ライフサイエンスコーパス: pulsed-field

1 etic fields up to 45 T (DC fields) and 60 T (pulsed fields).

2 magnetic atoms with the use of a sequence of pulsed fields.

3 Pulsed field ablation (PFA) can be myocardium selective,

4 o assess the safety and lesion durability of pulsed field ablation (PFA) for both PVI and LAPW ablati

5 Pulsed field ablation (PFA) is a nonthermal energy that

6 Pulsed field ablation (PFA) is a uniquely tissue-selecti

7 The tissue selectivity of pulsed field ablation (PFA) provides safety advantages o

8 We hypothesized that pulsed field ablation (PFA) would reduce PV stenosis ris

9 During pulsed field ablation (PFA), subsecond electric fields c

10 s with atrial fibrillation: electroporation (pulsed-field ablation), expandable lattice-tip radiofreq

11 pared to the wild-type ORF37, as assessed by pulsed-field and Gardella gel electrophoresis, electron

12 Two cohorts of 6 swine were treated with pulsed fields at low dose (PF(LD)) and high dose (PF(HD)

13 h experimental data found in the literature (pulsed field electrophoresis technique).

14 Pulsed field electrophoresis was performed on environmen

15 ficile strains (ribotype 027; North American pulsed-field electrophoresis 1 [NAP1]; restriction endon

16 IV DNA by isolating integrated HIV DNA using pulsed-field electrophoresis before performing sequencin

17 Here, we confirm by specific comet assay and pulsed-field electrophoresis that cells adapted to high

18 (Pulsed Fields for Persistent Atrial Fibrillation [PersAF

19 The degree of separation in pulsed field gel (PFG) depends on the size of DNA as wel

20 Pulsed field gel electrophoresis (PFGE) offers a high-re

21 on-Valentine leucocidin (PVL) screening, and pulsed field gel electrophoresis (PFGE) were performed t

22 Using quantitative pulsed field gel electrophoresis and sensitive DNA synth

23 Pulsed field gel electrophoresis determined that 91% of

24 zed FQ(R) C. coli isolates had similar PFGE (pulsed field gel electrophoresis) patterns and the same

25 ion of YAC DNA from yeast chromosomal DNA by pulsed field gel electrophoresis, concentration to a ran

26 Forty CR-Kp were genotyped by pulsed field gel electrophoresis, multilocus sequence ty

27 Pulsed-field gel analysis suggested that the R2 active a

28 olated in the United States were analyzed by pulsed-field gel electrophoresis (PFGE) after digestion

29 Pulsed-field gel electrophoresis (PFGE) analysis reveale

30 li isolates were compared using phylotyping, pulsed-field gel electrophoresis (PFGE) analysis, sequen

31 ersity of 248 strains was investigated using pulsed-field gel electrophoresis (PFGE) analysis.

32 itional molecular subtyping methods, such as pulsed-field gel electrophoresis (PFGE) and 7-gene multi

33 Outbreak-related cases were identified by pulsed-field gel electrophoresis (PFGE) and confirmed by

34 Isolates were further characterized by pulsed-field gel electrophoresis (PFGE) and emm typing.

35 Pulsed-field gel electrophoresis (PFGE) and multi-locus

36 d during the same period were compared using pulsed-field gel electrophoresis (PFGE) and multilocus s

37 -multiplex PCR) typing (SMT) with respect to pulsed-field gel electrophoresis (PFGE) and multilocus s

38 Pulsed-field gel electrophoresis (PFGE) and multilocus v

39 Pulsed-field gel electrophoresis (PFGE) and multiple-loc

40 le nucleotide polymorphisms (SNPs) than with pulsed-field gel electrophoresis (PFGE) and other method

41 gically evaluable patients were genotyped by pulsed-field gel electrophoresis (PFGE) and PCR for pvl

42 In this study, we combined pulsed-field gel electrophoresis (PFGE) and Southern hyb

43 robust molecular genetic approaches, such as pulsed-field gel electrophoresis (PFGE) and whole-genome

44 For evaluating the genotypic diversity, pulsed-field gel electrophoresis (PFGE) and/or enterobac

45 Isolates characterized as USA300 by pulsed-field gel electrophoresis (PFGE) are the predomin

46 Pulsed-field gel electrophoresis (PFGE) clonal type USA2

47 detection, toxinotyping, DNA sequencing, and pulsed-field gel electrophoresis (PFGE) DNA fingerprinti

48 ntification of Salmonella serotypes based on pulsed-field gel electrophoresis (PFGE) fingerprints.

49 d H. haemolyticus isolates were genotyped by pulsed-field gel electrophoresis (PFGE) following SmaI o

50 tandard method of SmaI restriction digestion pulsed-field gel electrophoresis (PFGE) for typing S. au

51 CR analysis for the spvA virulence gene, and pulsed-field gel electrophoresis (PFGE) genotyping were

52 Among the CA-MRSA isolates, the pulsed-field gel electrophoresis (PFGE) groups detected

53 Pulsed-field gel electrophoresis (PFGE) has been the gol

54 Pulsed-field gel electrophoresis (PFGE) is a common meth

55 Pulsed-field gel electrophoresis (PFGE) is a standard ty

56 Pulsed-field gel electrophoresis (PFGE) is considered th

57 AC) lung disease, but the "gold standard" of pulsed-field gel electrophoresis (PFGE) is time-consumin

58 strain is often determined by comparing its pulsed-field gel electrophoresis (PFGE) or multilocus se

59 solution, and it can be directly analyzed by pulsed-field gel electrophoresis (PFGE) or used in appli

60 All isolates had the same pulsed-field gel electrophoresis (PFGE) pattern, suggest

61 Pulsed-field gel electrophoresis (PFGE) patterns of the

62 y serotype 1/2a isolates with highly similar pulsed-field gel electrophoresis (PFGE) patterns.

63 lla serovar Typhimurium DT104 with different pulsed-field gel electrophoresis (PFGE) profiles were an

64 n of 55 virulence-associated genes, and XbaI pulsed-field gel electrophoresis (PFGE) profiling.

65 Comparison of raccoon pulsed-field gel electrophoresis (PFGE) pulse type data

66 tically distinct despite having the outbreak pulsed-field gel electrophoresis (PFGE) pulsotype.

67 patient was positive and molecular typing by pulsed-field gel electrophoresis (PFGE) revealed clonal

68 coli cases with an indistinguishable, novel pulsed-field gel electrophoresis (PFGE) subtyping patter

69 cassette chromosome mec (SCCmec) typing and pulsed-field gel electrophoresis (PFGE) subtyping.

70 nfection in the United States and to compare pulsed-field gel electrophoresis (PFGE) to the combinati

71 ts were used to investigate L. monocytogenes pulsed-field gel electrophoresis (PFGE) type diversity.

72 The pulsed-field gel electrophoresis (PFGE) type was determi

73 Pulsed-field gel electrophoresis (PFGE) was applied as a

74 Strain typing using pulsed-field gel electrophoresis (PFGE) was performed on

75 Pulsed-field gel electrophoresis (PFGE) was performed on

76 Pulsed-field gel electrophoresis (PFGE) was performed to

77 Pulsed-field gel electrophoresis (PFGE) was used to type

78 ction analysis of genomic DNA using SmaI and pulsed-field gel electrophoresis (PFGE) were both used t

79 Antimicrobial susceptibility testing and pulsed-field gel electrophoresis (PFGE) were performed o

80 stigated the use of whole-genome mapping and pulsed-field gel electrophoresis (PFGE) with isolates fr

81 By pulsed-field gel electrophoresis (PFGE), 8 of 10 environ

82 This protocol describes pulsed-field gel electrophoresis (PFGE), a method develo

83 Whole-genome-sequencing, pulsed-field gel electrophoresis (PFGE), and a mouse inf

84 hat can be performed within a clinical lab), pulsed-field gel electrophoresis (PFGE), and an antibiot

85 in, using multilocus sequence typing (MLST), pulsed-field gel electrophoresis (PFGE), and array-based

86 otyped by repetitive-sequence PCR (rep-PCR), pulsed-field gel electrophoresis (PFGE), and multilocus

87 sing surface protein profile identification, pulsed-field gel electrophoresis (PFGE), and multilocus

88 Susceptibility testing, pulsed-field gel electrophoresis (PFGE), and multilocus

89 acterial artificial chromosome (BAC) clones, pulsed-field gel electrophoresis (PFGE), and public arra

90 Typing was performed by PCR-ribotyping, pulsed-field gel electrophoresis (PFGE), and restriction

91 tine leukocidin (PVL) screening, and SCCmec, pulsed-field gel electrophoresis (PFGE), and spa typing.

92 erase chain reaction (PCR) detection of GES, pulsed-field gel electrophoresis (PFGE), and WGS for the

93 d thus further characterized by MLST typing, pulsed-field gel electrophoresis (PFGE), and whole genom

94 We also performed DNA sequencing, pulsed-field gel electrophoresis (PFGE), cultures of the

95 Currently, the standard typing technique, pulsed-field gel electrophoresis (PFGE), is laborious an

96 acter databases at the CDC and the FDA using pulsed-field gel electrophoresis (PFGE), multilocus sequ

97 nrelated to prevalent MRSA, as determined by pulsed-field gel electrophoresis (PFGE), multilocus sequ

98 -producing isolates were determined by using pulsed-field gel electrophoresis (PFGE), multilocus sequ

99 The typing methods included pulsed-field gel electrophoresis (PFGE), multilocus vari

100 March 2014) included Western blot analysis, pulsed-field gel electrophoresis (PFGE), polymerase chai

101 Pulsed-field gel electrophoresis (PFGE), ribotyping, and

102 isolate and all MRSA isolates were typed by pulsed-field gel electrophoresis (PFGE), screened for mu

103 pneumonia, we analyzed 24 paired isolates by pulsed-field gel electrophoresis (PFGE), serotyping, and

104 cal cassette chromosome mec (SCCmec) typing, pulsed-field gel electrophoresis (PFGE), spa typing, and

105 MRSA isolates were characterized by pulsed-field gel electrophoresis (PFGE), staphylococcal

106 relatedness of isolates was determined using pulsed-field gel electrophoresis (PFGE), Staphylococcus

107 Using pulsed-field gel electrophoresis (PFGE), the number of p

108 Using biochemical identification and pulsed-field gel electrophoresis (PFGE), we sought to id

109 revious molecular subtyping methods, such as pulsed-field gel electrophoresis (PFGE), were critical i

110 h were indistinguishable from one another by pulsed-field gel electrophoresis (PFGE), were obtained f

111 repetitive-sequence-based PCR (rep-PCR) and pulsed-field gel electrophoresis (PFGE), which showed th

112 Salmonella serotype Typhi, as determined by pulsed-field gel electrophoresis (PFGE), with onset duri

113 uded multiple representatives of a number of pulsed-field gel electrophoresis (PFGE)-defined types.

114 tested for antimicrobial susceptibility and pulsed-field gel electrophoresis (PFGE).

115 ental isolate relatedness was evaluated with pulsed-field gel electrophoresis (PFGE).

116 er a 5-year period by using CRISPR-MVLST and pulsed-field gel electrophoresis (PFGE).

117 ied fragment length polymorphism (AFLP), and pulsed-field gel electrophoresis (PFGE).

118 yping (MLST), spa typing, SCCmec typing, and pulsed-field gel electrophoresis (PFGE).

119 m infections, or endocarditis, were typed by pulsed-field gel electrophoresis (PFGE).

120 using multilocus sequence typing (MLST) and pulsed-field gel electrophoresis (PFGE).

121 bial susceptibility testing and subtyping by pulsed-field gel electrophoresis (PFGE).

122 hin ureaplasma serovars were investigated by pulsed-field gel electrophoresis (PFGE).

123 All isolates were subjected to pulsed-field gel electrophoresis (PFGE).

124 ically relevant level remains intangible for pulsed-field gel electrophoresis (PFGE).

125 istance genes, and plasmids and genotyped by pulsed-field gel electrophoresis (PFGE).

126 genes were compared to the data generated by pulsed-field gel electrophoresis (PFGE).

127 ab system (DL) to the results obtained using pulsed-field gel electrophoresis (PFGE).

128 at were previously characterized by MLST and pulsed-field gel electrophoresis (PFGE).

129 ing region of GyrA and ParC (ASLGP) and (ii) pulsed-field gel electrophoresis (PFGE).

130 s to identify genetically similar strains is pulsed-field gel electrophoresis (PFGE).

131 ral different clonal types, as determined by pulsed-field gel electrophoresis (PFGE).

132 REA), multilocus sequence typing (MLST), and pulsed-field gel electrophoresis (PFGE).

133 sence of 31 virulence genes and subjected to pulsed-field gel electrophoresis (PFGE).

134 h limited resolution, especially compared to pulsed-field gel electrophoresis (PFGE).

135 cus sequence typing (CRISPR-MVLST), and (iv) pulsed-field gel electrophoresis (PFGE).

136 well as SmaI macrorestriction patterns after pulsed-field gel electrophoresis (PFGE).

137 ose used for the interpretation of data from pulsed-field gel electrophoresis (PFGE).

138 the current gold standard subtyping method, pulsed-field gel electrophoresis (PFGE).

139 vailable Serratia isolates was determined by pulsed-field gel electrophoresis (PFGE).

140 Isolates were typed by pulsed-field gel electrophoresis (PFGE).

141 dvantages over length-based methods, such as pulsed-field gel electrophoresis (PFGE); however, conven

142 Isolates were characterized by pulsed-field gel electrophoresis (PFGE); SCCmec typing;

143 Montevideo infections with a rare pattern on pulsed-field gel electrophoresis (the outbreak strain) w

144 enes) and four groups of clonally linked (by pulsed-field gel electrophoresis [PFGE]) isolates.

145 ethod for determining bacterial relatedness (pulsed-field gel electrophoresis [PFGE]) remains essenti

146 ication using restriction digest technology (pulsed-field gel electrophoresis [PFGE]) to shotgun sequ

147 T to those of other means (traditional MLST, pulsed-field gel electrophoresis [PFGE], and single-nucl

148 f four molecular typing methods (ribotyping, pulsed-field gel electrophoresis [PFGE], random amplific

149 Pulsed-field gel electrophoresis analysis confirmed that

150 Standardized pulsed-field gel electrophoresis analysis facilitates st

151 Pulsed-field gel electrophoresis analysis indicated that

152 Pulsed-field gel electrophoresis analysis suggested that

153 Pulsed-field gel electrophoresis analysis yielded multip

154 confirmed by multilocus sequence typing and pulsed-field gel electrophoresis analysis.

155 All S. aureus isolates were characterized by pulsed-field gel electrophoresis and agr group.

156 Genomic analysis using pulsed-field gel electrophoresis and array based genomic

157 olates were closely related to each other by pulsed-field gel electrophoresis and contained a common

158 mosomal damage was directly visualized using pulsed-field gel electrophoresis and demonstrated repair

159 rUTI strains were characterized by pulsed-field gel electrophoresis and genomic virulence p

160 he formation of DNA DSBs, as demonstrated by pulsed-field gel electrophoresis and H2AX phosphorylatio

161 racterize possible transmission routes using pulsed-field gel electrophoresis and multi-locus variabl

162 ed both environmental and clinical ESBLEC by pulsed-field gel electrophoresis and multilocus sequence

163 ned laboratory characteristics of EAEC using pulsed-field gel electrophoresis and next-generation seq

164 sequence type 94, were indistinguishable by pulsed-field gel electrophoresis and optical mapping, an

165 ir proficiency in G0/G1 phase as measured by pulsed-field gel electrophoresis and repair focus resolu

166 performed two band-based typing techniques (pulsed-field gel electrophoresis and repetitive extragen

167 We used pulsed-field gel electrophoresis and restriction fragmen

168 urfaces were evaluated for relatedness using pulsed-field gel electrophoresis and staphylococcal cass

169 al isolates were characterized as CA-MRSA by pulsed-field gel electrophoresis and susceptibility test

170 solates from seven patients were analyzed by pulsed-field gel electrophoresis and VNTR typing.

171 lates from 15 other Belgian hospitals) using pulsed-field gel electrophoresis and WGS.

172 Pulsed-field gel electrophoresis and whole-genome sequen

173 terization of the 66 isolates was done using pulsed-field gel electrophoresis and whole-genome sequen

174 clinical isolates labeled according to their pulsed-field gel electrophoresis data for strain differe

175 determined by polymerase chain reaction and pulsed-field gel electrophoresis differed from that of B

176 Pulsed-field gel electrophoresis genotyping indicated th

177 tularensis isolates by DISA correlated with pulsed-field gel electrophoresis genotyping utilizing tw

178 identify irregular clusters of illness, and pulsed-field gel electrophoresis in conjunction with who

179 Although pulsed-field gel electrophoresis indicated that multiple

180 Pulsed-field gel electrophoresis of 174 of 179 NTHi isol

181 Pulsed-field gel electrophoresis of the CTX-M-positive i

182 tococcus pneumoniae serogroup 35 isolates by pulsed-field gel electrophoresis of the genome and pbp2b

183 m 6 confirmed cases had an indistinguishable pulsed-field gel electrophoresis pattern and belonged to

184 ak-associated E. coli O157:H7 or E. coli O61 pulsed-field gel electrophoresis pattern combinations, o

185 ak-associated E. coli O157:H7 or E. coli O61 pulsed-field gel electrophoresis pattern combinations, o

186 ed PCR strategy was used to analyze the AscI pulsed-field gel electrophoresis patterns of Listeria mo

187 Pulsed-field gel electrophoresis profiles of a sample of

188 ic resistance patterns and indistinguishable pulsed-field gel electrophoresis profiles.

189 Pulsed-field gel electrophoresis revealed the expected g

190 ut included (uniquely) K1 capsule and fimH64 Pulsed-field gel electrophoresis separated ST1193-H64 is

191 Results of pulsed-field gel electrophoresis showed 17 strain types.

192 ST-1 (which corresponds to pulsed-field gel electrophoresis strain type NAP1/riboty

193 reased age and infection with North American pulsed-field gel electrophoresis strains were associated

194 essus strains that were indistinguishable by pulsed-field gel electrophoresis testing.

195 icile isolates (n = 31) was also analyzed by pulsed-field gel electrophoresis to determine the circul

196 the fluoroquinolone-resistant North American pulsed-field gel electrophoresis type 1 (NAP1) strain in

197 The North American pulsed-field gel electrophoresis type 1 (NAP1) strain wa

198 ST-1-positive strains isolated, 6 (50%) were pulsed-field gel electrophoresis type USA200, multilocus

199 solates with chromosomal deletions, multiple pulsed-field gel electrophoresis types were identified,

200 s, repetitive-element-based PCR patterns, or pulsed-field gel electrophoresis types.

201 by multilocus sequence typing [MLST]) and 79 pulsed-field gel electrophoresis types.

202 Pulsed-field gel electrophoresis typing showed wide gene

203 index (TI) of Pa isolates were derived from pulsed-field gel electrophoresis typing.

204 Pulsed-field gel electrophoresis was conducted to strain

205 release of monomeric genomes as assessed by pulsed-field gel electrophoresis was greatly diminished,

206 Pulsed-field gel electrophoresis was performed on all av

207 Pulsed-field gel electrophoresis was used to determine c

208 erized (mecA confirmation, SCCmec typing and pulsed-field gel electrophoresis).

209 chain reaction (PCR) for 31 virulence genes, pulsed-field gel electrophoresis, and multilocus sequenc

210 erwent antimicrobial susceptibility testing, pulsed-field gel electrophoresis, and multiplex PCR for

211 rRNA gene sequence analysis, genotyped using pulsed-field gel electrophoresis, and phenotyped for a r

212 lates utilized multilocus sequence typing or pulsed-field gel electrophoresis, but high-resolution ex

213 T131 and its ESBL-associated H30Rx subclone, pulsed-field gel electrophoresis, extended virulence gen

214 Molecular analyses included strain typing by pulsed-field gel electrophoresis, mec and accessory gene

215 testing, sequencing of beta-lactamase genes, pulsed-field gel electrophoresis, multilocus sequence ty

216 to a single genetic clone, as determined by pulsed-field gel electrophoresis, multilocus sequence ty

217 hicillin susceptible) using a combination of pulsed-field gel electrophoresis, multilocus sequence ty

218 at 6 Canadian hospitals underwent typing by pulsed-field gel electrophoresis, multilocus sequence ty

219 hoc analysis using unique pathogens typed by pulsed-field gel electrophoresis, overall success rates

220 Isolates underwent pulsed-field gel electrophoresis, PCR for 33 putative vi

221 Pulsed-field gel electrophoresis, polymerase chain react

222 ilution, and selected isolates were typed by pulsed-field gel electrophoresis, repetitive sequence-ba

223 ates were evaluated for the MRSA genotype by pulsed-field gel electrophoresis, staphylococcal protein

224 (n = 92) were characterized by toxinotyping, pulsed-field gel electrophoresis, tcdC and cdtB PCR, and

225 Using pulsed-field gel electrophoresis, we determined chromoso

226 ee strains appeared to be clonal by standard pulsed-field gel electrophoresis, whole-genome sequencin

227 oquinolone resistance-determining loci), and pulsed-field gel electrophoresis.

228 yping of the E. coli isolates was done using pulsed-field gel electrophoresis.

229 and clonal relatedness was established using pulsed-field gel electrophoresis.

230 able to more arduous typing systems, such as pulsed-field gel electrophoresis.

231 elonged to 1 of 7 clonal types as defined by pulsed-field gel electrophoresis.

232 The isolates were subtyped by ribotyping and pulsed-field gel electrophoresis.

233 Isolates were typed by pulsed-field gel electrophoresis.

234 IV-negative patients; isolates were typed by pulsed-field gel electrophoresis.

235 dom amplification of polymorphic DNA PCR and pulsed-field gel electrophoresis.

236 llected from 2000 to 2008 were identified by pulsed-field gel electrophoresis.

237 and clonal relationships were determined by pulsed-field gel electrophoresis.

238 eus isolates were unrelated as determined by pulsed-field gel electrophoresis.

239 e the strains by standard techniques such as pulsed-field gel electrophoresis.

240 were identical by biochemical profiling and pulsed-field gel electrophoresis.

241 ns lacking the mre11 gene was observed using pulsed-field gel electrophoresis.

242 paced breaks yield DSBs that are observed by pulsed-field gel electrophoresis.

243 andom-amplified polymorphic DNA analysis and pulsed-field gel electrophoresis.

244 , IL, between 2004 and 2007 were analyzed by pulsed-field gel electrophoresis.

245 striction enzyme and size-fractionated using pulsed-field gel electrophoresis.

246 82 isolates, which were indistinguishable by pulsed-field gel electrophoresis.

247 ant, as determined by infectivity assays and pulsed-field gel electrophoresis.

248 -induced chromosomal DNA damage monitored by pulsed-field gel electrophoresis.

249 ominissuisisolates is easier and faster than pulsed-field gel electrophoresis.

250 sequencing for genospecies and genotyped by pulsed-field gel electrophoresis.

251 The pandemic sequence type (ST)8/pulsed-field gel type USA300 is the dominant CA-MRSA clo

252 migrations of the individual chromosomes in pulsed field gels.

253 the current study used Southern blotting of pulsed-field gels to localize the cpb gene to approximat

254 nt study used Southern blot hybridization of pulsed-field gels to test whether several toxin genes ar

255 In this study pulsed field gradient (PFG) (1)H NMR measurements of the

256 Pulsed field gradient (PFG) NMR measurements, combined w

257 In structural biology, pulsed field gradient (PFG) NMR spectroscopy for the cha

258 cled (SFC), rf pulse phase cycled (SPC), and pulsed field gradient (PFG) strength cycled (SGC) E.COSY

259 Microscopic diffusion measurement by the pulsed field gradient (PFG) technique of NMR offers the

260 niques of diffusion measurement, notably the pulsed field gradient (PFG) technique of NMR spectroscop

261 series of spectra collected under different pulsed field gradient conditions that differentially att

262 analysis of DGCR8/pri-mir-16 interactions by pulsed field gradient NMR lent further support to dynami

263 Pulsed field gradient NMR of the phosphatidylcholine (PC

264 In this study, we show by pulsed field gradient NMR spectroscopy that the monomeri

265 fluids in porous materials can be studied by pulsed field gradient nuclear magnetic resonance (NMR) n

266 ork was probed systematically by comparative pulsed field gradient nuclear magnetic resonance diffusi

267 combining Quasi Elastic Neutron Scattering, Pulsed Field Gradient Nuclear Magnetic Resonance, and Mo

268 , electrospray ionization mass spectrometry, pulsed field gradient spin echo NMR measurements, electr

269 nt optical and fluorescence spectroscopy and pulsed field gradient spin-echo (PGSE) NMR spectroscopy

270 , 9623 - 9629 ) and is based on the 1D (1)H pulsed field gradient stimulated echo (PFGSTE) NMR exper

271 This method, based on the pulsed field gradient stimulated echo (PGSTE) experiment

272 Pulsed-field gradient (PFG) NMR diffusion coefficient me

273 ownian motion of proteins, we performed (1)H pulsed-field gradient NMR and fluorescence correlation s

274 Pulsed-field gradient NMR diffusion experiments and 15N

275 Pulsed-field gradient NMR diffusion experiments, multian

276 be measured under identical conditions using pulsed-field gradient NMR diffusion measurements.

277 ich is understood using (129) Xe, (1) H, and pulsed-field gradient NMR spectroscopy.

278 tively coupled plasma mass spectrometry, and pulsed-field gradient stimulated echo (1)H NMR measureme

279 small-angle x-ray scattering experiments or pulsed-field-gradient NMR diffusion measurements, which

280 e here demonstrate an approach that combines pulsed-field-gradient NMR for translational diffusion an

281 Here we employ multi-axis pulsed-field-gradient NMR to measure diffusion anisotrop

282 cimetry at a high magnetic field with strong pulsed field gradients has clear advantages in terms of

283 By also accounting for imperfections in pulsed field gradients, LFCs were obtained that were vir

284 age caused by concentrated, highly energetic pulsed fields in plasmonic hotspots, and finally the pot

285 (X-ray diffraction, magnetic susceptibility, pulsed-field magnetization, heat capacity, and muon-spin

286 ultiple REA groups, and three North American pulsed-field (NAP) profiles contained both multiple REA

287 to determine the circulating North American pulsed-field (NAP) types that have been isolated in New

288 The pulsed-field operation provides arrival times without th

289 ystem can toggle between delivering biphasic pulsed field (PF) and radiofrequency energy from a 9-mm

290 ons from the mobility cell into the MS using pulsed-field sampling.

291 First, using pulsed-field transversal and longitudinal magnetostricti

292 e clone had multilocus sequence type 121 and pulsed-field type USA1200.

293 phylococcus aureus (CA-MRSA) strain known as pulsed-field type USA300 (USA300) is epidemic in the Uni

294 Staphylococcus aureus (MRSA) strains of the pulsed-field type USA300 are primarily responsible for t

295 methicillin-resistant Staphylococcus aureus pulsed-field type USA300 isolates collected at an ambula

296 istant clone had multilocus sequence type 8, pulsed-field type USA300, and SCCmec type IV and possess

297 All 9 MRSA isolates tested were pulsed-field type USA300.

298 MW2 (pulsed-field type USA400), the prototype CA-MRSA strain,

299 Although 188 unique pulsed-field types (PFTs) were identified from the colon

300 ultilocus sequence type clonal complexes and pulsed-field types.