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1 by systematic and measureable shifts in the mass spectrum.
2 tly 'stitched' together, creating a complete mass spectrum.
3 quencing stages with the experimental tandem mass spectrum.
4 ecies and their clusters in the negative ion mass spectrum.
5 identify important m/z values in the tandem mass spectrum.
6 face area of the section represented in each mass spectrum.
7 the different subpopulations to the overall mass spectrum.
8 ection sensitivity as well as the profile of mass spectrum.
9 oducts are separated by 68 mass units in the mass spectrum.
10 probable oligosaccharide structures from the mass spectrum.
11 n decarboxylation of YFP as indicated by the mass spectrum.
12 ange of m/z and abundance values within each mass spectrum.
13 hat is detected as the [M - H](-) ion in the mass spectrum.
14 er energy fragmentation pathways in the same mass spectrum.
15 tions are typically based on a single tandem mass spectrum.
16 probabilities are generated for each tandem mass spectrum.
17 ptimally packed peptide trimers dominate the mass spectrum.
18 atios of fragment ion abundances in a tandem mass spectrum.
19 e-interrupted) fatty acids in a single-stage mass spectrum.
20 sequence database and an experimental tandem mass spectrum.
21 as reflected in the electrospray ionization mass spectrum.
22 icon over the complementary strand in an ESI mass spectrum.
23 ctrum graph is used to preprocess the tandem mass spectrum.
24 rete masses that can be resolved in a single mass spectrum.
25 d accuracy in detecting heterozygotes in the mass spectrum.
26 of peaks may overlap with other peaks in the mass spectrum.
27 on alpha-Hb is also detected in the alpha-Hb mass spectrum.
28 r in the protein ion can be derived from the mass spectrum.
29 assisted laser desorption/ionization (MALDI) mass spectrum.
30 t comparison of the peptides within the same mass spectrum.
31 became the predominant ions observed in the mass spectrum.
32 unlabeled oligosaccharide is observed in the mass spectrum.
33 Hexamers were not observed in the mass spectrum.
34 om its collision-induced dissociation tandem mass spectrum.
35 fer but not in the conventional electrospray mass spectrum.
36 al from previously unobserved species in the mass spectrum.
37 d sequence to be deduced from a single-stage mass spectrum.
38 r mass-to-charge (m/z) value with the tandem mass spectrum.
39 peak pairs with a fixed mass difference in a mass spectrum.
40 ks, including noise and analyte, for a given mass spectrum.
41 ng binaries is formed in nature with a broad mass spectrum.
42 mass data and fine isotopic structure of the mass spectrum.
43 d-bound protein ions determined from the ESI mass spectrum.
44 lecular structures of unknown m/z peaks in a mass spectrum.
45 g an intense neutral loss product ion in the mass spectrum.
46 mportantly, correct pairing was confirmed by mass spectrum.
47 of the explosives were observed in the DESI mass spectrum.
48 up to thousands of components from a single mass spectrum.
49 ount both matched and unmatched peaks in the mass spectrum.
50 aphically summarizes results as an annotated mass spectrum.
51 nt this information while analyzing a tandem mass spectrum.
52 aric phosphopeptides sequenced from a single mass spectrum.
53 esulting in strong [OT + X](2+) peaks in the mass spectrum.
54 al resonance ejection can provide a complete mass spectrum.
55 otonated species of each in the positive ion mass spectrum.
56 ides were detected and identified based on a mass spectrum acquired from an individual spot of 7 mum
57 ased peptide identification compare a tandem mass spectrum against all peptides in a database whose m
59 mple, glyoproteins are refractory to careful mass spectrum analysis and often give anomalous retentio
60 Trp-containing proteins by HPLC; and third, mass spectrum analysis of the mixture of analogue-substi
62 Through affinity purification followed by mass spectrum analysis, we identified adaptor protein (A
65 higher than that for any previously reported mass spectrum and almost 3 times greater than that obtai
67 s from red blood cells revealed match of the mass spectrum and retention time of the compound with th
68 of which 87 were identified by comparison of mass spectrum and retention time to those of pure standa
69 yte complexes in the electrospray ionization mass spectrum and the enantiomeric composition of the an
70 rometry experiments whereby both the initial mass spectrum and the product ion spectrum are obtained
71 ase sequence match to an experimental tandem mass spectrum and to determine the level of significance
72 complicating the spectra (>12 000 peaks per mass spectrum and up to 63 peaks of the same nominal mas
73 extract peptide sequence tags from a tandem mass spectrum and use them as a filter to reduce the num
74 0 Da range, stitched into a single composite mass spectrum, and compare to a broad-band mass spectrum
75 eparation strategy reduces congestion in the mass spectrum, and experimental mobilities complement m/
77 determine whether the peaks observed in the mass spectrum are more likely to have been produced unde
80 he abundances of digest fragment ions in the mass spectrum, are increased relative to aqueous solutio
81 The base peak in the electrospray ionization mass spectrum arises from the loss of a water molecule f
82 a mass spectrometer and are represented in a mass spectrum as distinct isotopic clusters with a known
83 ention time and an identical electron impact mass spectrum as one of the two possible monomethyl este
84 ethyl salicylate in air gives a recognizable mass spectrum at 400 ppb in the ambient system, while us
86 instruments are capable of saving an entire mass spectrum at each pixel of an image, allowing for re
87 ht mass spectrometer (TOFMS) that provides a mass spectrum at every pixel of a two-dimensional image
88 For cycloalkanes, M(+*) species dominate the mass spectrum at lower capillary temperature (<100 degre
91 on Fourier transform ion cyclotron resonance mass spectrum (average mass resolving power of approxima
92 inct doublet mass peaks at each point in the mass spectrum beyond the mutation site, facilitating the
93 y identifies isotopic distributions within a mass spectrum, but also annotates matches between natura
94 e quality, and reduces the complexity of the mass spectrum by analyzing only one of the complementary
95 e metastable fragments may be focused into a mass spectrum by employing an ion mirror (reflectron) in
96 ]+ ion, which decomposes in the single-stage mass spectrum by loss of neutral methanol to form [M + 5
97 queries consider only a fraction of the full mass spectrum captured, and there are few tools to assis
99 ion mass spectrum (EI-MS) (i.e., the type of mass spectrum commonly generated by gas chromatography m
100 ionization detection (LC-APCI/MS) yielded a mass spectrum consistent with 3,3 '-dimethoxy-4,4'-biphe
101 A minor reaction product was observed with mass spectrum consistent with 3,3'-dimethoxy-4,4'-dihydr
102 as analyzed using LC-APCI/MS, a product with mass spectrum consistent with 3-methoxy-2',3',4-trihydro
103 HPLC with a retention time and electrospray mass spectrum consistent with prostaglandin E2 (PGE2).
104 position, ultraviolet absorbance maxima, and mass spectrum consistent with those characteristics of G
106 ntered around m/z = 733 amu in its MALDI-TOF mass spectrum, consistent with the formation of the [Ru2
107 with a high energy laser pulse to generate a mass spectrum consisting of multiply charged atomic ions
110 ecursor-ion scan of m/z 79 (PO-3) produces a mass spectrum containing only the molecular ions of the
112 ess heme, the predominant species in the ESI mass spectrum corresponds to the homotetramer beta*4, al
113 we have modified the method in which tandem mass spectrum data are acquired in 'shotgun' proteomic a
114 WUFlux is capable of directly correcting mass spectrum data of TBDMS (N-tert-butyldimethylsilyl-N
116 The algorithm formulates the problem of mass spectrum deconvolution as a classical statistical p
118 f genus Datura plants, we show here that the mass spectrum-derived chemical fingerprints for seeds of
119 een cytoplasmic and membrane subunits, and a mass spectrum dominated by large aggregates of detergent
121 roup in the gas phase to produce a signature mass spectrum during tandem mass spectrometric events.
122 putationally predicts an electron ionization mass spectrum (EI-MS) (i.e., the type of mass spectrum c
123 poration yields a protein whose electrospray mass spectrum (ESMS) shows peaks at the expected mass (M
125 peptide tandem mass spectrum to a predicted mass spectrum for an amino acid sequence within a databa
126 reproducibility demonstrated that the unique mass spectrum for each m/z 221 anion could be obtained f
127 lecular compounds in 3D by providing a MALDI mass spectrum for each spatial point of a 3D sample.
129 the reference protein method to correct the mass spectrum for the occurrence of nonspecific carbohyd
131 ed from the dominant [M - H]- ions in the ES mass spectrum formed with subnanomole amounts of oligosa
133 titis B virus (HBV) capsids and those of the mass spectrum from CRISPR-related cascade protein comple
134 he contributions to the overall droplet beam mass spectrum from the various species present under a g
135 tance was characterized by comparison of its mass spectrum, high-pressure liquid chromatography reten
136 ed flavins, as evidenced by the electrospray mass spectrum: hydroxy-FMN, FMN plus C(6)H(5)COCH(2)CH(2
137 neumococcal LTA (labeled LTA-9.5) that has a mass spectrum identical to that of pre-ion-exchange LTA
140 he functions include data format conversion, mass spectrum interpretation, detection, and verificatio
141 Thus, it is possible to break a broadband mass spectrum into 1-Da segments, rotate each segment by
142 ison) scorer converts an experimental tandem mass spectrum into a m/z profile of probability and then
145 Knowing the charge state of an ion in a mass spectrum is crucial to being able to assign a formu
146 racterization of individual DNA species in a mass spectrum is dependent solely upon the mass-to-charg
147 oduced to the MS for analysis, the resulting mass spectrum is free of non-extended primer peaks and t
149 ly accepted that a single 1D NMR spectrum or mass spectrum is usually not sufficient to establish the
150 sion efficiency, ionization probability, and mass spectrum, it is imperative to provide definitive ex
154 most widely used compound identification is mass spectrum matching, in which the dot product and its
155 ntains comprehensive targeted and untargeted mass spectrum metabolomics data for Arabidopsis mutants
156 y from the precursor peptide mass and tandem mass spectrum (MS/MS or MS(3)) fragment ions, without co
157 charge state is observed in the electrospray mass spectrum obtained from solutions containing 6.7% m-
158 he case of partially digested myoglobin, the mass spectrum obtained using a sample probe modified wit
161 with the observed drops in intensity in the mass spectrum of AgnV(+) clusters after 5, 7, and 14 Ag
164 by searching for the best match between the mass spectrum of an unidentified peptide and model spect
166 sotopic abundances are commonly based on the mass spectrum of carbon dioxide, but analysis of that sp
167 of 19, 23, 26, and 29, respectively, in the mass spectrum of charged argon clusters formed in a low-
169 der analysis of a deisotoped high-resolution mass spectrum of crude oil containing nearly 13,000 peak
171 xture be determined but an individual tandem mass spectrum of each component in the mixture can be ob
172 nged for protons, and (3) measurement of the mass spectrum of each histidine-containing peptide by LC
175 r desorption/ionization time-of-flight (TOF) mass spectrum of positive ELISA fractions revealed a mol
178 solution in Xmax enables us to determine the mass spectrum of the cosmic rays: we find a mixed compos
182 f several contaminants was identified in the mass spectrum of the HEPES matrix, including a prominent
184 ified in intact nucleic acids by obtaining a mass spectrum of the nucleic acid before and after deriv
187 qTOF mass spectrometer, by first obtaining a mass spectrum of the peptides in each sample spot in ord
188 Two additional peaks were observed in the mass spectrum of the photolabeled subunit with m/z 1931.
190 lkyl radicals with molecular oxygen, and the mass spectrum of the reacting mixture is monitored in ti
192 ng the amino acid sequence, each peak in the mass spectrum of the unlabeled subunit II could be assig
195 st abundant ion observed in the electrospray mass spectrum of this reaction mixture corresponds in ma
198 tersection spectra (2-D fragment correlation mass spectrum) often gives enough information to derive
199 ld be necessary to spread out a conventional mass spectrum over approximately 200 m in order to provi
200 control the false match frequency for tandem mass spectrum/peptide sequence matches, but reversal cre
205 e H-D exchange reaction is obtained from the mass spectrum reflecting the extent of deuterium incorpo
206 m representation of data sets, and the total mass spectrum representation of data sets, separately.
207 iguously identified as 1:2:1 triplets in the mass spectrum resulting from the binomial distribution o
210 on both two-dimensional retention times and mass spectrum similarity of fragment ions measured by Pe
212 unately, there are natural gaps in a typical mass spectrum, spaced 1 Da apart, because virtually no c
213 on of the ions of the holoprotein produces a mass spectrum that contains peaks corresponding to a low
214 cle composition is acquired in the form of a mass spectrum that must be subsequently interpreted in o
216 by, for example, the total ion count for the mass spectrum, the individual peak abundance, m/z value,
218 th shotgun proteomics match a peptide tandem mass spectrum to a predicted mass spectrum for an amino
220 information from its isotopic fine structure mass spectrum to increase the confidence in peptide and
221 MS) is achieved by matching the experimental mass spectrum to the mass spectra in a spectral library.
222 ons (x- and v-type ions) dominate the tandem mass spectrum up to 1 micros after the laser shot, but t
224 identify the isotopic distributions within a mass spectrum using a probabilistic classifier supplemen
225 y, a peak having the same retention time and mass spectrum was also generated pyrolytically when fura
230 ass spectrometry, a significant shift in the mass spectrum was observed, indicating labile modificati
231 al fatty acids, overlapping peaks in the ESI mass spectrum were deconvoluted generating a detailed mo
232 multimers (MCMs) present in the ion mobility/mass spectrum were unambiguously assigned by m/z selecti
233 lysis of ethyl cellulose are observed in the mass spectrum when the low-temperature plasma ion source
234 yte complexes in the electrospray ionization mass spectrum where the ratio of these complexes is depe
236 protoporphyrin IX as indicated by its MALDI mass spectrum, which showed an (M + H)(+) of m/z = 853.6
237 riment, based on data from a single discrete mass spectrum whose parameters are extracted by a least-
238 through non-IEPOX routes exhibits a notable mass spectrum with a characteristic fragment ion at m/z
239 aled elevated urinary bile acid excretion, a mass spectrum with intense ions at m/z 453 and m/z 510 c
240 loid beta 1-40 was detected in the full-scan mass spectrum with sufficient resolution to distinguish
241 e algorithm is demonstrated on a polystyrene mass spectrum with varying degrees of noise added either
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