1 m at the earth surface from near infrared to
near ultraviolet.
2 of the protein as inferred from visible and
near-ultraviolet absorption and circular dichroism spect
3 nd for porphyrins is usually observed in the
near-ultraviolet at approximately 400 nm, and few exampl
4 The tertiary structure
near ultraviolet CD signals of sigma N do not require re
5 Near-ultraviolet CD spectra of the enzyme-nucleotide com
6 , surface balance measurements, and far- and
near-ultraviolet circular dichroic spectroscopy.
7 Near-ultraviolet circular dichroism (near-UV CD) spectra
8 her drug is prebound, a novel application of
near-ultraviolet circular dichroism (UVCD) was developed
9 As we anticipated,
near-ultraviolet circular dichroism measurements and int
10 Far-ultraviolet and
near-ultraviolet circular dichroism spectroscopic analys
11 The
near-ultraviolet circular dichroism spectrum of this pro
12 obule characteristics of T. maritima IscU by
near-ultraviolet circular dichroism, 1-anilino-8-naphtha
13 cular lens that may be modified in vivo with
near ultraviolet energy.
14 Fiber-optic
near-ultraviolet evanescent-wave sensors have been const
15 les by up to three orders of magnitude using
near-ultraviolet excitation, depending on the substrate,
16 Upon
near-ultraviolet excitation, two new Pb-Cl and Pb-Br per
17 lfonium salts that are photosensitive in the
near-ultraviolet have been prepared.
18 After triplex formation and
near-ultraviolet irradiation (360 nm), DNA templates mod
19 Upon
near-ultraviolet irradiation (360 nm), psoralen-Asp41-Ta
20 Upon
near-ultraviolet irradiation (360 nm), this synthetic ps
21 ing the residual particles in a flow cell to
near-ultraviolet (
lambda>300 nm) radiation, we find that
22 During continuous irradiation with
near-ultraviolet light (l = 36510 nm; 16 mW/mm(2)) for 2
23 Mechanistic studies suggest that
near-ultraviolet light (lambdamax = 313 nm) photoinitiat
24 ted by harmful and poorly tissue-penetrating
near-ultraviolet light.
25 ase Ca2+ when cleaved upon illumination with
near-ultraviolet light.
26 atic absorption across large portions of the
near-ultraviolet (
NUV) to near-infrared (NIR) spectrum a
27 TRCD is monitored in the
near-ultraviolet,
over a time scale of 10 ps.
28 n spectrum with two distinctive peaks in the
near ultraviolet region.
29 phosphatase, increase the ellipticity in the
near-ultraviolet region of the CD spectrum of the enzyme
30 rough the appearance of intense bands in the
near-ultraviolet region of the spectrum (250-380 nm).
31 0 nm and a significant secondary peak in the
near-ultraviolet region of the spectrum.
32 nous pH-sensitive absorbance in the blue and
near-ultraviolet regions of light.
33 ioactive isotope of beryllium, (7)Be, in the
near-ultraviolet spectra of the classical nova V339 Del
34 ve inhibitor Li+ causes little change in the
near-ultraviolet spectrum in the absence or presence of
35 Near-ultraviolet stimulation of opsin regenerated with a
36 ), while anthracenes emit exclusively in the
near-ultraviolet to blue wavelength regime.
37 were shown to have tunable emission from the
near-ultraviolet to the near-infrared region.
38 the direct bandgap of this material from the
near-ultraviolet to the near-infrared region.
39 oader exploration of FRET with spectrum from
near-ultraviolet to visible wavelength.
40 ients of dispersed particulate matter in the
near ultraviolet (
UV) spectral region.
41 NPs absorb radiation in the
near-ultraviolet (
UV) range of the electromagnetic spect
42 The
near-ultraviolet/
visible circular dichroism spectrum als