ライフサイエンスコーパス: chemical species

1 therefore ideal for label-free detection of chemical species.

2 act on human health depends primarily on its chemical species.

3 and degradation of a locally produced single chemical species.

4 nvariant to the relative abundances of lipid chemical species.

5 ng in watts per meter squared, of individual chemical species.

6 ivity degraded by irreversible adsorption of chemical species.

7 ction between mechanical signals and mitosis chemical species.

8 concept of protection and remote release of chemical species.

9 otons and secondarily by reactive radiolytic chemical species.

10 echanical devices or to organize other large chemical species.

11 ctral and temporal information from multiple chemical species.

12 vels of activity of a number of intermediate chemical species.

13 irect electrical detection of biological and chemical species.

14 g transitions rather than the populations of chemical species.

15 values corresponding to the same fundamental chemical species.

16 for studying nanotubes in contact with other chemical species.

17 ulting in the quantification of 44 different chemical species.

18 lectrically based sensors for biological and chemical species.

19 that consider only the addition of monomeric chemical species.

20 the autonomous processing of a diversity of chemical species.

21 e stability with the progressive addition of chemical species.

22 es of reactions involving various phosphorus chemical species.

23 nsitions in selective response to particular chemical species.

24 a fast, nondestructive method for monitoring chemical species.

25 d demonstrate the identification of multiple chemical species.

26 a non-spherical nanoparticle using a single chemical species.

27 NMR is routinely used to quantitate chemical species.

28 widespread and accessible for characterising chemical species.

29 irect electrical detection of biological and chemical species.

30 cles to be internally mixed with two or more chemical species.

31 cording to the availability of a constituent chemical species.

32 oss-section determination, a large number of chemical species, 22 metabolites and 54 lipids, were ide

33 Virtually all chemical species absorb and have unique gas phase absorp

34 ngth range of 115-240nm, where virtually all chemical species absorb.

35 ments to control and regulate the passage of chemical species across them.

36 tal hydrolyzable amino acids and presence of chemical species affiliated with activated hydrocarbons,

37 ing platform can be extended to detect other chemical species and biomolecules such as proteins and s

38 l aerosol production in the troposphere, the chemical species and mechanism responsible for the growt

39 centrations among actively competitive ions, chemical species and molecular agents, and multi-cyclic

40 ively, but implicitly, define the individual chemical species and reactions that molecular interactio

41 V will be used to expose unidentified active chemical species and resolve pharmacodynamic interaction

42 Spectral similarities between known chemical species and the components identified by PARAFA

43 ation about both the identities of the major chemical species and their localization.

44 cells, (b) targeted imaging, (c) imaging of chemical species, and (d) imaging of temperature are giv

45 both abiotically, by a variety of inorganic chemical species, and biologically during anaerobic resp

46 of measured time series of concentrations of chemical species, another is on measurements of temporal

47 tection and quantification of biological and chemical species are central to many areas of healthcare

48 cle surface termination with specific plasma chemical species are proposed to provide an enhanced bar

49 In this work we use the time-integral of chemical species as a measure of a network's ability to

50 patial arrangement of the bulk and interface chemical species, as well as local potential energy vari

51 been demonstrated to neutralize free radical chemical species associated with many life-threatening d

52 s well as difficulties, in the separation of chemical species at atmospheric pressure.

53 However, chemotactically inactive chemical species at concentrations found in the human ga

54 sensitive and selective imaging of multiple chemical species at interfaces immersed in solution.

55 eal time and in situ monitoring of different chemical species at the electrolyte/electrode interfaces

56 rategy for estimating the concentration of a chemical species at the surface of a cell is presented.

57 Although we have not yet identified the chemical species being titrated, a likely candidate is l

58 pective model substrates and produce in situ chemical species (beta-nicotinamide adenine dinucleotide

59 rge differences in the distributions of many chemical species between different tissues of the maize

60 In this study, a non-native chemical species, bromodeoxyuridine (BrdU), was imaged w

61 electrophoretic analysis times of transient chemical species by inducing nascent, oppositely charged

62 P production required generation of reactive chemical species by mitochondria, NADPH oxidase, and typ

63 before it can initiate production of harmful chemical species by photosynthetic reaction centers.

64 fect the period, and how oscillations in one chemical species can be deduced from oscillations in oth

65 entration, pH and temperature, and different chemical species can be present.

66 Furthermore, we show that additional chemical species can be used to fine-tune the growth rat

67 These very reactive chemical species can damage proteins, lipids, nucleic ac

68 Exogenous and endogenous sources of chemical species can react, directly or after metabolic

69 Under irradiation, chemical species can redistribute in ways not expected f

70 Exposure of cells to toxic chemical species can result in reduced glutathione (GSH)

71 tonomous, periodic pulsations, which produce chemical species collectively referred to as the activat

72 Chemical species composed of light elements-such as hydr

73 S and similar techniques to extract the bulk chemical species concentration present in an ensemble of

74 ollected samples can be further analyzed for chemical species concentrations besides gravimetric anal

75 Observed emissions included many expected chemical species, dominantly ammonia and acetaldehyde, b

76 d radicals are some of the most investigated chemical species due to their preferential formation in

77 und to be capable of reducing many different chemical species en route to methanol through six sequen

78 The direct comparison of the chemical species evolved from the thermal degradation of

79 While many chemical species exhibit enhanced Bronsted acidity in th

80 hetic systems to shuttle both electronic and chemical species for the efficient oxidation of water.

81 otonumeric method is extensible to transient chemical species for which other methods are not availab

82 rst direct, in situ measurements of relevant chemical species formed on solid oxide fuel cell (SOFC)

83 predict biomarker levels (concentrations of chemical species found in the body that indicate exposur

84 nd quantification of over 50 major and minor chemical species from hydrogen and benzo[ghi]perylene we

85 Rhea reactions are described using chemical species from the Chemical Entities of Biologica

86 The chemical species giving rise to the reported biological

87 les while eliminating representations of the chemical species having relatively fast characteristic t

88 aining effective stochastic dynamics for the chemical species having relatively slow characteristic t

89 e upfield shifts in NMR, characteristic of a chemical species in a fullerene cage.

90 ogonal) the molar absorptivity curves of the chemical species in a model are, the less signal noise i

91 ects of a pulse change of concentration of a chemical species in a reaction network, either at equili

92 Monitoring of chemical species in breath offers an approach for the de

93 h high resolution provides a way to identify chemical species in cluttered environments and is of gen

94 ue utilizes the electrophoretic migration of chemical species in combination with variable hydrodynam

95 k for prediction of the dynamic evolution of chemical species in DNA amplification reactions, for any

96 ion, with the aim to control the delivery of chemical species in integrated systems.

97 arsenate [As(V)], the most prevalent arsenic chemical species in nature, causes severe depletion of e

98 orrelate with the biochemical roles of these chemical species in plant defense and photosynthesis.

99 th the antimicrobial assays using determined chemical species in solution in order to confirm the maj

100 ensive, quantitative kinetic modeling of all chemical species in the batch polymerization of 1-hexene

101 s show minimal nonspecific interactions with chemical species in the investigated sample and are thus

102 of certain siderophores for borate, a common chemical species in the marine but not the terrestrial e

103 biophysics: how are the free energies of the chemical species in the myosin-catalyzed ATP hydrolysis

104 The chemical species in the single and binary component solu

105 Consideration of charge donation from chemical species in the surface environment is critical

106 ate the physiology and pathology of reactive chemical species in their native environments with minim

107 Spatial resolved quantitation of chemical species in thin tissue sections by mass spectro

108 The major PM sources associated with these chemical species include residual/fuel oil combustion, t

109 ly possible when all other oxygen-containing chemical species, including hydroxyl, carboxyl, epoxide

110 detection of a wide range of biological and chemical species, including proteins, nucleic acids, sma

111 thm for detecting and quantifying co-eluting chemical species, including species that exist in multip

112 keite and show that the phase segregation of chemical species into discrete layers at the sub-nanomet

113 e cells, to induce necrosis and to introduce chemical species into live cells.

114 The determination of trace chemical species is a useful tool in paleoclimatology, a

115 hich the spatial distribution of the various chemical species is determined by scanning the DESI prob

116 Subsurface analysis of chemical species is imperative for biomedical diagnostic

117 point where the identification of individual chemical species is not possible.

118 tection and identification of a multitude of chemical species is required to fulfill the scientific o

119 d to study chemical interactions of multiple chemical species labeled with spectrally distinct fluoro

120 flow in porous media where several phases or chemical species may be present.

121 scope (SECM) for imaging the distribution of chemical species near a substrate.

122 ave identified nitric oxide (NO) and related chemical species (NOx) as having critical roles in neuro

123 cularly on differential dynamics of multiple chemical species of diacylglycerol.

124 al approach has been developed to derive the chemical species of each of the titanium layers.

125 ilitates the accurate spectral analysis of a chemical species of interest in the presence of overlapp

126 tudy we evaluated total Se and the different chemical species of Se in broccoli and carrots grown in

127 excess selenomethionine (SeMet, the dominant chemical species of Se in diets) via in ovo maternal tra

128 s change in viscosity, which varies with the chemical species of the vapors and the types of ionic li

129 led us to isolate and classify more than 500 chemical species of volatile organic compounds in urban

130 or imaging, but can originate from different chemical species on the surface.

131 mechanical action to induce the diffusion of chemical species out of synthetic vesicles, to enhance t

132 time we achieve uniform release of volatile chemical species over many hours for the first time, pav

133 limiting the response kinetics of the sensor-chemical species pair only to the reaction phenomena occ

134 inter-run variance in the retention time of chemical species poses a significant hurdle that must be

135 oxidation products confirmed the presence of chemical species potentially forming adducts with DNA.

136 The reagents are pure chemical species prepared from phosphoramidites synthesi

137 s, in that it tends to be dominated by those chemical species present at relatively higher concentrat

138 The other chemical species present in wastewater do not interfere

139 To better understand the chemical species produced when diisocyanates react with

140 of application reduces the flux of reactive chemical species reaching the sample, potentially limiti

141 ng effort to develop methods for identifying chemical species related to CW agent exposure.

142 the relative single proton peak areas of two chemical species represent the relative molar concentrat

143 metabolomics and proteomics to identify the chemical species responsible for the observed changes in

144 demonstrates their potential feasibility for chemical species sensing and bioimaging applications.

145 processes at biomembranes using EW-CRDS for chemical species showing optical absorbance in the visib

146 regate presentation of data for 48 different chemical species shows no correlation in either directio

147 odel leads to periodic rows and waves in the chemical species, similar to what is observed in experim

148 alysis is completely dominated by a very few chemical species, specifically alpha-glucose and fructos

149 des in the atmosphere, possibly by absorbing chemical species such as gaseous vanadium oxide and tita

150 ults in changes to the concentrations of key chemical species such as hydroxide, carbonate and bicarb

151 n invariant-that is independent of the other chemical species, such as free enzymes or enzyme-substra

152 Our ability to synthesize nanometre-scale chemical species, such as nanoparticles with desired sha

153 al manganese(IV) oxide reduction mediated by chemical species (sulfide and ferrous iron) and the comm

154 Among the chemical species tested for potential interferences (oth

155 ity of virgin olive oil can be controlled by chemical species that are linked to the production area.

156 analysis, can differentiate between diverse chemical species that are simultaneously retained by the

157 cord of numerous water-soluble and insoluble chemical species that are trapped in snow and ice offer

158 ron transfer (ECE) mechanism to generate new chemical species that are used for detection by fluoresc

159 l-suited to distinguish and characterize the chemical species that arise during the reaction.

160 In addition, by coupling a diffusing chemical species that can bind actin, such as myosin lig

161 in terms of identifying specific subsets of chemical species that contribute significantly to the op

162 sation, but their composition (and hence the chemical species that drive their production) remains an

163 sulfides and natural organic matter to form chemical species that include organic-coated mercury sul

164 ,3'-dideoxynucleosides (ddNs) are the active chemical species that inhibit viral DNA synthesis.

165 ns open the way to sharp signalling of small chemical species that perform critical biological functi

166 (or modules) that are aggregates of distinct chemical species that share similar chemistry and metabo

167 Identifying the form and role of the chemical species that traverse the stages of crystalliza

168 Specific chemical species that were determined by the feature sel

169 ic program that protects cells from reactive chemical species that, if left unchecked, would cause mu

170 lly coupled materials thus yielding peculiar chemical species (the colloidal QDs themselves), which d

171 e solution diffusion coefficients of the two chemical species, the depth of the evanescent field, and

172 strate the precisely controlled diffusion of chemical species through polymer networks.

173 n both 2D and 3D the spatial distribution of chemical species through the reconstruction of XANES spe

174 that allows for the comprehensive mapping of chemical species throughout biological tissues with typi

175 cavity of Ag colloids, and accessibility of chemical species to both inner and outer surface of the

176 lculation of heats of formation of the above chemical species to within 1.0 kcal/mol (1 kcal = 4.18 k

177 ombines simulations for each of the relevant chemical species, varying by protonation and ligation st

178 the capability of the technique in resolving chemical species, we first analyse a sample containing 2

179 New chemical species were then identified such as: citric (m

180 eacted subsequently with oxygen and formed a chemical species which reacted with either analysis solu

181 statistical analysis on a set of predefined chemical species, which might be chosen for their metabo

182 actors to allow detection of a wide range of chemical species while taking advantage of inexpensive b

183 Organic molecules containing redox centres-chemical species whose oxidation number, and hence elect

184 the experimentally measured coordinates and chemical species with 22 picometre precision can be used

185 Peroxynitrite is a highly reactive chemical species with antibacterial properties that are

186 The assemblies can be considered new chemical species with enhanced and tunable properties.

187 convolute spatial distributions of different chemical species with identical nominal mass.

188 enge, associated with simulating hundreds of chemical species with time scales varying from milliseco

189 hat incremental vaccination against a single chemical species within a multi-component mixture can be

190 estigated with regard to the quantitation of chemical species within individual ambient aerosol parti

191 We present progress toward imaging of chemical species within intact mammalian cells using sec

192 s capable of targeting and detecting salient chemical species within practical clinical timeframes.

193 n, mixing state, and spatial distribution of chemical species within single particles through the com

194 networks, which rests on elimination of fast chemical species without a loss of information about mes

195 ent of the pH-dependent emission to a single chemical species would be an oversimplification.

196 is synchronized with bulk homogenization of chemical species, yielding two distinct processes that a