ライフサイエンスコーパス: TEM

1 TEM also generates predictions that hippocampal remappin

2 TEM and IF demonstrate mislocalized basal bodies.

3 TEM cell death was prevented with neutralizing anti-IL-2

4 TEM hippocampal cells include place and landmark cells t

5 TEM imaging confirmed for C. lytica that the vesicles ar

6 TEM imaging revealed intact gram-positive bacterial and

7 TEM tomography and numerical simulations were used to mo

8 TEM, SEM-EDX, FT-IR, VSM techniques were applied for cha

9 TEM-NanoSIMS imaging revealed degraded cytoplasm and an

10 nsmission electron microscope tomography (3D TEM)] that chirality at the monomeric and intrachain lev

11 establishes a robust 'nanolab' platform in a TEM for in situ photoelectrical studies and provides val

12 cally stimulated within the liquid cell in a TEM to assemble into nanostructures.

13 tals, and collect and characterise them on a TEM grid.

14 rying class C (CMY-2 and DHA-1) and class A (TEM-1 and CTX-M-2) beta-lactamase enzymes, respectively.

15 -24/40 and OXA-48), as well as with class A (TEM-1, CTX-M-2) and class C (CMY-2, DHA-1) enzymes, is r

16 nchrotron radiation and spherical aberration TEM.

17 ls had a phenotype consistent with activated TEM/TEMRA cells.

18 Additionally, TEM images of spherical particles exhibited sintering-in

19 U were -77 HU for water and -990 HU for air; TEM precision improved with a reduction in variability f

20 Analytical TEM allowed assessing the homogeneous localization of bd

21 mobility mass spectrometry (IM-MS), AFM, and TEM.

22 stological, histomorphometric, micro-CT, and TEM analyses indicated no differences in enamel or denti

23 tection limit of synchrotron diffraction and TEM.

24 general morphological study such as DLS and TEM but by our SEE measurements.

25 SDS-PAGE, DLS, and TEM were used to confirm and characterize the formation

26 eformation bands, carried out using EBSD and TEM, revealed {332} <113> type primary bcc twins, contai

27 ing experiments, fluorescence microscopy and TEM revealed indigenous bacteria could obtain these vect

28 the FSPS samples was investigated by SEM and TEM imaging, and the observations were used to guide the

29 DES, which was further confirmed by SEM and TEM.

30 rmed with BET, FTIR, XRD, TGA, PZC, SEM, and TEM analyses.

31 calable pipeline coupled with the SONICC and TEM techniques to screen for microcrystal formation with

32 analyzed using FTIR, EDX, XRD, TGA, VSM, and TEM.

33 d, which was characterized by PXRD, XPS, and TEM techniques.

34 adsorption calorimetry, and in situ XRD and TEM to provide new insights into catalyst sintering.

35 Richter and Koon successfully applied TEM analysis of collagen to determine heating to modern

36 ighlight the utilization of state-of-the-art TEM technologies to explore dynamic MOF processes and ho

37 Various analytical techniques such as TEM, STEM, FESEM, XRD, RAMAN, EDX, ICP, and XPS confirme

38 nically feasible objective measure to assess TEM encoding in CI users.

39 find that increasing levels of IL-6 and bla(TEM) are associated with mortality, while decreasing IL-

40 DNA, and the antibiotic-resistance gene bla(TEM) with femtomolar sensitivity.

41 well as the antibiotic-resistance genes (bla(TEM), bla(KPC), and bla(CTX)).

42 xA) and the antibiotic-resistance genes (bla(TEM), tetA, and bla(CTX-M)).

43 nce genes, the examined strains harbored bla(TEM), bla(CTX-M), and tetA genes with a total prevalence

44 ound transposon, PTn6762, which harbours bla(TEM-1B).

45 Despite a significant increase in bla(TEM-1B) copy number, the TZP-resistant isolate does not

46 The bla(CTX-M), bla(TEM), and tetA genes are the main antibiotic-resistance

47 This mechanism of amplification of bla(TEM-1B) is an important consideration when using genomic

48 TUs, which increases the copy number of bla(TEM-1B,) leading to TEM-1B hyperproduction and TZP resis

49 Only bla(TEM), chlortetracycline, and tiamulin decreased signific

50 ve for bla(CTX-M), ESBL-type bla(SHV) or bla(TEM), or bla(OXA-48)-type carbapenemase genes, including

51 United States for bla(CTX-M), bla(SHV), bla(TEM), bla(KPC), bla(NDM), and bla(OXA-48)-type genes by

52 n Tn3 family but with a difference: the 'bla(TEM-1B) type' prophages exhibited a classic Tn2 transpos

53 nd cephalosporins, and are harboring the bla(TEM) and bla(CTX) genes.

54 , and carbapenems, and are harboring the bla(TEM), bla(CTX), and bla(KPC) genes.

55 e ARGs could be grouped into two types: 'bla(TEM-1B) ' and 'classic class 1 integron (IntI1)'.

56 c(6')Ib-cr (n = 13), bla-CTX-M (n = 51), bla-TEM (n = 117), tetA (n = 142) and tetB (n = 101).

57 rphological characteristics were assessed by TEM, SEM-EDX, X-ray photoelectron spectroscopy and vibra

58 to form materials that were characterized by TEM, EDX, Raman spectroscopy, rheometry, UV/Vis and NMR

59 nomaterials were thoroughly characterized by TEM, SEM, XPS, FTIR, and nitrogen-adsorption surface are

60 The nanocomposite was characterized by TEM, XRD, FTIR, XPS, TGA, BET, and CV using the redox co

61 The creation of nano-cargos was confirmed by TEM.

62 nt HDL preparations that are not detected by TEM.

63 Five pigments were evaluated by TEM, of which four had a size median below 100 nm, while

64 rate ligands) layer on nAu was observable by TEM, and was preserved after the retention by biochar, w

65 rticles were detected in all E172 samples by TEM or SAXS measurements.

66 id-vapor interface was imaged and videoed by TEM on the sample of electron irradiated sodium chloride

67 n correlated with higher percentages of CD4+ TEM and TTD cells.

68 ctive CD8 T cells with a CD28/DR/CD38/CD45RO TEM.

69 to characterize CD8 effector memory T cell (TEM) populations in the periphery and graft before and a

70 f missense mutations in the Escherichia coli TEM-1 beta-lactamase antibiotic resistance gene using gr

71 ed deacylation rate compared with the common TEM-1 beta-lactamase.

72 Crucially, TEM also aligns with empirically recorded representation

73 Cryo-TEM displays a polyhedral shape for eLNPs compared to sp

74 Cryo-TEM images reveal that R-6-AO molecules self-assemble in

75 Cryo-TEM revealed an average core metallocorrole particle siz

76 smission electron microscopies (AFM and cryo-TEM) tracked these transformations over angstrom to micr

77 ral information, gathered from SAXS and cryo-TEM, reveals that the distinct peptide domains maintain

78 The internal structure was observed by cryo-TEM with direct electron detection, which provides real-

79 ron microscopy at cryogenic conditions (cryo-TEM).

80 genic transmission electron microscopy (cryo-TEM) revealed key differences in the nature of DOX cryst

81 genic transmission electron microscopy (cryo-TEM) studies and subsequent three-dimensional-volume rec

82 genic transmission electron microscopy (cryo-TEM).

83 aring cells, which appear in two-dimensional TEM sections to form a separate population beneath the B

84 in the endothelium is required for efficient TEM in vivo.

85 In the endothelium, TEM requires the coordination of membrane movements and

86 recent advances in the use of environmental TEM and cryogenic electron microscopy in probing clean-e

87 e) and the beta-lactamase plasmid expressing TEM-135 are associated with distinct gonococcal lineages

88 that IQGAP1 in endothelial cells facilitates TEM by directing the LBRC to the site of TEM.

89 terized using different tools such as FESEM, TEM, EDX, XRD, DLS and zeta potential measurements.

90 FIB-TEM analysis of porated MG cells confirmed the non-agglo

91 icles appear core-shell like in bright field TEM images.

92 ron microscopy combined with energy-filtered TEM (EFTEM) elemental maps.

93 rovide thoughts on what the future holds for TEM in the study of MOFs.

94 Immunogold labelling for TEM confirmed that labelling was absent at P3, and showe

95 laser beam, and use it as a phase plate for TEM.

96 m the contra-lateral joint and processed for TEM.In WT and AKU mice novel microanatomical structures,

97 nt with the size and geometry extracted from TEM images.

98 characterized by UV-VIS spectroscopy, FTIR, TEM, DLS, and XRD.

99 acteria and beta-lactamase resistance genes (TEM-1) was observed over 6 months for any group (adjuste

100 However, TEM-1 exhibited a couple of hotspots for positive epista

101 Fluorescence spectroscopy, FT-IR, XRD and HR-TEM.

102 XRD, He-ion imaging, HR-TEM, EELS, PL, fluorescence lifetime imaging, Raman, FTI

103 olution transmission electron microscopy (HR-TEM) can provide valuable insight into the growth mechan

104 olution transmission electron microscopy (HR-TEM), high-angle annular dark-field scanning transmissio

105 ution Transmission Electronic Microscopy (HR-TEM).

106 small Pt nanoparticles (1.14 +/- 0.35 nm, HR-TEM), which have previously shown exceptional performanc

107 hesis process have been proposed based on HR-TEM observation and length analysis.

108 IR, XPS, XRD, Raman spectroscopy, FE-SEM, HR-TEM, AFM, UV-Vis and FL, revealed successful doping carb

109 on microscopy (TEM), high-resolution TEM (HR-TEM) and atom probe tomography analyses, we show that th

110 Quantitative immuno-TEM revealed IRX9 is present in a specific subdomain of

111 fitness effects occurred more frequently in TEM-1 than deleterious effects on antibiotic resistance

112 polypeptide, is required for its function in TEM.

113 tness effects of single amino acid InDels in TEM-1 beta-lactamase.

114 interactions between sequential mutations in TEM-1 beta-lactamase.

115 At least 42% of missense mutations in TEM-1 were deleterious, indicating that for some protein

116 eduction in the number of pilins observed in TEM and reduced surface adherence but still adsorb SSV9.

117 reactive oxygen species (ROS) production in TEM 4-18 cells.

118 dicating that STAT5 signaling drives RICD in TEM cells.

119 om a suite of biophysical methods, including TEM, AFM, high-resolution cryo-EM, and SAXS/WAXS measure

120 Interestingly, the double-hit-induced TEM increase was not due to decreased endothelial barrie

121 the local physicochemical conditions inside TEM liquid cells.

122 m to 23 nm (to match the mass loss to ions), TEM scans of particles retrieved from flow-cells showed

123 ied as hyperproduction of the beta-lactamase TEM.

124 ll transmission electron microscopy (LCTEM), TEM, and SCXRD, it was possible to ascertain that the ma

125 After learning, TEM entorhinal cells display diverse properties resembli

126 the LBRC and substantially reduced leukocyte TEM.

127 Our data strongly suggest that, like TEMs, OsRAV9/OsTEM1 has a conserved function as a repres

128 Post-mortem and identical location TEM analyses reveal that the Co/Fe spinel-like surface r

129 Using Lorentz TEM, it is observed that MNPs suspended in LC rotate to

130 This model for lymphatic TEM for various migrating and endothelial cell types pos

131 we introduce the Tolman-Eichenbaum machine (TEM).

132 Tie2-expressing monocytes/macrophages (TEMs) are a distinct subset of proangiogenic monocytes s

133 fferences in all tissue equivalent material (TEM) groups were measured.

134 Mature T effector memory TEM CD4+ T cells were expanded in patients with untreate

135 udied using transmission electron microcopy (TEM).

136 toelectric transmission electron microscope (TEM) holder.

137 -SEM), and transmission electron microscope (TEM) with EDAX.

138 resolution transmission electron microscope (TEM), Fourier-transform infrared spectroscopy (FT-IR), d

139 ope (SEM), transmission electron microscope (TEM), x-ray diffraction (XRD) method, cyclic voltammetry

140 ope (SEM), transmission electron microscope (TEM), x-ray diffraction (XRD), cyclic voltammetry (CV) a

141 rved under Transmission Electron Microscope (TEM).

142 Microscopic (TEM, AFM) and spectroscopic (steady-state UV-vis and flu

143 odium for transmission electron microscopic (TEM) observation.

144 utility of transmission electron microscopy (TEM) analysis of bone collagen for investigating prehist

145 Transmission electron microscopy (TEM) analysis reveals their microstructure to be nanocry

146 ined using transmission electron microscopy (TEM) and a novel scanning electron microscopy (SEM) meth

147 Transmission electron microscopy (TEM) and atomic-resolution scanning transmission electro

148 ualized by transmission electron microscopy (TEM) and Cryo-EM imaging, with diameters in the low tens

149 Transmission electron microscopy (TEM) and energy dispersive spectroscopy reveal that at t

150 ffraction, transmission electron microscopy (TEM) and energy dispersive X-ray spectroscopy (EDS) to i

151 ncement in transmission electron microscopy (TEM) and its direct application to MOF structure-propert

152 While transmission electron microscopy (TEM) and operando X-ray absorption spectroscopy showed t

153 n (p-XRD), transmission electron microscopy (TEM) and scanning electron microscopy (SEM).

154 opy (EDX), transmission electron microscopy (TEM) and scanning electron microscopy (SEM).

155 articles by ransmission electron microscopy (TEM) and selected area electron diffraction revealed met

156 nd in situ transmission electron microscopy (TEM) are combined to demonstrate Sb-based nanofibers com

157 ng in situ transmission electron microscopy (TEM) at atomic scale, we discover that, in stark contras

158 bon-coated transmission electron microscopy (TEM) grid supports, where in a single high-throughput ex

159 In situ transmission electron microscopy (TEM) has been extensively employed to provide mechanisti

160 Transmission electron microscopy (TEM) images of these NP-exposed bacterial cells show tha

161 ng in situ transmission electron microscopy (TEM) imaging reveals that the dissolution mechanism chan

162 ssisted by transmission electron microscopy (TEM) imaging.

163 lysis, and transmission electron microscopy (TEM) imaging.

164 iments and transmission electron microscopy (TEM) measurements of the fibril morphologies formed.

165 th DLS and transmission electron microscopy (TEM) measurements reveal nanostructured compartments of

166 a range of transmission electron microscopy (TEM) methods, we show that the surfaces of the as-synthe

167 aining and transmission electron microscopy (TEM) methods, we studied DDQ's beneficial effects in AD

168 Transmission electron microscopy (TEM) of rapidly frozen biological specimens, or cryo-EM,

169 al in situ transmission electron microscopy (TEM) offers a powerful tool for directly visualizing the

170 a, we used transmission electron microscopy (TEM) on wing imaginal discs temporally depleted of the E

171 nd in situ transmission electron microscopy (TEM) reveal unique CNT morphologies and growth character

172 Transmission electron microscopy (TEM) revealed sarcomere misalignment and changes to mito

173 nfocal and transmission electron microscopy (TEM) revealed SCW deposition is accompanied by a signifi

174 Transmission electron microscopy (TEM) revealed that POM clusters were individually immobi

175 Transmission electron microscopy (TEM) revealed that TFV and ADV-treated HK-2 cells had ac

176 Transmission electron microscopy (TEM) showed that the combined group displayed improvemen

177 ections by transmission electron microscopy (TEM) shows that GAG removal reduced the rate of reminera

178 by in situ transmission electron microscopy (TEM) studies.

179 tering and transmission electron microscopy (TEM) to investigate the high-pressure behaviors of CdS n

180 resolution transmission electron microscopy (TEM) to resolve nano-scale bending characteristic of rip

181 Using transmission electron microscopy (TEM) together with quantitative image analysis and blind

182 (IHC), and transmission electron microscopy (TEM) were used to analyze Ddr1 knockout (Ddr1(-/-)) mice

183 (AFM) and transmission electron microscopy (TEM) were used to confirm the few-layer nature of WS(2)

184 y (LM) and transmission electron microscopy (TEM), a study of ACC in wild type (WT) mice, and mice wi

185 p-ICP-MS), Transmission Electron Microscopy (TEM), Analytical Ultracentrifugation (AUC), and UV/Vis s

186 py (HVMA), transmission electron microscopy (TEM), and immunofluorescence analysis (IF).

187 ualised by transmission electron microscopy (TEM), but higher-resolution tools are needed to observe

188 e (FESEM), transmission electron microscopy (TEM), dynamic light scattering (DLS) and zeta potential,

189 rformed by transmission electron microscopy (TEM), dynamic light scattering (DLS), Fourier-transform

190 and using transmission electron microscopy (TEM), high-resolution TEM (HR-TEM) and atom probe tomogr

191 -sectional transmission electron microscopy (TEM), Landau-Ginzburg-Devonshire phenomenological theory

192 opy (SEM), transmission electron microscopy (TEM), scratch tests, MTT reduction cytotoxicity, HOS cel

193 Transmission electron microscopy (TEM), selected area electron diffraction, and scanning T

194 assay and transmission electron microscopy (TEM), showing good agreement between the techniques (Pea

195 rized with transmission electron microscopy (TEM), transmission electron cryomicroscopy (cryoTEM), an

196 scopy, and transmission electron microscopy (TEM), we also show that U(V) is generated and incorporat

197 ing immuno-transmission electron microscopy (TEM), we observed that a large number of intact IBDV vir

198 py, (SEM), transmission electron microscopy (TEM), X-ray diffraction (XRD), Raman spectroscopy, Ultra

199 opy (SEM), Transmission Electron Microscopy (TEM), X-ray Photoelectron Spectroscopy (XPS), and Nanopa

200 ing (DLS), Transmission Electron Microscopy (TEM), zeta-potential, Inductively Coupled Plasma-Mass Sp

201 nd ex situ transmission electron microscopy (TEM).

202 light and transmission electron microscopy (TEM).

203 resolution transmission electron microscopy (TEM).

204 nd in situ transmission electron microscopy (TEM).

205 analytical transmission electron microscopy (TEM).

206 imaged by transmission electron microscopy (TEM).

207 SdFFF) and transmission electron microscopy (TEM).

208 uated with transmission electron microscopy (TEM).

209 y (SEM), and transition electron microscopy (TEM).

210 V-Vis) and transmission electron microscopy (TEM).

211 oscopy and transmission electron microscopy (TEM).

212 (DLS), and transmission electron microscopy (TEM).

213 ence and transmission electronic microscopy (TEM).

214 te adhesion and trans-endothelial migration (TEM) and subsequent accumulation of leukocyte-derived fo

215 Transendothelial migration (TEM) of leukocytes across the endothelium is critical fo

216 Using neutrophil transendothelial migration (TEM) under physiological flow assays, we found that an L

217 ions within the terrestrial ecosystem model (TEM).

218 users rely on temporal envelope modulations (TEMs) to understand speech, and clinical outcomes depend

219 We found mouse "TEM-17" cells to be enriched within the intestinal epith

220 othelium synergistically enhanced neutrophil TEM when additionally treated with histamine, whereas th

221 at supported abluminal-to-luminal neutrophil TEM.

222 have severe secondary effects on neutrophil TEM in combination with an inflammatory stimulus.

223 histamine, whereas the effects on neutrophil TEM of the individual stimuli were moderate to undetecta

224 teracted the double-hit effect on neutrophil TEM.

225 Detailed characterization by NMR, TEM, mass spectrometry, and rheology provided the struct

226 s verified and supported by a combination of TEM, AFM, and multiscale simulation techniques.

227 First, the evolutionary development of TEM nanocells from the open-cell configuration to the cl

228 with BRR halted the in vivo proliferation of TEM cells and their ex vivo alloreactivity and resulted

229 X-ray diffraction study the main results of TEM study include: (1) a long range order that can be de

230 The signal sequence of TEM-1 tolerated InDels more than the mature protein.

231 tes TEM by directing the LBRC to the site of TEM.

232 Herein, we provide a perspective on TEM studies of MOFs and highlight the utilization of sta

233 ntimeter-sized graphene single crystals onto TEM grids to fabricate large-area and high-quality suspe

234 ize scale, relative average phase purity, or TEM-imaged phase separation but rather facilitates Y6 mi

235 Furthermore, single-particle TEM imaging and atomistic simulation of reaction traject

236 Proangiogenic TEMs in macrophage HIF-2alpha-deficient tumors presented

237 rintuitive prohypoxia role for proangiogenic TEMs in breast cancer which is, in part, suppressed by H

238 Reduced numbers of proangiogenic TEMs in macrophage HIF-1alpha-deficient tumors presented

239 we evolve the antibiotic resistance protein TEM-1 towards resistance on the antibiotic cefotaxime in

240 ly stable point mutants of a single protein, TEM-1 beta-lactamase.

241 factors HIF-1alpha and HIF-2alpha, regulates TEM function in the hypoxic tumor microenvironment.

242 Remarkably, TEM, rheology and SAXS studies indicate that a single co

243 n electron microscopy (TEM), high-resolution TEM (HR-TEM) and atom probe tomography analyses, we show

244 n vivo inside macrophages by high-resolution TEM following 12 months inhalation exposure.

245 Higher spatial resolution TEM (HRTEM) analysis reveals a FeO/MnO like structure in

246 scanning/transmission electron microscopy (S/TEM) combined with in situ indentation, we observe nanos

247 scanning transmission electron microscopy (S/TEM), and Raman spectroscopy were combined with first pr

248 cted area electron diffraction, and scanning TEM indicated no hydride formation in cryo-milled CP-Ti

249 omena revealed by atomic-resolution scanning TEM (STEM) and single-crystal diffraction using synchrot

250 xamined a 3D image stack from serial-section TEM (ssTEM) of the optic neuropiles of the miniature par

251 were confirmed by UV-vis spectroscopy, SEM, TEM and XRD analysis.

252 nocomposites were evaluated using, XRD, SEM, TEM, FT-IR and final contact angle.

253 In situ TEM analysis reveals that the inner Sb nanoparticles und

254 nd devices that have been enabled by in situ TEM are reviewed.

255 n to the introduction of an improved in situ TEM biasing technique.

256 xplored, followed by applications of in situ TEM for direct observation of electrocatalyst formation,

257 ng ZnO as a model system, we combine in situ TEM observations of single particle and ensemble assembl

258 ging opportunities and challenges in in situ TEM research of energy materials and devices are discuss

259 In situ TEM revealed an electron beam assisted transformation of

260 iceably, a great portion of previous in situ TEM studies has been focused on conversion-type material

261 Next, in situ TEM studies of rechargeable ion batteries in a practical

262 Herein, recent developments of in situ TEM techniques for investigation of dynamic phase transf

263 ndings that are uniquely obtained by in situ TEM to address fundamental questions and practical issue

264 ase transition is also visualized by in situ TEM, acquired under reactive conditions at 800 mbar pres

265 using SCLC, GIXRD, AFM, XPS, NEXAFS, R-SoXS, TEM, STEM, fs/ns TA spectroscopy, 2DES, and impedance sp

266 metre-scale secondary ion mass spectrometry (TEM-NanoSIMS) isotopic imaging to study (13) C-bicarbona

267 icroscopy/electron energy loss spectroscopy (TEM/EELS) to investigate the evolution of transition met

268 y with energy dispersive X-ray spectroscopy (TEM-EDX) for morphology and elemental composition.

269 d with energy dispersive X-ray spectroscopy (TEM-EDX) is a powerful tool for determining these partic

270 In this work, we used both negative stain TEM and cryo-EM to determine 3D maps of the full-length

271 FtsH dodecamer visualized by negative stain TEM suggests a lateral substrate entrance between the me

272 ning/transmission electron microscopes (STEM/TEM) provide a critical tool for understanding the micro

273 as previously overlooked in the well-studied TEM-1 beta-lactamase demonstrates the utility of exposon

274 d particles onto the TEM grid for subsequent TEM-EDX measurements.

275 high-pressure freezing, freeze-substitution, TEM, and confocal microscopy.

276 t subpopulation of CD4(+) effector memory T (TEM) cells that secrete IL-17A, but not IFN-gamma, was r

277 The TEM imaging showed penetration and infiltration of bacte

278 e factors in the quasi-2D confinement of the TEM fluid cell lead to abnormal diffusivities with times

279 position of the extracted particles onto the TEM grid for subsequent TEM-EDX measurements.

280 omes depend on the accuracy with which these TEMs are encoded by the electrically-stimulated neural e

281 tructural changes that can be viewed through TEM.

282 s the copy number of bla(TEM-1B,) leading to TEM-1B hyperproduction and TZP resistance.

283 In the absence of PD-ligands, both TS1 TEM and TN induced late-onset myocarditis.

284 ed this hypothesis and found that indeed TS1 TEM induced more severe skin and liver GVHD in the absen

285 fl/fl) /LysMcre mice and evaluated the tumor TEM population.

286 a significantly smaller percentage of tumor TEMs compared with control and HIF-2alpha (fl/fl) /LysMc

287 usly by almost all the bacterial cells under TEM.

288 Here we use TEM to show that ribose-5-phosphate (R5P) glycation of c

289 We used TEM to reconstruct a full segment of all 60 MNs and 236

290 y the oomycete Anisolpidium ectocarpii using TEM, in vivo autophagy markers and autophagy inhibitors.

291 obe has been characterized extensively using TEM, EDX, SAED, XRD, FE-SEM, FTIR, DIC, and electrochemi

292 lected during ABS printing was performed via TEM and electron energy loss spectroscopy, which indicat

293 sensor probe was characterized using UV-Vis, TEM, SAED, EDX, AFM, and electrochemical techniques incl

294 y relevant concentrations of 5 ng L(-1) with TEM-EDX and sp-ICP-MS measurements.

295 uNRs) were fabricated and characterized with TEM, SEM and XRD.

296 themselves are too short to be resolved with TEM.

297 themselves are too small to be resolved with TEM.

298 For UMNs, comparison of IM-MS results with TEM and N(2) physisorption yields quantitative agreement

299 e materials are characterized with SEM, XRD, TEM, SAED, EDX, XPS, UV-visible spectroscopy, and open-c

300 ciated with magnetic skyrmions, so that XRD, TEM, EDS, SAED and HREM investigations were carried out