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1 uick assessment, sorting and hole masking of electron micrographs.
2 nd a presynaptic dense projection protein in electron micrographs.
3 at previously estimated from the analysis of electron micrographs.
4 th basal dendrites reconstructed from serial electron micrographs.
5 oncentric rings when reconstructed from cryo-electron micrographs.
6 s, confirming findings that we obtained from electron micrographs.
7 os, and exhibited thicker fibers in scanning electron micrographs.
8 al repair was observed in nemaline muscle in electron micrographs.
9  explanation for the small ECS visualized in electron micrographs.
10 crystalline aggregates of protein and DNA in electron micrographs.
11  periodically arranged troponin complexes in electron micrographs.
12 rk-staining outer spore coat in thin-section electron micrographs.
13 le cell layer were reconstructed from serial electron micrographs.
14 apsids from cryo-negative stain transmission electron micrographs.
15 eurotransmitter release as well as examining electron micrographs.
16  to be identical to the wild-type virions in electron micrographs.
17 , thereby facilitating interpretation of the electron micrographs.
18 it bridges that are visible in reconstructed electron micrographs.
19 e-dimensional (3D) image reconstruction from electron micrographs.
20 ls constructed from stereo pairs of scanning electron micrographs.
21 he whole myosin-I tail in reconstructions of electron micrographs.
22 500 individual particles extracted from cryo-electron micrographs.
23 tructures that could be seen in thin-section electron micrographs.
24  the appearance of morphological features in electron micrographs.
25  thicker than those of epicotyl V-ATPases in electron micrographs.
26 se information from the Fourier transform of electron micrographs.
27  coarse subunit mapping onto 2-D images from electron micrographs.
28 e folds independently of their appearance in electron micrographs.
29 n osmiophilic precipitate that is visible in electron micrographs.
30 racterization of the leaves and to light and electron micrographs.
31  and performed unbiased disector counts from electron micrographs.
32 e particles with low detergent background in electron micrographs.
33 ic cells and reconstructed in 3D from serial electron micrographs.
34 ensional reconstructions from serial-section electron micrographs.
35 r the nanoscopic localization of proteins in electron micrographs.
36 ermined by single-particle reconstruction of electron micrographs a low-resolution, 3D structure of S
37         Correlation of immunofluorescent and electron micrographs allowed high resolution imaging of
38                                           On electron micrographs an average filament length of appro
39                                              Electron micrographs and biochemical data with a PFKL/PF
40  smooth muscle cells (SMCs) were observed in electron micrographs and by confocal microscopy.
41                                              Electron micrographs and immunofluorescence staining of
42 ascent flagellar filaments became visible in electron micrographs and over 40% of the cells exhibited
43                                              Electron micrographs and quantitative measurements show
44 9 mature seeds supported results of scanning electron micrographs and quantitatively showed depletion
45 microscopy, x-ray diffraction, simulation of electron micrographs, and molecular model building was u
46 r VGlut1-positive puncta, larger profiles in electron micrographs, and more release sites per profile
47 properties of a dimer, appears as a dimer in electron micrographs, and moves processively on actin fi
48               ClpP and proClpP(SA), which in electron micrographs appear to have subunits arranged in
49                        However, conventional electron micrographs are simply two-dimensional projecti
50               Helical 3D reconstruction from electron micrographs at 20 A resolution provides a struc
51                          As observed in cryo-electron micrographs, AVP-p treatment causes morphologic
52 ructural analysis by image reconstruction of electron micrographs based on averaging many identical p
53 uced thick-filament cross-sectional areas in electron micrographs by 44%.
54                                     Scanning electron micrographs confirm high imprint fidelity and p
55                                              Electron micrographs confirmed the lack of intact presyn
56                         Both amperometry and electron micrograph data were analyzed by statistical an
57                                           In electron micrographs, degenerating granule neurons displ
58 between nuclei in the cyst, and transmission electron micrographs demonstrate fusion between cyst nuc
59 he latter case, freeze-fracture transmission electron micrographs demonstrate that at least some of t
60                                              Electron micrographs demonstrated C3 molecules on the ce
61                      Examination of numerous electron micrographs demonstrated that enveloped virions
62                 Quantitative analysis of the electron micrographs demonstrated that the starch conten
63 t to pick out even quite large components in electron micrographs, despite nominally high resolution.
64          IR and X-ray absorption spectra and electron micrographs determine the structures and locati
65 alculated from disc membrane regions on such electron micrographs displayed a diffuse ring at approxi
66 icated that gastric glands were dilated, and electron micrographs displayed a distinct and striking a
67 nt concerns regarding the originality of the electron micrographs displayed in Fig. 1.
68 ve for three-dimensional reconstruction from electron micrographs due to the fact that projections of
69                                              Electron micrograph (EM) images of these mutants showed
70 ane resolution derived from a tilt series of electron micrographs established the solvent content of
71                                              Electron micrographs extended these findings and reveale
72                                              Electron micrographs first confirmed that the eukaryotic
73 e (EPS) in Mollicutes has been inferred from electron micrographs for over 50 years without conclusiv
74                      The 130 high resolution electron micrographs from aging rhesus monkey (Macaca mu
75                                              Electron micrographs from diabetic eNOS KO mice revealed
76                                 Transmission electron micrographs from humans and mice treated with i
77                                              Electron micrographs from previous studies show these pl
78                                              Electron micrographs from the 1960s revealed the presenc
79  As a case study, we analyze cross-sectional electron micrographs from the fornix of young and old rh
80 escence correlated with organelles imaged in electron micrographs from the same sections.
81 -scale acquisition of high-resolution serial electron micrographs from which neuronal arbors can be r
82 nal processes and synaptic connections using electron micrographs generated in a previous study of th
83 d 110 kDa, and single-particle processing of electron micrographs gives size estimates of 70-90 kDa.
84 ne caveolae and mitochondria (first noted in electron micrographs >50 yr ago) and caveolae-mitochondr
85 pecific proteins or cellular compartments in electron micrographs, however, remains challenging becau
86  "learns" from the thin section transmission electron micrograph image (2D) or the "seed and growth"
87                                In one study, electron micrograph image averages of the headpiece of i
88       Past attempts to detect tropomyosin in electron micrograph images of frozen-hydrated troponin-r
89 e we report a 3D single-particle analysis of electron micrograph images of negatively stained myosin
90    Single particle analysis of the resulting electron micrograph images, to which no symmetry was app
91     With three-dimensional reconstruction of electron micrograph images, we show that Hib pili compri
92 gle uniformity was quantified using scanning electron micrographs in cesa9 epidermal cells.
93                                              Electron micrographs indicate that chlamydiae possess ne
94                        Hydrodynamic data and electron micrographs indicate that the active state is e
95 s, as well as images from negatively stained electron micrographs, indicate that pore formation is as
96 atment reversibly inhibited vesicle cycling; electron micrographs indicated a dramatic reduction in t
97                                              Electron micrographs indicated that all of LMM 59 is loc
98                                              Electron micrographs indicated that modified epithelial
99                    Image reconstruction from electron micrographs indicates that a symmetric oligomer
100 ar NO3(-) chloride channel transporters plus electron micrographs indicating enlarged vacuoles sugges
101                                           In electron micrographs, individual CAR-deficient cardiomyo
102 omputational methods, we incorporated serial electron micrographs into a three-dimensional reconstruc
103 tion achieved in the image processing of the electron micrographs is on the order of 9 A in the merid
104 anisms in stained smears and in transmission electron micrographs is that of P. carinii, and P. carin
105 racting doublecortin domain observed in cryo-electron micrographs is the C-terminal domain rather tha
106 tein obstructions shown in many transmission electron micrographs led to a discussion about the mode
107         Its striated, periodic appearance in electron micrographs led to the idea that transverse fil
108 f the lattice and its appearance in filtered electron micrographs, molecular models were used to dete
109                  The field-emission scanning electron micrograph of the surface indicates nanostructu
110   We have applied correspondence analysis to electron micrographs of 2-D rafts of F-actin cross-linke
111 arrangement enabled serial reconstruction of electron micrographs of a flat, punctate zone, identifie
112                                              Electron micrographs of a JCSC1435 mutant with a deleted
113                  Interestingly, transmission electron micrographs of abscission zone regions from wil
114                                 We show that electron micrographs of acrosomal bundles in water are s
115 ifferences that have previously been seen in electron micrographs of actin filaments manifest themsel
116                               An analysis of electron micrographs of Al5Mn quasicrystals obtained by
117                                              Electron micrographs of aldehyde-fixed control PNJs, in
118                                              Electron micrographs of at least 15 keratocytes each fro
119                                              Electron micrographs of atrial myocytes show peripheral
120 ry of cytochrome oxidase, and morphometry of electron micrographs of biopsy specimens to determine wh
121 bed 50 years ago by analysis of transmission electron micrographs of bone marrow.
122                   The RNP polymer, viewed in electron micrographs of both virus RNP and RNP reconstit
123                                 In addition, electron micrographs of Cav-1-deficient lung capillaries
124 brane and have aberrant particle morphology; electron micrographs of cells expressing some of these m
125        Correlative thin-section transmission electron micrographs of cells fixed one second after irr
126                                              Electron micrographs of cells infected with the delta vp
127                                              Electron micrographs of CIP4-null megakaryocytes showed
128  1.5 and 1.8, respectively), consistent with electron micrographs of ClpAP that show a single tetrade
129                                              Electron micrographs of crosslinked, rotary shadowed spe
130      On the basis of our kinetic results and electron micrographs of depolymerizing fibers, we propos
131 ch calculations that image reconstruction of electron micrographs of disulfide cross-linked C41-C374
132                                 In addition, electron micrographs of Drosophila and other flies (e.g.
133                                       Immuno-electron micrographs of embryos expressing sAnxV::GFP or
134                   Embedment-free, immunogold electron micrographs of extracted cell whole mounts show
135                                              Electron micrographs of fibroblasts at 3 or 5 days posti
136  as well as from single-molecule imaging and electron micrographs of fixed cells, and provides the ma
137 ple structure are produced which are seen in electron micrographs of freeze-fracture replicas with pe
138                            Here we have used electron micrographs of frozen-hydrated two-dimensional
139 rough the nuclear pore, as observed in early electron micrographs of giant Balbiani ring mRNPs.
140 s in the junctional structure discernible in electron micrographs of glutaraldehyde-fixed cell materi
141                                 Transmission electron micrographs of GS52 silenced root nodules showe
142                                              Electron micrographs of hearts from TPC1/2 double knocko
143                                              Electron micrographs of HRP-containing axons as well as
144 in a model polymer electrolyte membrane from electron micrographs of individual acidic clusters.
145                                              Electron micrographs of infected cells revealed a large
146                                              Electron micrographs of insect mouthparts indicate that
147 y, using three-dimensional reconstruction of electron micrographs of interacting filaments, we have b
148                                              Electron micrographs of Listeria-infected hepatocytes de
149                                              Electron micrographs of livers from TgBP-1a mice showed
150                                           In electron micrographs of longitudinal sections of fast fi
151                                     Scanning electron micrographs of lung tissue, focusing on the int
152                        Furthermore, scanning electron micrographs of mitochondria from LKT-treated BL
153 o-stained histological sections and scanning electron micrographs of multiple stages of salivary glan
154                                              Electron micrographs of myosin-18A motor domain-decorate
155 ing that it corresponds to the hinge seen in electron micrographs of NCAM.
156                                              Electron micrographs of negatively stained ClpXP prepara
157                                              Electron micrographs of negatively stained E. faecalis c
158                                              Electron micrographs of negatively stained intact flagel
159 aments to c. 26 A resolution determined from electron micrographs of negatively stained preparations
160                                           In electron micrographs of negatively stained samples, Arp2
161              The Raman data are supported by electron micrographs of negatively stained specimens of
162 ipt cleavage factor GreB was determined from electron micrographs of negatively stained, flattened he
163                                     Scanning electron micrographs of neutrophils rolling on P-selecti
164 c reticulum (SR) network, as demonstrated by electron micrographs of osmium ferrocyanide-stained SR i
165                                              Electron micrographs of osmotically shocked cells showed
166                                              Electron micrographs of pancreas depicted macrophages in
167                                           In electron micrographs of permeabilized hippocampal synaps
168                                         Cryo-electron micrographs of purified Syn5 virions revealed t
169                                           In electron micrographs of quick-frozen, deep-etched sample
170 cern such relationships by inspection of the electron micrographs of rafts, but easy by examination o
171   The 1.93-A crystal structure of RVFV N and electron micrographs of ribonucleoprotein (RNP) reveal a
172 alyzed a reported distribution obtained from electron micrographs of RNA polymerase molecules along r
173                          Here we report that electron micrographs of rsh mutant cells lacking RSH ext
174 us cone terminals and their bipolar cells in electron micrographs of serial sections from macaque fov
175 were used to estimate numbers of synapses in electron micrographs of serial sections processed for po
176 Reconstructing neurons in macaque fovea from electron micrographs of serial sections, we identified s
177 Using three-dimensional reconstructions from electron micrographs of serial transverse sections, amph
178 15 MII spindles by using reconstruction from electron micrographs of serially sectioned meiotic cells
179 region T(iii) observed in computer-processed electron micrographs of sigma1 protein purified from vir
180 onstruction of biological molecules from the electron micrographs of single particles.
181 rating structures of variable size from cryo-electron micrographs of single particles.
182 ned by three-dimensional reconstruction from electron micrographs of single particles.
183 ical sections imaged by light microscopy, or electron micrographs of single ultrathin sections imaged
184                                              Electron micrographs of SOD2-deficient reticulocytes rev
185                                              Electron micrographs of spinal cords immunostained with
186 from T7 simulations are consistent with cryo-electron micrographs of T7 phage DNA.
187                                              Electron micrographs of the arrays are suitable for heli
188  immunostaining of fimbrial preparations and electron micrographs of the bacteria, revealed that surf
189                             Diffraction from electron micrographs of the crystals in negative stain e
190                                              Electron micrographs of the DeltaalgL mutant showed that
191                                              Electron micrographs of the F. tularensis LVS Delta ripA
192            This model is consistent with the electron micrographs of the fibre and it was supported b
193  labelled His tag by statistical analysis of electron micrographs of the gold-labelled photosystem II
194  Looking again at Larry's paper, I found the electron micrographs of the kDNA networks to be rather b
195            Flagellar stains and transmission electron micrographs of the motile S. pullorum culture s
196                                              Electron micrographs of the mutant revealed larger cells
197                   We present high-resolution electron micrographs of the OM usher PapC and show that
198        Collectively, our NMR spectra and the electron micrographs of the purified ECM inspire us to c
199                                              Electron micrographs of the purified inflammasome provid
200  glycocalyx depth (0.078 +/- 0.016 mum) from electron micrographs of the same portion of the same ves
201 hree dimensions to 23 A resolution from cryo-electron micrographs of the singly bound complex, PA200
202  of mitochondrial membrane integrity seen in electron micrographs of the transplanted 48-hr group.
203                                              Electron micrographs of the variant operon suggest that
204                                              Electron micrographs of thin sections of cells infected
205                                       Immuno-electron micrographs of thin sections of rat atrial myoc
206                                              Electron micrographs of this complex are presented, and
207                                         Cryo-electron micrographs of tilted Afp specimens (up to 60 d
208                       In this study, we used electron micrographs of tissues prepared using perfusion
209                                              Electron micrographs of toxin-induced cells showed no ob
210                                 Transmission electron micrographs of type I collagen fibrils in a pro
211 structure of the heterodimer determined from electron micrographs of unstained frozen-hydrated tubula
212                     Image reconstructions of electron micrographs of virus particles containing wild-
213 the axial density distribution of A-bands in electron micrographs of well-preserved specimens.
214                                     However, electron micrographs of WPBs at the Golgi apparatus show
215                                              Electron micrographs of ZapA-bundled FtsZ filaments show
216                                              Electron micrographs offer clear evidence of pores creat
217                                 Transmission electron micrographs on thin films of these composites s
218 loid-like peptides formed fibrils visible in electron micrographs or needle-like microcrystals showin
219                                     Based on electron micrographs, PAN and PAN(Delta1-73) apparently
220 +/-35 degree filaments seen in lamellipodial electron micrographs, requiring approximately 12 generat
221         Three-dimensional reconstructions of electron micrographs reveal a conformational difference
222                               Negative-stain electron micrographs reveal that filaments are apolar an
223                                 In addition, electron micrographs reveal the formation of tubular mye
224 a-catenin and E-cadherin, was increased, and electron micrographs revealed an apico-basal diffusion o
225                                              Electron micrographs revealed erythrostasis in tumor mic
226                               In this study, electron micrographs revealed fusion of differentiated m
227                                              Electron micrographs revealed large spaces between axons
228                                              Electron micrographs revealed lipid and mitochondrial ab
229 by plasma sputtering deposition and scanning electron micrographs revealed nano-clusters of metal cat
230                                     Scanning electron micrographs revealed presence of dents and fusi
231                                              Electron micrographs revealed stratified constructs with
232                                              Electron micrographs revealed that both water-deprived a
233                                              Electron micrographs revealed that D. mccartyi were abun
234                                     Scanning electron micrographs revealed that hair bundles exposed
235                        Furthermore, scanning electron micrographs revealed that KasA depletion result
236                                     Scanning electron micrographs revealed that the sonicated protein
237                                              Electron micrographs revealed that vesicular pools were
238                                              Electron micrographs revealed the cytoplasmic accumulati
239 citatory synapses, reconstructed from serial electron micrograph sections of mouse brain, and have co
240 legans adult male, reconstructed from serial electron micrograph sections.
241        Included are high-resolution scanning electron micrograph (SEM) images of the surface structur
242                       3D reconstruction from electron micrographs show a two-layer "simple" Z-band in
243                                              Electron micrographs show direct contact between endothe
244                                              Electron micrographs show mitochondria with swollen matr
245                                              Electron micrographs show morphological features indicat
246 ation of DNA-containing nuclear capsids, but electron micrographs show no enveloped virus particles i
247                 Published x-ray diagrams and electron micrographs show that fibers of synuclein, the
248                                              Electron micrographs show that the 100-A-thick fibers of
249                                              Electron micrographs show that the virion consists of a
250       Three-dimensional reconstructions from electron micrographs show that this peptide binds to the
251                                     Scanning electron micrograph showed well-shaped and smooth spheri
252                                     Scanning electron micrographs showed a protective shield of CP ar
253                                              Electron micrographs showed a stepwise entry and fusion
254                                              Electron micrographs showed collapsed capillaries, exten
255  was observed in SDS-PAGE while transmission electron micrographs showed complete dispersion of aggre
256                                              Electron micrographs showed gross abnormalities in the c
257                                     Scanning electron micrographs showed H. pylori arranged in a matr
258                                              Electron micrographs showed human fetal muscle myofibril
259                                              Electron micrographs showed human fetal muscle sarcomere
260                                     Scanning electron micrographs showed marked improvement in regula
261                                              Electron micrographs showed no significant difference in
262         Three-dimensional maps computed from electron micrographs showed that all three viruses have
263                                              Electron micrographs showed that in spoIIB mutant sporan
264                                 Thin-section electron micrographs showed that mutant cells did not fu
265                                              Electron micrographs showed that nebulin associates with
266        Furthermore, serial reconstruction of electron micrographs showed that postsynaptic cisterns o
267                                              Electron micrographs showed that the alternative conform
268                                              Electron micrographs showed that the bottom and top meta
269                                              Electron micrographs showed that these side polar filame
270                                              Electron micrographs showed the presence of the insectic
271                   A geometric model based on electron micrographs suggested that this surface is magn
272 t on active zone structure, as visualized by electron micrographs, suggesting that their contribution
273 e, the presence of intact axonal profiles in electron micrographs taken at the lesion site, and/or th
274                                 Transmission electron micrographs (TEM) of infected cells treated wit
275                                 Transmission electron micrographs (TEMs) were analyzed to determine f
276                                           In electron micrographs the M/T to granule cell synapse app
277                                           In electron micrographs, the AC is a highly vacuolated part
278                        In negatively stained electron micrographs, the isolated needles were 60-80 nm
279  for the number of mitochondrial profiles in electron micrographs, the levels of selected energy meta
280                                           In electron micrographs, the single fibers showed uniform e
281                                           In electron micrographs these filaments appeared sometimes
282 nnels are recognizable in negatively stained electron micrographs, these lattices are disordered and
283                     To aid interpretation of electron micrographs, three-dimensional model toroids we
284  achieved by taking a series of transmission electron micrographs tilted at different angles in vitre
285  cerevisiae has been reconstructed from cryo electron micrographs to a resolution of 35 A.
286 (BLiPs), whose size distribution is shown by electron micrographs to be skewed.
287 lly, we used serial morphometric analysis of electron micrographs to explore the basis for the progre
288 in the form of rings, which were observed in electron micrographs to have outside and inside diameter
289 three-dimensional reconstruction from serial electron micrographs to investigate two structural chang
290 pearance of the Z-band in transverse-section electron micrographs typically resembles a small-square
291                                Together with electron micrographs, visual inspection, and contact ang
292 rmine the lattice dimensions and analysis of electron micrographs was used to determine the lattice s
293                    From analysis of scanning electron micrographs, we find that median microvillar le
294 based on partial reconstructions from serial electron micrographs, we quantify synaptic circuits for
295                By reconstruction from serial electron micrographs, we show that L- and M-cone pedicle
296 optic nerve samples, light, and transmission electron micrographs were used to evaluate optic atrophy
297                     The article uses several electron micrographs which have been used in other publi
298  proliferation of the IM (up to 19 layers in electron micrographs) without significant effects on pla
299                                     Scanning electron micrographs, x-ray diffraction spectra, x-ray p
300 as monitored by (29)Si-MAS NMR, transmission electron micrographs, X-ray diffraction, and adsorption

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