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1  sub-pixel sweeping microscopy (SPSM) with a super-resolution algorithm, this system offers the abili
2 ly addressed using phase retrieval and pixel super-resolution algorithms, which utilize the diversity
3                    On the other hand, recent super resolution and single molecule results indicate th
4                                              Super-resolution and deconvolution microscopy analyses w
5 gh-throughput quantitative confocal imaging, super-resolution and electron microscopy to visualize or
6                                              Super-resolution and intravital imaging of developing Dr
7  is required for detailed imaging studies by super-resolution and live-cell microscopy.
8 space-bandwidth-products by performing pixel super-resolution and phase retrieval sequentially, they
9 odalities, including high-content screening, super-resolution and time-lapse microscopy, digital path
10 stical techniques underlying the analysis of super-resolution and, more broadly, imaging data.
11                    Biophysical measurements, super-resolution, and electron microscopy, as well as nu
12 e we use electron microscopy, SIM and dSTORM super-resolution, and live-cell TIRF microscopy to chara
13                  Both optical sectioning and super-resolution applications are supported.
14                     We developed a live-cell super-resolution approach to uncover the correlation bet
15 SH and structured illumination microscopy, a super-resolution approach, that mRNAs are spatially orga
16 strated the utility of proExM for multicolor super-resolution ( approximately 70 nm) imaging of cells
17                      Three dimensional (3D), super-resolution biplane fluorescence photoactivation lo
18               Here we demonstrate that pixel super-resolution can be merged into the color de-multipl
19              These results show promise that super-resolution chemical imaging may be used to differe
20 tinct techniques for preparing and acquiring super-resolution CLEM data sets for aldehyde-fixed speci
21                          We also demonstrate super-resolution correlative imaging with protein-specif
22   This new approach, termed Demosaiced Pixel Super-Resolution (D-PSR), generates color images that ar
23                          Cluster analysis of super-resolution data indicates that N-linked glycosylat
24   We subsequently break down the analysis of super-resolution data into four problems: the localizati
25                Imaging non-adherent cells by super-resolution far-field fluorescence microscopy is cu
26 n biofilms using correlative imaging between super resolution fluorescence microscopy and liquid time
27 anced preparations such as array tomography, super-resolution fluorescence imaging and electron micro
28                                              Super-resolution fluorescence imaging by photoactivation
29                               Here we use 3D super-resolution fluorescence imaging to determine the d
30 IM) is a versatile and accessible method for super-resolution fluorescence imaging, but generating hi
31 ue to the development of single-molecule and super-resolution fluorescence imaging, the subject of th
32 al microscopy (SECM) using three-dimensional super-resolution fluorescence imaging.
33 ins in mouse B lymphoma cell membranes using super-resolution fluorescence localization microscopy, d
34  of the NanoSIMS instrument or even the best super-resolution fluorescence methods.
35                  Prior to the development of super-resolution fluorescence microscopy (nanoscopy), in
36                          The introduction of super-resolution fluorescence microscopy (SRM) opened an
37                                              Super-resolution fluorescence microscopy allowed the pre
38                              Single-molecule super-resolution fluorescence microscopy and single-part
39                                              Super-resolution fluorescence microscopy has become an i
40                                              Super-resolution fluorescence microscopy has emerged as
41                                              Super-resolution fluorescence microscopy is distinct amo
42                  In this study, we have used super-resolution fluorescence microscopy supplemented by
43 ation for imaging in nanoscale topography)-a super-resolution fluorescence microscopy technique that
44  well as applications in single-molecule and super-resolution fluorescence microscopy.
45 ne, fluorophores are made to blink, enabling super-resolution fluorescence with 20-30 nm resolution o
46 useful for analysis of standard confocal and super-resolution FM images, where EM cross-validation is
47 ettiger et al. (2016) visualize chromatin in super-resolution, gaining unprecedented insight into chr
48                             It is shown that super-resolution image analysis methods can significantl
49   A variety of methods for obtaining both 3D super-resolution images and 3D tracking information have
50 ule localization microscopy (SMLM) generates super-resolution images by serially detecting individual
51                         Cross-correlation of super-resolution images gathered from point localization
52                          Taken together, our super-resolution images reveal distinct chromatin packag
53                                              Super-resolution images show that independent of labelin
54 ilitate acquisition of live-cell, two-color, super-resolution images, expanding the utility of nanosc
55 ecular complexes hidden in dense multi-color super-resolution images.
56             We report the use of multiplexed super-resolution imaging (Exchange-PAINT) followed by me
57                           Here, by combining super-resolution imaging (photoactivated localization mi
58                                The advent of super-resolution imaging (SRI) has created a need for op
59                                         This super-resolution imaging and analysis approach provides
60 unofluorescence labeling in combination with super-resolution imaging and average position determinat
61                The dye is a useful label for super-resolution imaging and constitutes a new scaffold
62                               We developed a super-resolution imaging and modeling platform that enab
63 en-source analytical framework that combines super-resolution imaging and naive single-particle analy
64 ew describes the growing partnership between super-resolution imaging and plasmonics, by describing t
65                      Selected examples of 3D super-resolution imaging and tracking are described for
66  structured illumination microscopy (iSIM, a super-resolution imaging approach) and a spot-detection
67                                 We present a super-resolution imaging approach, resolving single GPCR
68                    We achieve multiplexed 3D super-resolution imaging at sample depths up to 10 micr
69  laboratory microscope with high-performance super-resolution imaging capability.
70 ing both real-time dynamic visualization and super-resolution imaging for frozen systems.
71                                        While super-resolution imaging has greatly benefited from high
72 t efforts using single-molecule tracking and super-resolution imaging have begun to unravel the heter
73 nabling simultaneous multicolour tracking or super-resolution imaging in a single optical path.
74 the use of fluorogen activating proteins for super-resolution imaging in live bacterial cells.
75                  Using single-molecule based super-resolution imaging in the living cells, we capture
76  that CpcA-PEB and CpcA-PCB are suitable for super-resolution imaging in vivo.
77                                    Live-cell super-resolution imaging is rare, as it is generally ass
78 ng molecules in the pumped volume led to the super-resolution imaging of Eric Betzig and others, a ne
79                                              Super-resolution imaging of live cells over extended tim
80 luorescent proteins is a powerful method for super-resolution imaging of living cells with low light
81 rther demonstrated simultaneous multi-colour super-resolution imaging of microtubules and mitochondri
82 nabling dynamic single-molecule tracking and super-resolution imaging of N-linked sialic acids and O-
83     Example applications in conventional and super-resolution imaging of native and transfected cells
84                                    Moreover, super-resolution imaging of NM2 and M18A using fluoresce
85                                              Super-resolution imaging of Nup188 shows two barrel-like
86                          ExFISH thus enables super-resolution imaging of RNA structure and location w
87               Here we introduce a method for super-resolution imaging of the multiscale organization
88 f intracellular proteins at high density for super-resolution imaging of ultrastructural features wit
89                                Not only does super-resolution imaging offer a secondary feedback mech
90 ed in 2-7 d, are compatible with a number of super-resolution imaging protocols, and are broadly appl
91       We further applied photon localization super-resolution imaging reconstruction to the detected
92           Functional domain mapping based on super-resolution imaging reveals an unexpected role of a
93                                              Super-resolution imaging reveals that bicoid mRNA forms
94               Immuno-electron microscopy and super-resolution imaging show the budding of syntaphilin
95                    First, localization-based super-resolution imaging strategies, where molecules are
96            In the wake of reconstitution and super-resolution imaging studies, we are beginning to un
97                                     A recent super-resolution imaging study by Boettiger et al. elega
98         Here, we report a 3D single-molecule super-resolution imaging study using modulation interfer
99                                              Super-resolution imaging supports the existence of an IT
100 ly evolved, how it compares to other optical super-resolution imaging techniques, and what advantages
101 logies, such as electron microscopy (EM) and super-resolution imaging techniques, can provide the pre
102  it is possible to perform multi-dimensional super-resolution imaging to determine both the position
103 s supply process in living synapses, we used super-resolution imaging to track single vesicles at vol
104 scopy and provides an optional extension for super-resolution imaging using stimulated emission deple
105                 We place special emphasis on super-resolution imaging via single-molecule localizatio
106 inimal size of the probe allow for live-cell super-resolution imaging with very low background and na
107 elated approaches for sample preparation for super-resolution imaging within endogenous cellular envi
108                                 Biochemical, super-resolution imaging, and enzymology approaches esta
109 lly new capabilities to biochemical sensing, super-resolution imaging, and on-chip optical communicat
110                           Here we show using super-resolution imaging, biochemical approaches and in
111                                        Using super-resolution imaging, electrophysiology, and molecul
112 ntrast agents for both superlocalization and super-resolution imaging, offering benefits such as high
113                                  Here we use super-resolution imaging, operated in a charge-carrier-s
114 plication is an important research topic for super-resolution imaging, optical communications and qua
115               Here, we report the results of super-resolution imaging, optogenetic, and electrophysio
116                          In combination with super-resolution imaging, protein alkylation events may
117         By combining mutational analysis and super-resolution imaging, we identify membrane protein c
118                        Using live-tissue and super-resolution imaging, we uncover a centrosome-nuclea
119 on of a conventional confocal microscope for super-resolution imaging.
120 romatin in different epigenetic states using super-resolution imaging.
121 rom in vitro single-molecule measurements to super-resolution imaging.
122  determined by immunoelectron microscopy and super-resolution imaging.
123 ritical for single-molecule fluorescence and super-resolution imaging.
124 curve resolution method is then coupled with super-resolution in order to explore the heterogeneous s
125 irst time combines phase retrieval and pixel super-resolution into a unified mathematical framework a
126                             Conventional and super-resolution light microscopy identified significant
127                                              Super-resolution light microscopy of mutants, cryo-elect
128 ibuted in a toroid around the cartwheel, and super-resolution light microscopy studies have measured
129 nning ion conductance microscopy (SICM) is a super-resolution live imaging technique that uses a glas
130                       We demonstrate this by super-resolution live-cell imaging over timescales rangi
131 xpected results from these protocols include super-resolution localization ( approximately 10-50 nm)
132 cent proteins (pcFPs) are powerful tools for super-resolution localization microscopy and protein tag
133             This holds particularly true for super-resolution localization microscopy where high dema
134 nalyzing method for 3D particle tracking and super-resolution localization microscopy.
135  3D position in single-particle tracking and super-resolution localization microscopy.
136                                    Moreover, super-resolution localizations from these emission-coupl
137                 This novel fluorescence-free super-resolution method was applied to live HeLa cells t
138 ions of the genome using two single-molecule super-resolution methodologies.
139                                              Super-resolution methods such as Structured Illumination
140 eGFP or mEos2 and imaged with two orthogonal super-resolution methods: gated stimulated emission depl
141 owing range of fields and applications, from super-resolution microcopy and ultra-fast optical commun
142 Principle has it that even the most advanced super-resolution microscope would be futile in providing
143 nto the optical path of a localization-based super-resolution microscope, enabling all the informatio
144 n diffraction-limited instead of specialized super-resolution microscopes.
145                                  Here we use super-resolution microscopies to localize in 3D each com
146                         PET pharmacoimaging, super-resolution microscopies, and flow cytometry reveal
147                                  Here, using super resolution microscopy of fixed growth cones, we fo
148                              We also show by super resolution microscopy that DISC1 is localized to e
149                                  Here, using super resolution microscopy, live-cell imaging, and tau
150                           Here, by employing super resolution microscopy, we establish that the ParF
151                                     Applying super resolution microscopy, we were able to investigate
152 l-color stimulated emission depletion (STED) super resolution microscopy.
153  using multiple imaging techniques including super-resolution microscopy (3D-SIM) and live-cell imagi
154                                    Final, 3D super-resolution microscopy (SRM) images were obtained b
155                                  The rise of super-resolution microscopy (SRM) over the past decade h
156                                              Super-resolution microscopy allows biological systems to
157                                              Super-resolution microscopy allows optical imaging below
158                                  Here we use super-resolution microscopy and determine that S. aureus
159                         Here we have applied super-resolution microscopy and FRET to determine the na
160 cements that promise further improvements to super-resolution microscopy and its application to the p
161             By coupling biophysical methods, super-resolution microscopy and physiology, we decipher
162                                        Using super-resolution microscopy and single-particle tracking
163              Here, we used three-dimensional super-resolution microscopy and transmission electron mi
164 ination of genetic, quantitative imaging and super-resolution microscopy approaches to show that matu
165                            The resolution of super-resolution microscopy based on single molecule loc
166 ubcellular structures, opening new routes in super-resolution microscopy based on the encoding/decodi
167 opy and stimulated emission depletion (STED) super-resolution microscopy confirmed the presence of du
168                                              Super-resolution microscopy coupled with multiplexing te
169                                              Super-resolution microscopy demonstrates that COG sub-co
170                                Additionally, super-resolution microscopy established that LtgA locali
171                                              Super-resolution microscopy has revolutionized cellular
172                                  Advances in super-resolution microscopy have allowed membrane encoun
173              Recent advances in fluorescence super-resolution microscopy have allowed subcellular fea
174 ing the interaction of molecular clusters in super-resolution microscopy images.
175 e used optical stimulated emission depletion super-resolution microscopy in combination with fluoresc
176  nm axial resolution, now enabling DNA-based super-resolution microscopy in whole cells using standar
177 rganelles in living cells by long time-lapse super-resolution microscopy is challenging, as it requir
178       Recent advances in single-molecule and super-resolution microscopy methods help to overcome the
179                               In particular, super-resolution microscopy methods overcome the diffrac
180   Using stimulated emission depletion (STED) super-resolution microscopy of brain biopsies from patie
181             Live-cell immunofluorescence and super-resolution microscopy of epitope-tagged CaV1.3L re
182            Here, we combine conventional and super-resolution microscopy of replication sites in live
183                                              Super-resolution microscopy offers a significant gain in
184                        Single-molecule-based super-resolution microscopy offers researchers a unique
185                                              Super-resolution microscopy provides direct insight into
186                                              Super-resolution microscopy recently revealed that, unli
187 sion, photobleaching, immunofluorescence and super-resolution microscopy reveal polarized dynamics, a
188                                    Moreover, super-resolution microscopy revealed that mHtt toxicity
189 tact point submitochondrial fraction and, as super-resolution microscopy revealed, located more to th
190 function is conserved in human tauopathy, as super-resolution microscopy reveals a significantly disr
191 g axons-a phenomenon we call "actin trails." Super-resolution microscopy reveals intra-axonal deep ac
192                                   Video-rate super-resolution microscopy reveals movement of MOF part
193                                              Super-resolution microscopy reveals stable substructures
194                                              Super-resolution microscopy reveals that the ULK1 compar
195  interaction between Munc13-4 and Rab11, and super-resolution microscopy studies support the interact
196                                              Super-resolution microscopy techniques can detect specif
197           Single-molecule localization-based super-resolution microscopy techniques such as photoacti
198 e they colocalized to sites that appeared by super-resolution microscopy to be modified and to have h
199 g to fluorescently tag endogenous IP3Rs, and super-resolution microscopy to determine the geography o
200                                 Here we used super-resolution microscopy to image the E. coli transcr
201 ological processes at different scales, from super-resolution microscopy to in vivo imaging, using th
202                                  Here we use super-resolution microscopy to reveal the existence of h
203 ht some inherent challenges faced when using super-resolution microscopy to study membranes, and we d
204 a membrane and review recent applications of super-resolution microscopy to the study of membranes.
205 on and cell activity in the model system and super-resolution microscopy to visualize F-actin and lyt
206                In this issue, Liu et al. use super-resolution microscopy to visualize large COPII-coa
207       Successful application in localization super-resolution microscopy was demonstrated in phosphat
208 l techniques to align sequential images, and super-resolution microscopy was used to further define m
209 olymer that is physically expanded to enable super-resolution microscopy with ordinary microscopes.
210                                              Super-resolution microscopy with phase masks is a promis
211         Combining fluorescence polarization, super-resolution microscopy, and mathematical analyses,
212 ly of ratiometric pH sensors for use in STED super-resolution microscopy, and optimize their delivery
213                          Despite progress in super-resolution microscopy, discriminating and quantify
214          When viewed using three-dimensional super-resolution microscopy, F-actin foci often extended
215                   Fluorescence nanoscopy, or super-resolution microscopy, has become an important too
216                                        Using super-resolution microscopy, here we show that PcG prote
217 rkable developments in diffraction unlimited super-resolution microscopy, in vivo nanoscopy of tissue
218 on analyses, protein interaction assays, and super-resolution microscopy, Kolobova et al. now identif
219 ut few fluorescent proteins are suitable for super-resolution microscopy, particularly in the far-red
220 led via click chemistry and visualized using super-resolution microscopy, revealing higher resolution
221                    Here we report the use of super-resolution microscopy, single-molecule tracking, a
222      Using plasma membrane biotinylation and super-resolution microscopy, we demonstrate that ABCC4 i
223                                     Using 3D super-resolution microscopy, we demonstrate that depleti
224                                        Using super-resolution microscopy, we demonstrated that purino
225                                        Using super-resolution microscopy, we examined how fluorophore
226             By using a high-speed virtual 3D super-resolution microscopy, we have mapped the 3D spati
227 ar granule neuron system in combination with super-resolution microscopy, we investigate how these cy
228                              Using live-cell super-resolution microscopy, we visualize previously una
229  in ESCs and neural progenitors using 5C and super-resolution microscopy.
230 ls; and (d) use in affinity fluorescence and super-resolution microscopy.
231 t enables single-molecule localization-based super-resolution microscopy.
232  of telomeric chromatin in human cells using super-resolution microscopy.
233 with high-resolution electron tomography and super-resolution microscopy.
234 target proteins, in live mammalian cells, by super-resolution microscopy.
235 nabling long-time-scale protein tracking and super-resolution microscopy.
236 cules in complexes is challenging, even with super-resolution microscopy.
237 hromatin proximal to the NPC, as analysed by super-resolution microscopy.
238 ly enabled spectrally resolved, 'true-color' super-resolution microscopy.
239 nexplored protein family as novel probes for super-resolution microscopy.
240 ular fluorescence complementation (BiFC) and super-resolution microscopy.
241 eripheral region of the nucleus, as shown by super-resolution microscopy.
242 esses in primary human and rat beta cells by super-resolution microscopy.
243 otein copy number in cellular contexts using super-resolution microscopy.
244 ns in specific nanodomains, as determined by super-resolution microscopy.
245  that reproduces the structure identified by super-resolution microscopy.
246 ineage decisions by integrating high content super-resolution nanoscopy and imaging informatics of th
247 g on CRISPR/Cas9 gene-editing techniques and super-resolution nanoscopy, we explore the role of the s
248  using in situ imaging mass spectrometry and super resolution optical microscopy.
249                           Only the advent of super-resolution optical fluorescence microscopy now per
250 itted by individual molecules to reconstruct super-resolution optical images.
251                                              Super-resolution optical imaging based on the switching
252               Despite recent rapid progress, super-resolution optical imaging has yet to be widely ap
253 an atomic force microscope, magnetic tip, or super-resolution optical imaging.
254 yogenic transmission electron microscopy and super-resolution optical microscopy, we observed signatu
255                  Here, we present the use of super-resolution optical stimulated emission depletion m
256 n be further used for two-dimensional atomic super-resolution optical testing and sub-wavelength lith
257 o monitor dynamic processes in live cells at super-resolution over biologically relevant timescales.
258                             Here, we show by super-resolution photo-activated localization microscopy
259 ts to the main reading frame and thus offers super-resolution profiles for individual transcripts to
260 Here, we describe a new analytical approach, super-resolution radial fluctuations (SRRF), provided as
261 ent technique, termed shift-excitation blind super-resolution Raman spectroscopy (SEBSR), uses multip
262              Here, we developed a volumetric super-resolution reconstruction platform for large-volum
263                            We introduce a 3D super-resolution recovery algorithm that works for a var
264 electron microscopy and well correlated with super-resolution results.
265                                              Super-resolution scanning patch clamp showed that LTCCs
266                                              Super-resolution scanning patch-clamp, confocal and fluo
267 rms, and will promote routine application of super-resolution SIM imaging in cell biology.
268 ives and build a simple but high-performance super-resolution SMLM setup.
269 y satisfy the stringent labelling demands of super-resolution SMLM.
270 -field optical microscopy provides access to super-resolution spectroscopic imaging of the surfaces o
271  molecular assemblies in crowded three-color super-resolution (SR) images.
272                    The recent development of super-resolution (SR) light microscopy now allows the vi
273                     Here, using confocal and super-resolution STED imaging, force measurements, pharm
274 g fluorescence correlation spectroscopy on a super-resolution STED microscope.
275 gnificantly advanced by its combination with super-resolution STED microscopy (STED-FCS).
276 logies tested, including dendrites imaged by super-resolution STED microscopy in live brain tissue, s
277                Here, Chojnacki et al. employ super-resolution STED-FCS microscopy to study dynamics o
278                                              Super-resolution stimulated emission depletion (STED) mi
279 ic beta-cells, visualized using confocal and super-resolution stimulated emission depletion microscop
280                               However, using super-resolution stochastic optical reconstruction micro
281                           Furthermore, using super-resolution STORM microscopy, we revealed eukaryoti
282 e this, we used high-resolution confocal and super-resolution (STORM) microscopy in AD-like mice and
283                                              Super-resolution structured illumination microscopic ana
284                                              Super-resolution structured illumination microscopy show
285 oups developing their own implementations of super-resolution structured illumination microscopy, fai
286  an ideal candidate for use as a reagent for super-resolution structured illumination microscopy.
287                                        Using super-resolution structured illumination, atomic force,
288 e significant progress, high-speed live-cell super-resolution studies remain limited to specialized o
289        In the most challenging data sets for super-resolution, such as those obtained in low-illumina
290 Whole-brain CSD-based fiber tractography and super-resolution TDI mapping reveals abnormal fiber proj
291 ured illumination microscopy (3D-SIM) is the super-resolution technique of choice for multicolor volu
292                                              Super-resolution techniques are typically based on the n
293 pid multiplexed target detection with common super-resolution techniques such as (d)STORM, STED, and
294 ubcellular targeting, its compatibility with super-resolution techniques was investigated.
295 organisms in real time and space, also using super-resolution techniques.
296 y (SMLM) has become an essential part of the super-resolution toolbox for probing cellular structure
297 onvolution (CSD)-based tractography data and super-resolution track-density imaging (TDI) maps.
298                             Here, we combine super-resolution tracking of kinetochores with automated
299 beling, and its photoactivatable variant for super-resolution use.
300 ormance at low signal-to-noise ratios allows super-resolution using modern widefield, confocal or TIR

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