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1 te to exceed the limits imposed by far-field optical diffraction.
2 atial resolution is fundamentally limited by optical diffraction.
3 ned preparations, by electron microscopy and optical diffraction.
4 ssion electron microscopy, Fourier transform optical diffraction, and computer simulations to be well
5 cence imaging is indeed spatially limited by optical diffraction, and is thus unable to discriminate
6 eries of measurements were carried out using optical diffraction, atomic force microscopy, and normal
7 uorescent- or radiolabel-free self-assembled optical diffraction biosensor that utilizes rolling circ
8 ntibody grating alone produces insignificant optical diffraction, but upon immunocapture of cells, th
9 ac muscle and, using electron microscopy and optical diffraction, determined the effect of phosphoryl
12 of a target peptide, triggering a change in optical diffraction from a crystalline colloidal array o
13 asmon resonance imaging (GCSPRI) utilizes an optical diffraction grating embossed on a gold-coated se
14 f diagnostic markers using in situ assembled optical diffraction gratings in combination with immunom
15 monitored with a lateral resolution near the optical diffraction limit at an acquisition rate of ~1 H
16 lymer network, labels spaced closer than the optical diffraction limit can be isotropically separated
19 gle-molecule fluorescence imaging beyond the optical diffraction limit in 3 dimensions with a wide-fi
20 Label-free imaging of living cells below the optical diffraction limit poses great challenges for opt
21 genesis and LD dimensions, and can break the optical diffraction limit to detect small variation in l
23 microscopy can achieve resolution beyond the optical diffraction limit, partially closing the gap bet
24 s triggered and enlarges the AuNP beyond its optical diffraction limit, thereby making the invisible
36 he utility of these surfaces for biosensing, optical diffraction measurements of the hybridization ad
38 bility of the crossbridges inferred from the optical diffraction pattern correlated well with the rat
39 tro studies of muscle fibres and analysis of optical diffraction patterns obtained from living muscle
40 ace' techniques, which are either limited by optical diffraction to approximately 250 nm resolution o
42 jection structure calculated from measurable optical diffractions to 25 A revealed a pseudo-2-fold sy
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