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1 CARS imaging revealed that in the nuclei of proliferatin
2 CARS microscopy can be used to image the outer regions o
3 CARS microscopy could thus provide quantitative and semi
4 CARS microscopy detected changes in living hTMC morpholo
5 CARS microspectroscopy further indicated lower lipid flu
6 CARS-Cyp is expressed in a variety of tissues and cell t
7 CARSs also catalyze co-translational cysteine polysulfid
14 he sclera contained regions lacking TPAF and CARS fluorescence of approximately 3 to 15 mum in diamet
15 and coherent anti-Stokes Raman scattering (B-CARS) offers the same inherent chemical contrast as spon
18 lectron microscopy, the relationship between CARS signal strength and nanodiamond size is quantified.
19 ectroscopy technique that achieves broadband CARS measurements at an ultrahigh scan rate of more than
20 e's strength, we use it to perform broadband CARS spectroscopy of the transient mixing dynamics of to
21 s found between lipid volume data yielded by CARS microscopy and total fatty acid content obtained fr
28 stretching vibrational band, we demonstrate CARS imaging and spectroscopy of lipid-rich tissue struc
34 icles surrounding the nucleus is imaged by E-CARS at the frequency of the C-H stretching Raman band.
36 rger than the excitation wavelength, while E-CARS allows detection of smaller features with a high co
45 s is made possible by an integration of a FT-CARS system and a rapid-scanning retro-reflective optica
46 e basic principles of wide-field detected FT-CARS microscopy and demonstrate how it can be used as a
47 kes Raman scattering (wide-field detected FT-CARS) microscopy capable of acquiring high-contrast labe
49 rm coherent anti-Stokes Raman scattering (FT-CARS) spectroscopy technique that achieves broadband CAR
52 nd SFG imaging was faster, but hyperspectral CARS and SFG imaging has the potential to be applied to
53 es were used and compared: (i) hyperspectral CARS combined with principal component analysis (PCA) an
55 R patients with favorable characteristics, I-CARS suggests a 24% probability of successful LVAD expla
58 classified the 1,857 postmenopausal women in CARS as prior/current HRT users if they took HRT before
60 deuterated acyl chains that provide a large CARS signal from the symmetric CD(2) stretch vibration a
62 sruption of the genes encoding mitochondrial CARSs in mice and human cells shows that CARSs have a cr
64 ssed and unstained liver tissues, multimodal CARS imaging provides a wealth of critical information i
65 its sensitivity and versatility, multimodal CARS microscopy should be a powerful tool for the clinic
68 but experimentally simple SGH/TPEF/multiplex CARS multimodal imaging approach for a label-free charac
69 el image analysis approach for multispectral CARS data based on colocalization allows correlating spe
72 genes include RRM1, GOK (D11S4896E), Nup98, CARS, hNAP2 (NAP1L4), p57KIP2 (CDKN1C), KVLQT1 (KCNA9),
73 Here, unsupervised multivariate analysis of CARS datasets was used to visualize the subcellular comp
75 imental implementation for the generation of CARS by Bessel beam excitation using only passive optica
76 isted analysis of liver lipid level based on CARS signal intensity is consistent with triglyceride me
79 In addition, label-free and non-perturbative CARS imaging allow rapid screening of mitochondrial toxi
80 cattering of the intense forward-propagating CARS radiation in tissue gives rise to a strong epi-CARS
83 ratures low enough to freeze lumi, these PTR/CARS results provide the first detailed view of the vibr
84 The formation of lumiRT, monitored via PTR/CARS spectra recorded on the nanosecond time scale, can
87 eered to express chimeric antigen receptors (CARS), when activated peripheral blood mononuclear cells
89 elated, using childhood autism rating scale (CARS) and Vineland Adaptive scales, magnetic resonance i
90 ch as coherent anti-Stokes Raman scattering (CARS) and stimulated Raman scattering (SRS) microscopy p
91 ties, coherent anti-Stokes Raman scattering (CARS) and sum-frequency generation (SFG), were successfu
94 with coherent anti-Stokes Raman scattering (CARS) and two-photon excited fluorescence (TPEF) nonline
95 trong coherent anti-Stokes Raman scattering (CARS) at the sp(3) vibrational resonance of diamond.
97 lized coherent anti-Stokes Raman scattering (CARS) imaging to examine paclitaxel distribution in vari
98 iplex coherent anti-Stokes Raman scattering (CARS) imaging via supercontinuum excitation to probe mor
100 olved coherent anti-Stokes Raman scattering (CARS) is used as a probe for monitoring the vibrational
101 using coherent anti-Stokes Raman scattering (CARS) microscopy and isotopic perfusion experiments.
102 g the coherent anti-Stokes Raman scattering (CARS) microscopy and two-photon excited fluorescence (TP
103 dband coherent anti-Stokes Raman scattering (CARS) microscopy can be very useful for fast acquisition
104 gated coherent anti-Stokes Raman scattering (CARS) microscopy for monitoring lipid contents in living
105 modal coherent anti-Stokes Raman scattering (CARS) microscopy for the detection and characterization
106 ally, coherent anti-Stokes Raman scattering (CARS) microscopy images have been acquired and are compa
107 ctral coherent anti-Stokes Raman scattering (CARS) microscopy images of organic materials and biologi
109 -free coherent anti-Stokes Raman scattering (CARS) microscopy to mouse oocytes and pre-implantation e
110 e and coherent anti-Stokes Raman scattering (CARS) microscopy we identified that thirteen zooplankton
111 nning coherent anti-Stokes Raman scattering (CARS) microscopy with a lateral resolution of 0.25 mum.
112 nning coherent anti-Stokes Raman scattering (CARS) microscopy with fast data acquisition and high sen
113 se of coherent anti-Stokes Raman scattering (CARS) microscopy, a highly sensitive vibrational imaging
114 with coherent anti-Stokes Raman scattering (CARS) microscopy, a label-free vibrational imaging techn
115 ctral coherent anti-Stokes Raman scattering (CARS) microscopy, together with a quantitative image ana
116 using Coherent Anti-Stokes Raman Scattering (CARS) microscopy, which is used to selectively visualize
122 olved coherent anti-Stokes Raman scattering (CARS) with the advantages of time-resolved CARS spectros
125 ion to both coherent anti-Stokes scattering (CARS) and stimulated Raman scattering (SRS) spectroscopi
126 addition, we have demonstrated simultaneous CARS imaging of myelin and two-photon excitation fluores
127 and coherent anti-Stokes Raman spectroscopy (CARS) microspectroscopy allowed us to locally identify a
128 Coherent anti-Stokes Raman spectroscopy (CARS) uses vibrational resonances to study nuclear wavep
129 hat coherent anti-Stokes Raman spectroscopy (CARS), a nonlinear spectroscopy of great utility and pot
130 S), coherent anti-Stokes Raman spectroscopy (CARS), stimulated Raman spectroscopy (SRS) and surface e
133 The Coumadin Aspirin Reinfarction Study (CARS) database contains information on HRT use and menop
135 nsatory anti-inflammatory response syndrome (CARS; excessive anti-, but no/low proinflammatory mediat
142 ial CARSs in mice and human cells shows that CARSs have a crucial role in endogenous CysSSH productio
146 toplasm, and lipid droplets by analyzing the CARS spectra within the C-H stretching region only.
148 trong association was also identified at the CARS (cysteinyl-tRNA synthetase) locus (OR = 1.36, P = 3
149 od outer segments could be identified by the CARS signal from their lipid-rich plasma membranes.
150 chemical composition, are retrieved from the CARS intensity spectra using the causality of the suscep
152 alue decomposition on the square root of the CARS intensity, providing an automatic determination of
153 found that through the non-linearity of the CARS process in combination with the folded illumination
154 hly sensitive, camera-based detection of the CARS signal allows for fast and direct hyperspectral wid
157 osis in NIH 3T3 cells is monitored using the CARS signal from aliphatic C-H stretching vibration.
159 from human amelanotic melanomas subjected to CARS imaging exhibited strong pheomelanotic signals.
160 concentration from the difference of the two CARS intensities measured at the peak and dip frequencie
162 enic mouse adrenal cortical (Y-1) cells with CARS microscopy in real time without perturbations to th
163 ack collagen autofluorescence coincided with CARS signal, indicating the presence of stromal fibrobla
164 spectroscopic analysis was corroborated with CARS/TPEF multimodal imaging to visualize the distributi
165 taneous imaging of LDs and mitochondria with CARS and two-photon fluorescence microscopy clearly show
166 ing method as a classifier, was trained with CARS spectra using immunofluorescence images as a refere
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