ライフサイエンスコーパス: mass spectroscopy

1 detection of novel protein adducts (e.g. by mass spectroscopy).

2 in blood by liquid chromatography and tandem mass spectroscopy.

3 lid Phase Microextraction-Gas Chromatography/Mass Spectroscopy.

4 followed by PCR and electrospray ionization mass spectroscopy.

5 fluorescence in situ hybridization tests or mass spectroscopy.

6 o-high-performance liquid chromatography and mass spectroscopy.

7 ons determined by inductively coupled plasma mass spectroscopy.

8 analyze these foods using gas chromatography-mass spectroscopy.

9 artners of Cox4 by affinity purification and mass spectroscopy.

10 opic methods and deuterium-hydrogen exchange mass spectroscopy.

11 oncogene mutation screening was performed by mass spectroscopy.

12 Serum acrolein levels were estimated with mass spectroscopy.

13 haracterized through electrospray ionization mass spectroscopy.

14 d laser desorption ionization time-of-flight mass spectroscopy.

15 arated and detected using gas chromatography/mass spectroscopy.

16 teins and chromatin-associated factors using mass spectroscopy.

17 entified by a combination of proteolysis and mass spectroscopy.

18 ins using analytical ultracentrifugation and mass spectroscopy.

19 a selective vitamin D derivatizing agent and mass spectroscopy.

20 using thermal desorption-gas chromatography-mass spectroscopy.

21 14, 28, 35, and 50 by liquid chromatography-mass spectroscopy.

22 erformed to identify interacting proteins by mass spectroscopy.

23 assayed by natural abundance stable isotope mass spectroscopy.

24 ain histology and inductively coupled plasma-mass spectroscopy.

25 ere characterized by NMR, FT-IR, UV-vis, and mass spectroscopy.

26 rties of the complex using NMR and MALDI-TOF mass spectroscopy.

27 matrix-assisted laser desorption ionization mass spectroscopy.

28 ninfected cells were comparatively mapped by mass spectroscopy.

29 y high-resolution inductively coupled plasma mass spectroscopy.

30 ged cataract human lenses were identified by mass spectroscopy.

31 cleavage and to confirm the cleavage site by mass spectroscopy.

32 it liver membranes and identified as NPC1 by mass spectroscopy.

33 ure spectroscopy and nanoscale secondary ion mass spectroscopy.

34 quid chromatography tandem mass spectrometry/mass spectroscopy.

35 Trapped proteins were identified by mass spectroscopy.

36 with serum IgE of allergic individuals, and mass spectroscopy.

37 x RNA helicase CshA (NWMN_1985 or SA1885) by mass spectroscopy.

38 e electronic and emission spectroscopy), and mass spectroscopy.

39 ing gas and liquid chromatography coupled to mass spectroscopy.

40 mapimod using ATP-desthiobiotin pulldown and mass spectroscopy.

41 n be detected by functional assays and/or by mass spectroscopy.

42 d laser desorption ionization time of flight mass spectroscopy.

43 y high-performance liquid chromatography and mass spectroscopy.

44 ithiaporphyrin macrocycles were confirmed by mass spectroscopy, 1D and 2D NMR spectroscopy, and X-ray

45 2)C), i.e., in the same order as accelerator mass spectroscopy, achieved with a relatively inexpensiv

46 Detected antigens were identified by mass spectroscopy after 2-dimensional electrophoresis an

47 Fluorescence and mass spectroscopy analyses demonstrated that the STI rem

48 Mass spectroscopy analyses identify a cleavage preferenc

49 Mass spectroscopy analyses of Pcyt2 provided evidence fo

50 Abl-mediated nmMLCK phosphorylation sites by mass spectroscopy analysis (including Y231, Y464, Y556,

51 Deuterium exchange mass spectroscopy analysis further reveals that EPAC2-sp

52 Mass spectroscopy analysis now shows that HSP90 is prese

53 tography of the MW2 supernatant, followed by mass spectroscopy analysis of corresponding peaks, we id

54 Mass spectroscopy analysis of Gp78 phosphopeptides confi

55 Ultraperformance liquid chromatography/mass spectroscopy analysis of hepatic bile acids indicat

56 Mass spectroscopy analysis of N protein from ANDV-infect

57 Mass spectroscopy analysis of NSP2 complexes immunopreci

58 Cleavage sites were also analyzed by mass spectroscopy analysis of selected immunoprecipitate

59 hort-read-length DNA sequencing coupled with mass spectroscopy analysis of SNPs to study the molecula

60 Validating these findings, mass spectroscopy analysis revealed that S386 of ANDV N

61 High-performance liquid chromatography and mass spectroscopy analysis revealed that SleB is require

62 Inductively coupled plasma-mass spectroscopy analysis revealed variable levels of e

63 Mass spectroscopy analysis showed that single cysteine r

64 baseline samples using liquid chromatography-mass spectroscopy and a 2-site immunoassay, respectively

65 Next, studies using mass spectroscopy and a pharmacological inhibitor demons

66 Using liquid chromatography-mass spectroscopy and a VTC2-H238N mutant, we provide ev

67 The protein was then characterised by mass spectroscopy and an in vitro functional assay using

68 lution crystallographic data with structural mass spectroscopy and electron microscopic data to deriv

69 pH anion exchange chromatography, MALDI-TOF mass spectroscopy and FACS analysis with the plant lecti

70 igh performance liquid chromatography-tandem mass spectroscopy and gas chromatography-mass spectrosco

71 inal apelin secretion in vivo and ex vivo by mass spectroscopy and immunologic techniques.

72 ctroscopy and by fast atom bombardment (FAB) mass spectroscopy and it is shown that rapid exchange eq

73 n the supernate of activated platelets using mass spectroscopy and looking for proteins originating f

74 I-06 by an integrated approach using imaging mass spectroscopy and molecular networking, as well as c

75 Activity-guided fractionation, followed by mass spectroscopy and NMR analysis, resulted in the iden

76 ed under UV-visible, infra-red spectroscopy, mass spectroscopy and NMR techniques.

77 omatography (LC) fraction collection, LC-NMR-mass spectroscopy and one-dimensional and two-dimensiona

78 romatography (HPLC) and identified by tandem mass spectroscopy and proton nuclear magnetic resonance

79 chromatography, UV-visible spectroscopy, and mass spectroscopy and proved to be uroporphomethene, a c

80 icroextraction coupled to gas chromatography/mass spectroscopy and the determination of conventional

81 Mass spectroscopy and two-dimensional gel electrophoresi

82 djacent cysteine-366 thiol was was proved by mass spectroscopy and X-ray crystal structure studies.

83 Just as multidimensional separation in mass-spectroscopy and multidimensional spectra in NMR ha

84 TPD-MS (temperature-programmed decomposition-mass spectroscopy), and TGA-DSC (thermogravimetric analy

85 y NMR, UV-vis, fluorescence, high-resolution mass spectroscopies, and in many cases, X-ray crystallog

86 d laser desorption ionization time-of-flight-mass spectroscopy, and algorithmic means were employed t

87 xchange in the bulk solution, including NMR, mass spectroscopy, and Fourier transform infrared spectr

88 vitro and in vivo phosphorylation analysis, mass spectroscopy, and functional assays to identify two

89 TNFalpha-treated extracts was identified by mass spectroscopy, and its amino-terminal cleavage site

90 actions through photoaffinity, cross-linking/mass spectroscopy, and X-ray crystallographic studies.

91 By the use of UV spectrometry, mass spectroscopy, and x-ray crystallography, we have do

92 ectures assembled were characterized by NMR, mass spectroscopy, and X-ray crystallography.

93 C. trachomatis Incs to affinity purification-mass spectroscopy (AP-MS).

94 For mass spectroscopy applications, chemical identification

95 y uses a chiral liquid chromatography-tandem mass spectroscopy approach (LC-MS/MS) to quantify each s

96 Using a mass spectroscopy approach, we identified specific remod

97 stablished by nuclear magnetic resonance and mass spectroscopy as a heretofore unidentified alpha,bet

98 f F. nucleatum ATCC 23726 and identified via mass spectroscopy as members of the outer membrane famil

99 vo, and the target antigen was identified by mass spectroscopy as the alpha2 subunit of the alpha2bet

100 Thin-layer chromatography and mass spectroscopy assays demonstrated that these two rec

101 tation profiling was performed by using both mass spectroscopy-based genotyping and Sanger sequencing

102 However, new techniques, such as mass spectroscopy-based proteomics, were recently develo

103 To identify a repressor protein, we used a mass spectroscopy-based RNA-protein interaction system a

104 By applying mass spectroscopy-based sequencing and reverse-phase pro

105 Conventional approaches such as ELISA and mass spectroscopy cannot satisfy the needs of continual

106 but worse than continuous flow-isotope ratio mass spectroscopy (CF-IRMS) methods owing to memory effe

107 ectroscopy and nanometer-scale secondary ion mass spectroscopy confirm the carbon-nitrogen species in

108 de gel electrophoresis followed by MALDI/TOF mass spectroscopy confirmed high expression of beta-acti

109 Mass spectroscopy confirmed Leu- and Met-enkephalin in s

110 ers or pH inactivation of peroxynitrite, and mass spectroscopy confirmed nitration of conserved tyros

111 Mass spectroscopy corroborates that CYTL1 is specificall

112 f metal uptake by inductively coupled plasma mass spectroscopy demonstrated that ZIPB is selective fo

113 Liquid chromatography coupled with mass spectroscopy demonstrated the presence of many mono

114 Differential electrochemical mass spectroscopy (DEMS) is used to quantify the amounts

115 scopy (EIS) and differential electrochemical mass spectroscopy (DEMS) with high resolution.

116 Liquid chromatography-mass spectroscopy detected two chlorinated organic produ

117 e utilized amide hydrogen/deuterium exchange mass spectroscopy (DXMS) to assess potential conformatio

118 r water splitting by in situ electrochemical mass spectroscopy (EMS).

119 Electrospray ionization mass spectroscopy (ESI-MS) allows direct measurement of

120 R), fluorescence quenching, and electrospray mass spectroscopy (ESI-MS) were implemented to examine t

121 lity of using electrospray ionisation tandem mass spectroscopy (ESI-MS/MS) to unequivocally determine

122 ption energies of radicals detected from our mass-spectroscopy experiment provide an in-depth underst

123 found that high-throughput affinity capture-mass spectroscopy experiments can detect functional inte

124 The NMR ALARM assay, mass spectroscopy experiments, in vitro counter screenin

125 clinical chemistry analysis, 1D (1)H NMR and mass spectroscopy (FIA-MS/MS and LC-MS/MS) techniques.

126 the trapped substrate proteins identified by mass spectroscopy, five proteins, cathepsin G, glutaredo

127 ane, and then analysed by gas chromatography-mass spectroscopy/flame ionisation detector.

128 2 ginger samples using liquid chromatography-mass spectroscopy, followed by a principal component ana

129 ant species by the use of gas chromatography-mass spectroscopy, followed by detailed data mining and

130 nts, and then subjected selected antigens to mass spectroscopy for amino acid sequencing for comparis

131 n spectroscopy or inductively coupled plasma mass spectroscopy for total Se and X-ray absorption spec

132 Glycosylation was analyzed by mass spectroscopy; functionality was confirmed by antige

133 of chemical compounds by gas chromatography-mass spectroscopy (GC-MS) was also performed.

134 ic pollutants measured by gas chromatography-mass spectroscopy (GC-MS); all have theoretical and prac

135 itable derivatization, by gas chromatography-mass spectroscopy (GC/MS) analysis.

136 A series of gas chromatography/mass spectroscopy (GC/MS) measurements taken from the ef

137 on spectroscopy (XPS) and gas-chromatography/mass spectroscopy (GC/MS), this attachment strategy is d

138 s (TGA) coupled to online gas chromatography/mass spectroscopy (GC/MS).

139 Mass-spectroscopy genotyping for somatic gene mutations

140 d laser desorption ionization time-of-flight mass spectroscopy (GPC-MALDI ToF MS), which revealed the

141 Mass spectroscopy has revealed that ubiquitination of OA

142 chniques based on inductively coupled plasma mass spectroscopy (ICP-MS) and chlorodimetry illustrate

143 AF4) coupled with inductively coupled plasma mass spectroscopy (ICP-MS) for the speciation and quanti

144 roscopy (TEM) and inductively coupled plasma mass spectroscopy (ICP-MS).

145 quantified using inductively coupled plasma mass spectroscopy (ICPMS) and migration was found to occ

146 (AHG) interface to inductive coupled plasma mass spectroscopy (ICPMS) was developed for measuring ar

147 uantitatively via inductively coupled plasma mass spectroscopy (ICPMS), allowing for direct compariso

148 Liquid chromatography-mass spectroscopy identified 14-3-3 as one of the LNK-bi

149 Tandem mass spectroscopy identified a novel phosphorylation sit

150 Mass spectroscopy identified a single nitration site, lo

151 Chromatography and mass spectroscopy identified and quantitated 204 serum m

152 Immunoprecipitation coupled with mass spectroscopy identified eIF3 subunit b (eIF3b) as a

153 Immunoprecipitation and mass spectroscopy identified eight potential interacting

154 d chromatography and electrospray ionization mass spectroscopy identified selective accumulation of p

155 g ERK-dependent phosphorylation at Ser(319), mass spectroscopy identified two other ERK-phosphorylate

156 blotting and proteomic analyses using 2D-gel/mass spectroscopy identified vimentin and beta-catenin a

157 this issue, a correlative analysis combining mass spectroscopy imaging (MSI) and fluorescence imaging

158 Somatic mutations were analyzed using mass spectroscopy in 193 patients who underwent single-r

159 al lipid surveys using liquid chromatography-mass spectroscopy in nondiabetic, lean, predominantly no

160 emicals executed by using gas chromatography-mass spectroscopy in order to correlate the bioactivitie

161 sis followed by liquid chromatography tandem mass spectroscopy, including those involved in metabolis

162 Immunoprecipitation of FGFR1 coupled with mass spectroscopy indicated that FGFR1 forms a physical

163 Mass spectroscopy indicates that the beta-subunit bears

164 Results from electrospray ionization mass spectroscopy investigations showed that a single zi

165 ffers a cheaper alternative to isotope-ratio mass spectroscopy (IRMS), but its use in studying plant

166 measured delta(13)C-DIC using isotope ratio mass spectroscopy (IRMS).

167 y and capillary electrophoresis coupled with mass spectroscopy is presented.

168 _modeling package is an easy-to-use tool for mass spectroscopy isotopologue profile deconvolution inv

169 To aid the interpretation of the mass spectroscopy isotopologue profile, we have develope

170 ase liquid chromatography (LC) with ion trap mass spectroscopy (IT-MS), using positive polarity atmos

171 Using reverse phase HPLC and electrospray mass spectroscopy, it was determined that oligonucleotid

172 by laser ablation inductively coupled plasma mass spectroscopy (LA-ICP-MS).

173 bioassays supported by liquid chromatography-mass spectroscopy (LC-MS(n)).

174 ment of proteins using liquid chromatography-mass spectroscopy (LC-MS) analyses and does not necessar

175 Liquid chromatography-mass spectroscopy (LC-MS) analysis of culture supernatan

176 We have applied liquid chromatography-mass spectroscopy (LC-MS) based untargeted metabolite pr

177 matography (HPLC), and liquid chromatography-mass spectroscopy (LC-MS) pteridine urinalyses among oth

178 etection algorithm for liquid chromatography-mass spectroscopy (LC-MS).

179 pin ferric 2B4; liquid chromatography-tandem mass spectroscopy (LC-MS/MS) analysis shows that in this

180 By liquid-chromatography-mass spectroscopy (LC-MS/MS) we identified LTPs from two

181 Using liquid chromatography coupled with mass spectroscopy (LC-MS/MS), we detected 20 steroids wi

182 igh performance liquid chromatography tandem mass spectroscopy (LC/MS-MS) on plasma, urine, and lung

183 A4H aminopeptidase activity were detected by mass spectroscopy, LTA4H amounts were detected by ELISA,

184 matrix-assisted laser desorption ionization mass spectroscopy (MALDI-MS).

185 Three of the peptides detected by mass spectroscopy map to two ABC transport-related prote

186 lished mouse model and liquid chromatography-mass spectroscopy/mass spectroscopy-based lipidomics.

187 ce acceptors is analyzed using secondary ion mass spectroscopy measurements and traced to thermal acc

188 , high performance liquid chromatography and mass spectroscopy measurements are used to assess molecu

189 Here we report transport and mass spectroscopy measurements which establish that mono

190 whole genome gene expression and untargeted mass-spectroscopy metabolomics for MCF-7 cells.

191 ique liquid chromatography-mass spectrometry/mass spectroscopy method quantifying circulating and equ

192 ighly sensitive liquid chromatography-tandem mass spectroscopy method.

193 measured with an inductively-coupled-plasma mass spectroscopy method.

194 High-throughput sequencing, mass spectroscopy methods and advances in computational

195 Fourier transform spectroscopy (DRIFT), and mass spectroscopy (MS) analysis of RhAl2O3 catalyst unde

196 CV sT FLAG-affinity purification followed by mass spectroscopy (MS) analysis, which identified severa

197 The mass spectroscopy (MS) results show that the silica-lant

198 Mass spectroscopy (MS) shows the presence of AF1 in the

199 The Raman findings were complemented by mass spectroscopy (MS)-based metabolite analysis of 8 in

200 oassays (ELISA and RIA), or various types of mass spectroscopy (MS)-based protocols, semi-quantitativ

201 ment of the osmium moiety is demonstrated by mass spectroscopy (MS-MALDI-TOF) and cyclic voltammetry.

202 nstrate that optimization of a set of tandem mass spectroscopy (MS/MS) collision energies and automat

203 orous microarrays and their combination with Mass-Spectroscopy (MS) techniques, to protein properties

204 gen-deuterium exchange (HDX; as monitored by mass spectroscopy, MS).

205 matrix-assisted laser desorption/ionization mass spectroscopy, N-terminal sequencing, and improved c

206 Using nanoscale secondary ion mass spectroscopy (NanoSIMS) and a novel digital image p

207 e often prepared for nanoscale secondary ion mass spectroscopy (NanoSIMS) investigations by depositin

208 n Spectroscopy (XPS), and Nano Secondary Ion Mass Spectroscopy (NanoSIMS).

209 Mass spectroscopy of affinity-purified PIFTC3 revealed s

210 Mass spectroscopy of hexa-Fc reveals high-mannose, low-s

211 Mass spectroscopy of HOCl-treated human SP-D demonstrate

212 Mass spectroscopy of isolated lipid droplets from cgi-58

213 Mass spectroscopy of late passage MSC indicated a synerg

214 teins experimentally elucidated by proteomic mass spectroscopy of signalling complexes and proteins b

215 Induction-coupled plasma mass spectroscopy of single and double mutants showed th

216 The detection by mass spectroscopy of the reaction intermediates, in conj

217 tion by mammalian cell adhesion and by SAMDI mass spectroscopy of the SAMs.

218 tion magic angle spinning magnetic resonance mass spectroscopy on endometrial cancer surgical specime

219 as further supported by enzymatic assays and mass spectroscopy on recombinant protein, patient-derive

220 We initially identified, by mass spectroscopy, peptides from the Rv1681 protein in u

221 dissemination of the information beyond the mass spectroscopy proteomics community.

222 e in good agreement with inductively coupled mass spectroscopy ( R(2)=0.88, R(2)=0.75, P<0.001) and l

223 tion of (13)CO and O2 monitored by FT-IR and mass spectroscopy, respectively.

224 man spectroscopy and gas chromatography with mass spectroscopy, respectively.

225 d laser desorption/ionization time-of-flight mass spectroscopy revealed abnormal expression of a clus

226 from rodent ventricular lysates followed by mass spectroscopy revealed an interaction with junctophi

227 MALDI mass spectroscopy revealed hyperphosphorylation of myosi

228 Oil red O staining and quantitative mass spectroscopy revealed that esterified cholesterol c

229 Mass spectroscopy revealed that PrtA makes a major cut b

230 bitor screen, and a kinase trapping-Orbitrap mass spectroscopy screen to systematically identify esse

231 rement, peptide mapping analysis, and tandem mass spectroscopy sequencing.

232 Secondary ion mass spectroscopy (SIMS) analyses performed on Beach For

233 Using secondary ion mass spectroscopy (SIMS) analysis, we found that binding

234 gher than in the corresponding secondary-ion mass spectroscopy (SIMS) analysis.

235 Analyses by secondary ion mass spectroscopy (SIMS) of 11 specimens of five taxa of

236 s lower than the corresponding secondary ion mass spectroscopy (SIMS) signal, the mass spectra are si

237 ram quantities and fully characterized using mass spectroscopy, size exclusion chromatography (SEC),

238 g X-ray diffraction (XRD), Sputtered neutral-mass spectroscopy (SNMS), Scanning electron microscopy (

239 e single-particle inductively coupled plasma mass spectroscopy (SP-ICP-MS) analysis.

240 , we use single particle inductively coupled mass spectroscopy (SP-ICP-MS) to measure directly NP dia

241 e single particle-inductively coupled plasma mass spectroscopy (SP-ICPMS) to help quantify exposure t

242 , single-particle inductively coupled plasma mass spectroscopy (spICP-MS) with two different plant di

243 g single particle inductively coupled plasma mass spectroscopy (spICP-MS).

244 id Phase Micro Extraction-Gas Chromatography-Mass Spectroscopy (SPME-GC-MS), High-Performance Liquid

245 two-dimensional liquid chromatography-tandem mass spectroscopy strategy and functional network analys

246 Inhibitor and mass spectroscopy studies revealed that the fluorescence

247 Mass spectroscopy studies showed unequivocally the speci

248 nchrotron vacuum ultraviolet photoionization mass spectroscopy (SVUV-PIMS), which uncovers the existe

249 refined a derivatization gas chromatography-mass spectroscopy technique to measure 11 mono- and dica

250 Molecular and mass spectroscopy techniques are changing sepsis diagnos

251 ng pathways in human urothelial cells, using mass spectroscopy techniques, an agonist-dependent inter

252 ovel liquid chromatography-mass spectrometry/mass spectroscopy techniques.

253 they cannot be identified using conventional mass spectroscopy techniques.

254 ed controls using a combination of different mass spectroscopy techniques.

255 such as nucleic acid amplification tests and mass spectroscopy that allow clinical laboratories to de

256 ow, using electronic spectroscopy, HPLC, and mass spectroscopy, that in W191F partial formation of a

257 By tandem mass spectroscopy, the bands contained both liver and in

258 chromatography with electrospray-ionization mass spectroscopy, the first step of this transformation

259 By mass spectroscopy, the pentapeptide is rapidly formed fr

260 eric matrix protein (COMP) and confirmed, by mass spectroscopy, the presence of deamidated (Asp(64))

261 rystallography, NMR, terahertz spectroscopy, mass spectroscopy, thermodynamics, and computer simulati

262 reement with the molecular mass suggested by mass spectroscopy to be 83 kDa.

263 dem mass spectroscopy and gas chromatography-mass spectroscopy to discriminate global metabolites pro

264 odies in a far-Western technique followed by mass spectroscopy to identify the C3b acceptor molecule(

265 ied from human HMC-1 cells and identified by mass spectroscopy to include CTSB and CTSL.

266 scopy (XPS) and time-of-flight secondary ion mass spectroscopy (TOF-SIMS) are used to confirm sample

267 r, we performed time-of-flight secondary-ion mass spectroscopy (ToF-SIMS) measurements for quench-coo

268 Time-of-flight secondary ion mass spectroscopy (ToF-SIMS) was performed on the repres

269 acterized using Time-of-Flight Secondary Ion Mass Spectroscopy (ToF-SIMS), 2-D ToF-SIMS chemical imag

270 hniques, namely time-of-flight secondary ion mass spectroscopy (ToF-SIMS), atom probe tomography (APT

271 haracterized by time-of-flight-secondary ion mass spectroscopy (TOF-SIMS).

272 A/TGA) and temperature programmed desorption-mass spectroscopy (TPD-MS) in combination with X-ray dif

273 NAL were identified by liquid chromatography-mass spectroscopy (UHPLC-MS/MS).

274 uid and gas chromatography coupled to tandem mass spectroscopy (UPLC-MS/MS and GC-MS/MS).

275 igh performance liquid chromatography-tandem mass spectroscopy (UPLC-MS/MS) metabolomics on maternal

276 led using liquid chromatography coupled with mass-spectroscopy (UPLC) and PK parameters were calculat

277 -ethyl moiety by NMR spectroscopy, MALDI-TOF mass spectroscopy, UV-Vis spectroscopy, and titration an

278 In this work MALDI-TOF mass spectroscopy was investigated to characterise the b

279 Mass spectroscopy was most consistent with the presence

280 Mass spectroscopy was performed on BCE-ECM to examine th

281 Gas chromatography-mass spectroscopy was used to assess short-chain fatty a

282 Liquid chromatography-mass spectroscopy was used to determine incorporation of

283 mor-bearing mice, inductively coupled plasma mass spectroscopy was used to quantitatively and orthogo

284 Using mass spectroscopy we determined that recombinant Lac1 do

285 Using NanoSIMS (dynamic secondary ion mass spectroscopy), we show that the iron-phosphorus gra

286 advances and increased availability of lipid mass spectroscopy, we are now starting to discern the pa

287 tive integrated liquid chromatography-tandem mass spectroscopy, we characterize methylation of (i) re

288 Using mass spectroscopy, we confirmed that LM-MDSCs showed enh

289 Using high-resolution mass spectroscopy, we determined the structure of the py

290 Using mass spectroscopy, we found that Cox7c, a nuclear-encode

291 Using tandem mass spectroscopy, we have identified a number of oxidat

292 Using mass spectroscopy, we have previously identified three L

293 Using immunoaffinity purification and mass spectroscopy, we identified a stable complex of 174

294 By mass spectroscopy, we identified five serines in the hea

295 Using mass spectroscopy, we identified the catalytic subunit o

296 ing NMR and liquid chromatography coupled to mass spectroscopy, we identified the main compatible sol

297 h the use of the technique of time-of-flight mass spectroscopy, we obtain strong-field ionization yie

298 Here, using X-ray crystallography and mass spectroscopy, we report that ANQX forms two major p

299 Liquid chromatography and tandem mass spectroscopy were then employed to characterize the

300 We used hydroxy-radical foot printing with mass spectroscopy (XFMS) to track the solvent accessibil