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1 intained) and B2 (epithelium removed for the fluorescence analysis).
2 pproach, complemented by intrinsic extrinsic fluorescence analysis.
3 pheral EGF features, as quantified by radial fluorescence analysis.
4 y the Griess method and intracellular ROS by fluorescence analysis.
5 ial expression was evaluated by quantitative fluorescence analysis.
6 enylenediamine to form a product amenable to fluorescence analysis.
7 formation as determined by CD and tryptophan fluorescence analysis.
8 fferences in hybridization are determined by fluorescence analysis.
9 al to enhance scientific rigor in UV-vis and fluorescence analysis.
10  was studied by digital microscope and X-ray fluorescence analysis.
11 tlining common issues observed in UV-vis and fluorescence analysis.
12                           Our multiparameter fluorescence analysis allowed us to gain new insights in
13 shows that under the conditions used for the fluorescence analysis, alpha-synuclein is predominantly
14                              Single molecule fluorescence analysis and deterministic modeling reveal
15 he electrode surface was evaluated through a fluorescence analysis and measurement of the electrochem
16                             Leaf chlorophyll fluorescence analysis and thylakoid membrane composition
17                          Functional studies, fluorescence analysis, and citrullination experiments re
18                                              Fluorescence analysis by pulse-amplitude modulation fluo
19 parative analysis shows that the chlorophyll fluorescence analysis can accurately determine chloropla
20                                   The immuno-fluorescence analysis demonstrated enhanced peri-cryptal
21                    Homogeneous time-resolved fluorescence analysis demonstrated that the HTT1a transc
22                                      In vivo fluorescence analysis demonstrates that the proteins are
23  the combined method grazing incidence X-ray fluorescence analysis (GIXRF) and near edge X-ray absorp
24  confers tolerance to lower salt levels, and fluorescence analysis in 30% sucrose reveals instability
25 o using the purified proteins and in vivo by fluorescence analysis in human cells, using the split-EG
26                  Atomic force microscopy and fluorescence analysis in solution and on surfaces at the
27 te of O(2) evolution measured by chlorophyll fluorescence analysis in the PEPC mutant; this increase
28 of approximately 2:1 was found by Kalphabeta fluorescence analysis, indicating 2 Ni per [Fe(4)S(4)].
29  with the partially folded state observed in fluorescence analysis, interrogation of current versus t
30 n affinity similar to that of TnI(96-131) by fluorescence analysis (K(d)=380nM), its binding was not
31              3D and 2D-cross-sectional X-ray fluorescence analysis of biological material is a powerf
32                                         This fluorescence analysis of collagen-like peptides lays a f
33 d here via an unprecedented super-resolution fluorescence analysis of ex vivo tissue slices confirmin
34                                 Importantly, fluorescence analysis of fibroblast growth factor 2 and
35                        Using single molecule fluorescence analysis of MUTYH bound to abasic sites, we
36                        Using single-molecule fluorescence analysis of self-assembled DNA duplexes and
37 ace AMPA receptors in isolated synaptosomes: fluorescence analysis of single-synapse long-term potent
38 tical mass spectrometry-based proteomics and fluorescence analysis of single-synapse long-term potent
39                                              Fluorescence analysis of TcsL with 2-(p-toluidinyl) naph
40 's blood and milk samples was determined via fluorescence analysis of the functionalized QDs.
41 mbrane and their subsequent elution prior to fluorescence analysis of the quenching effect produced o
42                                              Fluorescence analysis of the subcellular localization of
43                                 Steady-state fluorescence analysis of these hybrids reveals that the
44                                 Double-label fluorescence analysis of these membranes indicated that
45                                  Multimarker fluorescence analysis of tissue specimens offers the opp
46                         We used quantitative fluorescence analysis of tissues to measure two fluoresc
47                                              Fluorescence analysis of wild-type, crd1, and sct1 strai
48 kage, "PyMca", primarily developed for X-ray fluorescence analysis offers an easy-to-use interface fo
49             Gamma-ray spectrometry and X-ray fluorescence analysis on a collected Pu particle indicat
50                        Using single-molecule fluorescence analysis on a prototypical superfamily 1 he
51 r cell metastasis was performed using immune-fluorescence analysis on lung and liver tissues.
52                                        Using fluorescence analysis over concentration based analysis
53                                      Protein fluorescence analysis provided evidence for conformation
54  procedures for Pb detection: portable X-ray fluorescence analysis (pXRF) and a simple colorimetric t
55                              Single-molecule fluorescence analysis revealed that instead of unwinding
56                                              Fluorescence analysis revealed that two native Trp resid
57                      Optical micrographs and fluorescence analysis show the successful topographic an
58                                   Tryptophan fluorescence analysis showed that all of the tested muta
59                                       CD and fluorescence analysis showed that it contained ordered t
60 the reactivity of free sulfhydryl groups and fluorescence analysis, showed that the increase of ethan
61                                              Fluorescence analysis shows a 3.38-3.5 times enhanced si
62 ter/early spring pine needles, time-resolved fluorescence analysis shows that extreme down-regulation
63                                  Chlorophyll fluorescence analysis shows that in vivo the Ndh complex
64                                Chlorophyll a fluorescence analysis suggested better performance of ph
65                      Although the tryptophan fluorescence analysis suggested that A2-17 and its analo
66 rough scanning electron microscopy and X-ray fluorescence analysis that highly Tl-enriched crystals o
67        We used rapid energy-dispersive x-ray fluorescence analysis to measure diagnostic elements in
68 llowing for a direct linking of quantitative fluorescence analysis to XPS quantification.
69   In a complementary approach, site-directed fluorescence analysis using an environmentally sensitive
70 pase activity and by performing quantitative fluorescence analysis using fluorescence-activated cell
71                                     However, fluorescence analysis using the typical flow cytometry m
72                        Using single-molecule fluorescence analysis, we showed that NS3 unwinds DNA in
73                                          The fluorescence analysis with avidin showed that target sam
74  absolute brightness values and quantitative fluorescence analysis with particle systems that can be