ライフサイエンスコーパス: in vivo imaging

1 rely on bulky optical elements that prevent in vivo imaging.

2 ical reporters for cell- and tissue-specific in vivo imaging.

3 ytochromes (BphPs) are of great interest for in vivo imaging.

4 ding pathogen, as visualized in real time by in vivo imaging.

5 orter of proteases has been demonstrated for in vivo imaging.

6 sition times and permitting highly sensitive in vivo imaging.

7 protein translation could be measured using in vivo imaging.

8 ethine dye designed and synthesized for SWIR in vivo imaging.

9 for the use of ADAPT probes for noninvasive in vivo imaging.

10 ar bacterial titers were monitored daily via in vivo imaging.

11 (III) has been viewed as a major obstacle to in vivo imaging.

12 f QD-bioconjugates for advanced in vitro and in vivo imaging.

13 er format with improved pharmacokinetics for in vivo imaging.

14 d (NIR) region are ideal for low back-ground in vivo imaging.

15 y encoded fluorescent probes for deep-tissue in vivo imaging.

16 pplication of IFPs for protein labelling and in vivo imaging.

17 d deposition was followed over 2 weeks using in vivo imaging.

18 ics as well as for biomarkers for diagnostic in vivo imaging.

19 ecruitment into the stroma was determined by in vivo imaging.

20 onal spectroscopy that has the potential for in vivo imaging.

21 ar cells (BCs) in the zebrafish retina using in vivo imaging.

22 d biomarkers for monitoring infections using in vivo imaging.

23 modulate olfactory responses in the MB with in vivo imaging.

24 reaction with fluorophores for in vitro and in vivo imaging.

25 in two different mouse strains by the use of in vivo imaging.

26 lanoma cells with potential significance for in vivo imaging.

27 bed the use of chemiluminescence systems for in vivo imaging.

28 ,5-tetrazines, particularly in live-cell and in vivo imaging, a major limitation has been the lack of

29 issue-mimicking phantoms and demonstrate its in vivo imaging ability of quantifying HbO2, HbR, sO2, c

30 of Bem1 to GTPase dynamics was borne-out by in vivo imaging: active Cdc42 was enriched at the cell p

31 We investigated this question by in vivo imaging activity in transgenic zebrafish express

32 hese novel quantum dots render them superior in vivo imaging agents compared with conventional quantu

33 great current interest as chemical sensors, in vivo imaging agents, and for photothermal therapeutic

34 vention as well as biomarkers for diagnostic in vivo imaging agents.

35 This may contribute to the understanding of in vivo imaging, allowing a better, noninvasive study of

36 histocompatibility antigen by phenotypic and in vivo imaging analyses.

37 a correlative gene-expression microarray and in vivo imaging analysis, and identified novel molecular

38 In vivo imaging and actuation of a swarm of magnetic hel

39 strate that iRFP713 is a progressive step in in vivo imaging and analysis that widens the optical ima

40 In vivo imaging and biodistribution studies showed a rap

41 d with the wild type mice as demonstrated by in vivo imaging and by elevated expression of angiogenes

42 re greatly promising for use as carriers for in vivo imaging and delivery.

43 powered microscopes which is unsuitable for in vivo imaging and diagnosis.

44 ht emission was quantitated in recipients by in vivo imaging and direct enzyme assay.

45 Novel in vivo imaging and electrophysiology methods allow long

46 Here we use in vivo imaging and genetic analysis in zebrafish to sho

47 Combining proteomics, in vivo imaging and genetic analysis of proteins linked

48 ir local and distant spread was monitored by in vivo imaging and histologic evaluation of the number

49 they develop quickly and are well suited for in vivo imaging and molecular approaches.

50 s), the second was 31 subjects who underwent in vivo imaging and postmortem histopathology for Abeta

51 Using real time in vivo imaging and subsequent composite fluorescence im

52 ritins can also be exploited as carriers for in vivo imaging and therapeutic applications, owing to t

53 tructural platforms required for integrating in vivo imaging and therapeutic response data with ex vi

54 then reviewed in terms of in vitro imaging, in vivo imaging, and cellular-process imaging, by means

55 c amyloid pathology and fibrillar amyloid on in vivo imaging, and increased numbers of activated huma

56 ed fluorescent proteins (IFPs) are ideal for in vivo imaging, and monomeric versions of these protein

57 Among these approaches is in vivo imaging, and specifically multiphoton intravital

58 The viability of the reagent for biological in vivo imaging application was also confirmed using Art

59 present the synthesis, characterization, and in vivo imaging applications of Copper-Caged Luciferin-1

60 le imaging modalities are often required for in vivo imaging applications that require both high prob

61 We developed an in vivo imaging approach for longitudinal tracking of sp

62 knowledge, S100A9 imaging represents a first in vivo imaging approach for the estimation of recruitme

63 The study evaluates an in vivo imaging approach to visualize peripheral blood m

64 This in vivo imaging approach will allow future detailed inve

65 Using a longitudinal in vivo imaging approach, we show how functional status

66 disease, using a combination of ex vivo and in vivo imaging approaches.

67 transplant method in adult zebrafish, using in vivo imaging as a non-invasive readout.

68 In vivo imaging at high spatiotemporal resolution is key

69 ion and emission spectra have advantages for in vivo imaging because of reduced scattering and absorp

70 excitation, hold promise for ultrasensitive in vivo imaging because they eliminate tissue autofluore

71 fluorescent proteins (FPs) are desirable for in vivo imaging because with these molecules less light

72 ltimate goal is to have clinical noninvasive in vivo imaging biomarkers of inflammation that will hel

73 ions in cell labeling, targeted in vitro and in vivo imaging, blood vessel imaging, cell tracing, inf

74 r-infrared (NIR) emission would be ideal for in vivo imaging but have proven difficult to engineer.

75 acoustic microscopy allows for label-free 3D in vivo imaging by detecting the acoustic response of a

76 We also demonstrate its utility for in vivo imaging by mapping the RFs of an array of bipola

77 New in vivo imaging clinical tools for noninvasive macrophag

78 eous over permanently fluorescent probes for in vivo imaging conditions of high autofluorescence and

79 In vivo imaging continues to reveal new insights on axon

80 In vivo imaging data were also fit well by the new PDE m

81 In vivo imaging data were supported by ex vivo biodistri

82 6 CRC cells that form viewable masses via an in vivo imaging device; genetically deficient mice were

83 Notably, in vivo imaging did not show measureable specific bindin

84 (19) F MRI is valuable for in vivo imaging due to the only trace amounts of fluorin

85 phytochromes attract attention as probes for in vivo imaging due to their near-infrared (NIR) spectra

86 d DNAzyme and inflammation were monitored by in vivo imaging (endoscopy) of mice.

87 r cortical area provide some of the earliest in vivo imaging evidence of prodromal Alzheimer's diseas

88 lantable bioengineered scaffold, amenable to in vivo imaging, ex vivo manipulation, and serial transp

89 These advances expand the potential of in vivo imaging experiments and facilitate experimentati

90 In vivo imaging experiments demonstrated that (18)F-FNDP

91 Results obtained during time-constrained in vivo imaging experiments may not be reproducible or a

92 ns to test in other animal model systems for in vivo imaging experiments.

93 In vivo imaging further revealed that in the initial pos

94 reby leukocytes enter sites of inflammation, in vivo imaging has been one of the key approaches used

95 usceptible mice; this is the first time such in vivo imaging has been performed under BSL-4 condition

96 this is the first time that antibody-guided in vivo imaging has been used for noninvasive diagnosis

97 Here we review how the use of in vivo imaging has contributed to our understanding of

98 In vivo imaging has revealed new details about how the m

99 minescence, vascular leakage by fluorescence in vivo imaging, histopathological changes by semiquanti

100 ransmissive multi-actuator adaptive lens for in vivo imaging in a mouse retina.

101 In vivo imaging in awake mice revealed that L2 cells had

102 e currently employed for in vitro as well as in vivo imaging in biology and medicine.

103 more, the use of confocal imaging of H2S and in vivo imaging in live zebra fish demonstrated FEPO's p

104 Using in vivo imaging in mice, we found that cocaine administr

105 BS device that allows for simultaneous live in vivo imaging in mice.

106 stability in aqueous media and were used for in vivo imaging in mice.

107 Using in vivo imaging in the developing brain of Xenopus laevi

108 crystals as promising fluorescent probes for in vivo imaging in this spectral region.

109 Using in vivo imaging in zebrafish, we demonstrate that Notch

110 ovide complementary molecular and functional in vivo imaging information on antiangiogenic treatment

111 The utility of NanoLuc for in vivo imaging is also demonstrated.

112 gning smart activatable probes for real-time in vivo imaging is also discussed.

113 In vivo imaging is critical, because the histopathologic

114 Feasibility of in vivo imaging is demonstrated by tracking a monomolecu

115 High-resolution in vivo imaging is of great importance for the fields of

116 hough T cells can be labeled for noninvasive in vivo imaging, little is known about the impact of suc

117 In vivo imaging may enable real-time follow-up of changi

118 Reflectance confocal microscopy (RCM) is an in vivo imaging method to get morphologic information ab

119 sibility of the use of a rapid, noninvasive, in vivo imaging method to measure fatty acid fractions o

120 In this study, we adapted a novel in vivo imaging method, originally developed in mouse re

121 her illustrate that, despite the challenges, in vivo imaging methods can be very powerful and provide

122 While in vivo imaging methods have demonstrated rapid changes

123 We used high-resolution mini-endoscopy and in vivo imaging methods to assess colitis progression.

124 tting more and more into the focus of modern in vivo imaging methods.

125 demonstrated in rat lungs by three different in vivo imaging modalities.

126 sitive and reliable preclinical longitudinal in vivo imaging model for this purpose, thereby facilita

127 Our in vivo imaging observations suggest that abnormalities

128 MR at 7 T enables in vivo imaging of (35)Cl in human brain and muscle in c

129 translational potential are demonstrated by in vivo imaging of a mouse colon, a rat esophagus, and s

130 alized for designing specific probes for the in vivo imaging of a variety of proteins and enzymes.

131 and screened regarding their suitability for in vivo imaging of alphavbeta6 integrin expression by PE

132 In vivo imaging of AS-PaRac1 revealed that a motor learn

133 ent and nuclear probe promises a new way for in vivo imaging of bacterial infections.

134 s the possibility of noninvasive, label-free in vivo imaging of BCCs that could reduce the time from

135 We performed longitudinal in vivo imaging of beta-cell calcium dynamics and islet

136 rerio) is an excellent vertebrate model for in vivo imaging of biological phenomena at subcellular,

137 t 1550 nm emitting nanoparticles enable fast in vivo imaging of blood vasculature in the mouse brain

138 the NSIN mice facilitated the monitoring and in vivo imaging of both leukemia and solid tumors.

139 ical 3.0-T MR imaging unit and were used for in vivo imaging of bound and pore water in cortical bone

140 emerged as a potential novel radiotracer for in vivo imaging of brain alpha2C adrenoceptors.

141 In vivo imaging of brain beta-amyloid, a hallmark of Alz

142 Here, we utilized in vivo imaging of C. muridarum infection in mice follow

143 ears the first reports of the feasibility of in vivo imaging of cancer with biocompatible SERS probes

144 behavioral learning, we performed two-photon in vivo imaging of cerebellar parallel fibers (PFs) in a

145 In vivo imaging of CSN activity during performance revea

146 In vivo imaging of cutaneous inflammation in the dorsal

147 bution profiles and both nuclear and optical in vivo imaging of Cy5-(111)In -DTPA-Tyr(3)-octreotate w

148 cortical hypodopaminergia in schizophrenia, in vivo imaging of dopamine release in the PFC has not b

149 we present a nanosensor for rapid, real-time in vivo imaging of drug-induced ROS and RNS for direct e

150 B1 accumulates at the flagellar tip, we used in vivo imaging of fluorescent protein-tagged EB1 (EB1-F

151 Using in vivo imaging of genetically encoded calcium reporters

152 Biochemical assays and in vivo imaging of H2O2 revealed that, relative to the c

153 ted DPA-713, a synthetic ligand of TSPO, for in vivo imaging of host response.

154 Here, by combining in vivo imaging of Hsp104-associated aggregates, a form

155 ection of PARPi-FL allowed for high contrast in vivo imaging of human OSCC models in mice with a surg

156 Here, we report direct in vivo imaging of hyperpolarized (29)Si nuclei in silic

157 hypoxia and inflammation was investigated by in vivo imaging of hypoxia and measurement of cytokines

158 In vivo imaging of implanted EMT6 murine and BT474 human

159 However, in vivo imaging of infected animals revealed persistentl

160 o our knowledge, this is the first report of in vivo imaging of infection with any member of the Pico

161 In vivo imaging of intact embryos of both sexes revealed

162 In vivo imaging of live zebrafish embryos revealed that

163 monstrated the capability of porphysomes for in vivo imaging of lung tumors in the mucosal/submucosal

164 Direct in vivo imaging of lymph flow is key to understanding ly

165 Here, we tested in vivo imaging of lymphoid cell death using a near-infr

166 me complementation approach for in vitro and in vivo imaging of lysine 9 (H3-K9 sensor) and lysine 27

167 werful potential applications such as direct in vivo imaging of mechanisms of action or hypoxia sensi

168 ered unsuitable as a specific PET ligand for in vivo imaging of mGluR2.

169 ntubation, our setup uniquely allows dynamic in vivo imaging of mucociliary clearance and steady-stat

170 Quantitative in vivo imaging of myelin loss and repair in patients wi

171 ewly developed technique for high-resolution in vivo imaging of myelinated axons in the brain, spinal

172 cardioCEST MRI enables in vivo imaging of myocardial fibrosis using endogenous

173 scent protein in cardiomyocytes, allowing an in vivo imaging of myofilaments.

174 In vivo imaging of N-methyl-d-aspartate (NMDA) glutamate

175 for extraction of classic Braak staging from in vivo imaging of neurofibrillary tau tangles have not

176 dent inflammatory responses were detected by in vivo imaging of NF-kappaB reporter mice with CDI that

177 Conclusion:(11)C-Me-NB1 is suitable for the in vivo imaging of NMDA GluN1/GluN2B receptors and the a

178 Multimodal dynamic in vivo imaging of NSC behaviors in the brain is necessa

179 CDy11 was further demonstrated for in vivo imaging of P. aeruginosa in implant and corneal

180 study showing the feasibility of noninvasive in vivo imaging of PD-L1 expression in tumors.

181 In vivo imaging of prodromal hippocampus CA1 subfield ox

182 GRPr affinity ligands have shown promise for in vivo imaging of prostate cancer with PET.

183 ion:(64)Cu-CBP7 is a promising candidate for in vivo imaging of pulmonary fibrosis.

184 uce a platform for large-scale, quantitative in vivo imaging of regenerating skin and reveal unantici

185 oglycans has a pathophysiologic validity for in vivo imaging of rheumatoid arthritis (RA) and its res

186 -2-deoxy-2-fluoroarabinose ([(18)F]DFA), for in vivo imaging of ribose salvage.

187 In vivo imaging of roots expressing a genetically encode

188 In vivo imaging of single optic tectal neurons coexpress

189 A-RGD PET for alphavbeta3 integrin molecular in vivo imaging of spontaneous PDAC occurring in Ptf1a(+

190 e demonstrate non-invasive, high resolution, in vivo imaging of subcortical structures within an inta

191 ocompatible near-infrared II fluorophore for in vivo imaging of TBI is designed.

192 In vivo imaging of the A1 adenosine receptor (A1AR) usin

193 Improved in vivo imaging of the cornea during acute hydrops has l

194 cortical areas directly beneath electrodes, in vivo imaging of the cortical vasculature via fluoresc

195 This molecular OCT method enables in vivo imaging of the expression profiles of lymphatic

196 Confocal in vivo imaging of the mouse EAE spinal cord reveals tha

197 Thus, the key preparation steps for in vivo imaging of the neural injury response described

198 Longitudinal in vivo imaging of the retina showed the relative anatom

199 However, repeated in vivo imaging of the same glomerulus over extended per

200 In vivo imaging of the spinal cord reveals the swift dev

201 Here, we establish in vivo imaging of the spinal cord, one of the main site

202 In vivo imaging of these receptors with selective 5HT4R

203 le, for the first time, specific, measurable in vivo imaging of this target protein, along with asses

204 99mTc-anti-CD56 is a promising tool for in vivo imaging of TINK cell trafficking.

205 In vivo imaging of transmission using synaptically targe

206 In vivo imaging of tumor angiogenesis was performed usin

207 Over the past several years, in vivo imaging of tumors using multiphoton microscopy h

208 In vivo imaging of VCAM-1 also demonstrated an acute dec

209 t-to-background ratio was suboptimal for the in vivo imaging of VCAM-1 expression in atherosclerotic

210 Using in vivo imaging of zebrafish and mouse tumor models, we

211 ctive candidate for material imaging such as in-vivo imaging of biological systems containing soft ti

212 Finally, near-infrared in vivo imaging performed in IL-7Ralpha(-/-) mice reveal

213 been devised as powerful potential tools for in vivo imaging, photothermal therapy, and drug delivery

214 rum over 24 hours, and (c) comparison of the in vivo imaging potential of the fragments was evaluated

215 the past decade has been the development of in vivo imaging probes targeted to amyloid beta protein,

216 tion and was critical for achieving suitable in vivo imaging properties, positioning [(18)F]5 and [(1

217 For a precise understanding of in vivo imaging results in terms of disease mechanisms d

218 In vivo imaging results were confirmed by postmortem tri

219 activity of preparations of both tracers on in vivo imaging results.

220 In vivo imaging revealed light-induced cycles in assimil

221 In vivo imaging revealed more ROS in joints of arthritic

222 In vivo imaging revealed sensory-evoked responses, inclu

223 When in vivo imaging revealed that dendritic spines are dynam

224 High-resolution in vivo imaging revealed that Erbb2 signaling regulates

225 In vivo imaging revealed that fetuses from mice that und

226 In vivo imaging revealed that intraglomerular NETs were

227 Multiphoton in vivo imaging reveals close to 30% loss of apical dend

228 In vivo imaging reveals that the dendritic filopodial dy

229 Novel in vivo imaging reveals that, in the developing mouse br

230 tending this knowledge by demonstrating with in vivo imaging sensitive to iron accumulation, one mark

231 Two-photon in vivo imaging showed a weaker visual response of PV-ce

232 time of reperfusion, indocyanine green-based in vivo imaging showed that CD47mAb-treated organs had g

233 In vivo imaging showed that siglec-E also promoted ROS i

234 In our study, in vivo imaging shows that after the immunization, SAM A

235 In vivo imaging studies have confirmed that synaptic pru

236 In vivo imaging studies in a monkey showed that the radi

237 In vitro binding studies and in vivo imaging studies in Wistar rats showed moderate b

238 In vivo imaging studies of alpha-synuclein-GFP transgeni

239 rain have been overturned in recent years by in vivo imaging studies revealing synaptic remodeling, n

240 The objective of the in vivo imaging studies was to determine the minimum num

241 for rational choice of optimal marker(s) for in vivo imaging studies.

242 n neural circuits is essential for long-term in vivo imaging studies.

243 Herein, we present an in vivo imaging study using positron emission tomography

244 In the in vivo imaging study we found that (18)F-dihydroxypheny

245 EC-infected mice by bioluminescence using an in vivo imaging system (IVIS).

246 ression of luciferase was quantitated via an in vivo imaging system (IVIS).

247 and after gestation were established with an in vivo imaging system (IVIS).

248 An in vivo imaging system study was conducted after injecti

249 By developing an in vivo imaging system to measure cyclic GMP production

250 Using a pneumococcal colonization model, an in vivo imaging system, and a multiplex assay for cytoki

251 es (ZOI) were measured visually and using an in-vivo imaging system (IVIS).

252 Additionally, use of in vivo imaging systems detecting light emitted from luc

253 n and precorneal retention were evaluated by in vivo imaging technique and ocular pharmacokinetics st

254 Diffusion tensor imaging (DTI) is a unique in vivo imaging technique that allows three-dimensional

255 The validity of QSM as a suitable in vivo imaging technique with which to monitor iron dys

256 confocal microscopy (RCM), a cellular-level, in vivo imaging technique, may be potentially used for m

257 ere we show, using a novel synchrotron-based in vivo imaging technique, that wild-type pigs display b

258 In vivo imaging techniques are powerful tools for evalua

259 State-of-the art in vivo imaging techniques are striving to achieve a sim

260 Yet, in vivo imaging techniques for measuring glutamate acros

261 TLPR) on serotonin transporter binding using in vivo imaging techniques have yielded inconsistent fin

262 In vivo imaging techniques including magnetic resonance

263 y in mice, which we detected using different in vivo imaging techniques.

264 Sensitive in vivo imaging technologies applicable to the clinical

265 Recent application of state-of-the-art in vivo imaging technologies is illuminating mechanisms

266 seful positron emitting isotope for use with in vivo imaging technology that potentially has extensiv

267 Although they can be used to in vivo imaging, their application has yet to be realize

268 Multi-photon in vivo imaging through a cranial window allowed us to c

269 clinically relevant to develop non-invasive in vivo imaging to detect this endothelial activation.

270 findings open the possibility of harnessing in vivo imaging to determine the contributions of strios

271 emistry, biology and materials science, from in vivo imaging to distance measurements in spin-labelle

272 We used in vivo imaging to investigate how bipolar cells transmi

273 The aim of this study was to use multimodal in vivo imaging to investigate the impact of systemic Ak

274 os promoter as well as time-lapse two-photon in vivo imaging to monitor neuronal activation triggered

275 l-model studies, and approaches ranging from in vivo imaging to novel neuroanatomical, molecular, epi

276 Forster and colleagues used in vivo imaging to tell a different story, in which each

277 Modern in vivo imaging tools can detect vascular narrowing and

278 uptake, internalization, hydrophobicity, and in vivo imaging using PET.

279 ar deprivation (MD) in adult V1 with chronic in vivo imaging using two-photon microscopy and determin

280 scales, from super-resolution microscopy to in vivo imaging, using the same probes.

281 ding cTK function in apoptotic cells and the in vivo imaging varies depending on the experiment.

282 In vivo imaging was complemented by ex vivo fluorescence

283 In vivo imaging was performed on 4 groups of CD1-deficie

284 consecutive S100A9 expression as depicted by in vivo imaging was significantly increased.

285 Using in vivo imaging we found that, early in hair growth, cel

286 Furthermore, by using real-time in vivo imaging we observed that CX3CR1(+) cells migrate

287 Using zebrafish mutants and in vivo imaging, we identified the Kif1B motor and its i

288 Through the use of real-time in vivo imaging, we observe disruption in thyroid follic

289 patient-derived melanoma cells and real-time in vivo imaging, we show a widespread distribution of mi

290 single-plane illumination microscopy (SPIM) in vivo imaging, we show that (1) the sequence of arriva

291 irradiation, bone marrow transplantation and in vivo imaging, we show that preserved muscle integrity

292 In vivo imaging, which enables us to peer deeply within

293 vided the mechanical stability necessary for in vivo imaging while allowing free movement between beh

294 Materials and Methods In vivo imaging with (129)Xe was performed in three heal

295 In vivo imaging with a fluorescent dye for new bone form

296 press these receptors in sufficient amounts, in vivo imaging with a single radioligand may not always

297 ange of mouse SPECT applications by enabling in vivo imaging with less than a megabecquerel of tracer

298 drive waveforms for in vitro biosensing and in vivo imaging with MPI.

299 In vivo imaging with PET may offer important insights in

300 pid, stable immobilization of planarians for in vivo imaging without injury or biochemical alteration