1 Here, by using
multiphoton ablation lithography to pattern surfaces wit
2 Using
multiphoton absorption and DNA cleavage at unique sites
3 Various emission mechanisms, such as
multiphoton absorption or emission, optical or dc field
4 visible (Vis) regions of the spectrum via a
multiphoton absorption process, known as upconversion.
5 ermeabilisation mechanism requires efficient
multiphoton absorption to produce free electrons but onc
6 h a very high degree of ionization, owing to
multiphoton absorption, which in a heteronuclear molecul
7 orescence-lifetime imaging microscopy/phasor
multiphoton analysis with confocal microscopy, implement
8 Live studies combining video-rate
multiphoton and confocal imaging in 4D demonstrate the p
9 ified Boyden chamber using three-dimensional
multiphoton and confocal time-lapse microscopy.
10 l and oxidative metabolism was visualized by
multiphoton and light sheet microscopy in cultured bovin
11 xtended semiclassical analysis, the roles of
multiphoton and multiple rescattering trajectories on th
12 Multiphoton and spinning disk confocal intravital micros
13 We used
multiphoton and time-lapse confocal microscopy to monito
14 ts for electron microscopy, optical imaging (
multiphoton),
and whole brain magnetic resonance imaging
15 Finally,
multiphoton-
and microPET/CT imaging indicate its abilit
16 Moreover, we discover that the
multiphoton-
and tunneling-ionization regimes in multipl
17 Tissues were imaged using
multiphoton autofluorescence and second harmonic generat
18 graphy in dysplasia using in vivo volumetric
multiphoton autofluorescence microscopy and second harmo
19 TPEF was collected through
multiphoton bandpass filters to obtain AF, SHG (collagen
20 Intravital
multiphoton calcium imaging revealed that 5-HT2C recepto
21 Here, we use
multiphoton calcium imaging to monitor cortical feedback
22 ed, including three-dimentional lithography,
multiphoton chirality transfer, polarization effects in
23 scein-conjugated gelatin and observed with a
multiphoton confocal microscope.
24 We demonstrate
multiphoton control by using a superconducting transmon
25 ulate a generalized method for measuring the
multiphoton cross section of fluorophores and use it to
26 complex mixtures of polymers using infrared
multiphoton decay (IRMPD) and electron capture dissociat
27 More advanced and accurate
multiphoton determinations of the glomerular sieving coe
28 essure cell of the QLT with a short infrared
multiphoton dissociation (IRMPD) activation in the low-p
29 otodissociation (UVPD) and 10.6-mum infrared
multiphoton dissociation (IRMPD) for the characterizatio
30 spectrometer was modified to permit infrared
multiphoton dissociation (IRMPD) in each of the two cell
31 n trap mass spectrometer to perform infrared
multiphoton dissociation (IRMPD) in the low-pressure tra
32 on-activated dissociation (CAD) and infrared
multiphoton dissociation (IRMPD) of Ag-adducted phosphol
33 n digests, we demonstrate selective infrared
multiphoton dissociation (IRMPD) of S-sulfonated peptide
34 nation of tandem mass spectrometry, infrared
multiphoton dissociation (IRMPD) spectroscopy, and DFT c
35 Infrared
multiphoton dissociation (IRMPD) was implemented in a no
36 sociation (AI-EDD) and negative ion infrared
multiphoton dissociation (IRMPD) were employed to invest
37 sion-induced dissociation (CID) and infrared
multiphoton dissociation (IRMPD).
38 brational transitions via resonance-enhanced
multiphoton dissociation detected by Ca(+) fluorescence.
39 on intermediates to applications of infrared
multiphoton dissociation spectroscopy (IRMPD) to interme
40 n intermediate was characterized by infrared
multiphoton dissociation spectroscopy and was trapped wi
41 anionic forms are characterized by infrared
multiphoton dissociation spectroscopy.
42 Collision-induced dissociation and infrared
multiphoton dissociation.
43 We find that the
multiphoton-
dominated trajectories only involve the elec
44 ion and development in harnessing the unique
multiphoton effect of UCNPs for photosensitive materials
45 ombs can be used to generate several bi- and
multiphoton entangled qubits, with direct applications f
46 ing photonic quantum gates and deterministic
multiphoton entanglement.
47 omerization interactions in living cells via
multiphoton excitation fluorescence correlation spectros
48 By simultaneous observation of
multiphoton excitation fluorescence emission and second
49 Multiphoton excitation fluorescence microscopy (MPM) can
50 Multiphoton excitation fluorescence microscopy is a powe
51 We demonstrate that
multiphoton excitation of DNA in live cells with visible
52 ined in all three spatial dimensions, making
multiphoton excitation of DNA with visible light an idea
53 We demonstrated this approach using
multiphoton excitation of the Blastochloris viridis phot
54 Excitation of this pair by a single
multiphoton excitation wavelength (MPE, 850 nm) yields w
55 d imaging of the fluorescence lifetime using
multiphoton excitation.
56 Thus, the novel
multiphoton-
excited 3D printing technique produces extra
57 Here, we used
multiphoton-
excited 3D printing to generate a native-lik
58 of ex vivo and in vivo rabbit corneas using
multiphoton fluorescence and second harmonic generation
59 Here, we present a
multiphoton fluorescence anisotropy microscopy live cell
60 s as a model of spontaneous albuminuric CKD,
multiphoton fluorescence imaging and single-vessel physi
61 nce energy transfer (FRET)-based assay using
multiphoton fluorescence lifetime imaging microscopy (FL
62 resonance energy transfer-based system using
multiphoton fluorescence lifetime imaging microscopy and
63 Using
multiphoton fluorescence lifetime imaging microscopy in
64 In conventional confocal/
multiphoton fluorescence microscopy, images are typicall
65 nging distortions from impedance mismatch in
multiphoton fluorescence microscopy.
66 ntial of this class of fluorescent probes in
multiphoton fluorescence microscopy.
67 Osteocyte responses are imaged by using
multiphoton fluorescence microscopy.
68 o differences in viscosity were detected via
multiphoton fluorescence recovery after photobleaching (
69 Multiphoton fluorescence recovery after photobleaching i
70 tion model broadens the applicability of the
multiphoton fluorescence recovery after photobleaching t
71 e use of a dorsal skinfold chamber model and
multiphoton fluorescence resonance energy transfer micro
72 evious studies based on spectrally resolved,
multiphoton fluorescence resonance energy transfer.
73 Moxifloxacin has bright intrinsic
multiphoton fluorescence, good tissue penetration and hi
74 iffusion with second harmonic generation and
multiphoton fluorescent recovery after photobleaching te
75 Multiphoton FRAP provided the specific binding constants
76 ubit can be used to realise both single- and
multiphoton frequency-conversion processes.
77 Multiphoton-
generated cyclooctynes undergo a SPAAC react
78 Multiphoton glutamate uncaging experiments revealed that
79 Multiphoton glutamate uncaging experiments revealed that
80 Multiphoton images were comparable to histologic section
81 nd brain vessels when measured by intravital
multiphoton imaging and immunohistochemistry.
82 in assemblies have been employed for in vivo
multiphoton imaging and lifetime-based oxygen measuremen
83 In vivo
multiphoton imaging and neural manipulations delineated
84 Here we use
multiphoton imaging and patch-clamp recording, and obser
85 We use in vivo
multiphoton imaging and show that mechanical forces duri
86 Our results demonstrate that
multiphoton imaging can be used for fast and sensitive c
87 Live,
multiphoton imaging demonstrated a selective vulnerabili
88 le cells (abGCs) in the olfactory bulb using
multiphoton imaging in awake and anesthetized mice.
89 In this study, we used
multiphoton imaging in Foxp3-GFP mice to examine the beh
90 Multiphoton imaging is a form of fluorescence microscopy
91 In vivo
multiphoton imaging of CD11c-EYFP mice revealed that int
92 Multiphoton imaging of developing mouse cortex reveals t
93 by Malpighi to the current use of single and
multiphoton imaging of intravital and isolated perfused
94 In this study, we used
multiphoton imaging of live rat kidney slices to investi
95 Multiphoton imaging of presynaptic NMDAR-mediated calciu
96 inflammatory events (day 3 of UUO), in vivo
multiphoton imaging of the intact kidney of CD11c report
97 We conducted in vivo time-lapse
multiphoton imaging of the rapidly developing and relati
98 ng the in vivo invasion assay and intravital
multiphoton imaging of tumor cell streaming.
99 We developed an in vivo
multiphoton imaging paradigm to study alpha-synuclein ag
100 Moreover, in vivo
multiphoton imaging revealed that deafening-induced chan
101 Intravital
multiphoton imaging revealed that inhibition of CSF1R in
102 Multiphoton imaging revealed that paxillin-deficient neu
103 Live
multiphoton imaging shows that selection is based on the
104 In brain slices of rat PFC, we employed
multiphoton imaging simultaneously with whole-cell elect
105 n combination with in vivo pharmacologic and
multiphoton imaging strategies to systematically test de
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 However, using in vivo
multiphoton imaging to observe tangles and activation of
109 ined molecular dynamics simulations, Laurdan
multiphoton imaging, and atomic force microscopy microin
110 the laser power required for adaptive optics
multiphoton imaging, and for facilitating integration wi
111 Intravital
multiphoton imaging, confocal imaging of cryosections an
112 lectrocardiography recordings and high-speed
multiphoton imaging, to assess Ca(2+) handling, revealed
113 Using in vivo longitudinal
multiphoton imaging, we found orchestrated activity-depe
114 Using intracranial
multiphoton imaging, we found that infusion of 100 ng of
115 By intravital
multiphoton imaging, we found that the motility of CD4(+
116 Using electrophysiology with concurrent
multiphoton imaging, we show that layer 6 pyramidal cell
117 cruitment by coupling mechanical loading and
multiphoton imaging.
118 multiple columns and layers using high-speed
multiphoton imaging.
119 grating online image analysis with automated
multiphoton imaging.
120 e combined with technologies such as in vivo
multiphoton imaging.
121 e clearance in aged Tg2576 mice with in vivo
multiphoton imaging.
122 Multiphoton in vivo imaging reveals close to 30% loss of
123 Using
multiphoton-
induced exposure of a commercial photoresist
124 Multiphoton infrared absorption from a focused, pulsed C
125 Multiphoton infrared irradiation of the protonated paren
126 isolation infrared absorption spectroscopy,
multiphoton infrared photodissociation (IRMPD) action sp
127 By multiple approaches, including
multiphoton intravital imaging, we found that antigen ca
128 Using mouse models and
multiphoton intravital imaging, we have identified a cru
129 Advances in techniques such as
multiphoton intravital microscopy (4, 5) have provided n
130 roaches is in vivo imaging, and specifically
multiphoton intravital microscopy (MP-IVM), which allows
131 Here, using a combination of
multiphoton intravital microscopy and genomic approaches
132 Here we used
multiphoton intravital microscopy in lymph nodes and tum
133 Multiphoton intravital microscopy revealed that in contr
134 Using
multiphoton intravital microscopy we showed that neutrop
135 Here, using
multiphoton intravital microscopy, we examine the dynami
136 lar dendritic cells, we used the approach of
multiphoton intravital microscopy.
137 itonitis was demonstrated using fluorescence
multiphoton intravital microscopy; however, no differenc
138 Direct infusion resonance-enhanced
multiphoton ionization (DI-REMPI) was performed on liqui
139 al carbon analyzer with a resonance-enhanced
multiphoton ionization (REMPI) mass spectrometer.
140 ation (SPI, 118 nm) or by resonance enhanced
multiphoton ionization (REMPI, 266 nm), and the molecula
141 romatography coupled to a resonance-enhanced
multiphoton ionization - time-of-flight mass spectrometr
142 ulations that for the first time incorporate
multiphoton ionization and dielectric models that are ne
143 On the other hand, the
multiphoton ionization regime is responsible for the eve
144 Resonance enhanced
multiphoton ionization spectroscopy (REMPI) generates si
145 olation, cavity ringdown, resonance enhanced
multiphoton ionization, and ion trapping have led to the
146 the PAHs, and a 193 nm laser, which requires
multiphoton ionization.
147 highly sensitive way via resonance-enhanced
multiphoton ionization.
148 Resonance-enhanced
multiphoton ionization/time-of-flight mass spectrometry
149 Multiphoton laser scanning in vivo microscopy showed tha
150 Here we integrated
multiphoton laser scanning microscopy and the registrati
151 Multiphoton laser scanning microscopy data showed for th
152 -3 could be tracked in the intestine through
multiphoton laser scanning microscopy in an ex vivo inte
153 y acid-binding protein (L-FABP) by real time
multiphoton laser scanning microscopy of novel fluoresce
154 Using
multiphoton laser scanning microscopy, we examined the s
155 Multiphoton laser-scanning microscopy (MPLSM) or optical
156 oactivatable fluorescent protein tracer with
multiphoton laser-scanning microscopy and flow cytometry
157 wake, lightly sedated, responsive mice using
multiphoton laser-scanning microscopy and novel genetic
158 ng, but the signal-to-noise ratio for a dim (
multiphoton)
light response is increased at night becaus
159 Multiphoton lithography (MPL) provides a means to create
160 In this report, we develop a versatile
multiphoton lithography method that enables rapid fabric
161 xploit the rapid prototyping capabilities of
multiphoton lithography to create and characterize a cel
162 rom a biocompatible precursor solution using
multiphoton lithography, an intrinsically 3D laser direc
163 Exploiting
multiphoton lithography, microchannel networks spanning
164 nanocrystalline platinum and palladium using
multiphoton lithography.
165 aptic triads with neuroanatomic analyses and
multiphoton live imaging of developing HCs, we found tha
166 Raman and
multiphoton luminescence together with transmission elec
167 on upon irradiation with NIR light through a
multiphoton mechanism.
168 uantitative analysis, we defined a numerical
multiphoton melanoma index (MMI) based on three-dimensio
169 ative to the scanning laser of a confocal or
multiphoton microscope and provides fully resolved three
170 view, we discuss the basic architecture of a
multiphoton microscope capable of such analysis and summ
171 ion of many cell types in vivo requires both
multiphoton microscope systems capable of expanding the
172 ent a procedure for constructing a two-laser
multiphoton microscope that extends the wavelength range
173 Here we develop an ultrafast random access
multiphoton microscope that, in combination with a custo
174 In this work, we used a clinical
multiphoton microscope to image in vivo and noninvasivel
175 We employ a clinical
multiphoton microscope to monitor in vivo and noninvasiv
176 that vastly improves the dynamic range of a
multiphoton microscope while limiting potential photodam
177 eloped an optical platform that integrates a
multiphoton microscope with a laser ablation unit for mi
178 Multiphoton microscopes are hampered by limited dynamic
179 be used in other imaging modalities, such as
multiphoton microscopes, and the field of view can be ex
180 l orders of magnitude lower than traditional
multiphoton microscopies.
181 We analyzed
multiphoton microscopy (MPM) images corresponding to 15
182 Multiphoton microscopy (MPM) is a nonlinear fluorescence
183 Here we report the development of serial
multiphoton microscopy (MPM) of the same glomeruli over
184 Recent translation of
multiphoton microscopy (MPM) to clinical practice raises
185 h signals, we used high-resolution live-cell
multiphoton microscopy (MPM) to directly observe cellula
186 e we developed an imaging approach that uses
multiphoton microscopy (MPM) to directly visualize podoc
187 By applying the new technique of
multiphoton microscopy (MPM) with clearing to a new mous
188 Multiphoton microscopy allows for deep tissue penetratio
189 d at depths beyond the reach of conventional
multiphoton microscopy and adaptive optics methods, albe
190 Using complementary
multiphoton microscopy and quantitative analyses in wild
191 By combining
multiphoton microscopy and sequencing, we show that tens
192 the recent preclinical insights gained using
multiphoton microscopy and suggests future advances that
193 By incorporating
multiphoton microscopy and the dsLNA biosensor, we perfo
194 hat circumvents the technical limitations of
multiphoton microscopy and, as a result, provides unprec
195 image-guided therapeutic interventions, and
multiphoton microscopy as the appropriate method of vali
196 Intravital
multiphoton microscopy data show that sunitinib induces
197 Multiphoton microscopy enables imaging deep into scatter
198 Multiphoton microscopy enables live imaging of the renal
199 Although intravital
multiphoton microscopy has addressed this limitation, th
200 veral years, in vivo imaging of tumors using
multiphoton microscopy has emerged as a powerful preclin
201 Multiphoton microscopy has enabled unprecedented dynamic
202 Intravital
multiphoton microscopy has provided powerful mechanistic
203 of tubular cell structure and function with
multiphoton microscopy in an intact, functioning organ.
204 Using
multiphoton microscopy in live cells, we show that free
205 ate cells (PSC) in culture and in situ using
multiphoton microscopy in pancreatic lobules.
206 Multiphoton microscopy is a powerful tool in neuroscienc
207 Multiphoton microscopy is the current method of choice f
208 As evidenced by intravital
multiphoton microscopy of Ccr2 reporter mice, CCR2(+) mo
209 Using longitudinal intravital
multiphoton microscopy of DC(GFP)/MC(RFP) reporter mice,
210 Multiphoton microscopy of kidney sections confirmed that
211 By high-resolution
multiphoton microscopy of mammary carcinoma in mice, we
212 al procedure suitable for time-lapse in vivo
multiphoton microscopy of mouse spinal cord without the
213 and MPT were detected by intravital confocal/
multiphoton microscopy of rhodamine 123, propidium iodid
214 We employed in vivo
multiphoton microscopy of the genetically encoded Ca(2+)
215 This study demonstrates that
multiphoton microscopy of the isolated perfused kidney i
216 Multiphoton microscopy revealed more efficient interacti
217 After induction of inflammation,
multiphoton microscopy revealed that approximately 20% o
218 Moreover, intravital
multiphoton microscopy revealed that Debio0719 reduced t
219 Resonant-scanning
multiphoton microscopy revealed that in vivo arterial st
220 Intravital
multiphoton microscopy reveals that Stat3 silencing comb
221 Here,
multiphoton microscopy reveals the direct transformation
222 the imaging of the skin hair follicles using
multiphoton microscopy showed that it opened the follicu
223 nte Carlo-based radiative transport model of
multiphoton microscopy signal collection in skin, establ
224 in probe choice and experimental design for
multiphoton microscopy studies.
225 t parasites combined with flow cytometry and
multiphoton microscopy techniques to understand the even
226 rm and methodology for label-free multimodal
multiphoton microscopy that uses a novel photonic crysta
227 Herein, we used in vivo
multiphoton microscopy to investigate NET formation in t
228 ident microglia in living mice and then used
multiphoton microscopy to monitor these cells over time.
229 Here, we use
multiphoton microscopy to obtain quantitative data of el
230 Here, we employed nonlinear
multiphoton microscopy to quantify collagen fiber organi
231 issue of Cell, Langen et al. use time-lapse
multiphoton microscopy to show how Drosophila photorecep
232 Here we use brain slice
multiphoton microscopy to show that substantia nigra dop
233 To address this, we used intravital
multiphoton microscopy to visualize immune cell interact
234 Here we used
multiphoton microscopy to visualize the dynamics and act
235 Using in vivo
multiphoton microscopy together with fluorescently label
236 METHODS AND
Multiphoton microscopy was used to image deep within car
237 Multiphoton microscopy was used to image renal dendritic
238 r scanning modalities including confocal and
multiphoton microscopy, and offers artifact free reconst
239 The diameter of vessels was assessed with
multiphoton microscopy, and the amount of renal collagen
240 tumor cell motility in the primary tumor by
multiphoton microscopy, as well as a dramatically reduce
241 Using a combination of intravital
multiphoton microscopy, genetically modified mice and no
242 re and exogenous contrast agents that enable
multiphoton microscopy, however, limit the ability to in
243 Here, we have used in vivo
multiphoton microscopy, laser speckle imaging of CBF, an
244 RECENT FINDINGS: Imaging modalities like
multiphoton microscopy, optical coherence tomography, Co
245 Using transcranial in vivo
multiphoton microscopy, we find that fmr1 KO mice have s
246 Using conditional mutants and intravital
multiphoton microscopy, we show here that the lipid medi
247 Using in vivo
multiphoton microscopy, we show that morpholino-mediated
248 Using
multiphoton microscopy, we show that, in vivo, CD11c(+)
249 Further, using
multiphoton microscopy, we show the utility of this tool
250 gical readouts, and sophisticated intravital
multiphoton microscopy-based imaging of liver in mice.
251 time to expected ovulation using intravital
multiphoton microscopy.
252 vapour deposited monolayer MoS2 samples with
multiphoton microscopy.
253 r optical properties of few-layer GaSe using
multiphoton microscopy.
254 when measured using intravital quantitative
multiphoton microscopy.
255 uorescently labelled ipRGCs visualized using
multiphoton microscopy.
256 onitored plaque formation in real time using
multiphoton microscopy.
257 nd closure up to 6 hours by autofluorescence
multiphoton microscopy.
258 e regulatory co-factor 2 (NHERF2-/- mice) by
multiphoton microscopy.
259 in CD were evaluated with flow cytometry and
multiphoton microscopy.
260 This result was further confirmed with
multiphoton microscopy.
261 olecules with deeper tissue penetration than
multiphoton microscopy.
262 er with teal fluorescent protein (mTFP1) for
multiphoton,
multicolor applications.
263 ning long-lived photoproducts resulting from
multiphoton,
multielectron processes.
264 The
multiphoton near-infrared, quantum cutting luminescence
265 ly polarized femtosecond laser, resulting in
multiphoton near-threshold ionization with little molecu
266 hat the observed behaviour is an interesting
multiphoton,
near-infrared, quantum cutting luminescence
267 photoinduced biological responses during the
multiphoton operation of neuronal glutamate receptors wi
268 Confocal and
multiphoton optical imaging techniques have been powerfu
269 conventional methods that require expensive
multiphoton optical sectioning setups, this technique is
270 sing - mediated by the Kerr nonlinearity and
multiphoton or tunnel ionization, respectively.
271 Here we present a new
multiphoton photo-excitation method, termed three-dimens
272 The CH radicals are prepared by 248 nm
multiphoton photolysis of CHBr(3) at 298 K and react wit
273 e theoretically predicted value of 50%), low
multiphoton probability (g(2)(0) <1%), and a significant
274 revented the use of this kind of entities as
multiphoton probes.
275 desorption mechanism involves a nonresonant,
multiphoton process, rather than thermal- or photoacoust
276 which applies independently of the nonlinear
multiphoton processes at the origin of waves and current
277 oscopy will now be a routine aid for probing
multiphoton processes.
278 Higher order
multiphoton-
pumped polarized lasers have fundamental tec
279 y open up a new route to the exploitation of
multiphoton-
pumped solid-state laser in single MOF micro
280 Such methods for verifying
multiphoton quantum behaviour are vital for achieving in
281 Our results suggest an important role of
multiphoton reactions and the previously described side
282 onstrated with some numerical studies of the
multiphoton resonance processes and quantum interference
283 fter one entangled photon propagates through
multiphoton-
scattering brain tissue slices with differen
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 ture through ET receptor activation, whereas
multiphoton time-lapse imaging shows that selective ET r
292 rious light microscopy techniques (confocal,
multiphoton,
total internal reflection, superresolution
293 ies, including short- and long trajectories,
multiphoton trajectories, resonance-enhanced trajectorie
294 eted including the influence of 1-photon and
multiphoton transitions.
295 Multiphoton-
triggered SPAAC (MP-SPAAC) enables high reso
296 -generation quadruplex ligand that acts as a
multiphoton turn-on fluorescent probe.
297 In
multiphoton,
two-mode systems, correlations may exist be
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.