1 Intravital 2-photon imaging revealed that CCR7 expressio
2 ng whole LN 3D imaging, histo-cytometry, and
intravital 2-photon microscopy, we have identified a spe
3 easurements were consistent with independent
intravital and ex vivo fluorescence microscopy studies a
4 Using both
intravital and explanted two-photon islet imaging, we de
5 Using
intravital and fluorescent microscopy, we found that all
6 ent use of single and multiphoton imaging of
intravital and isolated perfused lung preparations incor
7 Using
intravital and kidney slice two-photon imaging of the th
8 Using confocal,
intravital,
and superresolution microscopy, we find that
9 n vivo with no exogenous stain and show that
intravital autofluorescent images exhibited a distinctiv
10 Intravital blood vessel labeling and immunocytochemistry
11 plex biomolecular systems using non-invasive
intravital chemiluminescence imaging techniques.
12 Using
intravital confocal laser scanning microscopy we show th
13 interactions in real time and in vivo using
intravital confocal microscopy applied to inflamed crema
14 Intravital confocal microscopy performed immediately aft
15 Intravital confocal/two-photon microscopy continuously i
16 Multiplexed, phenotypic,
intravital cytometric imaging requires novel fluorophore
17 Using
intravital dye labeling and 3D imaging, we discovered th
18 unctional repair and recovery as assessed by
intravital dynamic imaging and behavioral tests.
19 mia, we present examples of the way in which
intravital FLIM can be applied to study kidney diseases
20 In conclusion,
intravital FLIM of intrinsic metabolites is a bias-free
21 Intravital FLIM revealed the metabolic signatures of S1
22 MR imaging findings were corroborated with
intravital fluorescence microscopy (IVM), where nearly 9
23 We used
intravital fluorescence microscopy to characterize Ang-4
24 Intravital fluorescence microscopy was used to determine
25 Intravital fluorescence microscopy, through extended pen
26 sculature were then quantified in vivo using
intravital fluorescence microscopy.
27 Using
intravital fluorescent microscopy, the extent of the ext
28 ples that infers H2O2 degradation rates from
intravital H2O2-biosensor imaging data.
29 However, to date there are no reports of
intravital high-resolution imaging of human tumours in t
30 nitors into immunodeficient mice, we used an
intravital imaging approach to follow cartilage maturati
31 Using advanced
intravital imaging approaches and newly created reporter
32 study, we track individual myeloma cells by
intravital imaging as they colonize the endosteal niche,
33 Intravital imaging demonstrated a transendothelial migra
34 Intravital imaging demonstrated MA cargo distributed bot
35 ic parasites combined with reporter mice and
intravital imaging demonstrated that replication in and
36 Therefore,
intravital imaging demonstrates that local myelin recogn
37 Intravital imaging enables to study dynamic tumour-strom
38 Using 3D, time-lapse
intravital imaging for direct visualization of the muscl
39 These findings stress the need for
intravital imaging for dissecting the fine mechanisms of
40 Using
intravital imaging in an antigen-loss CD19-negative rela
41 ose tissue, as demonstrated by single-photon
intravital imaging in mice.
42 Although
intravital imaging is a powerful tool for understanding
43 Intravital imaging is an invaluable tool for understandi
44 Intravital imaging of BRAF-mutant melanoma cells contain
45 s in shaping cell-mediated immunity by using
intravital imaging of CD4(+) T cell interactions with de
46 7BL/6 background provide a valuable tool for
intravital imaging of corneal lymphatic vessels and valv
47 Intravital imaging of CXCR4-expressing MCF-7 cells revea
48 Super-resolution and
intravital imaging of developing Drosophila melanogaster
49 Intravital imaging of fluorescently labeled amphiphilic-
50 Our approach combines
intravital imaging of growth cone dynamics in developing
51 platelet aggregometry, bleeding assays, and
intravital imaging of laser-induced arterial thrombus fo
52 cells using the novel approach of continuous
intravital imaging of Lgr5- Confetti mice.
53 A model system that allows long-term
intravital imaging of lymph nodes would facilitate the s
54 erized, we developed a facile method for the
intravital imaging of mammary cells in transgenic mice t
55 e, using retrospective study of patients and
intravital imaging of mice, we identify some of these ne
56 Intravital imaging of mouse LNs revealed persistent, but
57 Intravital imaging of nanoparticle extravasation and tum
58 Intravital imaging of post-ischemic kidneys revealed red
59 In this study, we used
intravital imaging of reactive lymph nodes (LNs) to show
60 Quantification of reporter mRNA and
intravital imaging of reporter expression in the outer s
61 Here we use
intravital imaging of signalling reporter cell-lines com
62 Intravital imaging of the bone marrow showed that CP tre
63 n imaging approach called LIMB (longitudinal
intravital imaging of the bone marrow) to analyze cellul
64 at the site of inflammation in the CNS using
intravital imaging of the brainstem of EAE-affected livi
65 ndow (CLNW) surgical preparation that allows
intravital imaging of the inguinal lymph node in mice.
66 s review, we examine the approaches used for
intravital imaging of the kidney and summarize the insig
67 Intravital imaging of the liver in mice confirmed that t
68 Stable, high-resolution
intravital imaging of the lung has become possible throu
69 ently implantable window for high-resolution
intravital imaging of the murine lung that allows the mo
70 se, and subsequently allows for longitudinal
intravital imaging of the murine lymph node and surround
71 In this study, using time-lapse
intravital imaging of the spleen, we identify a tropism
72 Intravital imaging revealed heterogeneous cell behaviour
73 The use of
intravital imaging revealed that activated CD4(+) T cell
74 Intravital imaging reveals that vessel growth in murine
75 Intravital imaging shows that CCT129254 or AT13148 treat
76 The
intravital imaging studies using a chronic calvarial bon
77 However,
intravital imaging suggests that early B-cell recognitio
78 Here we use
intravital imaging to demonstrate that secretion of exos
79 we use in vivo B cell competition models and
intravital imaging to examine the adhesive mechanisms go
80 y and transcriptomics, must be combined with
intravital imaging to fully understand a cell's phenotyp
81 FP-ki mice and performed single, nonterminal
intravital imaging to investigate BSCB permeability simu
82 Here, we used microfabricated channels and
intravital imaging to observe and manipulate T-cell kina
83 Here we use
intravital imaging to track the fate of mouse skin epith
84 We used
intravital imaging to visualize the behavior of human CL
85 The combination of functional analysis by
intravital imaging with cellular characterization has re
86 Intravital imaging with surgical exposure of the lymph n
87 Intravital imaging, coupled with mechanistic studies in
88 Here we used a combination of confocal
intravital imaging, genetically engineered mice, and ant
89 ting ways stem cells are being visualized by
intravital imaging, the intriguing discoveries that have
90 provides access to the mouse cerebellum for
intravital imaging, thereby allowing for a detailed char
91 Using
intravital imaging, we established that, upon anti-CD20
92 Using
intravital imaging, we found that selection is mediated
93 Using mouse models and multiphoton
intravital imaging, we have identified a crucial effect
94 Using
intravital imaging, we show that knockout of Ccn1 in end
95 By
intravital imaging, we show that the less malignant tumo
96 o and in vivo as shown by flow cytometry and
intravital imaging.
97 t membrane (3D rBM) cultures, and mice using
intravital imaging.
98 restore fibrin and platelet deposition in an
intravital laser injury model in hemophilia B mice.
99 Intravital laser-scanning microscopy revealed that, comp
100 CXCR4, we studied endothelial permeability,
intravital leukocyte adhesion, involvement of the Akt/WN
101 ate axonal co-transport of BRP and RBP using
intravital live imaging, with both proteins co-accumulat
102 in transferred and endogenous CTLs and with
intravital live-cell two-photon microscopy evidence for
103 To address this issue, we conducted
intravital,
longitudinal imaging analyses of cellular be
104 Using
intravital luminescence and fluorescence microscopy, we
105 In this study, we used a novel
intravital method that revealed spatiotemporal regulatio
106 aration and can be implemented into standard
intravital microscopes.
107 Intravital microscopic analysis indicated that the absen
108 Intravital microscopic images demonstrated significant b
109 microvascular leakage using a rat model with
intravital microscopic imaging.
110 io and colleagues report the use of a unique
intravital microscopic system to characterize an ontogen
111 Intravital microscopic tracking of individual animals re
112 As a preclinical tool,
intravital microscopy (IVM) allows for in vivo real-time
113 Intravital microscopy (IVM) is an ideal tool to provide
114 All animals underwent serial MR imaging and
intravital microscopy (IVM) up to 4 weeks after surgery.
115 n vivo imaging, and specifically multiphoton
intravital microscopy (MP-IVM), which allows for the inv
116 /-), and CX3CR1(gfp/+) mice were assessed by
intravital microscopy after PBS, IL-1beta, TNF-alpha, or
117 An
intravital microscopy and closed cranial window system,
118 10 to 1,000 nm in diameter, is studied using
intravital microscopy and computational modeling.
119 Here, using a combination of multiphoton
intravital microscopy and genomic approaches, we re-exam
120 Intravital microscopy and histologic analysis of tumor n
121 CV diseases, in rat mesenteric vessels using
intravital microscopy and in human arterial cells using
122 edicted tumor growth with that observed from
intravital microscopy and macroscopic imaging in vivo, f
123 Using spinning-disk confocal
intravital microscopy and mice with fluorescent reporter
124 r location and phenotype were examined using
intravital microscopy and time-of-flight mass cytometry.
125 ells was analyzed in vivo using conventional
intravital microscopy and two-photon microscopy.
126 r necrosis factor-alpha-stimulated tissue by
intravital microscopy applying the dorsal skinfold chamb
127 the last decade, the application of 2-photon
intravital microscopy as a tool to study cell interactio
128 col, we describe experimental procedures for
intravital microscopy based on a combination of thoracic
129 rdiac and respiratory cycles severely limits
intravital microscopy by compromising ultimate spatial a
130 Intravital microscopy demonstrated a decreased ability o
131 Intravital microscopy demonstrates that histamine-induce
132 Intravital microscopy demonstrates that platelet PDI is
133 Intravital microscopy demonstrates that the movement of
134 By using
intravital microscopy experiments, we demonstrated that
135 Intravital microscopy following laser-induced vascular i
136 Intravital microscopy has shown that microvascular units
137 cent developments in genetic engineering and
intravital microscopy have allowed further molecular and
138 tomatically removing motion artifacts during
intravital microscopy imaging of organs and orthotopic t
139 steroids on microvascular perfusion by using
intravital microscopy in a mice model and to investigate
140 Using
intravital microscopy in a murine model of polymicrobial
141 were conducted using catheter techniques and
intravital microscopy in animals subjected to different
142 Using
intravital microscopy in Lgr5(EGFP-Ires-CreERT2) mice, w
143 Here we show by
intravital microscopy in live mice that the regression p
144 Here we used multiphoton
intravital microscopy in lymph nodes and tumors to show
145 Using fluorescence
intravital microscopy in mice generated by crossing prot
146 interaction with dermal blood vessels, using
intravital microscopy in mice.
147 ecrosis of renal tubules, as demonstrated by
intravital microscopy in models of IRI and oxalate cryst
148 Using multicolor confocal
intravital microscopy in mouse models of sepsis, we obse
149 Using two-photon
intravital microscopy in mouse models of sterile injury
150 ral and spatial resolutions using high-speed
intravital microscopy in multiple channels of fluorescen
151 endothelium within minutes, as identified by
intravital microscopy in the cremaster model.
152 terized ASC differentiation and migration by
intravital microscopy in the lymph node (LN) by transfer
153 Using
intravital microscopy in the transparent larval zebrafis
154 through microfluidic studies in vitro and by
intravital microscopy in vivo.We showthatmargination,whi
155 Intravital microscopy is a key means of monitoring cellu
156 Intravital microscopy is a powerful tool in neuroscience
157 To test this, we developed a fetal
intravital microscopy model in pregnant mice and, using
158 Intravital microscopy of animals with chronic kidney fai
159 esion assays and during ex vivo perfusion or
intravital microscopy of carotid arteries.
160 Intravital microscopy of caveolae-immunotargeted fluorop
161 Using
intravital microscopy of cremasteric microvasculature of
162 Intravital microscopy of ischemic or tumor necrosis fact
163 using dual laser multichannel spinning-disk
intravital microscopy of joints, the CXCR6-GFP, which al
164 This was confirmed in rat
intravital microscopy of lipopolysaccharide-induced crem
165 Studies using
intravital microscopy of live mouse cremaster venules sh
166 windows in mice have been developed to allow
intravital microscopy of many different organs and have
167 By using
intravital microscopy of mouse cremaster muscle, the in
168 Intravital microscopy of mouse mesenteric venules demons
169 Intravital microscopy of NP spread in breast tumor tissu
170 Using
intravital microscopy of the bloodstream of mice infecte
171 A murine model for
intravital microscopy of the breathing lung under sealed
172 Intravital microscopy of the calvarium is the only nonin
173 Intravital microscopy of the carotid artery, the jugular
174 chamber assay of whole blood neutrophils and
intravital microscopy of the inflamed cremaster muscle t
175 Intravital microscopy of the mouse cremaster muscle conf
176 perties of Pyr1 were investigated in vivo by
intravital microscopy of tumor xenografts.
177 Using
intravital microscopy of tumour necrosis factor-alpha-ch
178 a new method for stable, long-term 2-photon
intravital microscopy of unrestrained large arteries in
179 dye-coupled nanoparticles can be tracked by
intravital microscopy or even non-invasively by multispe
180 ing ischemia and reperfusion injury in vivo,
intravital microscopy performed to study intravascular f
181 Intravital microscopy performed two hours following part
182 Intravital microscopy revealed a defect in LPS-induced n
183 Direct evaluation of renal morphology by
intravital microscopy revealed dilation of renal tubules
184 Intravital microscopy revealed IFNgamma-induced regressi
185 Whole-blood perfusion experiments and
intravital microscopy revealed increased recruitment of
186 In addition,
intravital microscopy revealed reduced leukocyte rolling
187 Kidney
intravital microscopy revealed that circulating neutroph
188 Intravital microscopy revealed that CX3CR1 is critical f
189 Intravital microscopy revealed that Cxcr3(-/-) T cells w
190 Multiphoton
intravital microscopy revealed that in contrast to CTLs,
191 Intravital microscopy revealed that in this setting, int
192 Multiphoton and spinning disk confocal
intravital microscopy revealed that monocytes patrol bot
193 Intravital microscopy showed that CYTH1 deficiency profo
194 mice in response to CCL20 or TNF-alpha, and
intravital microscopy studies demonstrated that CD43(-/-
195 In
intravital microscopy studies of intact or EC-denuded sk
196 Finally,
intravital microscopy studies of the mouse cremaster mic
197 Intravital microscopy studies reveal that CD47(-/-) Th1
198 Here, we used
intravital microscopy to assess the effects of Ang II on
199 Here, using
intravital microscopy to evaluate mice lacking specific
200 wild type (WT) were studied using time-lapse
intravital microscopy to examine leukocyte recruitment a
201 Furthermore, using
intravital microscopy to ferric chloride (FeCl3)-injured
202 Here, we used
intravital microscopy to investigate how fibrin is remov
203 Here, we have used multilaser spinning-disk
intravital microscopy to monitor the blood-borne stage i
204 ute lymphoblastic leukaemia (T-ALL) and used
intravital microscopy to monitor the progression of dise
205 Using
intravital microscopy to perform imaging studies of the
206 To test junctional function, we used
intravital microscopy to quantify the transport kinetics
207 Here, we use two-photon
intravital microscopy to show that immature B cell reten
208 d with mild TBI in humans and used long-term
intravital microscopy to study the dynamics of the injur
209 Through application of confocal
intravital microscopy to the mouse cremaster muscle, we
210 Using spinning-disk confocal
intravital microscopy to track MRSA-GFP in vivo, we iden
211 d, we used scanning electron and brightfield
intravital microscopy to visualize endothelial damage an
212 ay during retinal cell regeneration, we used
intravital microscopy to visualize neutrophil, macrophag
213 I-mediated thrombus formation was studied by
intravital microscopy using a mouse model of Hermansky-P
214 Intravital microscopy was used to visualize migration of
215 Using multiphoton
intravital microscopy we showed that neutrophils extrava
216 The studies combined high-resolution
intravital microscopy with a photo-activatable fluoresce
217 ell function in tumors, we combined confocal
intravital microscopy with depletion of CSF-1R-dependent
218 By using
intravital microscopy with DREAM-null mice and their bon
219 Here we have combined dynamic
intravital microscopy with ex vivo assessments of T cell
220 se the mouse hair follicle niche and combine
intravital microscopy with genetic lineage tracing to re
221 By using
intravital microscopy with mice lacking nicotinamide ade
222 e combination of whole body optical imaging,
intravital microscopy, and "in vivo fluorescence trappin
223 timeframe that is well suited to analysis by
intravital microscopy, and much has been learned in rece
224 In vivo
intravital microscopy, bone marrow reconstitution, and A
225 recruitment, migration, adhesion by means of
intravital microscopy, degranulation, TNF-alpha release,
226 Neutrophil function was assessed by using
intravital microscopy, flow chamber assays, and chemotax
227 erosclerotic plaques in vivo, as assessed by
intravital microscopy, flow cytometry, and histological
228 Using
intravital microscopy, in a 10% FeCl3-induced thrombosis
229 ion of histone citrullination, together with
intravital microscopy, showed that NETosis occurred in t
230 Here we demonstrate, using cerebral
intravital microscopy, that in response to liver inflamm
231 Thanks to the most recent advancements in
intravital microscopy, this approach has finally been ex
232 Although fluorescent proteins revolutionized
intravital microscopy, two major challenges that still r
233 Using real-time fluorescence
intravital microscopy, we demonstrated that short-term c
234 Using
intravital microscopy, we evaluated susceptibility to ca
235 By using spinning-disk confocal
intravital microscopy, we examined the molecular mechani
236 Using
intravital microscopy, we found that AML progression lea
237 Using
intravital microscopy, we found that antibody-dependent
238 Using
intravital microscopy, we found that cerebral ischemia/r
239 Finally, using
intravital microscopy, we observe that tumor spheroids d
240 Using lung
intravital microscopy, we observed the dynamic formation
241 Using confocal
intravital microscopy, we revealed that liver injury due
242 Using
intravital microscopy, we show distinct cell dynamics of
243 Using
intravital microscopy, we show that Arhgap25 deficiency
244 By repeated high-resolution
intravital microscopy, we show that biopsy-like injury i
245 ing early barrier permeability in vivo Using
intravital microscopy, we show that recurrent seizures a
246 Here, using confocal
intravital microscopy, we show that upon Toll-like recep
247 Finally, using
intravital microscopy, we show that, during CLA-induced
248 Here, we present an
intravital microscopy-based assay for the quantification
249 fully established breast carcinoma model by
intravital microscopy.
250 adhesion and extravasation as visualized by
intravital microscopy.
251 eritumoral pH were monitored over time using
intravital microscopy.
252 for the GCaMP2 transgene) were studied with
intravital microscopy.
253 tes in the rat peritoneal vascular bed using
intravital microscopy.
254 ility in KRIT1 heterozygous mice as shown by
intravital microscopy.
255 cerebral endothelial cells were analyzed by
intravital microscopy.
256 d-labeled rat serum albumin using two-photon
intravital microscopy.
257 TBI when studied using Evans blue assay and
intravital microscopy.
258 models of acute vasoocclusive episodes using
intravital microscopy.
259 Intravital microvascular imaging revealed a haphazard we
260 meningeal and brain vessels when measured by
intravital multiphoton imaging and immunohistochemistry.
261 tumors using the in vivo invasion assay and
intravital multiphoton imaging of tumor cell streaming.
262 Intravital multiphoton imaging revealed that inhibition
263 Intravital multiphoton imaging, confocal imaging of cryo
264 By
intravital multiphoton imaging, we found that the motili
265 As evidenced by
intravital multiphoton microscopy of Ccr2 reporter mice,
266 Using longitudinal
intravital multiphoton microscopy of DC(GFP)/MC(RFP) rep
267 Moreover,
intravital multiphoton microscopy revealed that Debio071
268 To address this, we used
intravital multiphoton microscopy to visualize immune ce
269 Using a combination of
intravital multiphoton microscopy, genetically modified
270 s, immunological readouts, and sophisticated
intravital multiphoton microscopy-based imaging of liver
271 amined over time to expected ovulation using
intravital multiphoton microscopy.
272 stmortem damage cannot be distinguished from
intravital occurrences, unless evidence of healing is pr
273 nd hemoglobin absorption, which act to limit
intravital optical techniques to large or subcutaneous t
274 ansport in neurons of adult animals requires
intravital or ex vivo imaging approaches, which are labo
275 Here we demonstrate
intravital quantification of the myelin molecular struct
276 ty compared with control when measured using
intravital quantitative multiphoton microscopy.
277 stom-built confocal microscope and performed
intravital real-time visualization of the absorption and
278 gate longitudinal responses, we developed an
intravital serial imaging approach that can directly vis
279 In this study, we use
intravital subcellular microscopy in live mice to study
280 Murine
intravital thrombosis studies demonstrated that CAP-PEs
281 Intravital thrombosis studies using ApoE(-/-) mice with
282 rasite, Trichinella spiralis, and multipoint
intravital time-lapse confocal microscopy of mouse calva
283 e T cell arrest in LNs that we confirm using
intravital two-photon data.
284 Concurrently,
intravital two-photon imaging revealed prompt peritubula
285 nto the blood and we have developed a stable
intravital two-photon lung imaging model in mice for dir
286 ism in vivo Here, we used the combination of
intravital two-photon microscopy and frequency-domain fl
287 icrobial niche by various methods, including
intravital two-photon microscopy and non-invasive whole-
288 Intravital two-photon microscopy imaging of Cxcr6(+/gfp)
289 Using
intravital two-photon microscopy in the mouse model of m
290 podocytes (wt1a:eGFP larvae) was observed by
intravital two-photon microscopy over extended periods o
291 In summary, we show by extended
intravital two-photon microscopy that podocytes are stat
292 g key cytoskeletal components and performing
intravital two-photon microscopy to visualize TRM cell b
293 Applying
intravital two-photon microscopy, we demonstrate the gat
294 Using
intravital two-photon microscopy, we observe that sympat
295 Using
intravital two-photon microscopy, we observed that local
296 vasculature in acute myeloid leukemia using
intravital two-photon microscopy.
297 platelets and CD4 T cells was analyzed using
intravital video fluorescence microscopy.
298 Morphometric analyses of
intravital video microscopy data showed that gammadelta
299 Intravital videomicroscopy was used to quantify adhesion
300 Moreover, using
intravital videomicroscopy, we demonstrate that the IL-1