ライフサイエンスコーパス: multiphoton

1 Here, by using multiphoton ablation lithography to pattern surfaces wit

2 Various emission mechanisms, such as multiphoton absorption or emission, optical or dc field

3 visible (Vis) regions of the spectrum via a multiphoton absorption process, known as upconversion.

4 ermeabilisation mechanism requires efficient multiphoton absorption to produce free electrons but onc

5 the emergence of nonlinear phenomena such as multiphoton absorption, biexcitons, and carrier multipli

6 h a very high degree of ionization, owing to multiphoton absorption, which in a heteronuclear molecul

7 crystals possess high PLQY of ~51.1%, a high multiphoton action cross-sections that can rival the cur

8 orescence-lifetime imaging microscopy/phasor multiphoton analysis with confocal microscopy, implement

9 Live studies combining video-rate multiphoton and confocal imaging in 4D demonstrate the p

10 testinal tissues were analyzed by histology, multiphoton and confocal microscopy, and real-time polym

11 l and oxidative metabolism was visualized by multiphoton and light sheet microscopy in cultured bovin

12 xtended semiclassical analysis, the roles of multiphoton and multiple rescattering trajectories on th

13 Multiphoton and spinning disk confocal intravital micros

14 We used multiphoton and time-lapse confocal microscopy to monito

15 Finally, multiphoton- and microPET/CT imaging indicate its abilit

16 Moreover, we discover that the multiphoton- and tunneling-ionization regimes in multipl

17 In this study, we present a novel multimodal multiphoton approach for quantifying hemoglobin concentr

18 Tissues were imaged using multiphoton autofluorescence and second harmonic generat

19 graphy in dysplasia using in vivo volumetric multiphoton autofluorescence microscopy and second harmo

20 TPEF was collected through multiphoton bandpass filters to obtain AF, SHG (collagen

21 Using multiphoton Ca(2+) imaging, we verified that activation

22 Using in vivo multiphoton calcium imaging from transgenic PUb-GCaMP6s

23 Here, we use multiphoton calcium imaging to monitor cortical feedback

24 nert at the high concentrations required for multiphoton chemical physiology.

25 ed, including three-dimentional lithography, multiphoton chirality transfer, polarization effects in

26 cal simplicity, representative sampling, and multiphoton compatibility.

27 scein-conjugated gelatin and observed with a multiphoton confocal microscope.

28 We demonstrate multiphoton control by using a superconducting transmon

29 ulate a generalized method for measuring the multiphoton cross section of fluorophores and use it to

30 complex mixtures of polymers using infrared multiphoton decay (IRMPD) and electron capture dissociat

31 essure cell of the QLT with a short infrared multiphoton dissociation (IRMPD) activation in the low-p

32 fragmentation methods are employed, infrared multiphoton dissociation (IRMPD) and electron-induced di

33 ectron transfer dissociation (AI-ETD) and IR multiphoton dissociation (IRMPD) experiments can be carr

34 Infrared multiphoton dissociation (IRMPD) has been used in mass s

35 n trap mass spectrometer to perform infrared multiphoton dissociation (IRMPD) in the low-pressure tra

36 n digests, we demonstrate selective infrared multiphoton dissociation (IRMPD) of S-sulfonated peptide

37 sociation (AI-EDD) and negative ion infrared multiphoton dissociation (IRMPD) were employed to invest

38 xture is isolated and fragmented by infrared multiphoton dissociation (IRMPD).

39 brational transitions via resonance-enhanced multiphoton dissociation detected by Ca(+) fluorescence.

40 on intermediates to applications of infrared multiphoton dissociation spectroscopy (IRMPD) to interme

41 n intermediate was characterized by infrared multiphoton dissociation spectroscopy and was trapped wi

42 anionic forms are characterized by infrared multiphoton dissociation spectroscopy.

43 racterization of phosphopeptides by infrared multiphoton dissociation two-dimensional mass spectromet

44 We find that the multiphoton-dominated trajectories only involve the elec

45 ion and development in harnessing the unique multiphoton effect of UCNPs for photosensitive materials

46 nal chromophore, as a first manifestation of multiphoton effects.

47 ombs can be used to generate several bi- and multiphoton entangled qubits, with direct applications f

48 ing photonic quantum gates and deterministic multiphoton entanglement.

49 recent achievements in the understanding of multiphoton excitation and the resulting photoluminescen

50 e heterogeneity, and poor compatibility with multiphoton excitation because of local heating.

51 omerization interactions in living cells via multiphoton excitation fluorescence correlation spectros

52 By simultaneous observation of multiphoton excitation fluorescence emission and second

53 We demonstrated this approach using multiphoton excitation of the Blastochloris viridis phot

54 py, a method integrating one-shot multicolor multiphoton excitation through wavelength mixing and ser

55 Excitation of this pair by a single multiphoton excitation wavelength (MPE, 850 nm) yields w

56 d imaging of the fluorescence lifetime using multiphoton excitation.

57 nue for the exploitation of high-performance multiphoton excited hybrid single microcrystal for futur

58 development of the photostable higher-order multiphoton-excited (MPE) upconversion single microcryst

59 Thus, the novel multiphoton-excited 3D printing technique produces extra

60 Here, we used multiphoton-excited 3D printing to generate a native-lik

61 on laser to follow the structural changes in multiphoton-excited bR from 250 femtoseconds to 10 picos

62 We introduce a compact, fast large area multiphoton exoscope (FLAME) system with enhanced molecu

63 te non-invasive imaging techniques, based on multiphoton fluorescence and quantitative second harmoni

64 of ex vivo and in vivo rabbit corneas using multiphoton fluorescence and second harmonic generation

65 Here, we present a multiphoton fluorescence anisotropy microscopy live cell

66 s as a model of spontaneous albuminuric CKD, multiphoton fluorescence imaging and single-vessel physi

67 Multiphoton fluorescence lifetime imaging microscopy (FL

68 resonance energy transfer-based system using multiphoton fluorescence lifetime imaging microscopy and

69 In conventional confocal/multiphoton fluorescence microscopy, images are typicall

70 Osteocyte responses are imaged by using multiphoton fluorescence microscopy.

71 nging distortions from impedance mismatch in multiphoton fluorescence microscopy.

72 o differences in viscosity were detected via multiphoton fluorescence recovery after photobleaching (

73 e use of a dorsal skinfold chamber model and multiphoton fluorescence resonance energy transfer micro

74 evious studies based on spectrally resolved, multiphoton fluorescence resonance energy transfer.

75 Moxifloxacin has bright intrinsic multiphoton fluorescence, good tissue penetration and hi

76 Multiphoton FRAP provided the specific binding constants

77 ubit can be used to realise both single- and multiphoton frequency-conversion processes.

78 Multiphoton-generated cyclooctynes undergo a SPAAC react

79 Multiphoton glutamate uncaging experiments revealed that

80 Multiphoton glutamate uncaging experiments revealed that

81 -guided genome mining) alongside multiplexed multiphoton-holography (MultiSLM), achieving control of

82 Multiphoton images were comparable to histologic section

83 nd brain vessels when measured by intravital multiphoton imaging and immunohistochemistry.

84 in assemblies have been employed for in vivo multiphoton imaging and lifetime-based oxygen measuremen

85 In vivo multiphoton imaging and neural manipulations delineated

86 Here we use multiphoton imaging and patch-clamp recording, and obser

87 We use in vivo multiphoton imaging and show that mechanical forces duri

88 Our results demonstrate that multiphoton imaging can be used for fast and sensitive c

89 Live, multiphoton imaging demonstrated a selective vulnerabili

90 le cells (abGCs) in the olfactory bulb using multiphoton imaging in awake and anesthetized mice.

91 motor behaviour are an inevitable problem of multiphoton imaging in awake behaving animals, particula

92 s of SN/CM co-cultures, ex vivo confocal and multiphoton imaging in clarified hearts, and biochemical

93 In this study, we used multiphoton imaging in Foxp3-GFP mice to examine the beh

94 resonance imaging, radiolabeled tracers, and multiphoton imaging in rodents to show instead that cere

95 Here, by combining chemoinformatics and multiphoton imaging in the mouse, we show that both the

96 In vivo multiphoton imaging of CD11c-EYFP mice revealed that int

97 Multiphoton imaging of developing mouse cortex reveals t

98 by Malpighi to the current use of single and multiphoton imaging of intravital and isolated perfused

99 inflammatory events (day 3 of UUO), in vivo multiphoton imaging of the intact kidney of CD11c report

100 ng the in vivo invasion assay and intravital multiphoton imaging of tumor cell streaming.

101 We developed an in vivo multiphoton imaging paradigm to study alpha-synuclein ag

102 Moreover, in vivo multiphoton imaging revealed that deafening-induced chan

103 Intravital multiphoton imaging revealed that inhibition of CSF1R in

104 Multiphoton imaging revealed that paxillin-deficient neu

105 In brain slices of rat PFC, we employed multiphoton imaging simultaneously with whole-cell elect

106 Multiphoton imaging suggested that most microspheres wer

107 e further demonstrate how this high-speed 3D multiphoton imaging system can be used to study neuronal

108 ation, we applied high-resolution intravital multiphoton imaging through the imaging window during in

109 We used multiphoton imaging to visualize genetically defined pro

110 ined molecular dynamics simulations, Laurdan multiphoton imaging, and atomic force microscopy microin

111 the laser power required for adaptive optics multiphoton imaging, and for facilitating integration wi

112 Intravital multiphoton imaging, confocal imaging of cryosections an

113 lectrocardiography recordings and high-speed multiphoton imaging, to assess Ca(2+) handling, revealed

114 Using in vivo longitudinal multiphoton imaging, we found orchestrated activity-depe

115 Using intracranial multiphoton imaging, we found that infusion of 100 ng of

116 By intravital multiphoton imaging, we found that the motility of CD4(+

117 Using electrophysiology with concurrent multiphoton imaging, we show that layer 6 pyramidal cell

118 grating online image analysis with automated multiphoton imaging.

119 e combined with technologies such as in vivo multiphoton imaging.

120 e clearance in aged Tg2576 mice with in vivo multiphoton imaging.

121 cruitment by coupling mechanical loading and multiphoton imaging.

122 multiple columns and layers using high-speed multiphoton imaging.

123 nile mice of both sexes, using widefield and multiphoton imaging.

124 Multiphoton in vivo imaging reveals close to 30% loss of

125 Using mouse models and multiphoton intravital imaging, we have identified a cru

126 roaches is in vivo imaging, and specifically multiphoton intravital microscopy (MP-IVM), which allows

127 Here, using a combination of multiphoton intravital microscopy and genomic approaches

128 Here we used multiphoton intravital microscopy in lymph nodes and tum

129 Multiphoton intravital microscopy revealed a mixing of b

130 Multiphoton intravital microscopy revealed that in contr

131 Using multiphoton intravital microscopy we showed that neutrop

132 Here, using multiphoton intravital microscopy, we examine the dynami

133 Resonance-enhanced multiphoton ionisation (REMPI) can be used to prepare mo

134 Direct infusion resonance-enhanced multiphoton ionization (DI-REMPI) was performed on liqui

135 Hs in aqueous samples, is resonance-enhanced multiphoton ionization (REMPI) coupled to external-membr

136 al carbon analyzer with a resonance-enhanced multiphoton ionization (REMPI) mass spectrometer.

137 ectrons) through a 2 + 1 resonantly-enhanced multiphoton ionization (REMPI) scheme targeting molecula

138 ation (SPI, 118 nm) or by resonance enhanced multiphoton ionization (REMPI, 266 nm), and the molecula

139 romatography coupled to a resonance-enhanced multiphoton ionization - time-of-flight mass spectrometr

140 ulations that for the first time incorporate multiphoton ionization and dielectric models that are ne

141 On the other hand, the multiphoton ionization regime is responsible for the eve

142 Resonance enhanced multiphoton ionization spectroscopy (REMPI) generates si

143 Using resonance-enhanced multiphoton ionization spectroscopy to investigate the p

144 olation, cavity ringdown, resonance enhanced multiphoton ionization, and ion trapping have led to the

145 highly sensitive way via resonance-enhanced multiphoton ionization.

146 the PAHs, and a 193 nm laser, which requires multiphoton ionization.

147 Resonance-enhanced multiphoton ionization/time-of-flight mass spectrometry

148 Multiphoton laser scanning in vivo microscopy showed tha

149 -3 could be tracked in the intestine through multiphoton laser scanning microscopy in an ex vivo inte

150 Using multiphoton laser scanning microscopy, we examined the s

151 Many IVM strategies employ a strong multiphoton laser that penetrates deeply into the tissue

152 Multiphoton laser-scanning microscopy (MPLSM) or optical

153 wake, lightly sedated, responsive mice using multiphoton laser-scanning microscopy and novel genetic

154 ng, but the signal-to-noise ratio for a dim (multiphoton) light response is increased at night becaus

155 In this report, we develop a versatile multiphoton lithography method that enables rapid fabric

156 xploit the rapid prototyping capabilities of multiphoton lithography to create and characterize a cel

157 rom a biocompatible precursor solution using multiphoton lithography, an intrinsically 3D laser direc

158 Exploiting multiphoton lithography, microchannel networks spanning

159 nanocrystalline platinum and palladium using multiphoton lithography.

160 Here, using multiphoton live cell imaging in mouse kidney tissue, FI

161 Raman and multiphoton luminescence together with transmission elec

162 on upon irradiation with NIR light through a multiphoton mechanism.

163 uantitative analysis, we defined a numerical multiphoton melanoma index (MMI) based on three-dimensio

164 view, we discuss the basic architecture of a multiphoton microscope capable of such analysis and summ

165 TPMDs were produced using a multiphoton microscope in Cal-520-AM loaded cells.

166 Here we develop an ultrafast random access multiphoton microscope that, in combination with a custo

167 In this work, we used a clinical multiphoton microscope to image in vivo and noninvasivel

168 We employ a clinical multiphoton microscope to monitor in vivo and noninvasiv

169 that vastly improves the dynamic range of a multiphoton microscope while limiting potential photodam

170 eloped an optical platform that integrates a multiphoton microscope with a laser ablation unit for mi

171 while scanning a single plane in a standard multiphoton microscope.

172 Multiphoton microscopes are hampered by limited dynamic

173 ts and takes advantage of commonly available multiphoton microscopes for the accurate positioning and

174 be used in other imaging modalities, such as multiphoton microscopes, and the field of view can be ex

175 l orders of magnitude lower than traditional multiphoton microscopies.

176 Through intravital multiphoton microscopy (IV-MPM), allowing the means to a

177 Multiphoton microscopy (MPM) has emerged as one of the m

178 We analyzed multiphoton microscopy (MPM) images corresponding to 15

179 Multiphoton microscopy (MPM) is a nonlinear fluorescence

180 Here we report the development of serial multiphoton microscopy (MPM) of the same glomeruli over

181 Recent translation of multiphoton microscopy (MPM) to clinical practice raises

182 h signals, we used high-resolution live-cell multiphoton microscopy (MPM) to directly observe cellula

183 e we developed an imaging approach that uses multiphoton microscopy (MPM) to directly visualize podoc

184 By applying the new technique of multiphoton microscopy (MPM) with clearing to a new mous

185 Multiphoton microscopy allows for deep tissue penetratio

186 d at depths beyond the reach of conventional multiphoton microscopy and adaptive optics methods, albe

187 s) to the drug-eluting scaffold and employed multiphoton microscopy and fluorescence lifetime imaging

188 Using complementary multiphoton microscopy and quantitative analyses in wild

189 By combining multiphoton microscopy and sequencing, we show that tens

190 the recent preclinical insights gained using multiphoton microscopy and suggests future advances that

191 By incorporating multiphoton microscopy and the dsLNA biosensor, we perfo

192 image-guided therapeutic interventions, and multiphoton microscopy as the appropriate method of vali

193 Multiphoton microscopy enables imaging deep into scatter

194 Multiphoton microscopy enables live imaging of the renal

195 veral years, in vivo imaging of tumors using multiphoton microscopy has emerged as a powerful preclin

196 Multiphoton microscopy has emerged as the primary imagin

197 Multiphoton microscopy has enabled unprecedented dynamic

198 Multiphoton microscopy has gained enormous popularity be

199 High resolution multiphoton microscopy imaged the spread across rat brai

200 (n=6) arterial wall damage was quantified by multiphoton microscopy in ex vivo samples.

201 Using multiphoton microscopy in live cells, we show that free

202 lasers have stimulated the broad adoption of multiphoton microscopy in the modern laboratory.

203 Using multiphoton microscopy in vivo, we imaged synaptic relea

204 Multiphoton microscopy is a powerful tool in neuroscienc

205 Multiphoton microscopy is the current method of choice f

206 As evidenced by intravital multiphoton microscopy of Ccr2 reporter mice, CCR2(+) mo

207 Using longitudinal intravital multiphoton microscopy of DC(GFP)/MC(RFP) reporter mice,

208 Multiphoton microscopy of kidney sections confirmed that

209 By high-resolution multiphoton microscopy of mammary carcinoma in mice, we

210 al procedure suitable for time-lapse in vivo multiphoton microscopy of mouse spinal cord without the

211 We employed in vivo multiphoton microscopy of the genetically encoded Ca(2+)

212 Multiphoton microscopy revealed more efficient interacti

213 After induction of inflammation, multiphoton microscopy revealed that approximately 20% o

214 Moreover, intravital multiphoton microscopy revealed that Debio0719 reduced t

215 Resonant-scanning multiphoton microscopy revealed that in vivo arterial st

216 Here, multiphoton microscopy reveals the direct transformation

217 the imaging of the skin hair follicles using multiphoton microscopy showed that it opened the follicu

218 Isothermal titration calorimetry and multiphoton microscopy showed that L9 and the other most

219 Multiphoton microscopy showed that the predominant orien

220 nte Carlo-based radiative transport model of multiphoton microscopy signal collection in skin, establ

221 t parasites combined with flow cytometry and multiphoton microscopy techniques to understand the even

222 rm and methodology for label-free multimodal multiphoton microscopy that uses a novel photonic crysta

223 Herein, we used in vivo multiphoton microscopy to investigate NET formation in t

224 ident microglia in living mice and then used multiphoton microscopy to monitor these cells over time.

225 Here, we use multiphoton microscopy to obtain quantitative data of el

226 Here, we employed nonlinear multiphoton microscopy to quantify collagen fiber organi

227 issue of Cell, Langen et al. use time-lapse multiphoton microscopy to show how Drosophila photorecep

228 Here we use brain slice multiphoton microscopy to show that substantia nigra dop

229 To address this, we used intravital multiphoton microscopy to visualize immune cell interact

230 Using in vivo multiphoton microscopy together with fluorescently label

231 Multiphoton microscopy was used to image renal dendritic

232 n vivo were assessed by combining intravital multiphoton microscopy with flow cytometry and functiona

233 We were also first to use multiphoton microscopy, a non-invasive and label-free im

234 bled intravital observation of xenografts by multiphoton microscopy, allowing us to visualise the ste

235 r scanning modalities including confocal and multiphoton microscopy, and offers artifact free reconst

236 The diameter of vessels was assessed with multiphoton microscopy, and the amount of renal collagen

237 tumor cell motility in the primary tumor by multiphoton microscopy, as well as a dramatically reduce

238 Using a combination of intravital multiphoton microscopy, genetically modified mice and no

239 Here, we have used in vivo multiphoton microscopy, laser speckle imaging of CBF, an

240 RECENT FINDINGS: Imaging modalities like multiphoton microscopy, optical coherence tomography, Co

241 eted to neuronal mitochondria and intravital multiphoton microscopy, we find increased mitochondrial

242 Using transcranial in vivo multiphoton microscopy, we find that fmr1 KO mice have s

243 Using conditional mutants and intravital multiphoton microscopy, we show here that the lipid medi

244 Using intravital multiphoton microscopy, we show previously unrecognized

245 Using in vivo multiphoton microscopy, we show that morpholino-mediated

246 Using multiphoton microscopy, we show that, in vivo, CD11c(+)

247 inescence (2PEL) - the processes crucial for multiphoton microscopy, which allows deeper imaging of t

248 gical readouts, and sophisticated intravital multiphoton microscopy-based imaging of liver in mice.

249 ic and collagen content and morphology using multiphoton microscopy.

250 in CD were evaluated with flow cytometry and multiphoton microscopy.

251 This result was further confirmed with multiphoton microscopy.

252 olecules with deeper tissue penetration than multiphoton microscopy.

253 time to expected ovulation using intravital multiphoton microscopy.

254 r optical properties of few-layer GaSe using multiphoton microscopy.

255 when measured using intravital quantitative multiphoton microscopy.

256 uorescently labelled ipRGCs visualized using multiphoton microscopy.

257 Kinetics of corneal leukocytes by intravital multiphoton microscopy.

258 vapour deposited monolayer MoS2 samples with multiphoton microscopy.

259 nd closure up to 6 hours by autofluorescence multiphoton microscopy.

260 er with teal fluorescent protein (mTFP1) for multiphoton, multicolor applications.

261 ning long-lived photoproducts resulting from multiphoton, multielectron processes.

262 The multiphoton near-infrared, quantum cutting luminescence

263 ly polarized femtosecond laser, resulting in multiphoton near-threshold ionization with little molecu

264 hat the observed behaviour is an interesting multiphoton, near-infrared, quantum cutting luminescence

265 photoinduced biological responses during the multiphoton operation of neuronal glutamate receptors wi

266 Confocal and multiphoton optical imaging techniques have been powerfu

267 sing - mediated by the Kerr nonlinearity and multiphoton or tunnel ionization, respectively.

268 Here we present a new multiphoton photo-excitation method, termed three-dimens

269 a direct momentum-space characterization of multiphoton photoemission from plasmonic gold nanostars

270 e theoretically predicted value of 50%), low multiphoton probability (g(2)(0) <1%), and a significant

271 revented the use of this kind of entities as multiphoton probes.

272 desorption mechanism involves a nonresonant, multiphoton process, rather than thermal- or photoacoust

273 which applies independently of the nonlinear multiphoton processes at the origin of waves and current

274 Higher order multiphoton-pumped polarized lasers have fundamental tec

275 y open up a new route to the exploitation of multiphoton-pumped solid-state laser in single MOF micro

276 Such methods for verifying multiphoton quantum behaviour are vital for achieving in

277 d quantum machine learning using specialized multiphoton quantum optical circuits.

278 Our results suggest an important role of multiphoton reactions and the previously described side

279 onstrated with some numerical studies of the multiphoton resonance processes and quantum interference

280 fter one entangled photon propagates through multiphoton-scattering brain tissue slices with differen

281 Using multiphoton-second harmonic generation imaging, we deter

282 mally invasive multimodal imaging technique: multiphoton-second harmonic generation.

283 We introduce chromatic multiphoton serial (ChroMS) microscopy, a method integra

284 nd enlarge the focal spot, which reduces the multiphoton signal.

285 Clearly discerned multiphoton signals are obtained by applying sub-nanosec

286 that takes advantage of the nonlinearity of multiphoton signals to determine and compensate for thes

287 We developed one-photon and multiphoton SiMView implementations and recorded cellula

288 Multiphoton SPIFI (MP-SPIFI) provides spatial resolution

289 e ability to generate and manipulate complex multiphoton states.

290 We improve multiphoton structured illumination microscopy using a n

291 rious light microscopy techniques (confocal, multiphoton, total internal reflection, superresolution

292 ies, including short- and long trajectories, multiphoton trajectories, resonance-enhanced trajectorie

293 mall dissipation strength in both single and multiphoton transition domains, revealing rich phase str

294 Multiphoton-triggered SPAAC (MP-SPAAC) enables high reso

295 -generation quadruplex ligand that acts as a multiphoton turn-on fluorescent probe.

296 In multiphoton, two-mode systems, correlations may exist be

297 ended pai-electron chromophore for efficient multiphoton uncaging on living neurons.

298 nic generation methods were performed with a multiphoton video-rate microscope to capture real time c

299 r and excitation rate, we can obtain typical multiphoton z-axis focal exclusive excitation.

300 ed localization of uncaging and imaging with multiphoton z-axis sectioning.