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