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1 he protection of surface Dirac fermions from backscattering.
2 was identified as a major contributor to the backscattering.
3 asurements of corneal sublayer thickness and backscattering.
4 states that are topologically protected from backscattering.
5 tes that are topologically protected against backscattering.
6 ing structures, it does not rely on multiple backscattering.
7 rized surface states that are protected from backscattering.
8 ropic nature of structures instead of strong backscattering.
9 clear NMR, mass spectrometry, and Rutherford backscattering.
10 analogy, we observe the suppression of 2k(F) backscattering, a characteristic of Dirac particles.
11 ering, which is thought to protect them from backscattering and localization.
12 xhibits parity asymmetry, can remove elastic backscattering and provides robustness against disorder.
13  laser scanning confocal microscopy, both in backscattering and transmission geometries.
14 tinuclear NMR, mass spectrometry, Rutherford backscattering, and density functional theory (DFT) simu
15 gher and temperatures above 14 K, and phonon backscattering, as manifested in the classical size effe
16  chemical systems show clear evidence for Cu backscattering at approximately 2.5 A.
17 cated Hg coordination by O atoms only and Fe backscattering atoms that is consistent with inner-spher
18 tion of Hg by Cl ligands, multiple Hg and Cl backscattering atoms, and concentration of Hg as small p
19 elative insensitivity to the geometry of the backscattering atoms.
20  that, despite strong atomic scale disorder, backscattering between states of opposite momentum and o
21 ntration is well correlated with the optical backscattering by particles suspended in seawater.
22 le-in-cell simulations that stimulated Raman backscattering can generate and amplify twisted lasers t
23 lation, in conjunction with retrieval of the backscattering coefficient from remote-sensing reflectan
24 e simultaneous measurement of its integrated backscattering coefficient related to the cell size and
25                   The spectrum of the single backscattering component is further analyzed to provide
26 sing light in between scattering layers in a backscattering configuration and show that the light int
27 raction imaging, we find unexpectedly strong backscattering contributions from low-Z atoms.
28 llary dual-bicell (DCDB) microinterferometic backscattering detection (MIBD) system was developed.
29 bstrate, followed by solvent evaporation and backscattering detection.
30  light scattering peak is the highest in the backscattering direction.
31 g non-local transport signals and suppressed backscattering due to the opposite spin polarizations of
32 c and aperiodic nanomeshes, and quantify the backscattering effect by comparing variable-pitch nanome
33 omagnetic waves around sharp corners without backscattering effects.
34 conventional SEM and FIB-SEM analyses was on backscattering efficiency, in some cases varying several
35 sualized using secondary-electron images and backscattering electron diffraction patterns.
36  (such as pig) cannot be imaged using purely backscattering electron wave packets without molecular a
37 ation of the free carrier response by strong backscattering expected from these heavily disordered pe
38 action (Michael addition) was monitored with backscattering fiber optics under strongly attenuated la
39  domain reflectometry methods that rely upon backscattering for spatially resolved detection.
40 a combination of optical gradient forces and backscattering forces, eliminating the need for electron
41 simulation of the experimental data involves backscattering from a histidine group with Cu-N of 1.92
42 small shear rates (0.001 s(-1)) can increase backscattering from blooms of large phytoplankton by mor
43 es it possible to distinguish between single backscattering from epithelial-cell nuclei and multiply
44               The new Ca EXAFS clearly shows backscattering from Mn at 3.4 A, a distance that agrees
45                                The increased backscattering from the base of the OS is explained by a
46 AFS spectrum was successfully interpreted by backscattering from two His residues (Fe-N at 1.99 A), a
47                                    Using the backscattering geometry at large photon momentum transfe
48 E focus is far from ideal, especially in the backscattering geometry, which is more practical in many
49 ieved in unstained tissues by using a simple backscattering geometry.
50 se materials are characterized by Rutherford backscattering, high-resolution electron microscopy, and
51 al nature of this system, we further observe backscattering-immune propagation of a nontrivial surfac
52 e only observe backward features, due to low backscattering in muscle.
53                             Stimulated Raman backscattering in plasma is potentially an efficient met
54 c states are topologically protected against backscattering in the absence of valley-mixing scatterin
55 , consistent with our calculation of reduced backscattering in this 1D system, and suggests that tran
56 rotection mechanism that strongly suppresses backscattering in zero magnetic field.
57 uantum matter exhibit unique protection from backscattering induced by disorders, making them ideal c
58          We show that DSL depth and acoustic backscattering intensity (a measure of biomass) can be m
59 el (I2, describing the angular change of the backscattering intensity in the model), which presented
60 extent of lipid collections, which had a low backscattering intensity, also were well documented.
61                            Here we show that backscattering interferometry (BSI) can accurately quant
62                                        Here, backscattering interferometry (BSI) has been shown to be
63                                              Backscattering interferometry (BSI) has been used to suc
64  first direct and quantitative comparison of backscattering interferometry (BSI) to fluorescence sens
65                  Here we describe the use of backscattering interferometry (BSI) to quantify the bind
66                             Here we employed backscattering interferometry (BSI), a free-solution lab
67 ce (SPR), biolayer interferometry (BLI), and backscattering interferometry (BSI), which can facilitat
68  based on refractive index (RI) sensing with backscattering interferometry (BSI).
69                               Finally, using backscattering interferometry and lipoparticles containi
70                             Here we show how backscattering interferometry in rectangular channels (B
71 in vitro is 6.5 +/- 1.0 nM, as determined by backscattering interferometry; KJ-Pyr-9 also interferes
72 ower, including all the mode reflections and backscattering, is below -40 dB, due to the adiabatic mo
73 el optical technology low-coherence enhanced backscattering (LEBS) spectroscopy, allows identificatio
74 tomic number of manganese enhances the X-ray backscattering, making it possible to identify.
75                                   Rutherford backscattering measurements show good stability of the t
76 aperture objective (NA = 0.7), necessary for backscattering measurements.
77 l in situations where the conventional Raman backscattering method is hampered or fails because of ex
78 is iTRUE technique enables light focusing in backscattering mode.
79                                     Rayleigh backscattering not only sets the intrinsic loss limit fo
80           The structural defects and maximum backscattering of light clearly localized to the posteri
81                                              Backscattering of light, a function of corneal haze and
82 shear rates (0.1 s(-1)) can increase optical backscattering of natural microbial assemblages by more
83  the current saturation appears to be set by backscattering of the charge carriers by optical phonons
84                                              Backscattering of the intense forward-propagating CARS r
85                                              Backscattering of these chiral Frenkel excitons is prohi
86  Using optical fibers with enhanced Rayleigh backscattering profiles as distributed temperature senso
87 lity is due to differences in absorption and backscattering properties of phytoplankton and related c
88 veraged description of texture, and electron backscattering provides spatially resolved surface measu
89 tivity than that available from conventional backscattering Raman spectroscopy.
90                                   Rutherford backscattering (RBS) was employed to understand this unu
91 tomic force microscope (AFM) tip utilizing a backscattering reflection configuration.
92                               Suppression of backscattering results in a transport lifetime 10(4) tim
93  The achieved structure exhibits an enhanced backscattering (see Figure), which has strong dependence
94 ion, more than 40-dB enhancement of Rayleigh backscattering signal was generated in silica fibers usi
95  perpendicular magnetic field suppresses the backscattering significantly and enables a junction 400
96 coupling within such crystals is probed with backscattering spectra, and the mode splitting (0.10 and
97                                  A high-flux backscattering spectrometer and a time-of-flight disk ch
98  structural analyses using HRTEM, Rutherford backscattering spectrometry (RBS) and laser excitation t
99 s of the membrane active layer by Rutherford backscattering spectrometry (RBS) revealed the incorpora
100 anning electron microscopy (SEM), Rutherford backscattering spectrometry (RBS), and nuclear reaction
101            Using 1.5 MeV (4)He(+) Rutherford backscattering spectrometry (RBS), each lab has demonstr
102 ed by X-ray diffraction (XRD) and Rutherford backscattering spectrometry (RBS).
103 dispersive spectroscopy (WDS) and Rutherford backscattering spectrometry (RBS).
104                                   Rutherford backscattering spectrometry and Fourier transform infrar
105 ques including Rutherford and non-Rutherford backscattering spectrometry and particle-induced X-ray e
106 oscopy characterization (TEM) and Rutherford backscattering spectrometry channeling (RBS-C) spectra s
107 etect the ligands after calcination, elastic backscattering spectrometry characterization demonstrate
108 scopy, X-ray diffractrometry, and Rutherford backscattering spectrometry to determine precisely struc
109  measurements were obtained using Rutherford backscattering spectrometry with samples prepared at a r
110 mug/cm(2) dendrimers G2 and G3 by Rutherford backscattering spectrometry with the aid of heavy ion pr
111 m elastically backscattered ions (Rutherford backscattering spectrometry).
112 e after each monomer addition via Rutherford backscattering spectrometry, X-ray photoelectron spectro
113                                   Rutherford backscattering spectroscopy (RBS) and microscopy demonst
114 infrared spectroscopy (FTIR), and Rutherford backscattering spectroscopy (RBS).
115  using incoherent neutron time-of-flight and backscattering spectroscopy on the picosecond to nanosec
116                                      Neutron backscattering spectroscopy showed that the mean square
117 0 K temperature region using high-resolution backscattering spectroscopy to measure an identical moti
118 e states and the associated valley-protected backscattering suppression around the curved waveguide a
119 as well as phonon particle effects including backscattering, the dominant mechanism responsible for t
120 topological insulators, a protection against backscattering through the spin-momentum locking mechani
121 l information on the frequency dependence of backscattering, which is descriptive of the histologic f

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