ライフサイエンスコーパス: mass spectrometry analyses

1 lidated in the H1N1 antigenic variants using mass spectrometry analyses.

2 re proposed based on amino acid analysis and mass spectrometry analyses.

3 ys and immunoblotting, quantitative PCR, and mass spectrometry analyses.

4 ed routinely in liquid chromatography tandem mass spectrometry analyses.

5 ich was confirmed by limited proteolysis and mass spectrometry analyses.

6 were subjected to electrophoresis and tandem mass spectrometry analyses.

7 ry as well as electrospray ionization-tandem mass spectrometry analyses.

8 ly verified by elemental and high-resolution mass spectrometry analyses.

9 d as casein kinase 2 (CK2) by immunoblot and mass spectrometry analyses.

10 s and subjected to amino acid sequencing and mass spectrometry analyses.

11 ity revealed by liquid chromatography/tandem mass spectrometry analyses.

12 detected by electrophoretic, immunoblot, and mass spectrometry analyses.

13 sonance spectrometry, and gas chromatography-mass spectrometry analyses.

14 romatography, 15N NMR, and gas chromatograph-mass spectrometry analyses.

15 re characterized using liquid chromatography-mass spectrometry analyses.

16 ines was confirmed by GC coupled with tandem mass spectrometry analyses.

17 usly assigned in conventional chromatography-mass spectrometry analyses.

18 to increase the sensitivity of crosslinking mass spectrometry analyses.

19 not been fully exposed by microscale or bulk mass spectrometry analyses.

20 e information obtainable from intact protein mass spectrometry analyses.

21 f chemical compounds is the ultimate goal of mass spectrometry analyses.

22 treat the wrappings using gas chromatography-mass spectrometry analyses.

23 y (LC-MS/MS) and qualitative high-resolution mass spectrometry analyses.

24 of LmrP, an observation supported by native mass spectrometry analyses.

25 e using co-immunoprecipitation combined with mass spectrometry analyses.

26 e peptide sequence and peak intensities from mass spectrometry analyses.

27 not been fully exposed by microscale or bulk mass spectrometry analyses.

28 using electron microscopy, biochemical, and mass spectrometry analyses.

29 h using molecular biology, biochemistry, and mass spectrometry analyses.

30 esonance Spectroscopy and Gas Chromatography-Mass Spectrometry analyses.

31 nuclear magnetic resonance spectroscopy and mass spectrometry analyses.

32 rine-64 residue, as observed by quantitative mass-spectrometry analyses.

33 sed on enzyme-linked immunosorbent assay and mass-spectrometry analyses.

34 -assisted laser desorption ionization-tandem mass spectrometry) analyses.

35 ytes as determined by Western immunoblot and mass spectrometry analyses, a finding replicated in HeLa

36 611 patients) and 4553 liquid chromatography-mass spectrometry analyses acquired through a single bat

37 Mass spectrometry analyses after administration of nanop

38 Furthermore, the hydron/deuterium exchange mass spectrometry analyses allowed us to identify dynami

39 Interestingly, biochemical and mass spectrometry analyses also showed that the compound

40 The results of gas chromatography-mass spectrometry analyses and bioassays indicated that

41 ging and, enabled by nanoscale secondary ion mass spectrometry analyses and dedicated image processin

42 s, we used liquid chromatography with tandem mass spectrometry analyses and immunoassays of human pla

43 rophages upon electrospray ionization-tandem mass spectrometry analyses, and their complex lipid comp

44 site-directed mutagenesis, thiol titration, mass spectrometry analyses, and three-dimensional modeli

45 Our structural and mass spectrometry analyses are consistent with PCPA form

46 C, but not at 20 degrees C, by SDS-page and mass spectrometry analyses as well as electron microscop

47 e diendoperoxide using liquid chromatography-mass spectrometry analyses as well as UV and NMR spectro

48 ated the phosphorylation of Dsh by combining mass-spectrometry analyses, biochemical studies, and in

49 Mass spectrometry analyses combined with molecular dynam

50 Tandem mass spectrometry analyses, combined with native gel ele

51 Mass spectrometry analyses confirmed expression of some

52 Mass spectrometry analyses confirmed that the N-terminal

53 The 1D and 2D NMR and mass spectrometry analyses confirmed the structures of t

54 duction was demonstrated by Western blot and mass spectrometry analyses confirming majority targeting

55 Mass spectrometry analyses defined two major overlapping

56 Structural and Hydrogen-Deuterium-Exchange mass spectrometry analyses demonstrate antibody interact

57 Our mass spectrometry analyses demonstrate that cells lackin

58 Gas chromatography/mass spectrometry analyses demonstrate that erg26-1ts et

59 Immunoblot and mass spectrometry analyses demonstrated monomeric cystat

60 conserved, potential N-linked sites, and our mass spectrometry analyses demonstrated that both N-link

61 chromatography-mass spectrometry and tandem mass spectrometry analyses demonstrated that methionine

62 Mass spectrometry analyses demonstrated that PMS can be

63 Data from trypsin digestion and mass spectrometry analyses demonstrated that the N448 gl

64 Additional gas chromatography/mass spectrometry analyses determining the levels of var

65 Fluorescence HPLC coupled to mass spectrometry analyses directly detected PC2 in the

66 incorporation of fluorescent amino acid and mass spectrometry analyses enabled trace of translation

67 Gas chromatography/mass spectrometry analyses examining different fatty aci

68 Using mass spectrometry analyses for NEK1 interactors and NEK1

69 Quantitative mass spectrometry analyses further reveal an increased a

70 The EPR measurements and mass spectrometry analyses further reveal that nitric ox

71 megaterium: identity of host proteins in our mass spectrometry analyses, genome sequence of the phage

72 Mass spectrometry analyses have shown that AnkB is modif

73 Cross-linking and mass spectrometry analyses help to discriminate among th

74 Two mass spectrometry analyses identified calreticulin in am

75 Tandem mass spectrometry analyses identified Cys(256) of serpin

76 Coimmunoprecipitation/mass spectrometry analyses identified cytoskeletal and p

77 In addition, mass spectrometry analyses identified elevated vimentin

78 Mass spectrometry analyses identified four flavonoids in

79 Immunoprecipitation and mass spectrometry analyses identified mitochondrial ribo

80 In addition, mass spectrometry analyses identified numerous component

81 Liquid chromatography-mass spectrometry analyses identified strombine as coral

82 Of these, our HPLC and mass spectrometry analyses identify riboflavin as the so

83 In conclusion, performing MALDI-TOF mass spectrometry analyses in oxidizing conditions, as c

84 per mille, which satisfactorily matches bulk mass spectrometry analyses in the same rock samples, sup

85 Gas chromatography-mass spectrometry analyses indicate that membrane sterol

86 Gas chromatography-mass spectrometry analyses indicated that both of these

87 Mass spectrometry analyses indicated the target of each

88 e described here by performing lipid imaging mass spectrometry analyses of a rat brain.

89 Electrospray ionization mass spectrometry analyses of brevetoxins have shown tha

90 Parallel gas chromatography-mass spectrometry analyses of bronchoalveolar lavage pro

91 iquid chromatography/electrospray ionization mass spectrometry analyses of chymotrypsin-digested pept

92 ion of spliceosomes coupled with advances in mass spectrometry analyses of complex mixtures.

93 opy of the powders and by gas chromatography-mass spectrometry analyses of compounds released upon th

94 Mass spectrometry analyses of copurified proteins reveal

95 Consistent with this hypothesis, our mass spectrometry analyses of CTCF interacting partners

96 NMR spectroscopy and mass spectrometry analyses of degraded LPS (OSA) fragmen

97 Front-end electron transfer dissociation mass spectrometry analyses of DP revealed six novel seri

98 Here, we report mass spectrometry analyses of endogenous lipids captured

99 h 86 were verified after immunoprecipitation mass spectrometry analyses of engineered, monoallelic ce

100 datasets obtained from liquid chromatography-mass spectrometry analyses of environmental samples.

101 Mass spectrometry analyses of FliI immunoprecipitates sh

102 Mass spectrometry analyses of hybrid Q10 polypeptides re

103 Mass spectrometry analyses of immunoprecipitates using c

104 Mass spectrometry analyses of lipid changes in the IL-4-

105 s chromatography coupled with time-of-flight mass spectrometry analyses of metabolite extracts using

106 aturally presented MR1 ligand using unbiased mass spectrometry analyses of MR1-bound metabolites.

107 Furthermore, quantitative mass spectrometry analyses of murine HCC samples (p53-/-

108 as chromatography- and liquid chromatography-mass spectrometry analyses of nasal microsomal DCBN meta

109 Often the limitation of mass spectrometry analyses of neuropeptides in complex t

110 Liquid chromatography-tandem mass spectrometry analyses of oxidized EPA demonstrated

111 Mass spectrometry analyses of oxPS species identify stru

112 High resolution mass spectrometry analyses of peptides revealed that sul

113 Notably, on-surface mass spectrometry analyses of polymer precursors provide

114 ophoretic mobility shift assays (EMSAs), and mass spectrometry analyses of proteins bound to porG pro

115 Tandem mass spectrometry analyses of proteins co-immunoprecipit

116 Linear ion trap-mass spectrometry analyses of rat liver mitochondria as

117 In-depth high resolution mass spectrometry analyses of reaction products formed i

118 Gas chromatography coupled to mass spectrometry analyses of SAR-related emissions of w

119 nalyzed using standard liquid chromatography-mass spectrometry analyses of separate extracts made spe

120 ption-ionization and electrospray ionization-mass spectrometry analyses of SERCA1 tryptic digests rev

121 Gas chromatography/mass spectrometry analyses of sterols in this mutant, de

122 Achieving parallel top-down and bottom-up mass spectrometry analyses of target proteins using a un

123 Mass spectrometry analyses of the 80-kDa cleaved product

124 or many of the multicomponent feed mixtures, mass spectrometry analyses of the displacement column ef

125 Mass spectrometry analyses of the intact antibody and N-

126 Mass spectrometry analyses of the lipolytic secretome id

127 on among BGCs are similarly exhibited across mass spectrometry analyses of the metabolomes of Escovop

128 Mass spectrometry analyses of the phosphorylated hGT-1 s

129 Mass spectrometry analyses of the purified FLAG-tagged 7

130 Nuclear magnetic resonance spectroscopy and mass spectrometry analyses of the reaction products demo

131 Argon cluster secondary ion mass spectrometry analyses of the reaction products reve

132 Mass spectrometry analyses of these isolated complexes i

133 wledge, we performed label-free quantitative mass-spectrometry analyses of glomerular and circulatory

134 asi-CRISPR to perform co-immunoprecipitation mass-spectrometry analyses of the autism-related protein

135 n the number and types of protein structural mass spectrometry analyses, particularly during the disc

136 stion result and hydrogen-deuterium exchange mass spectrometry analyses performed in this study.

137 igh-performance liquid chromatography-tandem mass spectrometry analyses performed on fasting plasma s

138 Liquid chromatography-tandem mass spectrometry analyses probed the cellular proteome

139 cations to CP2 based on crystallographic and mass spectrometry analyses results in variants with grea

140 Yet, high-resolution mass spectrometry analyses reveal a huge chemical divers

141 Mass spectrometry analyses reveal that DJ-1 is not only

142 Mass spectrometry analyses reveal that HIPK2 is at least

143 Gas chromatography-mass spectrometry analyses reveal that the innate cuticu

144 Importantly, immunoprecipitation and mass spectrometry analyses reveal that the tagged protei

145 ctor content, crystallographic, kinetic, and mass spectrometry analyses reveal that there are fundame

146 udies reported here, immunoprecipitation and mass spectrometry analyses reveal that Wdr82 additionall

147 Gas chromatography-mass spectrometry analyses revealed a restoration of the

148 ectroscopy, and time-of-flight secondary ion mass spectrometry analyses revealed degradation of proto

149 Our tandem mass spectrometry analyses revealed distinct fingerprint

150 ineage EVs by next-generation sequencing and mass spectrometry analyses revealed distinct microRNA an

151 Liquid chromatography-tandem mass spectrometry analyses revealed that gammaTE modulat

152 Mass spectrometry analyses revealed that lncEPAT specifi

153 Detailed mass spectrometry analyses revealed that LRAT undergoes

154 aking place, polysome/ribosome profiling and mass spectrometry analyses revealed that peptides can be

155 In vitro activity assays and mass spectrometry analyses revealed that STR18 stimulate

156 Liquid chromatography-mass spectrometry analyses revealed that tBPA forms a pr

157 Mass spectrometry analyses revealed that the 170-kDa fra

158 Specific labeling with (75)Se and mass spectrometry analyses revealed that the 5-kDa selen

159 volving enzyme digestion, chromatography and mass spectrometry analyses revealed that the arabinan of

160 Cell biological and mass spectrometry analyses revealed that the conversion

161 Quantitative label-free mass spectrometry analyses revealed that the injury effe

162 MALDI-TOF mass spectrometry analyses revealed the oxidation of thi

163 Indeed, genetic, biochemical, and mass spectrometry analyses show that a highly conserved

164 Glycosyl linkage and tandem mass spectrometry analyses show that the intact LPS core

165 The inductively coupled mass spectrometry analyses show that the purified [2Fe-2

166 ity-dependent biotin identification (Bio-ID) mass spectrometry analyses showed EBF4 binding to STAT3,

167 e(X) structures, MALDI-TOF and MALDI-TOF/TOF mass spectrometry analyses showed that 4-F-GlcNAc 1) red

168 Biochemical and mass spectrometry analyses showed that alpha cardiac act

169 Immunohistochemistry and mass spectrometry analyses showed that AMG+4 proteins we

170 Immunoprecipitation and mass spectrometry analyses showed that antibodies from p

171 Finally tandem mass spectrometry analyses showed that apoA-I in human a

172 cted mutagenesis and electrospray ionization mass spectrometry analyses showed that Cys-298 of AR was

173 Furthermore, our mass spectrometry analyses showed that KPT-6566 appeared

174 tra-performance liquid chromatography-tandem mass spectrometry analyses showed that kynoxazine is pre

175 Combined immunofluorescence and mass spectrometry analyses showed that LGI1 is enriched

176 Mass spectrometry analyses showed that regulatory cytosk

177 Mass spectrometry analyses showed that the fibrillin-1 f

178 ar magnetic resonance and gas chromatography-mass spectrometry analyses showed that the polysaccharid

179 Mass spectrometry analyses showed that the proteomic sig

180 Mass spectrometry analyses suggests that the physiologic

181 complementation, coimmunoprecipitation, and mass spectrometry analyses supported the existence of co

182 complementation, coimmunoprecipitation, and mass spectrometry analyses supported the existence of co

183 Based on detailed MALDI and ESI mass spectrometry analyses, the new cluster possesses a

184 approach combining structural evaluation and mass spectrometry analyses, the use of S. cerevisiae as

185 be obtained to carry out gas chromatography/mass spectrometry analyses, this variant was also devoid

186 coupled a bioinformatics-based approach with mass spectrometry analyses to demonstrate that CHD4 inte

187 s study, we use liquid chromatography-tandem mass spectrometry analyses to identify 21 phosphorylatio

188 this interaction, we used cross-linking and mass spectrometry analyses to identify residues required

189 We have used cross-linking and tandem mass spectrometry analyses to investigate the interactio

190 cent in situ hybridization and secondary ion mass spectrometry analyses, to identify anaerobic methan

191 cell culture (SILAC) quantitative proteomic mass spectrometry analyses-to identify cellular phenotyp

192 ments, but chemical crosslinking paired with mass spectrometry analyses traps a reproducible interact

193 , high pH anion exchange chromatography, and mass spectrometry analyses, truncation was demonstrated

194 Finally, immunoprecipitation-mass spectrometry analyses using PTHrP1-17-specific anti

195 Liquid chromatography mass spectrometry analyses using the racemic and enantio

196 Using an elaborate set of mass spectrometry analyses, we demonstrate that one of t

197 ce radiocarbon, and high resolution Orbitrap mass spectrometry analyses, we evaluated the sources of

198 By immunoprecipitation and mass spectrometry analyses, we found that CD2AP bound to

199 Using the targeted proteomic approach and mass spectrometry analyses, we have identified GRIN1 (G

200 Using mass spectrometry analyses, we identified 11 ubiquitinat

201 el electrophoresis and liquid chromatography mass spectrometry analyses, we identified 84 differentia

202 Using mass spectrometry analyses, we identify a cell surface p

203 Using targeted gas chromatography-mass spectrometry analyses, we quantified eight pesticid

204 Using mass-spectrometry analyses, we here for the first time c

205 Liquid chromatography/mass spectrometry analyses were performed on lipid extra

206 electrospray ionization quadrupole ion trap mass spectrometry analyses, which indicated that ATI is