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 Trapped proteins were identified by mass spectroscopy.

3 artners of Cox4 by affinity purification and mass spectroscopy.

4 opic methods and deuterium-hydrogen exchange mass spectroscopy.

5 oncogene mutation screening was performed by mass spectroscopy.

6 Serum acrolein levels were estimated with mass spectroscopy.

7 haracterized through electrospray ionization mass spectroscopy.

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

9 arated and detected using gas chromatography/mass spectroscopy.

10 teins and chromatin-associated factors using mass spectroscopy.

11 entified by a combination of proteolysis and mass spectroscopy.

12 ins using analytical ultracentrifugation and mass spectroscopy.

13 a selective vitamin D derivatizing agent and mass spectroscopy.

14 using thermal desorption-gas chromatography-mass spectroscopy.

15 14, 28, 35, and 50 by liquid chromatography-mass spectroscopy.

16 erformed to identify interacting proteins by mass spectroscopy.

17 assayed by natural abundance stable isotope mass spectroscopy.

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

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

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

21 matrix-assisted laser desorption ionization mass spectroscopy.

22 ninfected cells were comparatively mapped by mass spectroscopy.

23 y high-resolution inductively coupled plasma mass spectroscopy.

24 ged cataract human lenses were identified by mass spectroscopy.

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

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

27 ectroscopic methods including NMR, FTIR, and mass spectroscopy.

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

29 tension products are quantified by MALDI-TOF mass spectroscopy.

30 d laser desorption/ionization time-of-flight mass spectroscopy.

31 Bile acid composition was analyzed by mass spectroscopy.

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

33 isobaric tagging reagents (iTRAQ) and tandem mass spectroscopy.

34 ere studied using co-immunoprecipitation and mass spectroscopy.

35 ification-specific synuclein antibodies, and mass spectroscopy.

36 rption/ionization time-of-flight (MALDI-TOF) mass spectroscopy.

37 identified potential signaling molecules by mass spectroscopy.

38 yzed for 13C content by using stable-isotope mass spectroscopy.

39 content was measured by ion-coupled plasmon mass spectroscopy.

40 ing gas and liquid chromatography coupled to mass spectroscopy.

41 mapimod using ATP-desthiobiotin pulldown and mass spectroscopy.

42 d laser desorption ionization time of flight mass spectroscopy.

43 y high-performance liquid chromatography and mass spectroscopy.

44 in blood by liquid chromatography and tandem mass spectroscopy.

45 lid Phase Microextraction-Gas Chromatography/Mass Spectroscopy.

46 followed by PCR and electrospray ionization mass spectroscopy.

47 fluorescence in situ hybridization tests or mass spectroscopy.

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

49 ons determined by inductively coupled plasma mass spectroscopy.

50 analyze these foods using gas chromatography-mass spectroscopy.

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

52 peptide ligands that we sequenced by tandem mass spectroscopy, 5 were previously eluted from HLA cla

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

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

55 Fluorescence and mass spectroscopy analyses demonstrated that the STI rem

56 Mass spectroscopy analyses identify a cleavage preferenc

57 Mass spectroscopy analyses of isolated PEII alpha- and b

58 Mass spectroscopy analyses of Pcyt2 provided evidence fo

59 hromatography-electrospray ionization-tandem mass spectroscopy analyses, 15 proteins were identified

60 gned on the basis of 1D, 2D NMR (ROESY), and mass spectroscopy analyses.

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

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

63 Mass spectroscopy analysis now shows that HSP90 is prese

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

65 Mass spectroscopy analysis of Gp78 phosphopeptides confi

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

67 Mass spectroscopy analysis of NSP2 complexes immunopreci

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

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

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

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

72 Mass spectroscopy analysis showed that single cysteine r

73 ied N525, a site that cannot be recovered by mass spectroscopy analysis, as a glycosylation site.

74 d laser desorption ionization time-of-flight mass spectroscopy analysis.

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

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

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

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

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

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

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

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

83 ed during human infection were identified by mass spectroscopy and included both previously described

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

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

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

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

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

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

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

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

92 Mass spectroscopy and two-dimensional gel electrophoresi

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

94 cterized using both structural methods (NMR, mass spectroscopy) and photophysical measurements (UV-vi

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

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

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

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

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

100 sure liquid chromatography, characterized by mass spectroscopy, and subjected to kinetic analysis aga

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

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

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

104 For mass spectroscopy applications, chemical identification

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

106 Using a mass spectroscopy approach, we identified specific remod

107 that most, if not all, targets identified by mass spectroscopy are bona fide ISG15 targets.

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

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

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

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

112 trates, we used liquid chromatography tandem mass spectroscopy based sequencing to generate a complet

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

114 Using mass spectroscopy-based proteomics, we detected 117 prot

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

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

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

118 By mass spectroscopy-based studies, we identified Src tyros

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

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

121 Furthermore, liquid chromatography/tandem mass spectroscopy characterized 3 distinct types of post

122 layer chromatography and gas chromatography mass spectroscopy confirm that the intact molecule is se

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

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

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

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

127 In vitro cleavage assays and mass spectroscopy confirmed that three of the identified

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

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

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

131 matrix-assisted laser desorption/ionization mass spectroscopy detection is reported.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

152 Mass-spectroscopy genotyping for somatic gene mutations

153 Calibrated fluorescent images combined with mass spectroscopy give a transport rate of 0.06 ASP+/hNE

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

155 Mass spectroscopy has revealed that ubiquitination of OA

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

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

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

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

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

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

162 Tandem mass spectroscopy identified a novel phosphorylation sit

163 Mass spectroscopy identified a single nitration site, lo

164 Chromatography and mass spectroscopy identified and quantitated 204 serum m

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

166 Immunoprecipitation and mass spectroscopy identified eight potential interacting

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

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

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

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

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

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

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

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

175 Mass spectroscopy indicates that the beta-subunit bears

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

196 Biochemical and mass spectroscopy measurements revealed a 3.6-fold decre

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

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

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

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

201 ighly sensitive liquid chromatography-tandem mass spectroscopy method.

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

203 ontent cell screening, expression profiling, mass spectroscopy, mouse models of disease, and a post-l

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

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

206 rhodopsin chromophore was determined by HPLC-mass spectroscopy (MS) and the spectral properties by sp

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

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

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

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

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

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

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

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

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

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

217 Tandem mass spectroscopy of a tryptic digest of this 12.5 kDa p

218 Mass spectroscopy of affinity-purified PIFTC3 revealed s

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

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

221 Mass spectroscopy of isolated lipid droplets from cgi-58

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

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

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

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

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

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

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

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

230 ions by optical microscopy and secondary ion mass spectroscopy reveal that Ca is concentrated along t

231 Liquid chromatography/mass spectroscopy revealed a decrease in total adipose s

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

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

234 MALDI mass spectroscopy revealed hyperphosphorylation of myosi

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

236 Mass spectroscopy revealed that PrtA makes a major cut b

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

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

239 Analysis of the phosphotyrosine proteome by mass spectroscopy showed differential phosphorylation am

240 es by high performance liquid chromatography/mass spectroscopy showed that treatment with imatinib in

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

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

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

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

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

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

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

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

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

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

251 Inhibitor and mass spectroscopy studies revealed that the fluorescence

252 Mass spectroscopy studies showed unequivocally the speci

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

254 Molecular and mass spectroscopy techniques are changing sepsis diagnos

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

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

257 they cannot be identified using conventional mass spectroscopy techniques.

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

259 o-dimensional gel electrophoresis (2DIGE) or mass spectroscopy that represent unbiased approaches (as

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

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

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

263 By mass spectroscopy, the pentapeptide is rapidly formed fr

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

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

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

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

268 nd electrospray ionization-Fourier transform mass spectroscopy to follow the loading of the activated

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

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

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

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

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

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

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

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

277 Mass spectroscopy was most consistent with the presence

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

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

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

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

282 Using mass spectroscopy we determined that recombinant Lac1 do

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

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

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

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

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

288 Using co-immunoprecipitation and tandem mass spectroscopy, we found that HIV1 Vpr engages a DDB1

289 In this study, using linear ion trap mass spectroscopy, we have demonstrated that EVI5 exists

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

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

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

293 Using mass spectroscopy, we identified the catalytic subunit o

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

295 d laser desorption/ionization time-of-flight mass spectroscopy, we identified, out of the 100 cystein

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

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

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

299 ption spectroscopy and liquid chromatography-mass spectroscopy, which showed that the Se-tolerant mot

300 et-associated protein from the PAT family by mass spectroscopy, which was further confirmed by immuno