ライフサイエンスコーパス: intravital microscopy

1 fully established breast carcinoma model by intravital microscopy.

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

3 adhesion and extravasation as visualized by intravital microscopy.

4 eritumoral pH were monitored over time using intravital microscopy.

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

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

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

8 observed using a liver perfusion system and intravital microscopy.

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

10 cerebral endothelial cells were analyzed by 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 r diabetic fatty (ZDF) rat was quantified by intravital microscopy.

22 rization and cell viability were assessed by intravital microscopy.

23 leukocyte transmigration, as demonstrated by intravital microscopy.

24 the mouse blood-brain barrier by two-photon intravital microscopy.

25 ctivated microvenules of Adamts13-/- mice by intravital microscopy.

26 ucosal postcapillary venules with the use of intravital microscopy.

27 -dependent, PSGL-1-independent rolling using intravital microscopy.

28 ture of the jejunum was studied with in vivo intravital microscopy.

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

30 l thrombus formation in a living mouse using intravital microscopy.

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

32 models of acute vasoocclusive episodes using intravital microscopy.

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

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

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

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

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

38 Intravital microscopy analysis of the mesenteric venules

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

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

41 ry mouse neutrophils in whole blood by using intravital microscopy and autoperfused flow chambers.

42 An intravital microscopy and closed cranial window system,

43 10 to 1,000 nm in diameter, is studied using intravital microscopy and computational modeling.

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

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

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

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

48 Intravital microscopy and histologic analysis of tumor n

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

50 Ocular inflammation was assessed by intravital microscopy and histopathology.

51 cytes to the small intestine, as revealed by intravital microscopy and homing studies.

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

53 Intravital microscopy and in vivo tracking studies of B

54 Using intravital microscopy and laser-induced injury to cremas

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

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

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

58 Using intravital microscopy and the mouse model of Lyme borrel

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

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

61 ir ability to detect and quantify ileitis by intravital microscopy and transabdominal US.

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

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

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

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

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

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

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

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

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

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

72 Using intravital microscopy assays, we demonstrated that trans

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

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

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

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

77 and T1DM-MV patients using computer-assisted intravital microscopy (CAIM).

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

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

80 Intravital microscopy demonstrated a decreased ability o

81 Intravital microscopy demonstrates that histamine-induce

82 Intravital microscopy demonstrates that platelet PDI is

83 Intravital microscopy demonstrates that the movement of

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

85 Intravital microscopy experiments analyzing EC-HY-specif

86 Intravital microscopy experiments show that upon enterin

87 By using intravital microscopy experiments, we demonstrated that

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

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

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

91 Intravital microscopy following laser-induced vascular i

92 Intravital microscopy has been recognized for its abilit

93 Intravital microscopy has shown that microvascular units

94 Two-photon intravital microscopy has substantially broadened our un

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

96 Using intravital microscopy, histological analysis, alpha-smoo

97 Biodistribution was monitored using intravital microscopy, histology, and integrated single-

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

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

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

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

102 assays under physiologic flow conditions and intravital microscopy in a mouse inflammation model each

103 Using intravital microscopy in a murine model of polymicrobial

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

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

106 Two-photon intravital microscopy in bone marrow cavities showed tha

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

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

109 Here we describe the use of multiphoton intravital microscopy in intact BM to visualize platelet

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

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

112 By using multiphoton intravital microscopy in lymph nodes (LNs) of anesthetiz

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

114 Using fluorescence intravital microscopy in mice generated by crossing prot

115 Using intravital microscopy in mice, we demonstrated that quer

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

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

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

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

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

121 g or adhering to endothelium were counted by intravital microscopy in parietal subsurface venules thr

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

123 Intravital microscopy in the cremasteric vasculature rev

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

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

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

127 Using intravital microscopy in the transparent larval zebrafis

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

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

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

131 nses in cremasteric venules of KO animals by intravital microscopy indicated a defect in transmigrati

132 Intravital microscopy is a key means of monitoring cellu

133 Intravital microscopy is a powerful tool in neuroscience

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

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

136 Intravital microscopy (IVM) demonstrated that RvE1 rapid

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

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

139 Accordingly, intravital microscopy (IVM) of PLN HEVs revealed a defec

140 Intravital microscopy (IVM) provides quantitative, quali

141 Intravital microscopy (IVM) showed that TCMs roll effici

142 Intravital microscopy (IVM) techniques have been employe

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

144 performed adoptive transfer experiments and intravital microscopy (IVM) using both S1P1-/- lymphocyt

145 Intravital microscopy measurements of vascular length an

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

147 Using intravital microscopy, molecular techniques, and magneti

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

149 Intravital microscopy of adoptively transferred B cells

150 Intravital microscopy of animals with chronic kidney fai

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

152 Intravital microscopy of caveolae-immunotargeted fluorop

153 Intravital microscopy of chemotherapy-treated mouse mamm

154 Using intravital microscopy of cremasteric microvasculature of

155 Moreover, intravital microscopy of gingival vessels showed that le

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

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

158 Intravital microscopy of ischemic or tumor necrosis fact

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

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

161 Studies using intravital microscopy of live mouse cremaster venules sh

162 Multiphoton intravital microscopy of lymph nodes has revolutionized

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

164 Intravital microscopy of mesenteric venules showed that

165 Intravital microscopy of mouse cremaster muscle was perf

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

167 Intravital microscopy of mouse mesenteric venules demons

168 Intravital microscopy of NP spread in breast tumor tissu

169 Intravital microscopy of plt/plt subiliac lymph nodes sh

170 We used intravital microscopy of rat cremaster muscle microcircu

171 Using intravital microscopy of the bloodstream of mice infecte

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

173 Intravital microscopy of the calvarium is the only nonin

174 Intravital microscopy of the carotid artery, the jugular

175 Intravital microscopy of the dermis revealed histamine-i

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

177 Intravital microscopy of the mouse cremaster muscle conf

178 Using intravital microscopy of the mouse cremaster muscle, we

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

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

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

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

183 CD93 as an adhesion molecule was found using intravital microscopy or analyzing peritoneal cell recru

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

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

186 Intravital microscopy performed two hours following part

187 readily obtainable during the course of most intravital microscopy protocols from systemically inject

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

189 Intravital microscopy revealed a >3-fold increase in pla

190 Intravital microscopy revealed a defect in LPS-induced n

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

192 Intravital microscopy revealed IFNgamma-induced regressi

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

194 In addition, intravital microscopy revealed reduced leukocyte rolling

195 Intravital microscopy revealed reduced translocation and

196 Visualization by intravital microscopy revealed that administration of JW

197 Intravital microscopy revealed that at peak tumor accumu

198 Kidney intravital microscopy revealed that circulating neutroph

199 Intravital microscopy revealed that CX3CR1 is critical f

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

201 Time-lapse intravital microscopy revealed that enalapril reduces mo

202 Multiphoton intravital microscopy revealed that in contrast to CTLs,

203 Intravital microscopy revealed that in this setting, int

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

205 Intravital microscopy revealed that platelet depletion l

206 Intravital microscopy revealed that, in OVA-challenged P

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

208 Intravital microscopy showed that blockade was at the ca

209 Intravital microscopy showed that cancer cells adhered d

210 Intravital microscopy showed that CYTH1 deficiency profo

211 Intravital microscopy showed that minocycline and NIM811

212 Intravital microscopy showed that platelet and leukocyte

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

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

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

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

217 Finally, intravital microscopy studies of the mouse cremaster mic

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

219 Intravital microscopy studies revealed that activation o

220 Intravital microscopy studies revealed that these FucTVI

221 Using intravital microscopy that allows us to visualize the st

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

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

224 We show by intravital microscopy that cediranib significantly decre

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

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

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

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

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

230 When analyzed by intravital microscopy, there was a 43% inhibition of leu

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

232 Using intravital microscopy through a closed cranial window, h

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

234 Using intravital microscopy to assess the pial microvasculatur

235 We used computer-assisted intravital microscopy to characterize RBC flow velocity

236 Using intravital microscopy to create microscopic lesions in t

237 Here, using intravital microscopy to evaluate mice lacking specific

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

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

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

241 sitive fluorochrome and digital multichannel intravital microscopy to image unstimulated and stimulat

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

243 To address this issue we used intravital microscopy to investigate the temporal profil

244 We used intravital microscopy to measure leukocyte-endothelium i

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

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

247 Using intravital microscopy to perform imaging studies of the

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

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

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

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

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

253 We developed a novel model using fluorescent intravital microscopy to study the effect of atrial natr

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

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

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

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

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

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

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

261 When intravital microscopy was performed 3 days following inj

262 Intravital microscopy was performed during contrast-enha

263 Intravital microscopy was used to assess endothelium-dep

264 Intravital microscopy was used to examine the responses

265 Intravital microscopy was used to visualize migration of

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

267 Using multiphoton intravital microscopy we showed that neutrophils extrava

268 Using intravital microscopy, we demonstrate that PDI accumulat

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

270 Using intravital microscopy, we evaluated susceptibility to ca

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

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

273 Using intravital microscopy, we found that after mesenteric ar

274 Using intravital microscopy, we found that AML progression lea

275 Using intravital microscopy, we found that antibody-dependent

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

277 Using intravital microscopy, we found that endotoxemia in mice

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

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

280 Using lung intravital microscopy, we observed the dynamic formation

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

282 Using intravital microscopy, we show distinct cell dynamics of

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

284 Using intravital microscopy, we show that ADAMTS13 deficiency

285 Using intravital microscopy, we show that Arhgap25 deficiency

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

287 Using intravital microscopy, we show that local vasodilation i

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

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

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

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

292 By combining confocal, electron, and intravital microscopy, we showed that the fibroblastic r

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