ライフサイエンスコーパス: EM

1 EM, immune detection analysis, and assessment of aggrega

2 erall, GCs were frequent after 3 (DM: 53.9%; EM: 69.2%) and 6 months (DM: 76.9%; EM: 88.5%).

3 : 53.9%; EM: 69.2%) and 6 months (DM: 76.9%; EM: 88.5%).

4 rk demonstrates the feasibility of acquiring EM datasets at the scale of cortical microcircuits in mu

5 icle accelerators and enabling control of an EM field generating media including relativistic charge

6 rophoretic mobility macromolecular analysis, EM, X-ray crystallography, and enzyme assays.

7 otease fragmentation with mass analysis, and EM.

8 orescence microscopy, bulk actin assays, and EM to investigate how ExoY impacts actin dynamics.

9 eflection fluorescence (TIRF), confocal, and EM analyses, we show that the N-terminal N-BAR domain of

10 rom cell perturbation, correlative light and EM tomography, live-cell imaging, modeling, and high-res

11 tion of individually identified neurons, and EM data-based analyses of synaptic organization.

12 ombination of confocal, super-resolution and EM, we defined DAT localization and its membrane diffusi

13 tradeoffs between plant water retention and EM fungi under carbon-limiting conditions.

14 d during the standard technique used to blot EM grids and that these manifest in nonuniform ice after

15 Using a whole-brain EM dataset of a female Drosophila, we comprehensively de

16 vegetation as well as soil acidification by EM fungi, which are associated with greater diversity an

17 Pinus litter decay rates were decelerated by EM fungi and were associated with decoupling of litter C

18 Our collaborative EM algorithm is mathematically equivalent to the origina

19 onstructing deletion proteins guided by cryo EM structural knowledge.

20 Analysis of multiple cryo EM maps, further modelling and mutagenesis provide worki

21 Cryo-EM analyses of the pre-fusion spike incubated with EY6A

22 Cryo-EM and biochemical analyses of this subcomplex shows tha

23 Cryo-EM and mass spectrometry of tau filaments from CBD revea

24 Cryo-EM data generated by electron tomography (ET) contains i

25 Cryo-EM has rapidly gained popularity in recent years due to

26 Cryo-EM of the NTD dimer revealed a structural similarity to

27 Cryo-EM reveals that DNAs transported into E-S/E-K compartmen

28 Cryo-EM structures in the open and closed states reveal a dyn

29 Cryo-EM structures reveal that CTPS2 filaments dynamically sw

30 data using two-fold symmetry yielded a cryo-EM map in which both DNA ends appeared well ordered, ind

31 ational pipeline, where the inputs of a cryo-EM map, the corresponding atomistic structure, and the p

32 Here, we report a cryo-EM structure of a B. subtilis transcription activation c

33 We report a cryo-EM structure of a complex between the Mycobacterium smeg

34 We present a cryo-EM structure of an MCU-EMRE-MICU1-MICU2 holocomplex comp

35 We also report a cryo-EM structure of DNA-PK at 3.5- angstrom resolution and r

36 Here, we report a cryo-EM structure of human NPC1 bound to itraconazole, which

37 A cryo-EM structure of TerS(P76-26) revealed that it forms a ri

38 lour beetle, Tribolium castaneum, and a cryo-EM structure of the complex at 3.5 angstrom resolution.

39 A cryo-EM structure of the portal protein of thermostable virus

40 We report a cryo-EM structure of the S. cerevisiae RNase MRP holoenzyme s

41 A cryo-EM structure of the spastin-peptide complex at 4.2 angst

42 Here we present a cryo-EM structure of the strain 970 LH1-RC complex at 2.82 an

43 tag that binds 5-nm Ni-nanogold allowed cryo-EM tomography mapping of the C terminus of protein A to

44 o biochemistry, ribosome profiling, and cryo-EM to define molecular mechanisms that lead to these rib

45 rk, we used both negative stain TEM and cryo-EM to determine 3D maps of the full-length Aquifex aeoli

46 A 2.5- angstrom cryo-EM structure of a 1-18-BG505(SOSIP.664) Env complex reve

47 Here, we describe the 3.2 angstrom cryo-EM structure of human DEC-205, thereby illuminating the

48 d Gi protein and from the 3.5- angstrom cryo-EM structure of muOR-Gi complex after replacing the 168

49 Here we report the 3.2- angstrom cryo-EM structure of S.c. Pol delta in complex with primed DN

50 and ultimately solved the 4.9 angstrom cryo-EM structure of the DEC-205 tetramer to identify the unf

51 Our ~3.5 angstrom cryo-EM structure of the E. coli MCE protein LetB reveals an

52 Here, we present a 3.67 angstrom cryo-EM structure of the RSV polymerase (L:P) complex.

53 Here, we present a ~3.0- angstrom cryo-EM structure of trimeric human STEAP1 bound to three ant

54 We show here a 3.5- angstrom cryo-EM structure of yeast Pol epsilon revealing that the Dpb

55 ith a structure derived from asymmetric cryo-EM reconstructions.

56 which increases throughput in automated cryo-EM without degrading data quality.

57 f Cell, two papers report agonist-bound cryo-EM structures of the cannabinoid receptor, CB2, in compl

58 We have identified by cryo-EM a segment in CPSF100 that tethers mCF to mPSF, and we

59 We have compared the two capsids by cryo-EM at 3.5 angstrom resolution.

60 rest in extending structural studies by cryo-EM into the cell, where biological structures and proces

61 he structure of the PG16-Env complex by cryo-EM to an overall resolution of 4.6 angstrom.

62 ed reconstructions of mCF and CstF77 by cryo-EM, assembled around the mPSF core.

63 n of amyloids for structural studies by cryo-EM, but also pave the way to elucidate the structural ba

64 e of human SOAT1 (hSOAT1) determined by cryo-EM.

65 KCC4, in lipid nanodiscs determined by cryo-EM.

66 en captured at increasing resolution by cryo-EM.

67 le was visualized at high resolution by cryo-EM.

68 of the N-glycans could be visualized by cryo-EM.

69 We combine Cryo-EM and spectroscopy to determine the structure(-)functio

70 In contrast, cryo-EM structures of ribosomes from mutant cells lacking K63

71 ingle-particle electron cryomicroscopy (cryo-EM), computational modeling, and site-specific mass spec

72 Here we determine cryo-EM structures of Escherichia coli MlaFEDB in an apo stat

73 sub-module to the previously determined cryo-EM map of the S. cerevisiae CCAN-Cenp-ANuc complex.

74 We determined cryo-EM structures for RaTG13 S and for both furin-cleaved an

75 omorphic assemblies, we have determined cryo-EM structures of apo-CA hexamers and in complex with cyc

76 recognition and cleavage, we determined cryo-EM structures of Cas12i in multiple functional states.

77 By devising cryo-EM methodologies for exceedingly flexible and pleomorphi

78 lostery, protein quality control during cryo-EM construct optimization, and in the study of protein m

79 Here, yeast and human EMC cryo-EM structures reveal conserved intricate assemblies and

80 To interpret the experimental cryo-EM maps, we present molecular-dynamics-based methods for

81 hene-water interface, which facilitates cryo-EM 3D reconstruction of archaea 20S proteasomes at a rec

82 thod that, starting only from the final cryo-EM map, decomposes local resolution into the different p

83 The first cryo-EM structure of an HCN1 channel revealed that a novel st

84 Here, we report five cryo-EM structures, at resolutions of 3.0-3.3 angstrom, of hu

85 e design a fully automated approach for cryo-EM 3D density maps reconstruction (Auto3DCryoMap).

86 re we present a convenient workflow for cryo-EM structural analysis of MPs embedded in liposomes, usi

87 using models fitted to or derived from cryo-EM maps.

88 Furthermore, cryo-EM reveals a range of partially full, condensed DNA dens

89 Here, cryo-EM data were derived from filaments reconstituted with a

90 verified by electron microcopy imaging, cryo-EM tomography and in-situ X-ray scattering methods.

91 contributed to the principal methods in cryo-EM and identify persisting challenges and bottlenecks th

92 effective approach to pick particles in cryo-EM images automatically and accurately.

93 e used as a measure of resolvability in cryo-EM maps at various scales, from entire macromolecules do

94 he resolvability of individual atoms in cryo-EM maps, the map Q-score.

95 hy but in both phases and amplitudes in cryo-EM, and that half-maps with independent errors are avail

96 ith independent errors are available in cryo-EM.

97 xisting cryogenic electron microscopic (cryo-EM) maps, limit binding to incoming monomers, and flatte

98 Cryogenic electron microscopy (cryo-EM) analysis confirms that incubation of spike with CR30

99 Using cryo-electron microscopy (cryo-EM) and biochemical approaches, we show that PF846 inhib

100 ombination of electron cryo-microscopy (cryo-EM) and reconstituted translation initiation assays with

101 is present in cryo-electron microscopy (cryo-EM) density maps and it has not been utilized yet for de

102 Cryo-electron microscopy (cryo-EM) has become a leading technology for determining prot

103 Cryo-electron microscopy (cryo-EM) images show that new aggregates protrude from the en

104 ime course of electron cryo-microscopy (Cryo-EM) imaging reveals a crystalline intermediate wherein N

105 d progress of cryo-electron microscopy (cryo-EM) in structural biology has raised an urgent need for

106 particle electron cryogenic microscopy (cryo-EM) is presented.

107 Cryo-electron microscopy (Cryo-EM) is widely used in the determination of the three-dim

108 reported cryogenic electron microscopy (cryo-EM) open-state channel structure, multiple microseconds-

109 he results of cryo-electron microscopy (cryo-EM) reconstruction of multiple 3D DNA origami objects.

110 Electron cryo-microscopy (cryo-EM) reveals that the HIV stem-loop docks into the A site

111 Cryoelectron microscopy (cryo-EM) showed that engagement of both eIF2B regulatory site

112 Cryo-electron microscopy (cryo-EM) showed that the design is accurate and can simultane

113 Electron cryo-microscopy (cryo-EM) single-particle analysis has yielded protein structu

114 ngle-particle cryo-electron microscopy (cryo-EM) snapshots of ryanodine receptor type 1 (RyR1), a cal

115 3.4 angstrom cryo-electron microscopy (cryo-EM) structure of a neutralizing monoclonal Fab-spike com

116 etermined the cryo-electron microscopy (cryo-EM) structure of alpha-synuclein fibrils containing the

117 3.8- angstrom cryo-electron microscopy (cryo-EM) structure of CDT, a bipartite toxin comprised of the

118 5.8- angstrom cryoelectron microscopy (cryo-EM) structure of EEEV complexed with the HS analog hepar

119 rom resolution cryoelectron microscopy (cryo-EM) structure of gammaTuRC, combined with crosslinking m

120 we report the cryo-electron microscopy (cryo-EM) structure of Homo sapiens CHD4 engaged with a nucleo

121 solution cryogenic electron microscopy (cryo-EM) structure of palmitoleated human WNT8A in complex wi

122 determined the cryoelectron microscopy (cryo-EM) structure of Streptococcus thermophilus Rgg3 bound t

123 determine the cryoelectron microscopy (cryo-EM) structure of the channel functionally arrested by ta

124 we present a cryo-electron microscopy (cryo-EM) structure of the Escherichia coli 50S subunit at an

125 A cryoelectron microscopy (cryo-EM) structure of the IRP2-FBXL5-SKP1 complex reveals tha

126 3.3- angstrom cryoelectron microscopy (cryo-EM) structure of the serotype I FIPV spike (S) protein,

127 ow-resolution cryo-electron microscopy (cryo-EM) structure of this large membrane-bound protein compl

128 re, we report cryo-electron microscopy (cryo-EM) structures of an intact Escherichia coli class-II CA

129 determined the cryoelectron microscopy (cryo-EM) structures of chromatosomes containing 197 bp DNA an

130 gh-resolution cryo-electron microscopy (cryo-EM) structures of cucumber leaf spot virus and red clove

131 re, we report cryo-electron microscopy (cryo-EM) structures of DNA-bound Drosophila ORC with and with

132 we report the cryoelectron microscopy (cryo-EM) structures of DNA-PKcs (DNA-PK catalytic subunit) bo

133 e, we present cryo-electron microscopy (cryo-EM) structures of translationally inactive yeast and hum

134 we report the cryoelectron microscopy (cryo-EM) structures of two termination process intermediates.

135 we present two cryoelectron microscopy (cryo-EM) structures of UCN1-bound CRF1R and CRF2R with the st

136 igh-resolution cryoelectron microscopy (cryo-EM) structures reveal that the binding sites for PF 0688

137 Cryoelectron microscopy (cryo-EM) structures reveal the essential tubulin tail glutama

138 Recent cryoelectron microscopy (cryo-EM) studies of TRPM8 have shown distinct structural feat

139 hemistry, and cryo-electron microscopy (cryo-EM) to investigate the functions of two NPET-associated

140 genetics and cryo-electron microscopy (cryo-EM) to study the high-resolution solution structures of

141 enerated using cryoelectron microscopy (cryo-EM), cross-linking mass spectrometry, and homology model

142 Using cryo-electron microscopy (cryo-EM), we determined the structure of human cohesin bound

143 ngle-particle cryo-electron microscopy (cryo-EM), we present evidence for extensive interactions betw

144 ngle particle cryo-electron microscopy (cryo-EM), we report reconstructions of the core complex of th

145 Using cryoelectron microscopy (cryo-EM), we resolved the first three-dimensional (3D) struct

146 Using cryoelectron microscopy (cryo-EM), we show that KCNE3 tucks its single-membrane-spanni

147 ombination of cryo-electron microscopy (cryo-EM), x-ray crystallography, and computational prediction

148 P complexes by cryoelectron microscopy (cryo-EM).

149 l analysis by cryo-electron microscopy (cryo-EM).

150 ructure using cryo-electron microscopy (cryo-EM).

151 ing, and cryogenic electron microscopy (cryo-EM).

152 We report multiple cryo-EM and X-ray structures in four different states, includ

153 Q-score analysis of multiple cryo-EM maps of the same proteins derived from different labo

154 timized spectroscopy (TROSY)-based NMR, cryo-EM, and biochemical assays show that, on binding Bz-LL o

155 ever, it has proved difficult to obtain cryo-EM reconstructions with sufficient resolution to visuali

156 Using a combined approach of cryo-EM and atomistic molecular dynamics simulation, we prese

157 a route towards routine application of cryo-EM in high-throughput screening of small molecule modula

158 e developed a program for assessment of cryo-EM map quality.

159 y well with the estimated resolution of cryo-EM maps for both protein and RNA.

160 the sub-nanometer resolution imaging of cryo-EM.

161 scopy with use of the negative stain or cryo-EM imaging.

162 Using our cryo-EM structure as a testbed, we developed a program for as

163 uman Fzd5 determined by single-particle cryo-EM at 3.7 angstrom resolution, with the aid of an antibo

164 A single particle cryo-EM reconstruction of an ~160-kD N-terminal fragment of t

165 Here we present single-particle cryo-EM studies of ABCG2 in the apo state, and bound to the t

166 Here, we used single-particle cryo-EM to analyze the three-dimensional structure of the mat

167 We used single-particle cryo-EM to reveal the organisation and architecture of the co

168 Single-particle cryo-EM unveils that ArfB employs two modes of function depen

169 main was not visible in a postcatalytic cryo-EM structure.

170 Here, we present cryo-EM maps of SARM1 at 2.9 and 2.7 angstrom resolutions.

171 Here we present cryo-EM structures of human TMEM175 in open and closed confor

172 We present cryo-EM structures of piggyBac transpososomes: a synaptic com

173 We present cryo-EM structures of the Saccharomyces cerevisiae Polzeta ho

174 Recent cryo-EM analyses of mammalian and yeast complex I have revolu

175 However, recent cryo-EM studies of CENP-A NCP complexes comprising primarily

176 Here we report cryo-EM data for the substrate, creatine kinase (CKB) bound t

177 Here, we report cryo-EM reconstructions of a core complex lacking Cag3 and an

178 Here we report cryo-EM structures of bovine bestrophin-2 (bBest2) bound and

179 We report Cryo-EM structures of Glt(Ph) reconstituted into nanodiscs, i

180 Here we report cryo-EM structures of TRPC6 in both antagonist-bound and agon

181 t and present a 3.2 angstrom resolution cryo-EM reconstruction of the 50S-RsfS complex together with

182 ilament from a 3.5- angstrom-resolution cryo-EM reconstruction, and show that it has 11 protofilament

183 We developed a high-resolution cryo-EM refinement method that divides an imaged microtubule

184 re we report a ~3.9 angstrom resolution cryo-EM structure of activated Schizosaccharomyces pombe Arp2

185 e describe the 3.0- angstrom resolution cryo-EM structure of complex I from mouse heart mitochondria

186 e, we present a 3.1 angstrom resolution cryo-EM structure of the Desulfovibrio vulgaris type I-C Casc

187 We present the high-resolution cryo-EM structure of the human processive Pol delta-DNA-PCNA

188 , we report the 2.9 angstrom resolution cryo-EM structure of the TEN2-LPHN3 complex, and describe the

189 Furthermore, we present high-resolution cryo-EM structures of the Leishmania tarentolae proteasome in

190 ds, including TEM, AFM, high-resolution cryo-EM, and SAXS/WAXS measurements, reveals that the sheet a

191 ue that is ready to use for large-scale cryo-EM-based structure modeling and atomic-level density map

192 Using real and simulated cryo-EM data, we show that FTIP could be applied in the futur

193 To address this question, we solved cryo-EM structures of Msp1-substrate complexes at near-atomic

194 TYGRESS combines the advantages of SP-cryo-EM (images with good signal-to-noise ratio and contrast,

195 e-particle cryo-electron microscopy (SP-cryo-EM) routinely reaches near-atomic resolution of isolated

196 ESS) that is a hybrid of cryo-ET and SP-cryo-EM, and is able to achieve close-to-nanometer resolution

197 ic resonance (NMR) and H1 tail-swapping cryo-EM experiments revealed that the C-terminal tails of the

198 ying chain lengths, we demonstrate that cryo-EM can distinguish bilayer thickness differences as smal

199 Here, we report the cryo-EM and crystal structures of human STAT2 (hSTAT2) in com

200 g AAV Rep function, we investigated the cryo-EM and X-ray structures of Rep68-ssDNA complexes.

201 nd visualize the protein just above the cryo-EM grid surface.

202 New designs of the cryo-EM grids-aimed at preserving thin, uniform vitrified ice

203 remains a challenging early step in the Cryo-EM pipeline due to the diversity of particle shapes and

204 vement remain in various aspects of the cryo-EM single-particle analysis workflow (e.g., sample prepa

205 Here, we present the cryo-EM structure of a frog pannexin 1 (Panx1) channel at 3.0

206 We report here the cryo-EM structure of a six-protein core COMPASS subcomplex, w

207 ue, Malik et al. (2020) (1) present the cryo-EM structure of polymerase zeta and show how it catalyze

208 Here, the cryo-EM structure of PRC2 on dinucleosomes reveals how bindin

209 Here we report the cryo-EM structure of recombinant full-length hIAPP fibrils.

210 Here, we report the cryo-EM structure of the CENP-A 601 NCP determined by Volta p

211 Three recent papers report the cryo-EM structure of the complete ASFV virion, comprising a v

212 Here we report the cryo-EM structure of the complete EC* that contains RTF1, a d

213 Here, we present the cryo-EM structure of the UMOD filament core at 3.5 angstrom r

214 Here, we report the cryo-EM structure of VopQ bound to the V(o) subcomplex of the

215 The cryo-EM structure, combined with small-angle X-ray scattering

216 Here, we report the cryo-EM structures of heptameric PA channels with partially u

217 Here, we report the cryo-EM structures of human ZnT8 (HsZnT8) in both outward- an

218 mHsp10(7))(2) football complex, and the cryo-EM structures of the ADP-bound successor mHsp60(14)-(mHs

219 ng and storage of biopharmaceuticals to cryo-EM analysis of protein complexes.

220 ate image orientation using traditional cryo-EM.

221 Here, we report two cryo-EM structures of the intact V-ATPase from bovine brain w

222 Here, using cryo-EM single particle analysis we describe the equilibrium

223 Here, using cryo-EM, we determine the structures of human SERINC5 and its

224 chondrial ribosome (mitoribosome) using cryo-EM.

225 plex (NPC) continues to be refined with cryo-EM and x-ray crystallography, in vivo conformational cha

226 PCR in 40 patients with physician-diagnosed EM, 28 of whom were confirmed to have LB by skin biopsy

227 ence of the main drivers of ectomycorrhizal (EM) fungal communities along elevation and environmental

228 rarchical model by implementing an efficient EM algorithm.

229 To prevent the electromagnetic (EM) wakefields excitation, protect detectors from damage

230 ic SR and focused ion beam-milled block-face EM across entire vitreously frozen cells.

231 ngitudinal metagenomic count data and a fast EM-IWLS algorithm for fitting ZINBMMs.

232 tron microscopy (nsEM), a popular method for EM sample screening.

233 of the conventional materials, protect from EM fields and supress undesirable phenomena.

234 reparation of robust and ultraclean graphene EM grids remains challenging.

235 HPV-EM achieved 97-100% accuracy when benchmarked using cell

236 Using HPV-EM, we demonstrated HPV genotypic differences in recurre

237 Importantly, EM networks propagated NSC depletion and its negative ef

238 gal diversity and bacteria : fungi ratios in EM-dominated habitats are driven by monodominance of woo

239 n induced a similar rapid, early response in EM and TEMRA CD8(+) T cells, CD16 engagement resulted in

240 rimental difficulties at least partially, LP-EM has evolved into a new microscopy method with nanomet

241 cts in human naive (NV) and effector memory (EM) CD8(+) T cells under non-activated and activated (2

242 nstruction of a volume electron microscopic (EM) image of the female brain, we map all inputs and out

243 sed conformation, while electron microscopy (EM) and molecular dynamic (MD) simulations suggest a lar

244 Here we present cryo-electron microscopy (EM) data resolving the EC1 and EC1+2 domains of human CD

245 ment of high-resolution electron microscopy (EM) demands a background-noise-free substrate to support

246 lectron density maps or electron microscopy (EM) density maps, and export files for 3D printing.

247 Electron microscopy (EM) has been the gold standard for connectivity analysis

248 eomics measurements and electron microscopy (EM) imaging are used to further characterize the EVs and

249 Electron microscopy (EM) is widely used for studying cellular structure and n

250 Electron microscopy (EM) of primary hepatocytes or hepatocyte-derived cell li

251 amined these factors by electron microscopy (EM).

252 presenting with or without erythema migrans (EM) or an annular, expanding skin lesion and uninfected

253 reported for their electrophoretic mobility (EM) measurements.

254 We used eye movement (EM) monitoring during a partial-cue recognition memory t

255 of each other onto the surface of a nanowire EM grid, and the mixing reaction stops when the grid is

256 likelihood estimates, we developed a nested EM algorithm, in which closed-form updates are available

257 erved allow engineering materials capable of EM field control, instability suppression including thos

258 We found clear evidence of EM fungal suppression of C and N cycling in the Pinus-do

259 In contrast, increased frequency of EM CD8(+) T cells associated with reduced risk of graft

260 g the graphene grids and expand the scope of EM imaging.

261 cterization by x-ray crystallography, NMR or EM.

262 is mathematically equivalent to the original EM algorithm commonly used in GLMM construction.

263 putation, single imputation, and a penalized EM algorithm incorporating non-random missingness (PEMM)

264 Conductive foils or wires providing EM protection and required thermal and mechanical proper

265 As anticipated, PSMA-EMs showed increased cellular internalization in PSMA po

266 Participants reinstated encoding-related EMs following degraded retrieval cues and this reinstate

267 y via the recapitulation of encoding-related EMs or gaze reinstatement.

268 endrite that matched the previously reported EM-reconstructed synapse distributions.

269 level structural models using low-resolution EM density maps.

270 ns, which allow for low-to-medium resolution EM density map-guided structure modeling starting from a

271 Using negative stain EM analysis and functional assays, we demonstrate that h

272 we observe such structures by negative stain EM of in vitro assembly reactions.

273 Moreover, negative-stain EM with full-length antibodies disclosed a stable, ring-

274 two immunodominant effector memory CD4(+) T(EM) cell epitopes, amino acids (aa) 129 to 143 of VP11/1

275 he two immunodominant human VP11/12 CD4(+) T(EM) cell epitopes, but not with cryptic epitopes, induce

276 quency of antiviral effector memory CD4(+) T(EM) cells specific to two immunodominant epitopes derive

277 ld boost effector memory CD4(+) and CD8(+) T(EM) cell responses is discussed.

278 of multifunctional effector memory CD8(+) T(EM) cells in ASYMP individuals, the SYMP individuals pre

279 onist reduced hypertension-specific CD8(+) T(EM) cells in the bone marrow and reduced the hypertensiv

280 individuals presented dysfunctional CD8(+) T(EM) cells, expressing major exhaustion pathways.

281 Importantly, LN-derived T(EM) cells are a probable source of HIV-1 genomes capable

282 DNA sequences increased within PB-derived T(EM) cells.

283 persistence is particularly significant in T(EM) cells.

284 ming and survival of hypertension-specific T(EM) cells in the bone marrow after they are formed in hy

285 LN-derived effector memory T (T(EM)) cells contained HIV-1 DNA that was genetically iden

286 at the engineered anti-PSMA peptide-targeted EMs can be a promising drug delivery system for advanced

287 The targeted EMs were produced from anti-PSMA peptide, WQPDTAHHWATL,

288 cilities including particle accelerators the EM field control is required.

289 the first time the effect of dilution on the EM of U87 glioblastoma cell-derived and plasma-derived s

290 This indicates that the EM of EVs is only a function of the salt concentration o

291 rotein-protein docking of tropomyosin to the EM models.

292 Through EM reconstruction of all LC6 synaptic inputs to the glom

293 otential, and transfer of (13) CO(2) through EM to explore mechanisms linking stored NSCs to plant wa

294 Transmission EM revealed abundant autophagosome formation in response

295 Herein, we used transmission EM, biochemical assays, and solid-state NMR spectroscopy

296 es (LNCaP and C4-2B), compared to unmodified EMs.

297 Here, we used EM to show that actin filaments convert directly into gl

298 Using EM analysis, we demonstrate that in the absence of phosp

299 is and cell types, which are estimated using EM.

300 Using several biochemical assays along with EM and epifluorescence microscopy, to the best of our kn