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

4 Pulsed field electrophoresis was performed on environmen

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

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

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

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

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

10 These results reveal why pulsed field gel electrophoresis analysis of SmaI-digest

11 Using quantitative pulsed field gel electrophoresis and sensitive DNA synth

12 Pulsed field gel electrophoresis determined that 91% of

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

14 he induction of cellular DNA breaks based on pulsed field gel electrophoresis, comet analysis, and ga

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

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

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

18 The isolates had distinct ribotype and pulsed-field gel electorphoresis patterns and appeared i

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

20 Pulsed-field gel electrophoresis (PFGE) analysis reveale

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

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

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

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

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

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

27 udy compared the discriminatory abilities of pulsed-field gel electrophoresis (PFGE) and multilocus s

28 exists: the two most widely used methods are pulsed-field gel electrophoresis (PFGE) and multilocus s

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

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

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

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

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

34 ological and molecular techniques, including pulsed-field gel electrophoresis (PFGE) and plasmid prof

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

56 Pulsed-field gel electrophoresis (PFGE) played a key rol

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

58 They had indistinguishable plasmid and pulsed-field gel electrophoresis (PFGE) profiles.

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

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

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

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

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

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

65 These isolates were evaluated by pulsed-field gel electrophoresis (PFGE) to determine pos

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

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

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

69 LVA) for Staphylococcus aureus could predict pulsed-field gel electrophoresis (PFGE) types (i.e., USA

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

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

72 Pulsed-field gel electrophoresis (PFGE) was used to dete

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

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

75 Antimicrobial susceptibility testing and pulsed-field gel electrophoresis (PFGE) were performed f

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

126 hosphoglucose isomerase (pgi) genotyping and pulsed-field gel electrophoresis (PFGE).

127 mplified polymorphic DNA (RAPD) analysis and pulsed-field gel electrophoresis (PFGE).

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

145 Pulsed-field gel electrophoresis allows the number of DN

146 Pulsed-field gel electrophoresis analysis confirmed that

147 Standardized pulsed-field gel electrophoresis analysis facilitates st

148 Pulsed-field gel electrophoresis analysis indicated that

149 Pulsed-field gel electrophoresis analysis suggested that

150 Pulsed-field gel electrophoresis analysis using probes a

151 Pulsed-field gel electrophoresis analysis yielded multip

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

153 Pulsed-field gel electrophoresis and antimicrobial susce

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

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

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

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

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

159 Pulsed-field gel electrophoresis and hybridization analy

160 mpared with those from the United Kingdom by pulsed-field gel electrophoresis and integron analysis.

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 to the maximum parsimony trees inferred from pulsed-field gel electrophoresis and multilocus variable

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

165 University Hospital (SUH) were genotyped by pulsed-field gel electrophoresis and PCR for SCCmec and

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

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

168 We used pulsed-field gel electrophoresis and restriction fragmen

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

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

173 Pulsed-field gel electrophoresis demonstrated the epidem

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

175 Pulsed-field gel electrophoresis genotyping indicated th

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

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

178 Although pulsed-field gel electrophoresis indicated that multiple

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

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

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

182 Epidemiologic investigation and pulsed-field gel electrophoresis patterns indicated a cl

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

184 Isolates that differed in their pulsed-field gel electrophoresis patterns showed polymor

185 d to specific outbreaks and showed identical pulsed-field gel electrophoresis patterns were indisting

186 Pulsed-field gel electrophoresis profiles of a sample of

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

188 Pulsed-field gel electrophoresis revealed the expected g

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

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

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

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

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

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

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

196 table strain of Staphylococcus aureus with a pulsed-field gel electrophoresis type of USA300 and mult

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

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

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

200 Pulsed-field gel electrophoresis typing showed wide gene

201 Pulsed-field gel electrophoresis was conducted to strain

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

203 Pulsed-field gel electrophoresis was performed on all av

204 Pulsed-field gel electrophoresis was used to determine c

205 Pulsed-field gel electrophoresis was used to determine g

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

207 nly to MRSA isolates that were available for pulsed-field gel electrophoresis, 91% (159 of 175 isolat

208 zed by antimicrobial-susceptibility testing, pulsed-field gel electrophoresis, and detection of toxin

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 ts in less than 5 h and, in conjunction with pulsed-field gel electrophoresis, forms a very robust te

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

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

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

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

219 Pulsed-field gel electrophoresis, multilocus sequence ty

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

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

229 Isolates were typed by pulsed-field gel electrophoresis.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

245 hat of multilocus sequence typing (MLST) and pulsed-field gel electrophoresis.

246 treatment daptomycin-susceptible isolates by pulsed-field gel electrophoresis.

247 82 isolates, which were indistinguishable by pulsed-field gel electrophoresis.

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

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

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

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

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

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

254 migrations of the individual chromosomes in pulsed field gels.

255 Southern blotting of pulsed-field gels showed that the etx gene of type D iso

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

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

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

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

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

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

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

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

264 Pulsed field gradient NMR methods have determined the te

265 Pulsed field gradient NMR of the phosphatidylcholine (PC

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

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

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

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

273 Pulsed-field gradient NMR diffusion experiments and 15N

274 Pulsed-field gradient NMR diffusion experiments show lit

275 Pulsed-field gradient NMR diffusion experiments, multian

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

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

278 al fitting of the diffusional attenuation of pulsed-field gradient stimulated echo spectra and can, t

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

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

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

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

286 The pulsed-field operation provides arrival times without th

287 Recent computational research suggests that pulsed field protocols, however, should improve retentio

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

289 First, using pulsed-field transversal and longitudinal magnetostricti

290 trophoresis, 91% (159 of 175 isolates) had a pulsed-field type consistent with community-acquired MRS

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

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

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

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

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

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

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

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

299 umannii isolates were comprised of 18 unique pulsed-field types, with strains of clone A and clone B

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