1 cruited cell populations in combination with
intravital 2-photon microscopy, we demonstrate that mono
2 Moreover, using
intravital 2-photon microscopy, we found that 4-MUG (a n
3 ng whole LN 3D imaging, histo-cytometry, and
intravital 2-photon microscopy, we have identified a spe
4 Intravital 3D bioprinting could serve as an in vivo alte
5 We also show that
intravital 3D bioprinting of donor-muscle-derived stem c
6 Such
intravital 3D bioprinting-which does not create by-produ
7 Using
intravital analysis of the islet microcirculation in mic
8 Using both
intravital and explanted two-photon islet imaging, we de
9 Using
intravital and kidney slice two-photon imaging of the th
10 Future work should focus on
intravital applications.
11 Intravital biosensor imaging showed that wound peroxide
12 f bone tissue after tumor cell injection and
intravital bone microscopy revealed less tumor cells att
13 ading to eosinophil activation as we show by
intravital calcium imaging.
14 plex biomolecular systems using non-invasive
intravital chemiluminescence imaging techniques.
15 Using
intravital confocal laser scanning microscopy we show th
16 interactions in real time and in vivo using
intravital confocal microscopy applied to inflamed crema
17 Using
intravital confocal microscopy of Foxp3-GFP mice, we vis
18 Intravital confocal microscopy performed immediately aft
19 Multiplexed, phenotypic,
intravital cytometric imaging requires novel fluorophore
20 Using
intravital dye labeling and 3D imaging, we discovered th
21 unctional repair and recovery as assessed by
intravital dynamic imaging and behavioral tests.
22 mia, we present examples of the way in which
intravital FLIM can be applied to study kidney diseases
23 In conclusion,
intravital FLIM of intrinsic metabolites is a bias-free
24 Intravital FLIM revealed the metabolic signatures of S1
25 MR imaging findings were corroborated with
intravital fluorescence microscopy (IVM), where nearly 9
26 We used
intravital fluorescence microscopy to characterize Ang-4
27 sculature were then quantified in vivo using
intravital fluorescence microscopy.
28 Using
intravital fluorescent microscopy, the extent of the ext
29 ples that infers H2O2 degradation rates from
intravital H2O2-biosensor imaging data.
30 However, to date there are no reports of
intravital high-resolution imaging of human tumours in t
31 Intravital imaging and computational analyses have been
32 Using a combination of dynamic
intravital imaging and confocal multiplex microscopy, we
33 lumination, and offers new opportunities for
intravital imaging and control of cardiac function.
34 Intravital imaging and genetic approaches indicated that
35 also describe how to apply state-of-the-art
intravital imaging and hearing assessment techniques to
36 Using
intravital imaging and loss of function experiments, we
37 Using advanced
intravital imaging approaches and newly created reporter
38 LT-HSCs) and that is compatible with current
intravital imaging approaches in the calvarial bone marr
39 study, we track individual myeloma cells by
intravital imaging as they colonize the endosteal niche,
40 Intravital imaging demonstrated a transendothelial migra
41 ic parasites combined with reporter mice and
intravital imaging demonstrated that replication in and
42 Therefore,
intravital imaging demonstrates that local myelin recogn
43 Intravital imaging enables to study dynamic tumour-strom
44 Using 3D, time-lapse
intravital imaging for direct visualization of the muscl
45 Using
intravital imaging in an antigen-loss CD19-negative rela
46 Intravital imaging in live zebrafish embryos revealed th
47 ose tissue, as demonstrated by single-photon
intravital imaging in mice.
48 Although
intravital imaging is a powerful tool for understanding
49 Intravital imaging is an invaluable tool for understandi
50 Developing in vivo real-time
intravital imaging of alveoli revealed AMs crawling in a
51 Intravital imaging of BRAF-mutant melanoma cells contain
52 Using
intravital imaging of cardiac transplants, we uncover th
53 7BL/6 background provide a valuable tool for
intravital imaging of corneal lymphatic vessels and valv
54 Super-resolution and
intravital imaging of developing Drosophila melanogaster
55 Intravital imaging of fluorescently labeled amphiphilic-
56 Our approach combines
intravital imaging of growth cone dynamics in developing
57 Intravital imaging of immune cells can be negatively imp
58 Intravital imaging of livers in control mice revealed si
59 tal blood pressure analyzer and we performed
intravital imaging of livers of mice.
60 A model system that allows long-term
intravital imaging of lymph nodes would facilitate the s
61 erized, we developed a facile method for the
intravital imaging of mammary cells in transgenic mice t
62 e, using retrospective study of patients and
intravital imaging of mice, we identify some of these ne
63 Intravital imaging of mouse LNs revealed persistent, but
64 Intravital imaging of nanoparticle extravasation and tum
65 Through
intravital imaging of NSCs and their progeny, we identif
66 Intravital imaging of post-ischemic kidneys revealed red
67 In this study, we used
intravital imaging of reactive lymph nodes (LNs) to show
68 Here we use
intravital imaging of signalling reporter cell-lines com
69 n imaging approach called LIMB (longitudinal
intravital imaging of the bone marrow) to analyze cellul
70 Longitudinal analysis of mice using 2-photon
intravital imaging of the brain through cranial windows
71 and organic dyes that allow high-resolution
intravital imaging of the different mural cell subtypes.
72 ndow (CLNW) surgical preparation that allows
intravital imaging of the inguinal lymph node in mice.
73 s review, we examine the approaches used for
intravital imaging of the kidney and summarize the insig
74 the 1950s enabled imaging of live cells and
intravital imaging of the kidney; however, confocal micr
75 Intravital imaging of the liver in mice confirmed that t
76 Stable, high-resolution
intravital imaging of the lung has become possible throu
77 ently implantable window for high-resolution
intravital imaging of the murine lung that allows the mo
78 se, and subsequently allows for longitudinal
intravital imaging of the murine lymph node and surround
79 In this study, using time-lapse
intravital imaging of the spleen, we identify a tropism
80 Intravital imaging revealed heterogeneous cell behaviour
81 Intravital imaging revealed impaired bile secretion into
82 The use of
intravital imaging revealed that activated CD4(+) T cell
83 erstood "macrophage disappearance reaction."
Intravital imaging revealed that resident macrophages we
84 Real-time
intravital imaging revealed that the treatment with CCL5
85 Intravital imaging reveals that vessel growth in murine
86 Intravital imaging showed that CpG-C-activated microglia
87 Furthermore,
intravital imaging showed that virus spread and lesion f
88 Intravital imaging shows that CCT129254 or AT13148 treat
89 ransparent cranial windows normally used for
intravital imaging studies in mice to include a turnable
90 The
intravital imaging studies using a chronic calvarial bon
91 in vitro functional assays and confocal and
intravital imaging studies.
92 However,
intravital imaging suggests that early B-cell recognitio
93 Here we use
intravital imaging to demonstrate that secretion of exos
94 we use in vivo B cell competition models and
intravital imaging to examine the adhesive mechanisms go
95 y and transcriptomics, must be combined with
intravital imaging to fully understand a cell's phenotyp
96 Here, we used microfabricated channels and
intravital imaging to observe and manipulate T-cell kina
97 Here we use
intravital imaging to track the fate of mouse skin epith
98 We used
intravital imaging to visualize the behavior of human CL
99 mechanisms have been hindered by the lack of
intravital imaging tools capable of multiparametric prob
100 The combination of quantitative
intravital imaging with deep transcriptomes identified 4
101 Intravital imaging, coupled with mechanistic studies in
102 ng our recently developed quantitative liver
intravital imaging, RNA sequence analysis, and biochemic
103 provides access to the mouse cerebellum for
intravital imaging, thereby allowing for a detailed char
104 Using
intravital imaging, we also determined that high-avidity
105 Using mouse models and multiphoton
intravital imaging, we have identified a crucial effect
106 Using
intravital imaging, we observe that these dominant CAFs
107 Using
intravital imaging, we show that knockout of Ccn1 in end
108 Here, using
intravital imaging, we show that Kupffer cells (KCs) in
109 By
intravital imaging, we show that the less malignant tumo
110 Using
intravital imaging, we tracked interactions established
111 perties of brain T(RM) cells was revealed by
intravital imaging.
112 o and in vivo as shown by flow cytometry and
intravital imaging.
113 toxin as shown by compartmental staining and
intravital imaging.
114 ous reasons, from utilization in longer-term
intravital imaging.
115 e in situ requires animal models amenable to
intravital imaging.
116 restore fibrin and platelet deposition in an
intravital laser injury model in hemophilia B mice.
117 Intravital laser-scanning microscopy revealed that, comp
118 CXCR4, we studied endothelial permeability,
intravital leukocyte adhesion, involvement of the Akt/WN
119 in transferred and endogenous CTLs and with
intravital live-cell two-photon microscopy evidence for
120 Intravital microscopic images demonstrated significant b
121 microvascular leakage using a rat model with
intravital microscopic imaging.
122 receptor 2 (VEGFR2), which was confirmed by
intravital microscopic studies in a murine cremaster mod
123 Intravital microscopic tracking of individual animals re
124 As a preclinical tool,
intravital microscopy (IVM) allows for in vivo real-time
125 Intravital microscopy (IVM) and optical coherency tomogr
126 t 20 years, the application and evolution of
intravital microscopy (IVM) has vastly increased our abi
127 Intravital microscopy (IVM) is an ideal tool to provide
128 idative burst of murine neutrophils in vitro
Intravital microscopy (IVM) showed increased association
129 All animals underwent serial MR imaging and
intravital microscopy (IVM) up to 4 weeks after surgery.
130 Intravital microscopy (IVM) was used to observe changes
131 /-), and CX3CR1(gfp/+) mice were assessed by
intravital microscopy after PBS, IL-1beta, TNF-alpha, or
132 Here, using a combination of multiphoton
intravital microscopy and genomic approaches, we re-exam
133 y diameter and blood flow were recorded with
intravital microscopy and laser speckle imaging.
134 Using spinning-disk confocal
intravital microscopy and mice with fluorescent reporter
135 r location and phenotype were examined using
intravital microscopy and time-of-flight mass cytometry.
136 ells was analyzed in vivo using conventional
intravital microscopy and two-photon microscopy.
137 Taking advantage of
intravital microscopy and using African trypanosomes as
138 the last decade, the application of 2-photon
intravital microscopy as a tool to study cell interactio
139 col, we describe experimental procedures for
intravital microscopy based on a combination of thoracic
140 Moreover,
intravital microscopy demonstrated reduced post-traumati
141 Intravital microscopy demonstrates that histamine-induce
142 Intravital microscopy demonstrates that the movement of
143 Intravital microscopy experiments were performed using t
144 By using
intravital microscopy experiments, we demonstrated that
145 Intravital microscopy has shown that microvascular units
146 cent developments in genetic engineering and
intravital microscopy have allowed further molecular and
147 steroids on microvascular perfusion by using
intravital microscopy in a mice model and to investigate
148 Using
intravital microscopy in a murine model of polymicrobial
149 were conducted using catheter techniques and
intravital microscopy in animals subjected to different
150 Here we show by
intravital microscopy in humanized mice that perturbatio
151 Using
intravital microscopy in Lgr5(EGFP-Ires-CreERT2) mice, w
152 Here we show by
intravital microscopy in live mice that the regression p
153 interaction with dermal blood vessels, using
intravital microscopy in mice.
154 Using multicolor confocal
intravital microscopy in mouse models of sepsis, we obse
155 Using
intravital microscopy in the transparent larval zebrafis
156 through microfluidic studies in vitro and by
intravital microscopy in vivo.We showthatmargination,whi
157 Intravital microscopy is a powerful technique to observe
158 Intravital microscopy is a powerful tool in neuroscience
159 Intravital microscopy is increasingly used to capture th
160 ng of neutrophil recruitment, organ-specific
intravital microscopy methods are needed.
161 was detected by immunohistochemistry and by
intravital microscopy observation of platelet aggregates
162 by using real-time multichannel fluorescence
intravital microscopy of a tumor necrosis factor-alpha-i
163 Intravital microscopy of animals with chronic kidney fai
164 (2020) employ
intravital microscopy of colorectal cancer organoid xeno
165 Using
intravital microscopy of cremasteric microvasculature of
166 Thrombus formation was quantified by
intravital microscopy of laser-injured arterioles.
167 Studies using
intravital microscopy of live mouse cremaster venules sh
168 using spatially defined organotypic culture,
intravital microscopy of mammary tumours in mice and in
169 windows in mice have been developed to allow
intravital microscopy of many different organs and have
170 By using
intravital microscopy of mouse cremaster muscle, the in
171 Intravital microscopy of mouse mesenteric venules demons
172 Intravital microscopy of NP spread in breast tumor tissu
173 n and resistance programs cooperate, we used
intravital microscopy of orthotopic sarcoma and melanoma
174 Using
intravital microscopy of the bloodstream of mice infecte
175 Intravital microscopy of the carotid artery, the jugular
176 chamber assay of whole blood neutrophils and
intravital microscopy of the inflamed cremaster muscle t
177 on podocyte calcium levels in vivo, we used
intravital microscopy of the kidney in mice expressing t
178 Intravital microscopy of TNFalpha-inflamed cremaster mus
179 perties of Pyr1 were investigated in vivo by
intravital microscopy of tumor xenografts.
180 a new method for stable, long-term 2-photon
intravital microscopy of unrestrained large arteries in
181 Intravital microscopy performed two hours following part
182 Intravital microscopy provides evidence of neutrophil NE
183 Intravital microscopy revealed a defect in LPS-induced n
184 Multiphoton
intravital microscopy revealed a mixing of blood and bil
185 Intravital microscopy revealed heightened platelet adher
186 Intravital microscopy revealed IFNgamma-induced regressi
187 In addition,
intravital microscopy revealed reduced leukocyte rolling
188 Kidney
intravital microscopy revealed that circulating neutroph
189 Intravital microscopy revealed that CX3CR1 is critical f
190 Intravital microscopy revealed that Cxcr3(-/-) T cells w
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 decrease in leukocyte adhes
194 Intravital microscopy showed that CYTH1 deficiency profo
195 Intravital microscopy showed that liver colonization by
196 mice in response to CCL20 or TNF-alpha, and
intravital microscopy studies demonstrated that CD43(-/-
197 Finally,
intravital microscopy studies of the mouse cremaster mic
198 form was further exploited for studying with
intravital microscopy the extravasation of 0.58 kDa rhod
199 Here, we used
intravital microscopy to assess the effects of Ang II on
200 Here, we used
intravital microscopy to define lymphocyte trafficking r
201 Using state-of-the-art spinning disk
intravital microscopy to delineate the different compart
202 re included: (a) laser-Doppler flowmetry and
intravital microscopy to evaluate mesenteric perfusion;
203 The aim of this study was to use
intravital microscopy to investigate adhesion and transm
204 Here, we used
intravital microscopy to investigate how fibrin is remov
205 mbined contrast-enhanced ultrasonography and
intravital microscopy to measure IMVR and gracilis arter
206 Here, we have used multilaser spinning-disk
intravital microscopy to monitor the blood-borne stage i
207 ute lymphoblastic leukaemia (T-ALL) and used
intravital microscopy to monitor the progression of dise
208 ing pipeline using plus-end tip tracking and
intravital microscopy to quantify MT dynamics in live xe
209 To test junctional function, we used
intravital microscopy to quantify the transport kinetics
210 We further used 2-photon and
intravital microscopy to study endothelial activation an
211 Using spinning-disk confocal
intravital microscopy to track MRSA-GFP in vivo, we iden
212 ay during retinal cell regeneration, we used
intravital microscopy to visualize neutrophil, macrophag
213 Intravital microscopy via cranial window and flow cytome
214 Fluorescence
intravital microscopy was used to visualize cellular tra
215 Intravital microscopy was used to visualize migration of
216 The studies combined high-resolution
intravital microscopy with a photo-activatable fluoresce
217 By using
intravital microscopy with DREAM-null mice and their bon
218 By using
intravital microscopy with mice lacking nicotinamide ade
219 hen coupled the use of these biosensors with
intravital microscopy, a powerful tool that can be used
220 autoimmune encephalomyelitis (EAE), we used
intravital microscopy, assessing local cellular interact
221 In vivo
intravital microscopy, bone marrow reconstitution, and A
222 Neutrophil function was assessed by using
intravital microscopy, flow chamber assays, and chemotax
223 erosclerotic plaques in vivo, as assessed by
intravital microscopy, flow cytometry, and histological
224 Using
intravital microscopy, in a 10% FeCl3-induced thrombosis
225 ion of histone citrullination, together with
intravital microscopy, showed that NETosis occurred in t
226 Although fluorescent proteins revolutionized
intravital microscopy, two major challenges that still r
227 Using real-time fluorescence
intravital microscopy, we demonstrated that short-term c
228 Using
intravital microscopy, we evaluated susceptibility to ca
229 By using spinning-disk confocal
intravital microscopy, we examined the molecular mechani
230 Using
intravital microscopy, we found that AML progression lea
231 Using
intravital microscopy, we found that cerebral ischemia/r
232 Using
intravital microscopy, we found that Staphylococcus aure
233 Finally, using
intravital microscopy, we observe that tumor spheroids d
234 Using
intravital microscopy, we observed that neutrophilic rec
235 Here, through the application of confocal
intravital microscopy, we report that vascular permeabil
236 Using confocal
intravital microscopy, we revealed that liver injury due
237 Using
intravital microscopy, we show distinct cell dynamics of
238 Using
intravital microscopy, we show that Arhgap25 deficiency
239 By repeated high-resolution
intravital microscopy, we show that biopsy-like injury i
240 atical modelling, transplantation assays and
intravital microscopy, we show that haematopoiesis is re
241 ing early barrier permeability in vivo Using
intravital microscopy, we show that recurrent seizures a
242 Here, using confocal
intravital microscopy, we show that upon Toll-like recep
243 hird-order arterioles supplying the GM using
intravital microscopy.
244 ility in KRIT1 heterozygous mice as shown by
intravital microscopy.
245 cerebral endothelial cells were analyzed by
intravital microscopy.
246 d-labeled rat serum albumin using two-photon
intravital microscopy.
247 TBI when studied using Evans blue assay and
intravital microscopy.
248 models of acute vasoocclusive episodes using
intravital microscopy.
249 n a mouse model of arterial thrombosis using
intravital microscopy.
250 rial myeloid cell adhesion was quantified by
intravital microscopy.
251 microenvironment was observed in vivo using
intravital microscopy.
252 Intravital microvascular imaging revealed a haphazard we
253 meningeal and brain vessels when measured by
intravital multiphoton imaging and immunohistochemistry.
254 tumors using the in vivo invasion assay and
intravital multiphoton imaging of tumor cell streaming.
255 Intravital multiphoton imaging revealed that inhibition
256 transplantation, we applied high-resolution
intravital multiphoton imaging through the imaging windo
257 Intravital multiphoton imaging, confocal imaging of cryo
258 Through
intravital multiphoton microscopy (IV-MPM), allowing the
259 As evidenced by
intravital multiphoton microscopy of Ccr2 reporter mice,
260 Using longitudinal
intravital multiphoton microscopy of DC(GFP)/MC(RFP) rep
261 responses in vivo were assessed by combining
intravital multiphoton microscopy with flow cytometry an
262 icator targeted to neuronal mitochondria and
intravital multiphoton microscopy, we find increased mit
263 Using
intravital multiphoton microscopy, we show previously un
264 s, immunological readouts, and sophisticated
intravital multiphoton microscopy-based imaging of liver
265 amined over time to expected ovulation using
intravital multiphoton microscopy.
266 Kinetics of corneal leukocytes by
intravital multiphoton microscopy.
267 Here we describe an
intravital murine colonic window with a stabilizing ferr
268 ants into the ear pinna, this system enabled
intravital observation of xenografts by multiphoton micr
269 nd hemoglobin absorption, which act to limit
intravital optical techniques to large or subcutaneous t
270 Over the last few years, techniques such as
intravital,
optoacoustic and magnetic resonance imaging,
271 ansport in neurons of adult animals requires
intravital or ex vivo imaging approaches, which are labo
272 Here we demonstrate
intravital quantification of the myelin molecular struct
273 ty compared with control when measured using
intravital quantitative multiphoton microscopy.
274 Intravital real-time microscopy via cranial window revea
275 stom-built confocal microscope and performed
intravital real-time visualization of the absorption and
276 gate longitudinal responses, we developed an
intravital serial imaging approach that can directly vis
277 the first time: (1) the powerful utility of
intravital study of dendritic spine dynamics in the supe
278 In this study, we use
intravital subcellular microscopy in live mice to study
279 In addition,
intravital subcellular microscopy revealed that reduced
280 Using
intravital subcellular microscopy, we reveal that LTB4 e
281 Murine
intravital thrombosis studies demonstrated that CAP-PEs
282 Intravital thrombosis studies using ApoE(-/-) mice with
283 Therefore,
intravital two photon-based imaging of BDL mice was perf
284 fluoresce in vivo, thus allowing imaging by
intravital two-photon excitation microscopy.
285 t the LUXendin backbone can be optimized for
intravital two-photon imaging by installing a red fluoro
286 Concurrently,
intravital two-photon imaging revealed prompt peritubula
287 nto the blood and we have developed a stable
intravital two-photon lung imaging model in mice for dir
288 ism in vivo Here, we used the combination of
intravital two-photon microscopy and frequency-domain fl
289 icrobial niche by various methods, including
intravital two-photon microscopy and non-invasive whole-
290 Intravital two-photon microscopy demonstrated that LN ne
291 Using
intravital two-photon microscopy in the mouse model of m
292 were identified by immunohistochemistry and
intravital two-photon microscopy of kidneys of rats.
293 /-) CD8(+) T cells using in vitro assays and
intravital two-photon microscopy of lymphoid and nonlymp
294 g key cytoskeletal components and performing
intravital two-photon microscopy to visualize TRM cell b
295 Applying
intravital two-photon microscopy, we demonstrate the gat
296 vasculature in acute myeloid leukemia using
intravital two-photon microscopy.
297 Morphometric analyses of
intravital video microscopy data showed that gammadelta
298 f the ileal serosa or mucosa was recorded by
intravital videomicroscopy.
299 This removable
intravital window allowed manipulation and high-resoluti
300 No
intravital window has been developed for imaging the col