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

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

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

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

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

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

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

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

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

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

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

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

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

13 nuclear magnetic resonance spectroscopy and mass spectrometry analyses.

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

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

16 ed routinely in liquid chromatography tandem mass spectrometry analyses.

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

18 were subjected to electrophoresis and tandem mass spectrometry analyses.

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

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

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

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

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

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

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

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

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

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

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

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

31 Tandem mass spectrometry analyses, combined with native gel ele

32 Mass spectrometry analyses confirmed that the N-terminal

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

34 Mass spectrometry analyses defined two major overlapping

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

36 Immunoblot and mass spectrometry analyses demonstrated monomeric cystat

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

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

39 Mass spectrometry analyses demonstrated that PMS can be

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

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

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

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

44 Gas chromatography/mass spectrometry analyses examining different fatty aci

45 Quantitative mass spectrometry analyses further reveal an increased a

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

47 Mass spectrometry analyses have shown that AnkB is modif

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

49 Two mass spectrometry analyses identified calreticulin in am

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

51 In addition, mass spectrometry analyses identified elevated vimentin

52 Immunoprecipitation and mass spectrometry analyses identified mitochondrial ribo

53 Gas chromatography-mass spectrometry analyses indicate that membrane sterol

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

55 Mass spectrometry analyses indicated the target of each

56 Electrospray ionization mass spectrometry analyses of brevetoxins have shown tha

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

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

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

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

61 Mass spectrometry analyses of copurified proteins reveal

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

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

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

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

66 Mass spectrometry analyses of hybrid Q10 polypeptides re

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

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

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

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

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

72 Mass spectrometry analyses of oxPS species identify stru

73 High resolution mass spectrometry analyses of peptides revealed that sul

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

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

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

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

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

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

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

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

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

83 Mass spectrometry analyses of the 80-kDa cleaved product

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

85 Mass spectrometry analyses of the phosphorylated hGT-1 s

86 Mass spectrometry analyses of the purified FLAG-tagged 7

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

88 Mass spectrometry analyses of these isolated complexes i

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

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

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

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

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

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

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

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

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

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

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

100 Detailed mass spectrometry analyses revealed that LRAT undergoes

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

102 Mass spectrometry analyses revealed that the 170-kDa fra

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

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

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

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

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

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

109 Biochemical and mass spectrometry analyses showed that alpha cardiac act

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

111 Immunoprecipitation and mass spectrometry analyses showed that antibodies from p

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

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

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

115 Mass spectrometry analyses showed that regulatory cytosk

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

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

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

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

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

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

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

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

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

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

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

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

128 Liquid chromatography mass spectrometry analyses using the racemic and enantio

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

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

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

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

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

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

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