ライフサイエンスコーパス: TEM

1 TEM analyses of GO flakes confirm the size decrease of o

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

3 TEM characterization shows no sign of crystallization, H

4 TEM experiments showed that the AuNPs and AgNPs were cir

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

6 TEM observations exhibited spherical morphology of the N

7 TEM requires LBRC to move to the site at which TEM will

8 TEM revealed that the SiNPs were up-taken by the HCECs i

9 TEM showed that actin within the CR formed a dense and a

10 TEM-1 populations evolved in such strains endow host cel

11 ique single amino acid mutants of the TEM-1, TEM-17, TEM-19, and TEM-15 beta-lactamase alleles, which

12 gle amino acid mutants of the TEM-1, TEM-17, TEM-19, and TEM-15 beta-lactamase alleles, which constit

13 CD3(+) TILs were composed of 57% CD4(+) (82% TEM and 20% Tregs) and 36% CD8(+) cells.

14 We assayed a TEM-1 beta-lactamase variant and levoglucosan kinase (LG

15 boosting generates preternaturally abundant TEM that increases the total quantity of memory CD8 T ce

16 etection electron-counting camera to acquire TEM images of the MOF ZIF-8 with an ultralow dose of 4.1

17 -associated demethylated status but acquired TEM-associated programs.

18 sed surface expression of Le(x) on PMN after TEM, and blockade of terminal Le(x) regulated post-migra

19 at additional pathways restrain alloreactive TEM TS1 TN also caused more severe GVHD without PD-ligan

20 Analytical TEM allowed assessing the homogeneous localization of bd

21 on several other antibiotics that ancestral TEM-1 had been unable to deactivate.

22 id mutants of the TEM-1, TEM-17, TEM-19, and TEM-15 beta-lactamase alleles, which constitute an adapt

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

24 tems are easily synthesized in open air, and TEM indicates an average size of 2.4 +/- 0.6 nm for NAC@

25 on as primary central memory CD8 T cells and TEM Further analysis identified distinct TRM populations

26 ues on the PMN surface blocks chemotaxis and TEM while enhancing PMN-adhesive interactions with intes

27 in vitro system that models circulation and TEM, we showed that the small population of CLL cells th

28 cytes were deficient in in vivo crawling and TEM in the postcapillary venules.

29 tection limit of synchrotron diffraction and TEM.

30 DLS and TEM revealed a particle size about 170nm for the double

31 uding amyloid kinetics, dot blot, ELISA, and TEM show that 5 effectively inhibits both Abeta oligomer

32 of size ~24 nm by UV-visible, XRD, FTIR and TEM.

33 terized by light scattering, NMR, FT-IR, and TEM.

34 firmed experimentally using ion mobility and TEM measurements.

35 vocally characterized by NMR, ESI-IM-MS, and TEM techniques.

36 ifically required for targeted recycling and TEM.

37 haracterized by XRD, SEM, XPS, XRF, SAED and TEM measurements.

38 SEM and TEM analysis showed that TRIP-1 promoted the nucleation

39 SEM and TEM characterization results indicated that graphene in-

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

41 nd transmission electron microscopy (SEM and TEM), Fourier transformed infrared (FT-IR) spectroscopy

42 constitutive activity between CD8(+) TCM and TEM are due to differential regulation by SH2 domain-con

43 tral and effector memory CD8 T cell (TCM and TEM, respectively) homeostatic proliferation, maintenanc

44 XRD, Raman, TPO, and TEM analysis confirmed that the deactivation of monometa

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

46 e tension of uncharacterized origin works at TEM boundaries to limit their widening.

47 dely endemic resistance mechanisms (e.g. bla TEM, bla CTX-M) suggests that it may become similarly pr

48 road-spectrum beta-lactam AR genes (ARG; bla(TEM), bla(SHV), bla(OXA) and bla(CTX-M)) and class-1 int

49 Synthesized materials were characterized by TEM, SEM, UV-Vis, XRD, XPS, EIS, fluorescence, and photo

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

51 weakly aggregate, a prediction confirmed by TEM.

52 istribution comparable to that determined by TEM, and a random NP distribution on the UME surface.

53 on on heating to 150 degrees C, as judged by TEM and SAXS.

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

55 s, with an obvious release stage observed by TEM.

56 Together, our findings identify CD4(+) TEM cells as a key effector of TSS and reveal a novel ro

57 ice, this patient exhibited increased CD4(+) TEM cells in the peripheral blood.

58 Notably, CD4(+) TEM cells from the patient were strikingly resistant to

59 -stimulation, such as effector/memory (CD4(+)TEM and CD8(+)TCM) and regulatory (T reg) T cells.

60 nt IFN-gamma production in CD4(+) and CD8(+) TEM cells.

61 estored the number of local antiviral CD8(+) TEM and CD8(+) TRM cells associated with protection agai

62 cy of effector memory CD8(+) T cells (CD8(+) TEM cells) specific to three epitopes derived from the H

63 omised the mobilization of functional CD8(+) TEM and CD8(+) TRM cells within latently infected trigem

64 obust and polyfunctional HSV-specific CD8(+) TEM cells associated with strong protective immunity aga

65 *02:01 transgenic mice with the three CD8(+) TEM-cell epitopes from ASYMP individuals induced robust

66 *02:01 transgenic mice with the three CD8(+) TEM-cell epitopes from ASYMP individuals induced robust

67 ICP-MS) measurements, corroborated the CeFFF-TEM results.

68 ) CD62L(low) CD8(+) effector memory T cells (TEM cells) in ASYMP individuals than SYMP individuals.

69 function of effector memory CD8(+) T cells (TEM) and tissue-resident memory CD8(+) T cells (TRM), bu

70 Effector memory T cells (TEM) are less capable of inducing graft-versus-host dise

71 We show in mouse effector memory T cells (TEM) that >50% of lymphocyte-specific protein tyrosine k

72 ission electron microscopy characterization (TEM) and Rutherford backscattering spectrometry channeli

73 Cryo-TEM, used together with SAXS to determine fibril dimensi

74 olving the correlation of cryo-SHXM and cryo-TEM data sets from the same specimen area, is broadly ap

75 s monitored by HATR-FTIR, NMR, DSC, and cryo-TEM.

76 genic transmission electron microscopy (cryo-TEM) and synchrotron hard X-ray microprobe (SHXM) data s

77 genic transmission electron microscopy (cryo-TEM).

78 Biophysical evidence from TEM, cryo-TEM, SAXS, AFM, and STEM measurements on the 3FD-IL nano

79 mission electron microscopy (TEM), cryogenic TEM, and (55)Fe as an isotope tracer to observe changes

80 ations and explore their role in determining TEM's specificity.

81 PMN-MPs secreted by activated PMNs during TEM displayed a high level of enzymatically active matri

82 analytical techniques including FESEM, EDS, TEM, AFM, FTIR, Raman, Fluorescence and Absorption Spect

83 ized and characterized with FT-IR, SEM, EDX, TEM, UV-Visible, XRD and TG/DTA techniques.

84 sufficient to augment GVHD caused by either TEM or TN, indicating that donor PD-ligand-expressing AP

85 Also, we first try to employ TEM information quantitatively to offer probable referen

86 e presence of an actomyosin cable encircling TEMs.

87 ial measurements, sedimentation experiments, TEM images, and modified DLVO calculations all indicated

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

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

90 sisted transmission electron microscopy (FIB-TEM) and validated by a numerical simulation model.

91 s, whereas ERK was additionally required for TEM across dermal MVECs.

92 Biophysical evidence from TEM, cryo-TEM, SAXS, AFM, and STEM measurements on the 3

93 site was characterised by UV-vis, XRD, FTIR, TEM, XPS and Raman spectroscopy techniques.

94 Furthermore, TEM reveals important local structural features of ZIF-8

95 i stacking two clean single-crystal graphene TEM grids, in which atomic-scale resolution imaging and

96 mon absorbance, and the NPs are imaged by HR-TEM.

97 olution-transmission electron microscopy (HR-TEM), vibrating sample magnetometer (VSM), X-ray diffrac

98 The HR-TEM image shows that the average size of the prepared N-

99 ual appearance of new crystalline domains in TEM images and new diffraction maxima in selected area e

100 rved superior cytotoxic effector function in TEM compared with TCM, and we provide evidence that this

101 observed enhanced Zap-70 phosphorylation in TEM following TCR ligation compared with TCM Furthermore

102 dicating that STAT5 signaling drives RICD in TEM cells.

103 al cellular dewetting framework to interpret TEM physical parameters that are quantitatively determin

104 cells resulted in phenotypic conversion into TEM cells and was coupled to increased methylation of th

105 recovery procedure, we show that intravenous TEM activation determines neutrophil and monocyte recrui

106 o better than 3-A resolution using a 200-keV TEM.

107 Lorentz transmission electron microscopy (L-TEM).

108 enterica subsp. arizonae The beta-lactamase TEM-1 reporter system showed that SeoC is translocated b

109 kines influenced LEC phenotype and leukocyte TEM.

110 targeted recycling of the LBRC and leukocyte TEM.

111 wall shear stress (WSS) dependent leukocyte TEM and compensatory arterial remodeling obeying Glagov'

112 er, using the model, we have found leukocyte TEM increases monotonically with decreases in luminal vo

113 y resulting in sudden increases in leukocyte TEM suggesting lumen volumes that will give rise to rapi

114 , we present a multiscale model of leukocyte TEM and plaque evolution in the left anterior descending

115 sult in a representative number of leukocyte TEM as compared to pulsatile flow, whereas passing WSS a

116 hed an in vitro system to evaluate lymphatic TEM for various cell types across primary mouse and huma

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

118 together we conclude that during lymphocyte TEM, ICAM-1 signaling diverges into pathways regulating

119 tion of paxillin was required for lymphocyte TEM and converged functionally with VE-cadherin phosphor

120 Transendothelial cell macroaperture (TEM) tunnels control endothelium barrier function and ar

121 (HLA-DR(+)) T cells with an effector memory (TEM) profile are enriched in such lesions.

122 ry human naive, short-lived effector memory (TEM), and longer-lived central memory (TCM) and stem cel

123 ed subsets, such as TTM and effector memory (TEM).

124 sitional memory [TTM], TCM, effector memory [TEM], and TSCM cells, respectively).

125 Transmission electron micrographs (TEM) of infected cells treated with endocytosis inhibito

126 nventional transmission electron microscope (TEM) and too slow for ultrafast electron microscopy.

127 nts with a transmission electron microscope (TEM) show that nano-Se particles synthesized by P. putid

128 systematic transmission electron microscope (TEM) study revealed a similar structural transition from

129 (SEM) and transmission electron microscope (TEM) techniques were used for phase identification as we

130 y (FESEM), transmission electron microscope (TEM), energy dispersive X-ray spectroscopy (EDX), X-ray

131 rved under Transmission Electron Microscope (TEM).

132 -corrected transmission electron microscope (TEM).

133 g 300-keV transmission electron microscopes (TEMs).

134 (AFM) and Transmission Electron Microscopic (TEM) images support the presence of an array like semi c

135 bserved by transmission election microscopy (TEM).

136 ether with transmission electron microscopy (TEM) analyses, we could assess the extent of both homo-

137 Transmission Electron Microscopy (TEM) analysis confirmed the presence of small metallic n

138 nd ex situ transmission electron microscopy (TEM) and compare them with solid Si nanoparticles and na

139 ng in situ transmission electron microscopy (TEM) and consecutive ion-irradiations: 1 MeV Kr(2+) (sim

140 merulus by transmission electron microscopy (TEM) and conventional scanning electron microscopy (SEM)

141 Transmission electron microscopy (TEM) and cryogenic electron tomography (cryo-ET) results

142 ization to transmission electron microscopy (TEM) and dynamic light scattering (DLS) and confirmed th

143 ion (XRD), transmission electron microscopy (TEM) and dynamic light scattering (DLS) techniques.

144 ualized by transmission electron microscopy (TEM) and enhanced dark-field (EDF) microscopy.

145 icroscopy, transmission electron microscopy (TEM) and gene expression analyses in order to assess div

146 (SAXS) and Transmission electron microscopy (TEM) and holds great promise for potential applications

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

148 ualized by transmission electron microscopy (TEM) and Prussian Blue staining, and quantified using an

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

150 pported by transmission electron microscopy (TEM) and scanning tunneling microscopy (STM).

151 pproaches: transmission electron microscopy (TEM) and serial block face scanning EM (SBF-SEM) with 3D

152 epared for transmission electron microscopy (TEM) and subsequent high-spatial-resolution NanoSIMS ima

153 t employed transmission electron microscopy (TEM) and X-ray diffraction (XRD) to interpret the supers

154 opy (SEM), transmission electron microscopy (TEM) and X-ray photoelectron spectroscopy (XPS).

155 g (DLS)and transmission electron microscopy (TEM) are used to determine nanoparticle size and morphol

156 sis (EDX), transmission electron microscopy (TEM) combined with EDX, and micro-Raman spectroscopy.

157 (AFM) and transmission electron microscopy (TEM) confirmed the efficient immobilization of the antib

158 MOFs with transmission electron microscopy (TEM) due to the extreme instability of MOFs upon electro

159 ication of transmission electron microscopy (TEM) grids bearing graphene oxide (GO) sheets that have

160 g improved transmission electron microscopy (TEM) images and image averages of the rosette-type CSC,

161 (SEM) and transmission electron microscopy (TEM) images revealed the spherical nanostructure of the

162 (APT), and transmission electron microscopy (TEM) is compared.

163 by in situ transmission electron microscopy (TEM) is reported.

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

165 s article, transmission electron microscopy (TEM) observation of hexagonal Moire patterns with unusua

166 ge through transmission electron microscopy (TEM) of quartz nanopipets for SECM imaging of single sol

167 nd ex situ transmission electron microscopy (TEM) results show that the lithiation is suppressed by t

168 d from the transmission electron microscopy (TEM) results.

169 L3 XAS and transmission electron microscopy (TEM) reveal that initially sorbed U(VI) species recrysta

170 Transmission electron microscopy (TEM) revealed that Mkx(-/-) mice presented collagen fibr

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

172 Transmission electron microscopy (TEM) revealed two intergrown domains with slight structu

173 nalysis by transmission electron microscopy (TEM) suggested a membrane lytic mechanism of action for

174 g advanced transmission electron microscopy (TEM) technique combined with first-principles theory.

175 f advanced transmission electron microscopy (TEM) techniques, including spherical aberration-correcte

176 um replica transmission electron microscopy (TEM) to determine the structural organization of actin a

177 ironmental transmission electron microscopy (TEM) under an oxygen environment, we image the product m

178 ironmental transmission electron microscopy (TEM) when operated under realistic conditions and a lack

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

180 kinetics, transmission electron microscopy (TEM), and atomic force microscopy (AFM) show that ADH-41

181 light and transmission electron microscopy (TEM), and electroretinography (ERG) were used to analyze

182 in-section transmission electron microscopy (TEM), and general morphological features of the VLPs by

183 opy (SEM), transmission electron microscopy (TEM), and X-ray photoelectron spectroscopy (XPS).

184 ochemical, transmission electron microscopy (TEM), atomic force microscopy (AFM) and Fourier transfor

185 esolved by transmission electron microscopy (TEM), consistent with amyloid fibers.

186 s and used transmission electron microscopy (TEM), cryogenic TEM, and (55)Fe as an isotope tracer to

187 terized by Transmission Electron Microscopy (TEM), FTIR, UV-Visible absorption and Photoluminiscence

188 by ex situ transmission electron microscopy (TEM), in situ scanning transmission electron microscopy

189 th in situ transmission electron microscopy (TEM), in situ X-ray diffraction (XRD), and in situ elect

190 opy (SEM), transmission electron microscopy (TEM), Raman spectroscopy and X-ray diffractometry (XRD)

191 d by using transmission electron microscopy (TEM), scanning electron microscopy (SEM), atomic force m

192 iquid cell transmission electron microscopy (TEM), scanning transmission X-ray microscopy (STXM) and

193 terized by transmission electron microscopy (TEM), UV and Fourier transform infrared (FTIR) spectrosc

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

195 ermined by transmission electron microscopy (TEM), with corresponding larger NP diffusion coefficient

196 opy (SEM), transmission electron microscopy (TEM), X-ray diffraction (XRD) and ultraviolet-visible ab

197 opy (SEM), transmission electron microscopy (TEM), x-ray diffraction (XRD), Raman-spectroscopy, elect

198 opy (SEM), transmission electron microscopy (TEM), x-ray diffraction (XRD), x-ray photo-electron spec

199 opy (SEM), transmission electron microscopy (TEM), X-ray photoelectron spectroscopy (XPS), X-ray diff

200 chnique of transmission electron microscopy (TEM).

201 (SEM) and transmission electron microscopy (TEM).

202 imaged by transmission electron microscopy (TEM).

203 nfirmed by transmission electron microscopy (TEM).

204 uated with transmission electron microscopy (TEM).

205 roplets by transmission electron microscopy (TEM).

206 terized by transmission electron microscopy (TEM).

207 SdFFF) and transmission electron microscopy (TEM).

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

209 (SEM) and transmission electron microscopy (TEM).

210 support of transmission electron microscopy (TEM).

211 cess using transmission electron microscopy (TEM).

212 yzed using transmission electron microscopy (TEM).

213 gated by transmission electronic microscopy (TEM) and scanning electron microscopy (SEM).

214 oscopy and transmission electron microscopy, TEM) can only provide 2D simplifications of size and sha

215 d imaging (transmission electron microscopy, TEM, and scanning transmission X-ray microscopy, STXM) t

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

217 Trans-endothelial migration (TEM) is essential for leukocyte circulation.

218 t upconversion via triplet energy migration (TEM) occurs as well as materials for stimulated emission

219 cells to undergo transendothelial migration (TEM) and enter the proliferation centers of the LNs.

220 Lymphocyte transendothelial migration (TEM) is critically dependent on intraendothelial signali

221 t promotes their transendothelial migration (TEM).

222 is critical for transendothelial migration (TEM).

223 is glycans during transepithelial migration (TEM) has not been well characterized.

224 leukocyte (PMN)] transepithelial migration (TEM) is a hallmark of inflammatory mucosal disorders.

225 ions within the terrestrial ecosystem model (TEM).

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

227 On the basis of TEM analysis, it has been estimated that as small as app

228 9 regulates a step at or close to the end of TEM.

229 unted to be less than 50 nm with the help of TEM.

230 Reducing the number of TEM cells through a depletion recovery procedure, we sho

231 We take advantage of the high resolution of TEM to demonstrate that laser-pulled quartz nanopipets r

232 High-throughput sequencing of TEM-1 populations shows that this advantage is associate

233 st that targeting of the LBRC to the site of TEM precedes VE-cadherin clearance.

234 ole in clearing VE-cadherin from the site of TEM.

235 stabilizing actin filaments at the edges of TEMs, thereby favouring their crosslinking by NMIIa.

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

237 Here, the authors combine liquid-phase TEM and single particle tracking to observe the dynamics

238 op preparations facilitated increases in PMN TEM.

239 Seventy produced TEM, SHV, or CTX-M ESBLs, with 15 coproducing an AmpC an

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

241 onstrate that deep vein thrombosis-recruited TEM receive an immediate antigen-independent activation

242 n imaging with NanoSIMS, which could replace TEM for localization in ultrahigh resolution imaging ana

243 High-resolution TEM analysis demonstrates that most dislocations emerge

244 High-resolution TEM of carbon pipettes was used to attain better underst

245 nd the X-ray diffraction and high-resolution TEM testified that the NYS compound belongs to the apati

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

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

248 Cross-sectional TEM images reveal the BiFeO3 film consists of two zones

249 These findings along with results from SEM, TEM, and XRPD studies support our hypothesis that water

250 rial by microscopy techniques including SEM, TEM and confocal microscopy is presented.

251 anoparticles were characterized by XRD, SEM, TEM, FTIR, TGA, DSC and UV-visible spectroscopy.

252 Ex situ TEM characterization is conducted to further investigate

253 situ SAXS measurements supported by ex situ TEM indicate that initially Fe13 Keggin clusters (radius

254 Complementary time-dependent ex situ TEM studies were also performed.

255 sually with atom-resolved imaging by in situ TEM and quantitatively with sample-averaged measurements

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

257 harmonic generation polarimetry and in situ TEM electrical testing on single-crystalline GeTe nanowi

258 y elaborately modifying the existing in situ TEM experimental technique, rapid lithium-ion diffusion

259 Ex situ and in situ TEM measurements demonstrate catalyzed nanowire growth i

260 imescales too short to capture using in situ TEM.

261 terization by FTIR, XPS, Raman Spectroscopy, TEM, XRD, TOC, collectively demonstrates that oxidized C

262 tioning transmission electron microscopy (SS-TEM) were used to better resolve the fluorescent Gag-con

263 Negatively stained TEM images confirmed the absence of tailocins and reveal

264 sion electron microscopy system (in-situ STM-TEM).

265 signaling in the death of effector memory T (TEM) cells in mice and humans.

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

267 nd Ca(2+) influx in human effector memory T (TEM) cells.

268 en for rapid semi-automated processing of TB-TEM dark field data acquired using this method.

269 Here we report that TEMPRANILLO (TEM) genes negatively control trichome initiation not on

270 We infer from these findings that TEM grids modified with GO-NTA are a useful tool that re

271 geny, leading us to test the hypothesis that TEM induce less GVHD because of increased sensitivity to

272 Moreover, we show that TEM also acts as a link between GA and cytokinin signali

273 The TEM images of urease NPs showed their size in the range,

274 The TEM quasi-single mode THz waveguide excitation and non-d

275 The TEM/HRTEM results confirm that these bundles are compose

276 vivax, the fungus Aspergillus niger, and the TEM-family of beta-lactamase associated with antibiotic

277 ion data and particle size obtained from the TEM images were used to calculate the nanoparticle densi

278 ,500 unique single amino acid mutants of the TEM-1, TEM-17, TEM-19, and TEM-15 beta-lactamase alleles

279 can be inter-converted by simply tilting the TEM specimen following designated directions.

280 tension at the cell boundary surrounding the TEMs by promoting the formation of an actomyosin ring.

281 ion to endothelial cells and enhancing their TEM.

282 sizing (with results that are comparable to TEM) despite charges of only fC being measured.

283 sing micro-Raman spectroscopy, Transmission (TEM) and Scanning (SEM) Electron Microscopy on Focused I

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

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

286 found that cell-intrinsic properties of TS1 TEM reduced their GVHD potency relative to TS1 TN Posttr

287 tency relative to TS1 TN Posttransplant, TS1 TEM progeny expressed higher levels of PD-1 than did TS1

288 ells or those with the propensity to undergo TEM.

289 Using TEM and optical modelling, we show that the spiders' sca

290 xygenate production, and characterized using TEM.

291 show loss of the ciliary ODAs in humans via TEM and immunofluorescence (IF) analyses.

292 M requires LBRC to move to the site at which TEM will take place and for VE-cadherin to move away.

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

294 d lens tissues, fibers are not observed with TEM, but highly ordered beta-sheets of amyloid secondary

295 themselves are too short to be resolved with TEM.

296 themselves are too small to be resolved with TEM.

297 ails using FT-IR, UV/vis., FESEM, XEDS, XPS, TEM, and XRD techniques.

298 a solution process and characterized by XRD, TEM, EDS, and XPS.

299 l state of the art techniques including XRD, TEM, SEM and XPS.

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