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1 using a label-free approach, confocal Raman microspectroscopy.
2 r transform infrared (FTIR) spectroscopy and microspectroscopy.
3 nformation or present confounding effects in microspectroscopy.
4 inside a somatic mammalian cell using Raman microspectroscopy.
5 with the high specificity and speed of Raman microspectroscopy.
6 ted biomolecular specificity for vibrational microspectroscopy.
7 for "spectral" cytology of urine using Raman microspectroscopy.
8 ed S and von Kossa staining as well as Raman microspectroscopy.
9 zation mass spectrometric imaging, and Raman microspectroscopy.
10 ated nerve fiber by means of polarized Raman microspectroscopy.
11 Saos-2 and SW-1353 cells by utilizing Raman microspectroscopy.
12 in desiccated specimens using confocal Raman microspectroscopy.
13 copic information obtained by FTIR and Raman microspectroscopy.
14 ried and spectra were collected by using MIR-microspectroscopy.
15 y an improved approach of sensitive infrared microspectroscopy.
16 rovided by a combination of Raman macro- and microspectroscopy.
17 herent anti-Stokes Raman spectroscopy (CARS) microspectroscopy allowed us to locally identify acylgly
18 sis using Fourier-transform infrared (FT-IR) microspectroscopy, an evolving method that allows the no
19 ese observations, Fourier transform infrared microspectroscopy analysis revealed that the ech and yip
21 least fivefold faster than spontaneous Raman microspectroscopy and can be used to generate maps of bi
22 ascitic fluid is possible by means of Raman microspectroscopy and chemometrical evaluation with the
23 onalities of the SOA were probed using X-ray microspectroscopy and compared with other laboratory gen
25 ted here should enable the routine use of IR microspectroscopy and imaging for the molecular analysis
27 ated on aluminum foils and analyzed by Raman microspectroscopy and subsequently by electron microscop
28 ynchrotron Fourier transform infrared (FTIR) microspectroscopy and synchrotron micro-X-ray fluorescen
29 xidation characteristics obtained with Raman microspectroscopy and temperature programmed oxidation,
30 ssion scanning electron microscopy, infrared microspectroscopy, and biochemical characterization of s
31 nation of compound-specific chemical assays, microspectroscopy, and electron microscopy to show that
32 structively analyzed by laser tweezers Raman microspectroscopy, and information on their composition
33 ynchrotron radiation FTIR (S-FTIR) and Raman microspectroscopy are powerful complementary techniques
34 ttenuated total internal reflection infrared microspectroscopy as a detector for high-performance liq
35 this study, we present the ability of Raman microspectroscopy as a novel analytical technique for a
36 ing NYscFv as probe in combination with SERS microspectroscopy at a single laser excitation wavelengt
37 pores were analyzed by using nonlinear Raman microspectroscopy based on coherent anti-Stokes Raman sc
38 gorous theory is presented for IR absorption microspectroscopy by using Maxwell's equations to model
39 thermal Fourier-transform infrared (PT-FTIR) microspectroscopy can also be employed using the same pr
44 carbon electrode using synchrotron infrared microspectroscopy combined with protein film electrochem
45 sue using Fourier-transform infrared (FT-IR) microspectroscopy, confocal Raman microspectroscopy (CRM
46 n-based Fourier transform infrared (SR-FTIR) microspectroscopy coupled with multivariate analysis was
50 ed (FT-IR) microspectroscopy, confocal Raman microspectroscopy (CRM), and matrix-assisted laser desor
54 hermal-Fourier transform-infrared (PT-FT-IR) microspectroscopy employs a thermal probe mounted in a s
55 advent of automated algorithms, vibrational microspectroscopy excels in the field of spectropatholog
56 cornea were collected by using a synchrotron microspectroscopy facility at Daresbury Laboratory (Unit
57 nt two-dimensional multifocus confocal Raman microspectroscopy featuring the tilted-array technique i
58 rove of the diagnostic capabilities of FT-IR microspectroscopy for monitoring in real-time the bioche
61 demonstrate the capability of confocal Raman microspectroscopy for the discrimination and identificat
63 (SEM) analysis, a Fourier-transform infrared microspectroscopy (FTIRM) method was employed to monitor
66 f microbiological samples with optical Raman microspectroscopy has been the inability to acquire pre-
69 monstrates for the first time that NIR Raman microspectroscopy has the potential for the reagentless
71 In this report, we employ coherent Raman microspectroscopy in a combination with a hierarchical c
73 dent identification procedure by using Raman microspectroscopy in combination with innovative chemome
75 ctance Fourier transform infrared (SR FT-IR) microspectroscopy in conjunction with discriminant analy
76 n vivo by mixed stable isotope-labeled Raman microspectroscopy in conjunction with multivariate curve
78 monstrate here by synchrotron based infrared microspectroscopy in transmission and attenuated total r
79 trochemical microcell for in situ soft X-ray microspectroscopy in transmission, dedicated for nonvacu
86 the combination with microscopy, vibrational microspectroscopy is currently emerging as an important
91 mark method in pollen analysis, the infrared microspectroscopy method offers better taxonomic resolut
92 morphological and Fourier transform infrared microspectroscopy (mFTIR) analyses of intact sediments a
93 of attenuated total reflectance mid-infrared microspectroscopy (MIR-microspectroscopy) was evaluated
95 determined experimentally by polarized Raman microspectroscopy of oriented fd fibers, using the amide
96 ions of Tyr 21 and Tyr 24 by polarized Raman microspectroscopy of oriented Ff fibers, utilizing a nov
97 ntroduce a novel sampling setup for infrared microspectroscopy of pollens preventing strong Mie-type
98 in hardening using uniaxial tensile loading, microspectroscopy of polymer chain alignment, and theory
100 investigated by synchrotron radiation FT-IR microspectroscopy on connective tissue and in muscle fib
101 lysis of the solid surface by confocal Raman microspectroscopy performed at a constant focal distance
102 d have implications for the utility of Raman microspectroscopy process analysis for the generation of
103 ed that synchrotron FTIR and synchrotron XRF microspectroscopies provide complementary information on
105 determination, Fourier-transformed infrared microspectroscopy, quantitative reverse transcription-PC
106 emonstrate the power of synchrotron infrared microspectroscopy relative to conventional infrared meth
107 emical imaging by Fourier transform infrared microspectroscopy revealed large differences in the dist
114 and the limitations of stable isotope Raman microspectroscopy (SIRM), resonance SIRM, and SIRM in co
118 emonstrated using synchrotron-based infrared microspectroscopy that the striatum and the cortex of pa
119 gans plants using Fourier transform infrared microspectroscopy, that TE lignification occurs postmort
120 itored by Fourier transform-infrared (FT-IR) microspectroscopy the response of live breast cancer MCF
123 This study highlights the potential of FTIR microspectroscopy to acquire useful structural informati
124 te the applicability of synchrotron infrared microspectroscopy to adsorbed proteins by reporting pote
127 Hence, we demonstrate the potential of Raman microspectroscopy to directly sort pellets containing L.
129 of high-resolution bench top-based infrared microspectroscopy to investigate the microstructure of T
132 nced catalytic conversion, as detected by IR microspectroscopy, to areas with high concentration of A
133 orce microscopy, x-ray tomography, and Raman microspectroscopy, to assess the properties of bone matr
134 of surface-enhanced Raman scattering (SERS) microspectroscopy using glass-coated, highly purified SE
137 ation of NIR spectroscopy and FTIR and Raman microspectroscopy was used to elucidate the effects of d
141 lectance mid-infrared microspectroscopy (MIR-microspectroscopy) was evaluated as a rapid method for d
143 e field-effect transistor (FET) and infrared microspectroscopy, we demonstrate a gate-controlled, con
145 ods of high-resolution mass spectrometry and microspectroscopy were utilized for molecular analysis o
146 using confocal spontaneous Raman scattering microspectroscopy, which exploits the intrinsic vibratio
148 . compared Fourier transform infrared (FTIR) microspectroscopy with histological pathology to evaluat
149 , bleaching-corrected polarized fluorescence microspectroscopy with nanometer spectral peak position
151 impetus for this approach was that SR FT-IR microspectroscopy would offer several advantages over co
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