ライフサイエンスコーパス: intravital microscopy

1 n a mouse model of arterial thrombosis using intravital microscopy.

2 rial myeloid cell adhesion was quantified by intravital microscopy.

3 fully established breast carcinoma model by intravital microscopy.

4 adhesion and extravasation as visualized by intravital microscopy.

5 eritumoral pH were monitored over time using intravital microscopy.

6 for the GCaMP2 transgene) were studied with intravital microscopy.

7 tes in the rat peritoneal vascular bed using intravital microscopy.

8 in response to IVIG in vivo, using real-time intravital microscopy.

9 observed using a liver perfusion system and intravital microscopy.

10 ulation was analyzed at 0 hr and 2 hrs using intravital microscopy.

11 chronically infected mouse dermis imaged by intravital microscopy.

12 ment was evaluated by using flow chamber and intravital microscopy.

13 Uveitis was assessed by traditional and intravital microscopy.

14 tored in vivo at the single-cell level using intravital microscopy.

15 Cs display robust osteotropism visualized by intravital microscopy.

16 t plasma cells (PCs) in mouse lymph nodes by intravital microscopy.

17 el of sickle cell vaso-occlusion analyzed by intravital microscopy.

18 c cells, we used the approach of multiphoton intravital microscopy.

19 y response within the iris was quantified by intravital microscopy.

20 and MitoTracker fluorescence was detected by intravital microscopy.

21 microenvironment was observed in vivo using intravital microscopy.

22 hird-order arterioles supplying the GM using intravital microscopy.

23 ility in KRIT1 heterozygous mice as shown by intravital microscopy.

24 cerebral endothelial cells were analyzed by intravital microscopy.

25 d-labeled rat serum albumin using two-photon intravital microscopy.

26 TBI when studied using Evans blue assay and intravital microscopy.

27 models of acute vasoocclusive episodes using intravital microscopy.

28 Intravital microscopy(3), in which a tumor or organ is e

29 Advances in techniques such as multiphoton intravital microscopy (4, 5) have provided new insights

30 hen coupled the use of these biosensors with intravital microscopy, a powerful tool that can be used

31 ous oxidative burst capacity ex vivo, and by intravital microscopy, a reduced level of neutrophil mig

32 /-), and CX3CR1(gfp/+) mice were assessed by intravital microscopy after PBS, IL-1beta, TNF-alpha, or

33 an be extended for single cell imaging using intravital microscopy, allowing real-time tracking of an

34 t HSPCs, as well as how to perform calvarium intravital microscopy and analyze the resulting images.

35 The combination of intravital microscopy and animal models of disease has p

36 An intravital microscopy and closed cranial window system,

37 10 to 1,000 nm in diameter, is studied using intravital microscopy and computational modeling.

38 Here, using intravital microscopy and elemental analysis, we compare

39 ed DCs rather than macrophages, we performed intravital microscopy and ex vivo analyses after infecti

40 Using dynamic intravital microscopy and flow cytometry, we observed a

41 Here, using a combination of multiphoton intravital microscopy and genomic approaches, we re-exam

42 Intravital microscopy and histologic analysis of tumor n

43 and cellular infiltration was quantified by intravital microscopy and histologic assessment.

44 Ocular inflammation was assessed by intravital microscopy and histopathology.

45 CV diseases, in rat mesenteric vessels using intravital microscopy and in human arterial cells using

46 Intravital microscopy and in vivo tracking studies of B

47 y diameter and blood flow were recorded with intravital microscopy and laser speckle imaging.

48 edicted tumor growth with that observed from intravital microscopy and macroscopic imaging in vivo, f

49 Using spinning-disk confocal intravital microscopy and mice with fluorescent reporter

50 rior and posterior chamber was visualized by intravital microscopy and scanning laser ophthalmoscopy.

51 Using intravital microscopy and the mouse model of Lyme borrel

52 , Clay et al. provide unique insights, using intravital microscopy and the zebrafish-embryo model of

53 r location and phenotype were examined using intravital microscopy and time-of-flight mass cytometry.

54 ells was analyzed in vivo using conventional intravital microscopy and two-photon microscopy.

55 Taking advantage of intravital microscopy and using African trypanosomes as

56 e combination of whole body optical imaging, intravital microscopy, and "in vivo fluorescence trappin

57 optic bronchoscopy, in lung parenchyma using intravital microscopy, and in the whole body using fluor

58 timeframe that is well suited to analysis by intravital microscopy, and much has been learned in rece

59 fferent gene-deficient mice in flow chamber, intravital microscopy, and peritonitis studies.

60 ukocytes to the inflamed CNS, as assessed by intravital microscopy, and with a blunted inflammatory r

61 Leukocyte recruitment was analyzed by intravital microscopy; angiogenesis was evaluated by imm

62 r necrosis factor-alpha-stimulated tissue by intravital microscopy applying the dorsal skinfold chamb

63 the last decade, the application of 2-photon intravital microscopy as a tool to study cell interactio

64 irculation (n = 6/group) were obtained using intravital microscopy, as well as macrohemodynamic param

65 Using intravital microscopy assays, we demonstrated that trans

66 autoimmune encephalomyelitis (EAE), we used intravital microscopy, assessing local cellular interact

67 col, we describe experimental procedures for intravital microscopy based on a combination of thoracic

68 Here, we present an intravital microscopy-based assay for the quantification

69 In vivo intravital microscopy, bone marrow reconstitution, and A

70 rdiac and respiratory cycles severely limits intravital microscopy by compromising ultimate spatial a

71 By use of intravital microscopy, CRAMP was found to be deposited b

72 recruitment, migration, adhesion by means of intravital microscopy, degranulation, TNF-alpha release,

73 Intravital microscopy demonstrated a decreased ability o

74 Moreover, intravital microscopy demonstrated reduced post-traumati

75 Intravital microscopy demonstrates that histamine-induce

76 Intravital microscopy demonstrates that platelet PDI is

77 Intravital microscopy demonstrates that the movement of

78 ry venules under conditions of blood flow by intravital microscopy, exhibiting enhanced slow rolling

79 Intravital microscopy experiments show that upon enterin

80 Intravital microscopy experiments were performed using t

81 By using intravital microscopy experiments, we demonstrated that

82 As shown by intravital microscopy, FcgammaRIIA but not FcgammaRIIIB-

83 Neutrophil function was assessed by using intravital microscopy, flow chamber assays, and chemotax

84 erosclerotic plaques in vivo, as assessed by intravital microscopy, flow cytometry, and histological

85 Intravital microscopy following laser-induced vascular i

86 Intravital microscopy has been recognized for its abilit

87 Intravital microscopy has shown that microvascular units

88 Two-photon intravital microscopy has substantially broadened our un

89 cent developments in genetic engineering and intravital microscopy have allowed further molecular and

90 demonstrated using fluorescence multiphoton intravital microscopy; however, no differences in cytoki

91 tomatically removing motion artifacts during intravital microscopy imaging of organs and orthotopic t

92 orescence background allowed high-resolution intravital microscopy imaging of tumour vessels beneath

93 steroids on microvascular perfusion by using intravital microscopy in a mice model and to investigate

94 Using intravital microscopy in a murine model of polymicrobial

95 Previous studies using intravital microscopy in a sickle cell disease (SCD) mou

96 were conducted using catheter techniques and intravital microscopy in animals subjected to different

97 C-theta in neutrophil adhesion, we performed intravital microscopy in cremaster venules of mice recon

98 Here we show by intravital microscopy in humanized mice that perturbatio

99 Real-time intravital microscopy in immunocompromised (NOD/SCID) mi

100 Using intravital microscopy in Lgr5(EGFP-Ires-CreERT2) mice, w

101 Here we show by intravital microscopy in live mice that the regression p

102 Here we used multiphoton intravital microscopy in lymph nodes and tumors to show

103 Using fluorescence intravital microscopy in mice generated by crossing prot

104 Using intravital microscopy in mice, we demonstrated that quer

105 interaction with dermal blood vessels, using intravital microscopy in mice.

106 ecrosis of renal tubules, as demonstrated by intravital microscopy in models of IRI and oxalate cryst

107 Using multicolor confocal intravital microscopy in mouse models of sepsis, we obse

108 Using two-photon intravital microscopy in mouse models of sterile injury

109 ral and spatial resolutions using high-speed intravital microscopy in multiple channels of fluorescen

110 endothelium within minutes, as identified by intravital microscopy in the cremaster model.

111 Intravital microscopy in the cremasteric vasculature rev

112 Amorphous GFP+ deposits were visualized by intravital microscopy in the entheses of antibiotic-trea

113 terized ASC differentiation and migration by intravital microscopy in the lymph node (LN) by transfer

114 Here we used intravital microscopy in the salivary glands of live rod

115 Using intravital microscopy in the transparent larval zebrafis

116 through microfluidic studies in vitro and by intravital microscopy in vivo.We showthatmargination,whi

117 In this study we used confocal intravital microscopy in wild-type and Foxp3-GFP mice to

118 Using intravital microscopy, in a 10% FeCl3-induced thrombosis

119 Intravital microscopy is a key means of monitoring cellu

120 Intravital microscopy is a powerful technique to observe

121 Intravital microscopy is a powerful tool in neuroscience

122 Intravital microscopy is increasingly used to capture th

123 As a preclinical tool, intravital microscopy (IVM) allows for in vivo real-time

124 Intravital microscopy (IVM) and optical coherency tomogr

125 sease, we used multimodal imaging, including intravital microscopy (IVM) combined with bioluminescenc

126 Intravital microscopy (IVM) demonstrated that RvE1 rapid

127 t 20 years, the application and evolution of intravital microscopy (IVM) has vastly increased our abi

128 We imaged this process by intravital microscopy (IVM) in the ear skin of transgeni

129 Intravital microscopy (IVM) is an ideal tool to provide

130 Intravital microscopy (IVM) provides quantitative, quali

131 idative burst of murine neutrophils in vitro Intravital microscopy (IVM) showed increased association

132 All animals underwent serial MR imaging and intravital microscopy (IVM) up to 4 weeks after surgery.

133 Intravital microscopy (IVM) was used to observe changes

134 Intravital microscopy measurements of vascular length an

135 ng of neutrophil recruitment, organ-specific intravital microscopy methods are needed.

136 To test this, we developed a fetal intravital microscopy model in pregnant mice and, using

137 Using intravital microscopy, molecular techniques, and magneti

138 n vivo imaging, and specifically multiphoton intravital microscopy (MP-IVM), which allows for the inv

139 was detected by immunohistochemistry and by intravital microscopy observation of platelet aggregates

140 by using real-time multichannel fluorescence intravital microscopy of a tumor necrosis factor-alpha-i

141 Intravital microscopy of animals with chronic kidney fai

142 esion assays and during ex vivo perfusion or intravital microscopy of carotid arteries.

143 Intravital microscopy of caveolae-immunotargeted fluorop

144 Intravital microscopy of chemotherapy-treated mouse mamm

145 (2020) employ intravital microscopy of colorectal cancer organoid xeno

146 Using intravital microscopy of cremasteric microvasculature of

147 CD47(-)/(-) endothelium was corroborated by intravital microscopy of inflamed cremaster muscle micro

148 leukocytes to the endothelium as assessed by intravital microscopy of inflamed vessels of the cremast

149 Intravital microscopy of ischemic or tumor necrosis fact

150 using dual laser multichannel spinning-disk intravital microscopy of joints, the CXCR6-GFP, which al

151 Thrombus formation was quantified by intravital microscopy of laser-injured arterioles.

152 This was confirmed in rat intravital microscopy of lipopolysaccharide-induced crem

153 Studies using intravital microscopy of live mouse cremaster venules sh

154 using spatially defined organotypic culture, intravital microscopy of mammary tumours in mice and in

155 windows in mice have been developed to allow intravital microscopy of many different organs and have

156 Intravital microscopy of mesenteric venules showed that

157 Intravital microscopy of mouse cremaster muscle was perf

158 By using intravital microscopy of mouse cremaster muscle, the in

159 Intravital microscopy of mouse mesenteric venules demons

160 Intravital microscopy of NP spread in breast tumor tissu

161 n and resistance programs cooperate, we used intravital microscopy of orthotopic sarcoma and melanoma

162 We used intravital microscopy of rat cremaster muscle microcircu

163 Using intravital microscopy of the bloodstream of mice infecte

164 A murine model for intravital microscopy of the breathing lung under sealed

165 Intravital microscopy of the calvarium is the only nonin

166 Intravital microscopy of the carotid artery, the jugular

167 chamber assay of whole blood neutrophils and intravital microscopy of the inflamed cremaster muscle t

168 on podocyte calcium levels in vivo, we used intravital microscopy of the kidney in mice expressing t

169 Intravital microscopy of the mouse cremaster muscle conf

170 Using intravital microscopy of the mouse cremaster muscle, we

171 Intravital microscopy of TNFalpha-inflamed cremaster mus

172 perties of Pyr1 were investigated in vivo by intravital microscopy of tumor xenografts.

173 iogenic activity was further evidenced using intravital microscopy of tumors grown within dorsal skin

174 Using intravital microscopy of tumour necrosis factor-alpha-ch

175 a new method for stable, long-term 2-photon intravital microscopy of unrestrained large arteries in

176 dye-coupled nanoparticles can be tracked by intravital microscopy or even non-invasively by multispe

177 ing ischemia and reperfusion injury in vivo, intravital microscopy performed to study intravascular f

178 Intravital microscopy performed two hours following part

179 Intravital microscopy provides evidence of neutrophil NE

180 ontrolling regulated secretion and show that intravital microscopy provides unique opportunities to a

181 Intravital microscopy revealed a defect in LPS-induced n

182 Multiphoton intravital microscopy revealed a mixing of blood and bil

183 Direct evaluation of renal morphology by intravital microscopy revealed dilation of renal tubules

184 Intravital microscopy revealed heightened platelet adher

185 Intravital microscopy revealed IFNgamma-induced regressi

186 Whole-blood perfusion experiments and intravital microscopy revealed increased recruitment of

187 In addition, intravital microscopy revealed reduced leukocyte rolling

188 Intravital microscopy revealed reduced translocation and

189 Visualization by intravital microscopy revealed that administration of JW

190 Intravital microscopy revealed that at peak tumor accumu

191 Kidney intravital microscopy revealed that circulating neutroph

192 Intravital microscopy revealed that CX3CR1 is critical f

193 Intravital microscopy revealed that Cxcr3(-/-) T cells w

194 Time-lapse intravital microscopy revealed that enalapril reduces mo

195 Multiphoton intravital microscopy revealed that in contrast to CTLs,

196 Intravital microscopy revealed that in this setting, int

197 Multiphoton and spinning disk confocal intravital microscopy revealed that monocytes patrol bot

198 Intravital microscopy revealed that platelet depletion l

199 Intravital microscopy revealed that, in OVA-challenged P

200 In vivo studies using intravital microscopy show that PDI appears rapidly afte

201 Intravital microscopy showed decrease in leukocyte adhes

202 Intravital microscopy showed that blockade was at the ca

203 Intravital microscopy showed that cancer cells adhered d

204 Intravital microscopy showed that CYTH1 deficiency profo

205 Intravital microscopy showed that liver colonization by

206 Intravital microscopy showed that platelet and leukocyte

207 ion of histone citrullination, together with intravital microscopy, showed that NETosis occurred in t

208 mice in response to CCL20 or TNF-alpha, and intravital microscopy studies demonstrated that CD43(-/-

209 E-selectin-deficient endothelial cells, and intravital microscopy studies demonstrated that Th17 cel

210 In intravital microscopy studies of intact or EC-denuded sk

211 Finally, intravital microscopy studies of the mouse cremaster mic

212 Intravital microscopy studies reveal that CD47(-/-) Th1

213 Intravital microscopy studies revealed that activation o

214 Using intravital microscopy that allows us to visualize the st

215 We have demonstrated using intravital microscopy that anti-beta(2)-GP1 autoantibodi

216 ntly developed experimental techniques using intravital microscopy that are capable of directly probi

217 We show by intravital microscopy that cediranib significantly decre

218 ptical frequency domain imaging (OFDI) as an intravital microscopy that circumvents the technical lim

219 We adapted techniques of intravital microscopy that permitted TPM of organs maint

220 Here we demonstrate, using cerebral intravital microscopy, that in response to liver inflamm

221 form was further exploited for studying with intravital microscopy the extravasation of 0.58 kDa rhod

222 s, despite no physical contact with them; by intravital microscopy, the clustering of Ag-specific T c

223 According to intravital microscopy, the probe rapidly bound to beta-c

224 Thanks to the most recent advancements in intravital microscopy, this approach has finally been ex

225 Using intravital microscopy through a closed cranial window, h

226 Here, we used intravital microscopy to assess the effects of Ang II on

227 Using intravital microscopy to assess the pial microvasculatur

228 Using intravital microscopy to create microscopic lesions in t

229 Here, we used intravital microscopy to define lymphocyte trafficking r

230 Using state-of-the-art spinning disk intravital microscopy to delineate the different compart

231 re included: (a) laser-Doppler flowmetry and intravital microscopy to evaluate mesenteric perfusion;

232 Here, using intravital microscopy to evaluate mice lacking specific

233 wild type (WT) were studied using time-lapse intravital microscopy to examine leukocyte recruitment a

234 Furthermore, using intravital microscopy to ferric chloride (FeCl3)-injured

235 Here we apply intravital microscopy to identify a subpopulation of B c

236 The aim of this study was to use intravital microscopy to investigate adhesion and transm

237 Here, we used intravital microscopy to investigate how fibrin is remov

238 mbined contrast-enhanced ultrasonography and intravital microscopy to measure IMVR and gracilis arter

239 We used intravital microscopy to measure leukocyte-endothelium i

240 Here, we have used multilaser spinning-disk intravital microscopy to monitor the blood-borne stage i

241 ute lymphoblastic leukaemia (T-ALL) and used intravital microscopy to monitor the progression of dise

242 Using intravital microscopy to perform imaging studies of the

243 ing pipeline using plus-end tip tracking and intravital microscopy to quantify MT dynamics in live xe

244 To test junctional function, we used intravital microscopy to quantify the transport kinetics

245 Here we use quantitative intravital microscopy to reveal distinct steps of granul

246 er, in this issue of the JCI, Shi et al. use intravital microscopy to reveal that brain invasion by C

247 Here, we use two-photon intravital microscopy to show that immature B cell reten

248 We further used 2-photon and intravital microscopy to study endothelial activation an

249 d with mild TBI in humans and used long-term intravital microscopy to study the dynamics of the injur

250 Through application of confocal intravital microscopy to the mouse cremaster muscle, we

251 Using spinning-disk confocal intravital microscopy to track MRSA-GFP in vivo, we iden

252 d, we used scanning electron and brightfield intravital microscopy to visualize endothelial damage an

253 ay during retinal cell regeneration, we used intravital microscopy to visualize neutrophil, macrophag

254 ccount novel nanotechnology, biosensing, and intravital microscopy tools to monitor animal cancer mod

255 Although fluorescent proteins revolutionized intravital microscopy, two major challenges that still r

256 I-mediated thrombus formation was studied by intravital microscopy using a mouse model of Hermansky-P

257 Intravital microscopy via cranial window and flow cytome

258 When intravital microscopy was performed 3 days following inj

259 Intravital microscopy was performed during contrast-enha

260 Intravital microscopy was used to assess endothelium-dep

261 Intravital microscopy was used to examine the responses

262 Fluorescence intravital microscopy was used to visualize cellular tra

263 Intravital microscopy was used to visualize migration of

264 Here, using intravital microscopy we show that after infection of mi

265 Using multiphoton intravital microscopy we showed that neutrophils extrava

266 Using intravital microscopy, we demonstrate that PDI accumulat

267 Using real-time fluorescence intravital microscopy, we demonstrated that short-term c

268 Using intravital microscopy, we evaluated susceptibility to ca

269 Here, using multiphoton intravital microscopy, we examine the dynamic behaviour

270 By using spinning-disk confocal intravital microscopy, we examined the molecular mechani

271 Using intravital microscopy, we found that after mesenteric ar

272 Using intravital microscopy, we found that AML progression lea

273 Using intravital microscopy, we found that antibody-dependent

274 Using intravital microscopy, we found that cerebral ischemia/r

275 Using intravital microscopy, we found that endotoxemia in mice

276 Using intravital microscopy, we found that Staphylococcus aure

277 Finally, using intravital microscopy, we observe that tumor spheroids d

278 Furthermore, using intravital microscopy, we observed functional platelet-m

279 Using intravital microscopy, we observed that neutrophilic rec

280 Using lung intravital microscopy, we observed the dynamic formation

281 Here, through the application of confocal intravital microscopy, we report that vascular permeabil

282 Using confocal intravital microscopy, we revealed that liver injury due

283 Using intravital microscopy, we show distinct cell dynamics of

284 eractions in inflamed tissues using confocal intravital microscopy, we show how pericytes facilitate

285 Using intravital microscopy, we show that ADAMTS13 deficiency

286 Using intravital microscopy, we show that Arhgap25 deficiency

287 By repeated high-resolution intravital microscopy, we show that biopsy-like injury i

288 atical modelling, transplantation assays and intravital microscopy, we show that haematopoiesis is re

289 Using mouse models and intravital microscopy, we show that migrating PMNs expan

290 ing early barrier permeability in vivo Using intravital microscopy, we show that recurrent seizures a

291 Here, using confocal intravital microscopy, we show that upon Toll-like recep

292 Finally, using intravital microscopy, we show that, during CLA-induced

293 Using intravital microscopy, we showed that the number of leuk

294 (2)) and to activated venular endothelium on intravital microscopy were similar for MB(Ab) and MB(YSP

295 The studies combined high-resolution intravital microscopy with a photo-activatable fluoresce

296 ell function in tumors, we combined confocal intravital microscopy with depletion of CSF-1R-dependent

297 By using intravital microscopy with DREAM-null mice and their bon

298 Here we have combined dynamic intravital microscopy with ex vivo assessments of T cell

299 se the mouse hair follicle niche and combine intravital microscopy with genetic lineage tracing to re

300 By using intravital microscopy with mice lacking nicotinamide ade