocol parameter, such as type of anesthesia, preparation, or post-injection medication, increased the
243              Combined with the simple sample preparation, our method represents a valuable tool to be
244 terization of pure, homogeneous nanomaterial preparations, particle sizing and counting remains diffi
245 ative (EMD) added to papilla reflection/root preparation (PR/RP) could enhance clinical and inflammat
246 moothness; moreover, an additional substrate preparation procedure which involves (1) a modified subs
247                        Overall, this library preparation process allows for highly accurate small RNA
248  In this study, we developed a novel library preparation process using randomized splint ligation wit
249                             The whole sample preparation process was carried out at less than 3 min,
250        Testing 54 intravenous immunoglobulin preparations, produced from plasma collected in Europe a
251                    Following nanoPOTS sample preparation, protein digests from single cells were sepa
252 of the advantages of the filter aided sample preparation protocol are maintained.
253                                   The sample preparation protocol included a simple and rapid extract
254 cal modalities through this universal sample preparation protocol offers the ability to study tissues
255  speeding up the classic filter aided sample preparation protocol, FASP, from overnight to 2.5 h.
256 The two labs used the same silylation sample preparation protocols but different instrumentation, dat
257               Data collection included colon preparation quality, based on the Boston Bowel Preparati
258 tatin depending on its interaction with CDC: Preparations responding to CDC with an increase in insul
259 eparation quality, based on the Boston Bowel Preparation Scale, and a questionnaire given to all subj
260 l be useful to diversify the range of sample preparation schemes and analytical methods enabled by 3D
261                                      Mito-AP preparations showed a strong enrichment with typical mit
262 at balances scalability, high-fidelity state preparation, site-resolved readout and preservation of a
263 cific VR headsets; rely on complicated model-preparation software; and/or require the user to install
264  nonoptimal modifications to upstream sample preparation steps, limit the throughput of high-volume w
265 consuming and labor-intensive offline sample preparation steps.
266        Here we describe a cellular O-glycome preparation strategy, Preparative Cellular O-Glycome Rep
267 d etch steps common to conventional sapphire preparation, suggesting potential industrial application
268 were collected using Nissl and fiber stained preparations, supplemented with acetylcholinesterase and
269 ed this artifact, and this microcrystal-free preparation suppressed LPS- or MSU crystal-induced monoc
270 tform by incorporating a microfluidic sample preparation system, termed nanoPOTS (nanodroplet process
271 ion procedure is chosen as an optimal sample preparation technique for the TXRF analysis of tea.
272                Using our improved chromosome preparation technique, we were able to unequivocally cou
273                      Here, we explore sample preparation techniques relevant to a range of clinically
274          This Review summarizes the specific preparation techniques, details process operating condit
275 a general preconcentration method for sample preparation that can be performed on a variety of specim
276                                            A preparation that does not meet the sufficient dose can b
277 lth depends on treatment with immunoglobulin preparations that need to contain neutralizing antibodie
278 ions were less impaired by atorvastatin than preparations that were nonresponsive to CDC.
279                                    Including preparation, the protocol takes 31 h to complete.
280 tive of the present study was to compare the preparation time for transplantation in children of diff
281                               To shorten the preparation time of the NMR sample, the following protoc
282 lumina dye sequencing, and requires 1-2 h of preparation time, 1/2 d for sequencing preparation and 2
283 s protocol typically takes 2-3 d from sample preparation to data acquisition, with an additional day
284 eous biological mixtures, methods for sample preparation to detect (1)H-, (13)C-, (15)N-, and (31)P-l
285 lution, enabling direct transfer from sample preparation to dNAAT.
286 e the passive viscoelastic properties of the preparation to isolate forces contributed by nonmuscle s
287 ental procedure takes approximately 3 d from preparation to MS.
288                                     Hospital preparations to expand crisis capacity are further dimin
289 ion as well as demonstrates SPME as a sample preparation tool for nucleic acid analysis in plasma.
290 re, we explore this effect with a variety of preparation types, microbial lineages and isotope labels
291                      Studies on invertebrate preparations usually examine synaptic changes at specifi
292           A custom-made, lytic bacteriophage preparation was administered to the patient in December
293 ratory gloves or reagents used during sample preparation was investigated.
294                                        Bowel preparation was poor in 19% of index colonoscopies, and
295 days of incubation) mounted on a Langendorff preparation were exposed to IR (30 min ischaemia) after
296                    Two commercial fibrinogen preparations were used, a monodisperse and a polydispers
297 354 patients received prebiotic or symbiotic preparations, whereas 1369 patients in the control arm r
298    We further found that the feeding of meat preparations with added nitrate to rats resulted in hype
299 ssue in single arterially perfused brainstem preparations with respect to the ongoing respiratory mot
300 s represents an important strategy for their preparation, yet current methods are limited in their al

 
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