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1  are the only structure contributing to RNFL birefringence.
2  to evaluate the contribution of MTs to RNFL birefringence.
3 of microgears based on the principle of form birefringence.
4  MTs make a significant contribution to RNFL birefringence.
5 ution using the method of transient electric birefringence.
6  objective information on RNFL thickness and birefringence.
7 -spaced dielectric nanostructures with shape birefringence.
8 s then adjusted to minimize anterior segment birefringence.
9 ured birefringence largely reflects the RNFL birefringence.
10 oscopy by exploiting the angle dependence of birefringence.
11  control of alignment, domain structure, and birefringence.
12 changes occurred in the absence of Congo red birefringence.
13 ods such as light and neutron scattering and birefringence.
14 perties of macromolecules, specifically form birefringence.
15 ctrophoretic mobility and transient electric birefringence.
16 ansgenic muscle only rarely showed Congo red birefringence.
17 hering our understanding of textural or form birefringence.
18 ules, using the method of transient electric birefringence.
19 the length of the waveguide and quantify its birefringence.
20 croscopy and in situ quantification of light birefringence.
21 ings are used to overcome the limitations of birefringence.
22 aterials, based on the phenomenon of optical birefringence.
23 onodomain hydrogel that exhibits significant birefringence.
24 s, functions in the formation of gut granule birefringence.
25 LAR XYLEM 10-L (IRX10-L) and ESKIMO1/TRICOME BIREFRINGENCE 29 (ESK1/TBL29), catalyze these respective
26  bend angle determined by transient electric birefringence, 38 degrees +/- 7 degrees.
27 recently developed technique, PSOCT measures birefringence, a material property that is elevated in t
28 smonic metamaterials explored herein exhibit birefringence, a skin depth approaching that of pure met
29 red-positive material producing bright green birefringence also developed outward from AEF precipitat
30 l interference contrast (DIC) microscopy and birefringence also show crystal formation rather than th
31                     The variation of corneal birefringence among individuals is substantial enough to
32             In addition, we demonstrate that birefringence amplitude data can be used to provide mode
33                                              Birefringence analysis showed root PDL reattachment for
34 re examined via DPI, with changes in bilayer birefringence analyzed as a function of the peptide mass
35 ce and optical activity (linear and circular birefringence and dichroism) can be controlled by a wave
36 olarization, cross-polarization, directional birefringence and dichroism.
37                                              Birefringence and force produced by pig tracheal smooth
38 of seven candidate chemicals restored normal birefringence and increased survival of dystrophin-null
39                   The method is resilient to birefringence and light dispersion.
40                                          The birefringence and linear dichroism of anisotropic thin f
41 ed states, as well as measurements of linear birefringence and linear dichroism of mixed crystals, we
42                         Commonly, the linear birefringence and linear dichroism of these films resemb
43 stretching structural transitions, increased birefringence and morphological alignment were demonstra
44 velength thickness optical manifestations of birefringence and optical activity (linear and circular
45 ssed substrates, as indicated by behavioral, birefringence and small angle X-ray scattering analyses.
46 e aligned nanofiber bundles, enhancing their birefringence and structural integrity.
47                  The origin of the anomalous birefringence and the assignment of the absolute configu
48 esigned to minimize spherical aberration and birefringence and to detect light from a particular dire
49 esolution images of skin structure, collagen birefringence, and blood flow.
50         The hydrogel string shows remarkable birefringence, and highly aligned nanofibers are visible
51 r layer (RNFL) thickness, phase retardation, birefringence, and reflectance using polarization sensit
52 d IOP and RNFL thickness, phase retardation, birefringence, and reflectance were characterized in sev
53 iation of RNFL thickness, phase retardation, birefringence, and reflectance with elevated intraocular
54 ively long polyGln peptide exhibit Congo red birefringence, and this birefringence is only observed i
55 ng in anisotropic rocks leads to scattering, birefringence, and waves with hybrid polarizations.
56 he peptide HPA3; significantly, the mass and birefringence are constrained by the same set of kinetic
57 the (dis)order in the LCN and its associated birefringence are evidenced at all temperatures.
58 rted by quantitative simulations of circular birefringence arising from crystallite twisting and spla
59      Consequently, when a spatially constant birefringence around the ONH is assumed, the conversion
60 is study was to evaluate the distribution of birefringence around the optic nerve head (ONH) in norma
61 ich in oriented collagen and exhibits higher birefringence, as confirmed with co-located histology.
62 thmic variations of both linear and circular birefringence, as determined by Mueller matrix microscop
63                        With a quick and easy birefringence assay, we have identified seven small mole
64                                      Resting birefringence at the longest length was 30% greater than
65                                              Birefringence, B-type crystallites and acid hydrolysis d
66 arimeter to calculate and neutralize corneal birefringence based on an intact Henle's layer.
67 ound integration, inflammation, and collagen birefringence between the two strains of mice.
68          Both fibril types display Congo red birefringence, bind Thioflavin-T and have X-ray fibre di
69 al methods (e.g., intrinsic UV fluorescence, birefringence, bright-field image analysis, etc.) is oft
70 alizes cytoskeletal filaments based on their birefringence but differs from the standard polarization
71 veals radial oscillations in not only linear birefringence, but also circular birefringence, whose or
72 , the magnitude and axis of anterior segment birefringence can be determined from a polarimetry image
73                                       Muscle birefringence, caused mainly by parallel thick filaments
74                                         RNFL birefringence changes after acute RGC injury are associa
75 s images related to linear dichroism, linear birefringence, circular dichroism, and anomalous circula
76 ic ring patterns and radial variation of the birefringence color.
77 logies, Inc., San Diego, CA) so that corneal birefringence could be corrected on a subject-specific v
78                                          The birefringence decay behavior of the loop-containing RNA
79 sing two variably phased bends, the relative birefringence decay times depend on the flexibility of e
80                                         RNFL birefringence declined before and faster than RNFL thick
81                                         RNFL birefringence declined by 15% 1 week after ONT (P = 0.04
82                                          The birefringence (Deltan) depends on the density and compos
83 e changes in the vibration angle (theta) and birefringence (Deltan) on the (001) face of the crystal
84           Congo red staining and apple green birefringence demonstrated vitreous amyloidosis.
85                                        Light birefringence demonstrates a substantial decrease in cry
86                              The increase in birefringence did not occur in the presence of the aggre
87                             In contrast, the birefringence did not vary significantly as a function o
88 nal nerve fiber layer (RNFL) exhibits linear birefringence due to the oriented cylindrical structure
89 ivity of the crystal has no influence on the birefringence during Q-switching if the quarter wave pla
90 ultaneous real-time measurements of mass and birefringence during the binding and dissociation of the
91 embrane structure through the measurement of birefringence during the binding of magainin 2 (Mag2) an
92 ulent array of topological defects, and (iv) birefringence-enabled visualization of microflow generat
93                        The nanobelts exhibit birefringence enhanced by 1 order of magnitude as a resu
94                            Previous electric birefringence experiments have shown that the actin-acti
95                            Previous electric birefringence experiments on minifilaments showed a larg
96 mental data obtained from transient electric birefringence experiments.
97  the optical effects of transmission, linear birefringence, extinction, linear dichroism, and orienta
98 utomated CD spectrometer equipped with a low-birefringence flow-through cell that is coupled to a thr
99  RNFL thickness and mean retinal nerve fiber birefringence for each of 48 sectors on a circle were de
100 onstruct images of the depth-resolved tissue birefringence free of artefacts.
101 curs in skeletal muscle, where a decrease in birefringence has been correlated with crossbridge movem
102         In contrast, the phenomenon of x-ray birefringence has been demonstrated only recently and ha
103                                  Unlike RNFL birefringence, however, which totally disappears after c
104 hat is typical of confocal images; and (3) a birefringence image.
105 rt analysis of conventional bright-field and birefringence images were performed.
106  ca. 5 mum) form interwoven patterns seen in birefringence images, Piezo-Force Microscopy (PFM) and R
107            Here, we report a technique-x-ray birefringence imaging (XBI)-that enables spatially resol
108                In our scheme, we exploit the birefringence in a single-mode polarization maintaining
109 a tissue diagnosis demonstrating apple-green birefringence in Congo Red-stained sections viewed micro
110                         The decrease of RNFL birefringence in glaucoma may indicate a loss of MTs.
111 s, while measuring the Lorentz force-induced birefringence in graphene at Terahertz frequencies in ma
112 rimetry (SLP) reveals abnormal retardance of birefringence in locations of the edematous peripapillar
113 strate that PSOCT enables the measurement of birefringence in plaques and in fibrous caps of necrotic
114 rs stain with Congo red and show apple-green birefringence in polarized light, characteristic of amyl
115 tested) by their ability to prevent abnormal birefringence in sapje.
116  more robust measure of the anterior segment birefringence in some eyes with macular disease.
117 pic modeling revealed a significant positive birefringence in the layer, suggesting oriented protein
118 inferior (P = 0.021) regions, decreased RNFL birefringence in the nasal (P = 0.002) and inferior (P =
119  long lengths, and that approximately 35% of birefringence in the resting muscle at the longest lengt
120       Neurotubules are the primary source of birefringence in the RNFL of the primate retina.
121 etry endothermic peak enthalpies and loss of birefringence in the starch were found, indicating starc
122 onstructed using polymers that exhibit large birefringence in their indices of refraction.
123 of solid-state absorption, fluorescence, and birefringence, in response to external electric fields.
124                     Using this approach, the birefringence, including the formation of spatially patt
125 ic range because of their high orientational birefringence, incorporate a dye designed to have a larg
126                         During contractures, birefringence increased by 25 and 18% at the shortest an
127                               During tetani, birefringence increased with approximately the same time
128 binant sericin fibrils exhibited apple-green birefringence, indicating long-range order in the array
129  S. cerevisiae showed an aggregation-induced birefringence indicative of order on the cell surface.
130                                      Corneal birefringence is an important source of variance in SLP,
131 onantly coupling out unwanted modes, whereas birefringence is engineered by fabricating an asymmetric
132  the twisted fibril structure with Congo red birefringence is not the predominant form in the polyGln
133 de exhibit Congo red birefringence, and this birefringence is only observed in a small portion of the
134                                 The circular birefringence is shown to be a consequence of misoriente
135 s for strongly aligned tissues, where linear birefringence is the dominant optical property.
136 th the described method so that the measured birefringence largely reflects the RNFL birefringence.
137 ype II transmembrane protein with a Trichome Birefringence-Like domain and a domain of unknown functi
138 e AXY9 protein is distinct from the TRICHOME BIREFRINGENCE-LIKE proteins, reported to be polysacchari
139 es the REDUCED WALL ACETYLATION and TRICHOME BIREFRINGENCE-LIKE proteins.
140 d plasmonic surface in conjunction with high birefringence liquid crystals, we demonstrate a tunable
141  changes in retinal nerve fiber layer (RNFL) birefringence may both precede clinically detectable gla
142                         Measurements of RNFL birefringence may provide a means to detect early subcel
143                                         RNFL birefringence measured by SLP decreased over time in all
144         X-ray powder diffraction and optical birefringence measurements confirm that these are amyloi
145 by performing a series of transient electric birefringence measurements on bovine mtRNASer(AGY) const
146  series of time-resolved, transient electric birefringence measurements was conducted in an effort to
147 ime-resolved flow velocimetry and full-field birefringence microscopy to study the behavior of a seri
148                                Abnormal RNFL birefringence occurs in sectors corresponding to regiona
149 nts an interplay between linear and circular birefringence of a laser cavity along with light induced
150 the longer peptides, we report here that the birefringence of a small drop of peptide solution can su
151 mple to determine and correct for the linear birefringence of an aligned sample.
152                                              Birefringence of healthy RNFL is constant as a function
153 ll-established radial oscillations in linear birefringence of many polycrystalline ensembles is accom
154  enables spatially resolved mapping of x-ray birefringence of materials, representing the x-ray analo
155                         We have measured the birefringence of microtubules (MTs) and of MT-based macr
156 r small size and belt geometry exceeding the birefringence of naturally occurring minerals, including
157   The magnitude and axis of anterior segment birefringence of normal eyes were determined from a pola
158                    Furthermore, the measured birefringence of protein fibers in the thin lamellipodia
159                                              Birefringence of root PDL reattachment was also evaluate
160  detectable in principle, are unclear due to birefringence of the components of the cytoplasm and nuc
161         Thus, the analysis elucidates on the birefringence of the dilute-As GaNAs alloys and comparis
162                                              Birefringence of the modified protein was induced when i
163                 One reason for an ARP is the birefringence of the sclera.
164                                     The form birefringence of the solution is calculated as the diffe
165 que incidence of the beam on the sample, and birefringence of the tissue.
166                                          The birefringence of this phase can be switched by applicati
167 ween 0.10 and 0.35 deg/microm, equivalent to birefringences of 1.2 x 10(-4) and 4.1 x 10(-4) respecti
168 er bundles was used to follow change of RNFL birefringence over time.
169 s defined as a TSS of 80 to 100 and abnormal birefringence pattern (ABP) as TSS <or= 79.
170 ased on the typical scan score (TSS): Normal birefringence pattern (NBP) was defined as a TSS of 80 t
171 had been expected from the change in optical birefringence patterns and which is consistent with a ra
172                                      Macular birefringence patterns were classified as well defined,
173 igate the effect of the presence of atypical birefringence patterns, as measured by the typical scan
174                     Spatially averaged PSOCT birefringence, Phi, was measured and compared with plaqu
175               The sedimentation and electric birefringence properties of minifilaments formed by rods
176 also provide insight into directional tissue birefringence properties to monitor pathological changes
177 sted eyes, the magnitude of anterior segment birefringence ranged from 21.7 to 86.3 nm, and the slow
178 , with normal electrophoretic mobilities and birefringence relaxation times.
179  calcium increase caused by stimulation, the birefringence response inverted, suggesting crossbridge
180 lose agreement of AFM and transient electric birefringence results validates the suitability of both
181                                 The measured birefringence retardation of kinetochore fibers is propo
182  radial actin bundles, as displayed by their birefringence retardation, also is preserved during retr
183 scence, and the congo red spectral shift and birefringence show that these aggregates contain intermo
184 ility by about 10-fold, as inferred from the birefringence signal amplitude increase.
185       Erroneously corrected anterior segment birefringence significantly affects PP RNFL retardation
186                                              Birefringence studies showed a loss of typical Maltese c
187  carried out modeling and transient electric birefringence studies to determine the angle between the
188        The interocular similarity of corneal birefringence suggests deterministic control of corneal
189 brafish results in abnormal muscle, with low birefringence, tears at the myosepta, and increased embr
190    Using a combination of transient electric birefringence (TEB) and gel electrophoretic measurements
191 ules can be identified by transient electric birefringence (TEB) because they exhibit rotational rela
192 ue, we describe a form of transient electric birefringence (TEB) measurement in which the rotational
193       Using the method of transient electric birefringence (TEB), and by changing the helical torsion
194 as utilized the method of transient electric birefringence (TEB), which is highly sensitive to change
195    Our approach is to use transient electric birefringence techniques to measure changes in hydrodyna
196 ers were generally more sensitive to retinal birefringence than mean-based parameters.
197 s is accompanied by oscillations in circular birefringence that cannot be explained by the natural op
198 he retinal nerve fiber layer (RNFL) exhibits birefringence that is due to the oriented cylindrical st
199  with 1 g mL-1 fluorescent dye and polarized birefringence), the cells failed to elongate, and the co
200 ommercial optical fibers, the absence of any birefringence, the presence of technologically inaccessi
201 xplore the application of Transient Magnetic Birefringence (TMB) to study these weak interactions, us
202 otation, determined using transient electric birefringence to measure rates of rotational Brownian mo
203  stained with Congo Red to produce the green birefringence typical of amyloid.
204 ng, monitored by characteristic yellow-green birefringence under crossed polarization has been used a
205 pearance by electron microscopy and generate birefringence under polarized light when stained with Co
206 ining with Congo red and examining for green birefringence under polarized light.
207 s of long-range order despite retaining some birefringence under polarized microscopy.
208                  In particular, we show that birefringence upon CR binding is due to the anisotropic
209 lar strategies for neutralization of corneal birefringence using SLP-VCC can fail if Henle's layer is
210                  Both the RNFL thickness and birefringence varied as a function of sector around the
211                                         RNFL birefringence varies with position around the ONH.
212                                              Birefringence was calculated along circular scan paths a
213 d magnitude so that compensation for corneal birefringence was eye specific.
214 er of amyloid deposits measured by Congo Red birefringence was increased in the double ACT/amyloid pr
215                                         RNFL birefringence was measured by scanning laser polarimetry
216                                         RNFL birefringence was measured by SLP before injection and e
217  soluble than the wild-type sequence, and no birefringence was observed with Congo Red staining.
218                            Moreover, a giant birefringence was observed, and the refractive index dif
219 ted THz pulse with zero ellipticity, and the birefringence was quantified.
220                                      Corneal birefringence was well correlated between the two eyes o
221 ls bind Congo Red and exhibit dramatic green birefringence when observed between crossed polarizers,
222 of beta-sheet structure, and exhibited green birefringence when stained with Congo Red.
223 account for the observed changes in mass and birefringence, whereas for the unsaturated phospholipid
224 e cells to the substratum lead to changes in birefringence, which can be measured and recorded by the
225 ive measurements provide the means to assess birefringence, which is elevated in oriented collagen fi
226 ogear), we can fabricate microgears of known birefringence, which may be readily rotated by manipulat
227 only linear birefringence, but also circular birefringence, whose origin is explained through slight
228 ed amyloid deposits confirmed by apple-green birefringence within dermal collagen, sweat glands, and
229 scribed that determines the anterior segment birefringence without relying on the presence of macular
230     This was manifest as a reduction of RNFL birefringence, without alteration of RNFL thickness, sug

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