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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
42 ascent flagellar filaments became visible in electron micrographs and over 40% of the cells exhibited
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
52 ructural analysis by image reconstruction of electron micrographs based on averaging many identical p
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
63 t to pick out even quite large components in electron micrographs, despite nominally high resolution.
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
68 ve for three-dimensional reconstruction from electron micrographs due to the fact that projections of
70 ane resolution derived from a tilt series of electron micrographs established the solvent content of
73 e (EPS) in Mollicutes has been inferred from electron micrographs for over 50 years without conclusiv
79 As a case study, we analyze cross-sectional electron micrographs from the fornix of young and old rh
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"
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
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
100 ar NO3(-) chloride channel transporters plus electron micrographs indicating enlarged vacuoles sugges
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
108 f the lattice and its appearance in filtered electron micrographs, molecular models were used to dete
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
115 ifferences that have previously been seen in electron micrographs of actin filaments manifest themsel
120 ry of cytochrome oxidase, and morphometry of electron micrographs of biopsy specimens to determine wh
124 brane and have aberrant particle morphology; electron micrographs of cells expressing some of these m
128 1.5 and 1.8, respectively), consistent with electron micrographs of ClpAP that show a single tetrade
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
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
140 s in the junctional structure discernible in electron micrographs of glutaraldehyde-fixed cell materi
144 in a model polymer electrolyte membrane from electron micrographs of individual acidic clusters.
147 y, using three-dimensional reconstruction of electron micrographs of interacting filaments, we have b
153 o-stained histological sections and scanning electron micrographs of multiple stages of salivary glan
159 aments to c. 26 A resolution determined from electron micrographs of negatively stained preparations
162 ipt cleavage factor GreB was determined from electron micrographs of negatively stained, flattened he
164 c reticulum (SR) network, as demonstrated by electron micrographs of osmium ferrocyanide-stained SR i
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
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
183 ical sections imaged by light microscopy, or electron micrographs of single ultrathin sections imaged
188 immunostaining of fimbrial preparations and electron micrographs of the bacteria, revealed that surf
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
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.
211 structure of the heterodimer determined from electron micrographs of unstained frozen-hydrated tubula
218 loid-like peptides formed fibrils visible in electron micrographs or needle-like microcrystals showin
220 +/-35 degree filaments seen in lamellipodial electron micrographs, requiring approximately 12 generat
224 a-catenin and E-cadherin, was increased, and electron micrographs revealed an apico-basal diffusion o
229 by plasma sputtering deposition and scanning electron micrographs revealed nano-clusters of metal cat
239 citatory synapses, reconstructed from serial electron micrograph sections of mouse brain, and have co
246 ation of DNA-containing nuclear capsids, but electron micrographs show no enveloped virus particles i
255 was observed in SDS-PAGE while transmission electron micrographs showed complete dispersion of aggre
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
279 for the number of mitochondrial profiles in electron micrographs, the levels of selected energy meta
282 nnels are recognizable in negatively stained electron micrographs, these lattices are disordered and
284 achieved by taking a series of transmission electron micrographs tilted at different angles in vitre
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
292 rmine the lattice dimensions and analysis of electron micrographs was used to determine the lattice s
294 based on partial reconstructions from serial electron micrographs, we quantify synaptic circuits for
296 optic nerve samples, light, and transmission electron micrographs were used to evaluate optic atrophy
298 proliferation of the IM (up to 19 layers in electron micrographs) without significant effects on pla
300 as monitored by (29)Si-MAS NMR, transmission electron micrographs, X-ray diffraction, and adsorption
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