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1                                              NIR displayed better performance for the evaluation of p
2                                              NIR imaging is comfortable for patients and is commonly
3                                              NIR light adsorption heats the HGN, inducing vapor nanob
4                                              NIR spectra were obtained in the wavenumber range 11100-
5                                              NIR spectral bands characterising dehydration, proteolys
6                                              NIR technique should be a useful tool for industry insof
7                                              NIR-ASM was successfully used to detect and image the en
8                                              NIR-guided SLN mapping may improve staging and outcomes
9                                              NIR-II fluorescence enables deep-tissue imaging with mic
10                                              NIR-II fluorophores have shown great promise for biomedi
11                                              NIR-II photoacoustic (PA) molecular imaging (PMI) is eme
12                                              NIR-II PMI results reveal the excellent targeting abilit
13 e isotope ratios [13C/12C (CIR) and 15N/14N (NIR)] are promising dietary biomarkers.
14                                            A NIR fluorochrome was conjugated to a cyclic peptide that
15                                            A NIR II emissive dye was synthesized by the C-H bond func
16 ved 2.5 mg/mL WST-D and was illuminated by a NIR diode laser (755 nm, 10 mW/cm(2)).
17 ted by conjugating the drug pamidronate to a NIR fluorescent gold nanocluster.
18                                  Activatable NIR fluorescent probes have been extensively used for di
19  quinone oxidoreductase 1 (NQO1)-activatable NIR fluorescent probe (NIR-ASM) by conjugating dicyanois
20                                    Although, NIR to Vis TTA-UC is known since 2007, the recent five y
21 fluorescent proteins (FPs), we engineered an NIR Forster resonance energy transfer (FRET)-based genet
22 played significant lower StO2 (p = 0.02) and NIR perfusion indices, 15 min after reperfusion (p < 0.0
23                The combination of MoS(2) and NIR light may provide new approaches to regulate and dir
24  reveals significant influence of MoS(2) and NIR stimulation of MoS(2) on integrins, cellular migrati
25                The interaction of MoS(2) and NIR stimulation of MoS(2) with human stem cells is inves
26  flecks which are hyper AF in both SW-AF and NIR-AF corresponded to the subretinal macrophages fully
27                         Normalized SW-AF and NIR-AF images appeared darker in all patients with mutat
28  that qualitative and quantitative SW-AF and NIR-AF images can serve as biomarkers of deficiencies sp
29 itative analysis of non-normalized SW-AF and NIR-AF images; signal intensities were significantly low
30 d by the colocalization of lipofuscin-AF and NIR-AF under the fluorescence microscope.
31  (30 degrees and 55 degrees : blue/SW-AF and NIR-AF; 200 degrees : ultrawide-field, UWF-AF), excitati
32 nventional blue autofluorescence (B-AF), and NIR-AF imaging.
33 iguration constitute a new class of blue and NIR-II luminophores, which complement the classical esta
34 l photocatalyst for both full broadband- and NIR-mediated CRP in aqueous conditions.
35 s to evaluate plasma, RBCs, and hair CIR and NIR as biomarkers of fish, meat, and sugar-sweetened bev
36                             Overall, CIR and NIR discriminated between dietary fish and meat, and to
37 cts of fish, meat, and SSB intake on CIR and NIR were evaluated using a balanced factorial design, wi
38 nanoparticles that combine mRNA delivery and NIR imaging hold promise as an applicable future approac
39 of gastrointestinal peristalsis disorder and NIR-II FI-guided intestinal obstruction surgery.
40   Our results demonstrate that NIR-GECO2 and NIR-GECO2G provide substantial improvements over NIR-GEC
41  NIR GECI variants, designated NIR-GECO2 and NIR-GECO2G, derived from NIR-GECO1.
42 tial nanocatalytic therapy in both NIR-I and NIR-II biowindows is proposed, which innovatively change
43 ging system with the detection of NIR-II and NIR-I (700-900 nm in wavelength) fluorescence (by using
44                   The multimodal imaging and NIR-triggered drug release capabilities of the proposed
45 sis of choroidal nevi imaged with SS OCT and NIR.
46 mice, reduced 11-cis-retinal levels, qAF and NIR-AF intensities, and photoreceptor loss were consiste
47 hesized in water under blue, green, red, and NIR light irradiation.
48  in broad absorptions across the visible and NIR regions (E(g) ~ 1.2 eV).
49            The text also covers visible- and NIR-light-induced photosensitized release using molecula
50  (complexes) that absorb in the visible- and NIR-range to release various leaving groups and gasotran
51                        The TCZ-PNPs-assisted NIR-II PMI provides a new strategy for RA theranostics,
52 uding near-infrared fundus autofluorescence (NIR-AF), blue autofluorescence (B-AF), optical coherence
53  (SW-AF) and near-infrared autofluorescence (NIR-AF) modalities correlating with reduced levels of bi
54 th decreased near-infrared autofluorescence (NIR-AF) provided evidence for retinal pigment epithelial
55      Compared to rare earth and silver-based NIR-II emitters, RNase-A@AuNCs had excellent biocompatib
56 t development of D-A type thiopyrylium-based NIR-II fluorophores with frequency upconversion luminesc
57 een gradings in GA area measurements between NIR and FAF were assessed by mean difference, overlap ra
58 rate and accuracy were satisfactory for both NIR and MIR datasets.
59 ced sequential nanocatalytic therapy in both NIR-I and NIR-II biowindows is proposed, which innovativ
60 xcitation wavelength deep into the NIR, both NIR one-photon absorption cross-section and photoisomeri
61 escence in aqueous solution but emits bright NIR fluorescence at 725 nm after incubation with beta-ga
62                                           By NIR laser irradiation, a controlled release of angiotens
63 port on the feed frame allows measurement by NIR or Raman spectroscopy of the blends just before tabl
64 on, the therapeutic evaluation of RA mice by NIR-II PMI is shown to be consistent with clinical micro
65                  Composed of a peptide-caged NIR signaling moiety linked with a hydrophilic poly(ethy
66  Golgi staining reagent, NBD C(6) -ceramide, NIR imaging in the Golgi apparatus has been demonstrated
67 s have been extensively developed to combine NIR-II PTT with other therapeutic modalities for improve
68                    Finally, proof-of-concept NIR-I imaging using the PDs is demonstrated to show grea
69                        Ninety-seven confocal NIR images (Heidelberg HRA + Spectralis) and FAF images
70 ingly, deeper parts of caves still contained NIR, an effect likely attributable to the reflectance of
71 nterior and posterior stroma in healed WST-D/NIR corneas and untreated controls revealed no obvious d
72 ng treatment confirms the potential of WST-D/NIR therapy as a means of safely stiffening the cornea.
73 oscopy data were collected from paired WST-D/NIR treated and untreated rabbit corneas.
74                          Unlike BphP-derived NIR FPs, miRFP670nano is highly stable to denaturation a
75 ort 2 improved NIR GECI variants, designated NIR-GECO2 and NIR-GECO2G, derived from NIR-GECO1.
76                     This combination of dual-NIR-II image-guided surgery can be performed under brigh
77 anual segmentation of the GA lesions on each NIR and FAF image using GNU Image Manipulation Program s
78 eat potential of DCNP@PDA NP as an efficient NIR-II/PAI dual-modal contrast agent for precision medic
79                                    Elevating NIR expression dissolves cytoplasmic RBP aggregates, res
80 , and not to undifferentiated MSCs, and emit NIR fluorescence for functional detection.
81  which are the brightest genetically encoded NIR probes.
82 IR) molecular probe with far-red excitation, NIR emission, and high "turn-on" ratio upon senescence-a
83                       However, there are few NIR fluorescent materials known and suitable for biomedi
84 er nanoparticles (PNPs) to develop the first NIR-II theranostic nanoplatform, named TCZ-PNPs, for PA-
85 ormal-tissue toxicity over traditional first NIR PTT (750-1000 nm).
86 ), emerging as unrivaled contrast agents for NIR-II preclinical bioimaging.
87 tic efficacy remain the major challenges for NIR-II PTT.
88 specific detectivity around 10(12) Jones for NIR spectral region up to 1010 nm, close to that of a co
89 us, this study offers a typical paradigm for NIR-II imaging-guided NIR-light-triggered remote control
90 ce quantum yield (FQY) of 16.6% reported for NIR FPs, whereas the initial iRFP appeared to be a mixtu
91 from FAF images and 7.65 +/- 7.83 mm(2) from NIR, with a mean nonsignificant difference of 0.31 +/- 0
92 nated NIR-GECO2 and NIR-GECO2G, derived from NIR-GECO1.
93 ation rates were higher than 94% for both FT-NIR and FT-MIR range by using a cut-off limit set at 2 u
94 as successfully applied to a multivariate FT-NIR spectroscopic method for the screening of durum whea
95          We investigated the potential of FT-NIR spectroscopy combined with Linear Discriminant Analy
96              These findings indicate that FT-NIR, as well as FT-MIR analysis, might be a promising, i
97 study was to develop a robust model using FT-NIR and PLS-DA to discriminate extra virgin olive oil sa
98        Success rates indicate that ATR-FTIR, NIR reflectance spectroscopy, and LIBS coupled with mach
99  91, 97, and 70% success rates for ATR-FTIR, NIR reflectance spectroscopy, LIBS, and XRF, respectivel
100 s rates of 99, 81, 76, and 66% for ATR-FTIR, NIR reflectance spectroscopy, LIBS, and XRF, respectivel
101            Our previously reported NIR GECI, NIR-GECO1, has these advantages but also has several dis
102 a typical paradigm for NIR-II imaging-guided NIR-light-triggered remote control of the CRISPR/Cas9 sy
103  to these results, the new low-cost handheld NIR spectrometers can be used to monitor umbu fruit qual
104 cal performance of two new low-cost handheld NIR spectrometers for the determination of umbu fruit (S
105 luate the use of hyperspectral imaging (HSI)-NIR spectroscopy to assess the presence of DON and ergos
106 first set of bulk samples was scanned by HSI-NIR and divided into two subsamples, one that was analys
107 e of near infrared hyperspectral images (HSI-NIR) combined with pattern recognition analysis, partial
108 ral imaging in the near-infrared region (HSI-NIR) and multivariate pattern recognition, to study and
109                 The results confirm that HSI-NIR may be a suitable technique for ergosterol quantific
110                        Validation of the HSI-NIR method and subsequent analysis was realized using 15
111 photodetectors (PDs) toward near-infrared I (NIR-I) photons (700-900 nm), the so-called "optical wind
112                            Near-infrared II (NIR-II) imaging at 1100-1700 nm shows great promise for
113        Here, a multiplexed-near-infrared-II (NIR-II) in vivo imaging system using nonoverlapping NIR-
114  use of Near Infrared-Hyperspectral Imaging (NIR-HSI), together with machine learning methods, is val
115 d using near infrared hyperspectral imaging (NIR-HSI).
116                   Here, we report 2 improved NIR GECI variants, designated NIR-GECO2 and NIR-GECO2G,
117 caves characterized by low light enriched in NIR and inhabited by cyanobacteria producing NIR-absorbi
118 arger part of the solar spectrum and (ii) in NIR stimulated biological applications where the deep pe
119 ot visible in color fundus photographs or in NIR images.
120 els (StO2), near infrared perfusion indices (NIR), organ hemoglobin indices (OHI) and tissue water in
121 ity in mouse IBD models using near infrared (NIR) detection.
122 rescent optical imaging using near infrared (NIR) dyes tagged to tumor specific target will benefit s
123          Picosecond pulses of near infrared (NIR) light provided by a two-photon microscope, or by a
124  the entire visible (VIS) and near infrared (NIR) range, 500- 3000 nm, as well as the characterizatio
125 tonic applications, efficient near infrared (NIR) to Vis upconversion is preferred.
126  cornea and illumination with Near Infrared (NIR), has been identified as a promising therapy for sti
127 y attenuation coefficient and near-infrared (NIR) absorbance, excellent light-to-heat conversion effi
128 -cumulene moieties leading to near-infrared (NIR) absorption in neutral and protonated forms of macro
129 onor materials developed with near-infrared (NIR) absorption that are well matched to the existing ef
130  evaluated the suitability of near-infrared (NIR) and mid-infrared (MIR) spectroscopies for the devel
131 n this work, the potential of near-infrared (NIR) and mid-infrared (MIR) spectroscopy along with chem
132              We evaluate both near-infrared (NIR) and Raman spectroscopy for use in PAT applications
133 sublingual administration for near-infrared (NIR) and short-wave infrared (SWIR) optical imaging.
134  applications centered in the near-infrared (NIR) and short-wave infrared (SWIR) wavelength regimes r
135 iarylmethane, phenazinium and near-infrared (NIR) cyanine cationic dyes, respectively.
136              In addition, the near-infrared (NIR) dye Cy5.5 was coupled to the polymer providing live
137 xhibited promising far-red to near-infrared (NIR) emission, large Stoke shifts, broad full width at h
138 ght-harvesting system becomes near-infrared (NIR) emissive (675 nm).
139 , a novel method for targeted near-infrared (NIR) fluorescence imaging of glucagonlike peptide 1 rece
140                  Although the near-infrared (NIR) fluorescence intensity of SWCNTs at 998 nm is eithe
141       Herein, renal-clearable near-infrared (NIR) fluorescent macromolecular reporters are synthesize
142 rt the generation of two new, near-infrared (NIR) fluorescent probes for use in the molecular imaging
143 e present a design of turn-on near-infrared (NIR) fluorescent probes with intrinsically high signal-t
144              Bright monomeric near-infrared (NIR) fluorescent proteins (FPs) are in high demand as pr
145           Using two monomeric near-infrared (NIR) fluorescent proteins (FPs), we engineered an NIR Fo
146 escence intensity of specific near-infrared (NIR) fluorophore-labeled oligodeoxyribonucleotide duplex
147      Here, we present a novel near-infrared (NIR) free fatty acid (FFA) tracer suitable for in vivo i
148                               Near-infrared (NIR) genetically encoded calcium ion (Ca2+) indicators (
149 s (PBD) for mRNA delivery and near-infrared (NIR) imaging in vitro and in vivo.
150 x (biological) samples in the near-infrared (NIR) is beneficial due to reduced light scattering, abso
151 lution of GNPs with an 808 nm near-infrared (NIR) laser and measuring the temperature increase of the
152 x, and subsequent narrow-band near-infrared (NIR) laser excitation to give 1cc.
153 iciencies were acquired after near-infrared (NIR) laser irradiation.
154        Sensitive detection of near-infrared (NIR) light enables many important applications in both r
155 tion (PBM) by far-red (FR) to near-infrared (NIR) light has been demonstrated to restore the function
156                          Upon near-infrared (NIR) light irradiation, this pro-nanoenzyme not only gen
157 chemically benign visible and near-infrared (NIR) light.
158 have developed an activatable near-infrared (NIR) molecular probe with far-red excitation, NIR emissi
159 ared spectroscopy (ATR-FTIR), near-infrared (NIR) reflectance spectroscopy, laser-induced breakdown s
160 s that absorb and emit in the near-infrared (NIR) region are potentially noninvasive, high-resolution
161 ned with insights provided by near-infrared (NIR) spectroscopy and time-dependent density functional
162  zero-field (57)Fe Mossbauer, near-infrared (NIR) spectroscopy, and X-ray crystallography techniques.
163 owed energy absorption in the near-infrared (NIR) wavelength range.
164 coustic imaging in the second near-infrared (NIR) window and T(1) -MR imaging due to the released Mn(
165 ltrasensitive and sustainable near-infrared (NIR)-emitting piezoluminescence is observed from noncent
166 otor that can be activated by near-infrared (NIR)-irradiation for the triggered delivery of internal
167                               Near-infrared (NIR)-light-induced tumor photothermal therapy has been s
168  recent years, broadband- and near-infrared (NIR)-mediated polymerizations have been of particular in
169           Strong magnetic and near-infrared (NIR)-responsive plasmonic properties of the engineered n
170  short-wavelength (SW-AF) and near-infrared (NIR-AF) autofluorescence images of ten patients with mut
171 atform combining broadband Vis/near-infrared(NIR) spectroscopy and electrophysiology with studying E-
172 h overt (visible) and covert (near-infrared, NIR) properties, with concomitant multi-emissive spectra
173 is readily photoexcited using near-infrared, NIR, and light through two-photon absorption, TPA.
174                     The use of low-intensity NIR light to operate molecular switches offers several p
175 nce emission of Au nanoclusters (AuNCs) into NIR-II region with improved quantum yields (QY) could be
176  ball milling and facile tip sonication into NIR fluorescent nanosheets (EB-NS).
177  compared with NIR-I imaging, intraoperative NIR-II imaging provided a higher tumour-detection sensit
178 TLs with cellular resolution by non-invasive NIR-IIb light sheet microscopy.
179 s of 2 phase I clinical trials investigating NIR-guided SLN mapping utilizing ICG in patients with su
180 rrent organic photodetectors suffer from low NIR sensitivity typically due to early absorption cutoff
181                  To date, few small-molecule NIR-II fluorophores have been discovered with donor-acce
182          Using spectrally distinct monomeric NIR FP variants, we perform two-color live-cell STED mic
183 sign to engineer a complete set of monomeric NIR FPs, which are the brightest genetically encoded NIR
184                                         Most NIR-IIb fluorophores are nanoparticle-based probes with
185 e, nanomedicine and biology, multifunctional NIR-II photothermal inorganic or organic materials have
186  We characterized the performance of the new NIR GECIs in cultured cells, acute mouse brain slices, a
187 8 nm, blue/SW-AF; 532 nm, UWF-AF and 787 nm, NIR-AF) and image processing.
188 of torsionally restrictive N-substituted non-NIR fluorescent rosol dyes based on density functional t
189  in vivo imaging system using nonoverlapping NIR-II probes with markedly suppressed photon scattering
190               To address this, here, a novel NIR-light-responsive and injectable DNA-mediated upconve
191 his work aimed to investigate the ability of NIR-HSI and augmented Multivariate Curve Resolution-Alte
192 adients generated by plasmonic absorbance of NIR irradiation, with velocities ranging up to 6.2+/-1.1
193 his review summarizes the recent advances of NIR-II photothermal combinational theranostics pertinent
194     Here we demonstrate that J-aggregates of NIR fluorophore IR-140 can be prepared inside hollow mes
195 ectively, demonstrating the applicability of NIR-HSI and MCR-ALS in the identification of fiber in pa
196                           The application of NIR-II emitters for gastrointestinal (GI) tract imaging
197 els, but is limited by the low brightness of NIR-II probes, which prevents imaging at low excitation
198 tested the hypothesis that a brief course of NIR (830 nm) PBM would preserve mitochondrial metabolic
199  ureters displayed a significant decrease of NIR perfusion with increased distance to the renal pelvi
200 t here the first successful demonstration of NIR imaging of DNA damage-induced senescence both in vit
201 pectral imaging system with the detection of NIR-II and NIR-I (700-900 nm in wavelength) fluorescence
202 strate for the first time a direct effect of NIR PBM on retinal mitochondrial redox status in a well-
203  deep penetration and non-invasive nature of NIR light coupled to TTA-UC offers new opportunities.
204     The results demonstrate the potential of NIR-HSI to quantify pectin content in orange peels, prov
205          This indicates an important role of NIR-driven oxygenic photosynthesis in primary production
206                 The increased sensitivity of NIR readouts for colon permeability is shown using dextr
207 emonstrate that the enhanced miRFP series of NIR FPs, which combine high effective brightness in mamm
208 ent has hindered the clinical translation of NIR-II imaging.
209                                        GA on NIR/FAF images was defined in accordance to recently pub
210 use this approach to design reliable turn-on NIR fluorescent sensors for detecting specific protein t
211                           In this case, only NIR showed a good performance with regression coefficien
212 hing and high brightness compared with other NIR fluorophores.
213 GECO2G provide substantial improvements over NIR-GECO1 for imaging of neuronal Ca2+ dynamics.
214 eneral design strategy for direct one-photon NIR photoswitches based on negative photochromic dihydro
215 heses and require UV, visible, or two-photon NIR light to trigger release.
216 his study investigated the use of a portable NIR spectrometer combined with chemometric tools to disc
217  1 (NQO1)-activatable NIR fluorescent probe (NIR-ASM) by conjugating dicyanoisophorone (ASM) fluoroph
218 NIR and inhabited by cyanobacteria producing NIR-absorbing pigments.
219 bacteria to harvest near-infrared radiation (NIR) at 700-780 nm for oxygenic photosynthesis.
220 enables them to use near-infrared-radiation (NIR) for oxygenic photosynthesis.
221  with a high signal-to-low noise ratiometric NIR fluorescence response.
222 oscope, including near-infrared reflectance (NIR), green fundus autofluorescence (G-FAF), confocal ps
223 ndus photography, near-infrared reflectance (NIR), spectral-domain (SD) and swept-source (SS) optical
224 tial and temporal resolution, and remarkable NIR-II image-guided photothermal therapy.
225                      Our previously reported NIR GECI, NIR-GECO1, has these advantages but also has s
226        We elicit a clear, spatially-resolved NIR signal from deep organs (brain, liver and kidney) wi
227 neously illuminated tumors via pH-responsive NIR imaging.
228                               SVPII selected NIR regions correlated with coffee components, and the f
229  as compared to laser ignition with a single NIR pulse.
230 icantly higher (2-3 times, P < .01) specific NIR FI in the nuclei and cytoplasm of islets cells than
231  and exhibited strong tumor uptake, specific NIR-II signals with high spatial and temporal resolution
232 The TCZ-PNPs are demonstrated to have strong NIR-II extinction coefficient, high photostability and e
233 sed O(2) imaging, we demonstrate substantial NIR-driven oxygenic photosynthesis by endolithic, Chl f-
234 blish an approach for developing superbright NIR-II contrast agents based on the synergy between chem
235 ures, and upconversion-mitochondria-targeted NIR-II dyes have not been reported.
236 tection and less day-to-day variability than NIR spectroscopy.
237                 Our results demonstrate that NIR-GECO2 and NIR-GECO2G provide substantial improvement
238            Our result also demonstrated that NIR can accurately quantify phenolics even at low concen
239                   The results indicated that NIR spectroscopy can be useful for an approximate quanti
240                                          The NIR method avoids the tedious extraction and TPC assay p
241                                          The NIR spectra obtained from individual seeds were used to
242 , which comprises a DCNP core, acting as the NIR-II optical imaging agent, and a PDA shell, acting as
243                  We infer that combining the NIR-I/II spectral windows and suitable fluorescence prob
244 FWHM) of <50 nm, and tunability to cover the NIR-I range are highlighted.
245 that are significantly blue-shifted from the NIR-II region (<850 nm) and may thus ultimately compromi
246                             Importantly, the NIR emitting NPS-SC4AD-NiB system exhibits an ultrahigh
247 e to strong absorptions and emissions in the NIR region.
248 arkable responsivity over 0.5 A W(-1) in the NIR spectral region (920-960 nm), which is the highest a
249 ule sensitivity has not been achieved in the NIR-II window due to lack of suitable bio-probes.
250  for primary/metastatic tumor imaging in the NIR-IIa (1100-1300 nm) window.
251 visualize cancer-invaded sentinel LNs in the NIR-IIb (>1500 nm) window.
252 ting the excitation wavelength deep into the NIR, both NIR one-photon absorption cross-section and ph
253 r two-photon absorption bands reach into the NIR-II region of the electromagnetic spectrum.
254                   Herein, we investigate the NIR-to-UV/visible emission of sub-15 nm alkaline-earth r
255 al transition was shifted beyond 900 nm, the NIR cross-section was enhanced by two orders of magnitud
256                  The 702-900 nm range of the NIR spectrum was associated with the chalky grain trait.
257 e identified on the FAF image but not on the NIR image, translating into a sensitivity of 94.8%.
258                       The results showed the NIR spectroscopy can better predict the origin of sample
259   Second near-infrared photothermal therapy (NIR-II PTT, 1000-1500 nm) has recently emerged as a new
260 monly obtained along with OCT, and therefore NIR-based GA assessment may be a useful surrogate in cli
261  apparatus has been demonstrated using these NIR emissive nanoparticles.
262 ort presents the first D-A type thiopyrylium NIR-II theranostics for synchronous upconversion-mitocho
263 ofuscin granules were found to contribute to NIR-AF, indicated by the colocalization of lipofuscin-AF
264 ations, including emission in the far-red to NIR region, large Stokes' shifts, and high photostabilit
265 ies of bionic PDs with selective response to NIR-I photons, the merits of a narrowband response with
266 st time, the design of fixable cell-tracking NIR fluorophores (CTNFs) with high optical properties, e
267         We demonstrate dye degradation under NIR illumination using SrYbF:1 %Tm(3+) @CaF(2) , highlig
268 otential, and tumor growth suppression under NIR laser radiation are the main biomedical research are
269              In total, 66 patients underwent NIR-guided SLN mapping and lymphadenectomy after peritum
270  the core-shell nanostars were released upon NIR illumination due to the heat generation from the cor
271  enable in vivo swallowing evaluations using NIR/SWIR imaging.
272 erapy by the regulation of Ppa release using NIR illumination.
273  be identified and quantified reliably using NIR images in many cases, though eyes with a thin choroi
274 ((MIR values - NIR values)/0.5 (MIR values + NIR values) x 100%) for cow and camel milk were, for pro
275 an of the relative difference ((MIR values - NIR values)/0.5 (MIR values + NIR values) x 100%) for co
276 generation of miRFPs should become versatile NIR probes for multiplexed imaging across spatial scales
277      To date, N0 status when established via NIR SLN mapping seems to be associated with decreased re
278       However, the lack of clinically viable NIR-II equipment has hindered the clinical translation o
279 es of the isolated peaks by NMR, MS, and vis-NIR spectra revealed that the major products were four t
280 ombining electrophysiology and broadband Vis-NIR spectroscopy, to monitor neurodevelopment in brain o
281 es with 10 fs duration across the entire VIS-NIR spectral range.
282         Taking together the experimental vis-NIR spectra, NMR assignments, and the computed relative
283 persive X-ray (EDX) spectroscopy, and UV-Vis-NIR absorption spectroscopy.
284  and 1:2 complexes were determined by UV-vis-NIR denaturation titration, using pyridine as a competin
285                                   The UV-vis-NIR spectra of this partially fused nanoring show that p
286 y, Ultraviolet-visible-near infrared (UV-Vis-NIR) spectroscopy, and Hall Effect measurements.
287 ts show that visible and near infra-red (Vis/NIR) spectroscopy can classify rice according to sub-pop
288              These results indicate that Vis/NIR can be used for non-destructive high throughput phen
289                                      In vivo NIR fluorescence imaging of CHL-GLP-1R xenografts was pe
290 -1R xenografts were visualized using in vivo NIR fluorescence imaging.
291 -mitochondria-targeted cell imaging, in vivo NIR-II osteosarcoma imaging and excellent photothermal e
292 hotoresponsive at near-infrared wavelengths (NIR).
293 perating in the second near-infrared window (NIR-II, 1,000-1,700 nm), where tissues are highly transp
294 e advantages of second near-infrared window (NIR-II, 1000-1700 nm) fluorescence imaging (FI) and phot
295  imaging in the second near-infrared window (NIR-II, ~1000-1350 nm) is advantageous for in vivo studi
296  The second near-infrared wavelength window (NIR-II, 1,000-1,700 nm) enables fluorescence imaging of
297                 We found that, compared with NIR-I imaging, intraoperative NIR-II imaging provided a
298 Intratumoral injection of HD/Se/ICG gel with NIR laser irradiation provided the most efficient tumor
299           Dot SDDs were well identified with NIR (83.1% sensitivity; 91.4% specificity) and G-FAF (84
300       In 2-D cell cultures, irradiation with NIR light at low power results in precisely focused phot

 
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