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1  recording optical voltammograms in a single micrograph.
2 haracteristic footprint seen in the electron micrograph.
3 lowed us to identify this morphotype in STEM micrographs.
4  measured by direct counts of tiled confocal micrographs.
5 ubunit mapping onto 2-D images from electron micrographs.
6 itting an equation to widefield fluorescence micrographs.
7 e beads was measured using image analysis of micrographs.
8 ndependently of their appearance in electron micrographs.
9 ilic precipitate that is visible in electron micrographs.
10 tion of the leaves and to light and electron micrographs.
11 es with low detergent background in electron micrographs.
12 n relative chloroplast volume estimated from micrographs.
13 and reconstructed in 3D from serial electron micrographs.
14  on the spiral anode is clearly shown in SEM micrographs.
15 d the extremely low signal-to-noise ratio of micrographs.
16 reconstructions from serial-section electron micrographs.
17 oscopic localization of proteins in electron micrographs.
18 ynaptic dense projection protein in electron micrographs.
19 usly estimated from the analysis of electron micrographs.
20 dendrites reconstructed from serial electron micrographs.
21  rings when reconstructed from cryo-electron micrographs.
22 ming findings that we obtained from electron micrographs.
23 xhibited thicker fibers in scanning electron micrographs.
24  was observed in nemaline muscle in electron micrographs.
25 ed resolution is comparable to that of still micrographs.
26 ion for the small ECS visualized in electron micrographs.
27 ne aggregates of protein and DNA in electron micrographs.
28 tween immunogold particles in immunoelectron micrographs.
29 aset of 16227 scanning transmission electron micrographs.
30 roach for single particle picking in cryo-EM micrographs.
31 f a large number of candidate particles from micrographs.
32  document it with drawings and light and SEM micrographs.
33 ssment, sorting and hole masking of electron micrographs.
34  recognition of particle images from cryo-EM micrographs.
35 ormed unbiased disector counts from electron micrographs.
36 known 3D structures, in single electron cryo-micrographs.
37 ayer were reconstructed from serial electron micrographs.
38 y single-particle reconstruction of electron micrographs a low-resolution, 3D structure of S. cerevis
39 hometric features extracted from the digital micrographs, along with other non-morphometric data to p
40                                  On electron micrographs an average filament length of approximately
41                                 Cryoelectron micrograph analyses and 3D reconstructions showed that t
42 tility to the cryoEM community for improving micrograph and tomogram interpretability and acceleratin
43  results, negative-stain electron microscopy micrographs and a crystal structure of the Anbu particle
44                                     Electron micrographs and biochemical data with a PFKL/PFKP chimer
45  conditioned meshes generated from segmented micrographs and boundary marked tetrahedral meshes which
46 c methods were used to analyze the resultant micrographs and determine the age-related changes of the
47              We demonstrate by cryo electron micrographs and elongated tracer particles imaging, that
48                                      Optical micrographs and fluorescence analysis show the successfu
49 automatically traces nerve fibers in corneal micrographs and generates measures based on these traces
50                                     Electron micrographs and immunofluorescence staining of rat CB se
51                                     Electron micrographs and quantitative measurements show that glyc
52 seeds supported results of scanning electron micrographs and quantitatively showed depletion of secon
53 omimetic was characterized with fluorescence micrographs and temperature-dependent fluorescence recov
54 ortions from two-photon excited fluorescence micrographs and through data simulations was found to ex
55 ption signatures are correlated with optical micrographs and western blot tests.
56 racy on Ginkgo scanning electron microscropy micrographs, and 94.2% transfer accuracy when tested on
57 positive puncta, larger profiles in electron micrographs, and more release sites per profile.
58 s of a dimer, appears as a dimer in electron micrographs, and moves processively on actin filaments.
59               However, conventional electron micrographs are simply two-dimensional projections of th
60 es and PD dimensions (measured from electron micrographs) are both used as methods to predict PD tran
61      Helical 3D reconstruction from electron micrographs at 20 A resolution provides a structure of f
62                 As observed in cryo-electron micrographs, AVP-p treatment causes morphological change
63 analysis by image reconstruction of electron micrographs based on averaging many identical particles.
64 k-filament cross-sectional areas in electron micrographs by 44%.
65   Absorption spectra of different parts of a micrograph can readily be compiled using white-light ill
66 aining on a dataset composed of thousands of micrographs collected across a wide range of imaging con
67                            Scanning electron micrographs confirm high imprint fidelity and precision
68                                      The AFM micrographs confirmed a nanometric film of Fc-GO and PEI
69                                     Electron micrographs confirmed the lack of intact presynaptic ter
70                                      The SEM micrographs confirmed the successful capturing of E. col
71                Both amperometry and electron micrograph data were analyzed by statistical and machine
72                            Using an electron micrograph dataset for an entire Drosophila melanogaster
73 evident from pin-holes and eroded surface in micrographs, decreased % crystallinity and FTIR peaks.
74                                  In electron micrographs, degenerating granule neurons displayed a un
75 uclei in the cyst, and transmission electron micrographs demonstrate fusion between cyst nuclei.
76  case, freeze-fracture transmission electron micrographs demonstrate that at least some of the soluti
77             Examination of numerous electron micrographs demonstrated that enveloped virions were hou
78                   Immunofluorescent confocal micrographs demonstrated the enveloping membranous struc
79              Here we present scanning helium micrographs demonstrating image contrast arising from a
80                                          SEM micrographs depicted smoother surface for gelatin-MMT an
81  out even quite large components in electron micrographs, despite nominally high resolution.
82 IR and X-ray absorption spectra and electron micrographs determine the structures and locations of th
83 at gastric glands were dilated, and electron micrographs displayed a distinct and striking absence of
84 ns regarding the originality of the electron micrographs displayed in Fig. 1.
85                                           EM micrographs displayed packets of cellular material conta
86 ree-dimensional reconstruction from electron micrographs due to the fact that projections of these fi
87                                     Electron micrograph (EM) images of these mutants showed assembled
88                        Using serial electron micrograph (EM) reconstruction, we re-evaluate here the
89 ages from negative-stain electron microscopy micrographs (EM), a 3D density map from single-particle
90 ngle-particle recognition from noisy cryo-EM micrographs, enabling automated particle picking, select
91 eruginosa (CF-PA) isolates in vitro using 3D micrographs, Fiji and MATLAB.
92                        The electron scanning micrograph for the composite film was homogeneous, witho
93 he enrichment of single cells based on their micrographs for further downstream processing and analys
94 n Mollicutes has been inferred from electron micrographs for over 50 years without conclusive data to
95             The 130 high resolution electron micrographs from aging rhesus monkey (Macaca mulatta), p
96                                     Electron micrographs from diabetic eNOS KO mice revealed an injur
97                        Transmission electron micrographs from humans and mice treated with imatinib s
98                                     Electron micrographs from previous studies show these plaques to
99 tic 512 x 512 scanning transmission electron micrographs from spiral, jittered gridlike, and other pa
100                                     Electron micrographs from the 1960s revealed the presence of an S
101 e study, we analyze cross-sectional electron micrographs from the fornix of young and old rhesus monk
102 orrelated with organelles imaged in electron micrographs from the same sections.
103 quisition of high-resolution serial electron micrographs from which neuronal arbors can be reconstruc
104                      Atomic force microscopy micrographs further support the model of ganglioside-ind
105 , and single-particle processing of electron micrographs gives size estimates of 70-90 kDa.
106 r scale crystallographic defects in electron micrographs governed by complex contrast mechanisms is s
107 ae and mitochondria (first noted in electron micrographs >50 yr ago) and caveolae-mitochondria intera
108             Transmission electron microscope micrographs have confirmed the presence of wormlike fibr
109 roteins or cellular compartments in electron micrographs, however, remains challenging because of dif
110  from the thin section transmission electron micrograph image (2D) or the "seed and growth" model ima
111 ions requires watertight meshing of electron micrograph images into 3D volume meshes, which can then
112 rt a 3D single-particle analysis of electron micrograph images of negatively stained myosin filaments
113 rmity was quantified using scanning electron micrographs in cesa9 epidermal cells.
114 tomated particle extraction from raw cryo-EM micrographs in the absence of a template.
115                                     Electron micrographs indicate that chlamydiae possess needle fila
116               Hydrodynamic data and electron micrographs indicate that the active state is extended,
117           Image reconstruction from electron micrographs indicates that a symmetric oligomer is prese
118  chloride channel transporters plus electron micrographs indicating enlarged vacuoles suggested vacuo
119                                  In electron micrographs, individual CAR-deficient cardiomyocytes wit
120           Denoising with this model improves micrograph interpretability and allows us to solve 3D si
121 nal methods, we incorporated serial electron micrographs into a three-dimensional reconstruction of t
122 oublecortin domain observed in cryo-electron micrographs is the C-terminal domain rather than the N-t
123 ructions shown in many transmission electron micrographs led to a discussion about the mode of phloem
124 ts striated, periodic appearance in electron micrographs led to the idea that transverse filaments wi
125 ectrons per atom contributing to an electron micrograph may enable diffraction measurements of single
126 umber initially decreased (relative area per micrograph of 64+/-10% at baseline vs. 39+/-13% at 8 h f
127  1947, Sulzberger and colleagues published a micrograph of a blocked acrosyringium in a patient with
128 hest resolution (11-13 nm) x-ray diffraction micrograph of biological specimens, and a demonstration
129 nce intensity, emulsifying properties, light micrograph of emulsions and in vitro antioxidant activit
130         The field-emission scanning electron micrograph of the surface indicates nanostructured lamel
131  applied correspondence analysis to electron micrographs of 2-D rafts of F-actin cross-linked with al
132                                     Electron micrographs of a JCSC1435 mutant with a deleted cap regi
133         Interestingly, transmission electron micrographs of abscission zone regions from wild-type an
134                        We show that electron micrographs of acrosomal bundles in water are similar to
135                                     Electron micrographs of aldehyde-fixed control PNJs, in which TBs
136                                     Electron micrographs of atrial myocytes show peripheral SR cister
137                                Additionally, micrographs of bacteria adhered on a nanopatterned cicad
138                 Scanning electron microscopy micrographs of biofilms exposed to taurocholate revealed
139                                  Using BRIM, micrographs of biomarkers whose expression correlates wi
140  breast cancer aggressiveness are divided by micrographs of biomarkers whose expression negatively co
141 ars ago by analysis of transmission electron micrographs of bone marrow.
142          The RNP polymer, viewed in electron micrographs of both virus RNP and RNP reconstituted from
143  quantitative image analysis of fluorescence micrographs of cells undergoing apoptosis verifies that
144                                 Atomic-force micrographs of CH3-Ge(111) surfaces indicated that the s
145                                     Electron micrographs of CIP4-null megakaryocytes showed an altere
146 d generate a vascular area mask (VAM) in H&E micrographs of clear cell renal cell carcinoma (ccRCC) c
147                                              Micrographs of cultured cells exposed to the nanoparticl
148      The particle size analysis and confocal micrographs of digesta also suggest the size of fat and
149                        In addition, electron micrographs of Drosophila and other flies (e.g. the hous
150                                     Confocal micrographs of EGFP fusion proteins localized at key cel
151                              Immuno-electron micrographs of embryos expressing sAnxV::GFP or sGFP::La
152                                     Electron micrographs of fibroblasts at 3 or 5 days postinfection
153 as from single-molecule imaging and electron micrographs of fixed cells, and provides the mathematica
154 traightforward strategy to calibrate digital micrographs of fluorescent surfaces such as planar cellu
155 ture are produced which are seen in electron micrographs of freeze-fracture replicas with periodiciti
156 ection of single particles from low-contrast micrographs of frozen hydrated biomolecules by cryo-elec
157  nuclear pore, as observed in early electron micrographs of giant Balbiani ring mRNPs.
158                        Transmission electron micrographs of GS52 silenced root nodules showed that ea
159                                     Electron micrographs of hearts from TPC1/2 double knockout mice s
160                  The confocal laser scanning micrographs of HeLa cells confirmed the cell permeabilit
161                                              Micrographs of historical interest are presented that ar
162 l polymer electrolyte membrane from electron micrographs of individual acidic clusters.
163                                     Electron micrographs of infectious virions depict particle-associ
164                                     Electron micrographs of insect mouthparts indicate that the prism
165                                              Micrographs of kernel showed pigments concentrated in pe
166                                     Electron micrographs of myosin-18A motor domain-decorated F-actin
167 it corresponds to the hinge seen in electron micrographs of NCAM.
168 rkflow using GAMer 2 to a series of electron micrographs of neuronal dendrite morphology explored at
169                                     Electron micrographs of pancreas depicted macrophages in close co
170 d/pore diffusion mechanism based on confocal micrographs of percolating pores in the polymer, not pre
171            From direct measurements on light micrographs of polytene chromosomes, we then deduce the
172                                Cryo-electron micrographs of purified Syn5 virions revealed that the c
173 3-A crystal structure of RVFV N and electron micrographs of ribonucleoprotein (RNP) reveal an encapsi
174 reported distribution obtained from electron micrographs of RNA polymerase molecules along rrn operon
175                 Here we report that electron micrographs of rsh mutant cells lacking RSH extensin cor
176  to estimate numbers of synapses in electron micrographs of serial sections processed for postembeddi
177 indles by using reconstruction from electron micrographs of serially sectioned meiotic cells.
178 on of biological molecules from the electron micrographs of single particles.
179 ions imaged by light microscopy, or electron micrographs of single ultrathin sections imaged by trans
180 larger serum pores were observed in confocal micrographs of soymilk added with ODPEPS.
181                                     Electron micrographs of spike protein suggests that heparin enhan
182 pheroidal fluorescent shell image to optical micrographs of spores incorporating fluorescent fusion p
183 imulations are consistent with cryo-electron micrographs of T7 phage DNA.
184                                        Light micrographs of the dorsal root entry zone show the perip
185 econstruction from negative-stained electron micrographs of the ectodomain and multidomain constructs
186                                     Electron micrographs of the F. tularensis LVS Delta ripA mutant d
187 again at Larry's paper, I found the electron micrographs of the kDNA networks to be rather beautiful.
188                                     Electron micrographs of the mutant revealed larger cells with div
189 llectively, our NMR spectra and the electron micrographs of the purified ECM inspire us to consider t
190                                     Electron micrographs of the purified inflammasome provide unprece
191 yx depth (0.078 +/- 0.016 mum) from electron micrographs of the same portion of the same vessel.
192 ed from this growth model, polarized optical micrographs of the self-assembled fibrillar networks (SA
193                                Cryo-electron micrographs of tilted Afp specimens (up to 60 degrees) w
194              In this study, we used electron micrographs of tissues prepared using perfusion fixation
195                                     Electron micrographs of toxin-induced cells showed no obvious mem
196                               Higher quality micrographs of untilted specimens were processed to prod
197 NM IIA and NM IIB typically seen in confocal micrographs of well-polarized cells is reflected in the
198  density distribution of A-bands in electron micrographs of well-preserved specimens.
199                            However, electron micrographs of WPBs at the Golgi apparatus show that the
200 epository of biological images, housing 1500 micrographs of yeast cells carrying stained proteins.
201                                     Electron micrographs of ZapA-bundled FtsZ filaments showed the mo
202                                     Electron micrographs offer clear evidence of pores created on cel
203  peptides formed fibrils visible in electron micrographs or needle-like microcrystals showing a cross
204 is the identification of single particles in micrographs (particle picking).
205 tations to terrace heights from atomic force micrographs proves that the end chains are interdigitate
206 tailed schematic drawings and representative micrographs provide examples of how best to identify hum
207                                     The CLSM micrographs provided evidence of the substantial disinte
208                                              Micrographs provided images of the changing morphology o
209 lates with aggressiveness to create computed micrographs reflecting aggressiveness.
210                     Particle picking from 2D micrographs remains a challenging early step in the Cryo
211 ree filaments seen in lamellipodial electron micrographs, requiring approximately 12 generations of s
212                      Negative-stain electron micrographs reveal that filaments are apolar and made of
213                                Cryo-electron micrographs reveal that the V18S substitution causes fib
214  and E-cadherin, was increased, and electron micrographs revealed an apico-basal diffusion of AJs.
215                 Proximate analysis and light micrographs revealed higher migration of red rice protei
216                                     Electron micrographs revealed lipid and mitochondrial abnormaliti
217  sputtering deposition and scanning electron micrographs revealed nano-clusters of metal catalyst in
218                            Scanning electron micrographs revealed presence of dents and fusion of ric
219                                     Electron micrographs revealed stratified constructs with multiple
220                                     Electron micrographs revealed that both water-deprived and NaCl-t
221                                     Electron micrographs revealed that D. mccartyi were abundant with
222                            Scanning electron micrographs revealed that hair bundles exposed to fragme
223                            Scanning electron micrographs revealed that modified okara particles had a
224                                        Light micrographs revealed that NaCl roughened the surface of
225                     In the resulting pastes, micrographs revealed that starch gelatinization depended
226                            Scanning electron micrographs revealed that the sonicated protein isolates
227                                     Electron micrographs revealed that vesicular pools were not reduc
228             Immunogold labelling in electron micrographs revealed that YSD1_22 forms the main shaft o
229                                     Electron micrographs revealed the cytoplasmic accumulation of lip
230 ult male, reconstructed from serial electron micrograph sections.
231 cluded are high-resolution scanning electron micrograph (SEM) images of the surface structures, along
232 dpoles (EC(50) = 16 microM) and fluorescence micrographs show 1-AMA localized to brain and olfactory
233                                   Individual micrographs show clear ultrastructure that allowed direc
234                                     Electron micrographs show direct contact between endothelial cell
235                                     Electron micrographs show mitochondria with swollen matrices that
236                                     Electron micrographs show morphological features indicating a pro
237                                     Cryo-TEM micrographs show that SWNTs stabilized using p-PNCPA tra
238 ee-dimensional reconstructions from electron micrographs show that this peptide binds to the RAD-51 N
239                            Scanning electron micrograph showed well-shaped and smooth spherical morph
240                                         SPEF micrographs showed a decrease in cellular area followed
241                            Scanning electron micrographs showed a protective shield of CP around the
242                 Additionally, immunoelectron micrographs showed A9 in tubules containing protein disu
243 rved in SDS-PAGE while transmission electron micrographs showed complete dispersion of aggregates and
244 herms, polarized light and scanning electron micrographs showed crystallized lactose in low protein p
245 ster loaded saponin micelles (LMS), cryo-TEM micrographs showed depending on the composition of the m
246                                              Micrographs showed different mechanisms of actuation of
247                                     Electron micrographs showed human fetal muscle myofibrils elongat
248                                     Electron micrographs showed human fetal muscle sarcomeres are not
249                            Scanning electron micrographs showed marked improvement in regular three-d
250                                     Electron micrographs showed that at physiological molar ratios, s
251                                      Optical micrographs showed that lime disrupted the integrity of
252                        The cryo-SEM and CLSM micrographs showed that minimum porosity was observed at
253                        Thin-section electron micrographs showed that mutant cells did not fully separ
254                                     Electron micrographs showed that nebulin associates with elongate
255                                Anterior view micrographs showed that posterior zonular fibers origina
256 rthermore, serial reconstruction of electron micrographs showed that postsynaptic cisterns of BKalpha
257                                     Electron micrographs showed that these side polar filaments are v
258 e construct, whereas quick-freeze, deep-etch micrographs showed the details of the matrix interaction
259                Observations are supported by micrographs showing coherent networks with reduced size
260 ting a steady SPR signal decrease, with SPEF micrographs showing extensive collapse of cell actin str
261  for high throughput analysis of fluorescent micrographs such as 2D-myelinating cultures and statisti
262 ve zone structure, as visualized by electron micrographs, suggesting that their contribution to activ
263                                              Micrographs taken during the first 4 days during healing
264                        Transmission electron micrographs (TEM) of infected cells treated with endocyt
265                        Transmission electron micrographs (TEMs) were analyzed to determine fibril pos
266                                 Fluorescence micrographs, TGA, DSC and FTIR spectra suggested the hyp
267 era, they assembled a stunning collection of micrographs that illustrated how L. monocytogenes enters
268 of approximately 10 nm were also observed in micrographs that were attributed to alpha-lac/CMD-b-PEG
269                                  In electron micrographs the M/T to granule cell synapse appeared to
270                                  In electron micrographs, the AC is a highly vacuolated part of the c
271                                     In light micrographs, the density of TM radial collagen fibers wa
272 number of mitochondrial profiles in electron micrographs, the levels of selected energy metabolites a
273 patterns seen in transverse section electron micrographs; the so-called small-square and basketweave
274 tion; from the model of producing only a few micrographs, through the current state where many images
275        Particle extraction from experimental micrographs thus can be laborious and presents a major p
276  by taking a series of transmission electron micrographs tilted at different angles in vitreous ice:
277 whose size distribution is shown by electron micrographs to be skewed.
278 tion process by allowing lower electron dose micrographs to be used for analysis.
279 ensional reconstruction from serial electron micrographs to investigate two structural changes that c
280 rystals, measured from transmission electron micrographs, to be from 10 to 30 nm.
281 of the Z-band in transverse-section electron micrographs typically resembles a small-square lattice o
282 f both new and previously published electron micrographs update previous results and include data on
283 easuring their length, diameter, and area on micrographs using imaging software.
284                       Together with electron micrographs, visual inspection, and contact angle measur
285 on the appearance of nerve fibers in corneal micrographs was explored.
286 partial reconstructions from serial electron micrographs, we quantify synaptic circuits for two other
287                              Two-dimensional micrographs were collated into a three-dimensional array
288 m to overcome many of these problems.Digital micrographs were obtained from cone photoreceptor mosaic
289 ve samples, light, and transmission electron micrographs were used to evaluate optic atrophy postmort
290            The article uses several electron micrographs which have been used in other publications a
291 ecular results are supported by fluorescence micrographs, which show the presence of mitochondrial DN
292 le to obtain phase-contrast and fluorescence micrographs with more than 18,000 single cells per image
293 eld multi-pass polarization and transmission micrographs with variance reductions of 4.4+/-0.8 dB (11
294 ize particle-like objects from noisy cryo-EM micrographs without the need of labeled training data or
295 ation of the IM (up to 19 layers in electron micrographs) without significant effects on plant growth
296                            Scanning electron micrographs, x-ray diffraction spectra, x-ray photoelect
297 red by (29)Si-MAS NMR, transmission electron micrographs, X-ray diffraction, and adsorption isotherms
298  this molecular assembly in negative-stained micrographs yielded a three-dimensional asymmetric recon
299  single particles in cryoelectron microscopy micrographs yields a confirmatory 15% of defective parti
300  averaging of small subsets of digitized TEM micrographs yields an averaged projection image that is

 
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