ライフサイエンスコーパス: UV

1 ons, as did temperature (but not rainfall or UV).

2 es far less damage to organic molecules than UV.

3 ions were also observed for other metrics of UV.

4 tracts were characterized by GC-FID and HPLC-UV.

5 Concurrently, GA + UV-A also inhibits the activity of superoxide dismutase

6 lude a large absorption cross-section in the UV-A and UV-B spectral regions and the availability of o

7 UV-A exposed PG caused oxidative damage to the cell and

8 UV-A has been reported to lower blood pressure, possibly

9 higher damage to the cell membrane than GA + UV-A treatment, explaining its higher effectiveness than

10 xplaining its higher effectiveness than GA + UV-A treatment.

11 nimal erythemal doses to monochromatic UV-B, UV-A, and visible radiation and broadband provocation te

12 igands were observed, including decreases in UV absorbance and shifts in the molecular composition of

13 the only amino acid that exhibited specific UV absorbance of nitrosamines at 335nm, supporting the a

14 diation at 310-410 nm, due to differences in UV absorbance properties of components.

15 The change in UV absorbance showed loss of protein solubility dependin

16 (poly)saccharide taylorgrams, including non-UV absorbing polymers.

17 phototoxicity problems encountered with many UV-absorbing photocages.

18 romatograms of the expected [M-H](-) ion and UV absorption revealed the presence of five possible rea

19 s been measured by broadband cavity enhanced UV absorption.

20 Based on specific UV-absorption (SUVA), aromatic DOM was preferentially ad

21 d into the gel through methacrylamide can be UV-activated multiple times to photocapture protein.

22 cals (Cl(*)) is an attractive alternative to UV alone or chlorination for disinfection because of the

23 pounds were analysed using spectrophotometry-UV and GC-MS-SPME, respectively.

24 wed us to present spatiotemporally modulated UV and green luminance in any region of the visual field

25 y, absorption and action spectroscopy in the UV and IR regions, and microwave spectroscopy.

26 ation exchange column for (2)D, coupled with UV and LC1MS2 detection.

27 y RPS3 along with nuclear interaction during UV and oxidative stress may serve to modulate active DNA

28 Herein, we use UV and visible radiation as both excitatory and inhibito

29 o-step extraction was developed for use with UV and/or tandem mass spectrometry (SRM) detection.

30 The combined ultraviolet (UV) and free chlorine (UV-chlorine) advanced oxidation p

31 synthesis is often inhibited by ultraviolet (UV) and intense photosynthetically available radiation (

32 ne pathogens of humans and wildlife to solar UV, and use the DNA action spectrum to model how differe

33 rface charge properties and exhibit superior UV- and visible-light photocatalytic activity for ammoni

34 he AlN/GaN DA for mid- and deep-ultraviolet (UV) applications.

35 The latter is due to its viral or UV-associated carcinogenesis.

36 ardial BV, the additional use of endocardial UV at normal BV sites improves the diagnostic accuracy r

37 rom polar areas subject to periodic enhanced UV-B due to depletion of stratospheric ozone.

38 rise and accumulate in the nucleus following UV-B exposure, similar to Arabidopsis UVR8, but M. polym

39 precursor of the active gibberellin, GA1, by UV-B in this zone, which is regulated, at least in part,

40 In addition, UV-B increased leaf quercetin content and total antioxid

41 Protective effects of UV-B radiation against nonmelanoma skin cancer (NMSC) ar

42 rge absorption cross-section in the UV-A and UV-B spectral regions and the availability of one or mor

43 Our results indicate that UV-B supplementation may provide a method to manipulate

44 ith minimal erythemal doses to monochromatic UV-B, UV-A, and visible radiation and broadband provocat

45 hat phospho-Pak1 and Pak1 levels are high in UV-B-exposed hairless SKH mouse model skin samples as co

46 ak1 confers protection to keratinocytes from UV-B-induced apoptosis and DNA damage via ATR.

47 nd reduced recurrent ocular herpes following UV-B-induced reactivation.

48 UV-based advanced oxidation processes (AOPs) effectively

49 ng of compounds varying in polarity, such as UV blockers and biocide compounds in water, and the data

50 he sanitizers revealed a detectable level of UV-C (1.9 nWcm(-2)nm(-1)), modest surface temperature (6

51 form synthesis of stilbenes is induced after UV-C irradiation, whereas a more localized synthesis of

52 except for C difficile, for which bleach and UV-C were used); bleach; and bleach and UV-C.

53 adienes (CBDs) in aqueous solution by ozone, UV-C(254 nm) photolysis, and the corresponding advanced

54 non-ionizing, short-wavelength ultraviolet (UV-C) light source.

55 and UV-C were used); bleach; and bleach and UV-C.

56 m disinfectant and disinfecting ultraviolet [UV-C] light except for C difficile, for which bleach and

57 ovement in both the spectral performance and UV capabilities of the instrument.

58 induced DNA damage and repair and ultimately UV carcinogenesis.

59 in mind before common interventions such as UV catheterizations.

60 including heterocomplex pulldown assays, far-UV CD spectroscopy, the thioflavin T binding assay, tran

61 in macrophages differentiated from the BM of UV-chimeric mice.

62 planted into naive mice, the recipient mice (UV-chimeric) had reduced accumulation of elicited monocy

63 combined ultraviolet (UV) and free chlorine (UV-chlorine) advanced oxidation process that produces hi

64 HPLC-UV chromatographic data was further treated by partial l

65 sponding to polyphenolic peak areas and HPLC-UV chromatographic fingerprints were then analyzed by ex

66 ant EHMT1 p.P809L was also studied using far UV circular dichroism spectroscopy and intrinsic protein

67 Far-UV circular dichroism spectroscopy was used to confirm t

68 h are most important in determining the near-UV circular dichroism spectrum.

69 d substitutions, electronic absorption, near-UV circular dichroism, and electron paramagnetic resonan

70 etal-modified DNA films was characterized by UV, circular dichroism (CD), and X-ray photoelectron spe

71 fish, although quite different from rods and UV cones, RGB cones (red, green, and blue cones) are str

72 and cytoplasmic fractions are prepared from UV-crosslinked cells and then subjected to iCLIP.

73 r4 (TRAMP complex) and Nab3 (NNS complex) by UV crosslinking immediately following glucose withdrawal

74 UV crosslinking immunoprecipitation and sequencing (CLIP

75 Currently applied UV cutoff values are based on studies that lacked epicar

76 This study aimed to define endocardial UV cutoff values using computed tomography-derived fat i

77 We also generated time-resolved UV damage maps of both CPDs and (6-4)PPs by HS-Damage-se

78 ion is facilitated in the genomic context by UV-damaged DNA-binding protein 2 (DDB2), which is part o

79 in 2 (DDB2), which is part of a multiprotein UV-DDB ubiquitin ligase complex.

80 ights, but understanding of non-ultraviolet (UV)-derived CMs remains limited.

81 nated by structural variation and absence of UV-derived mutation signatures.

82 nternal quantum efficiency for mid- and deep-UV device application.

83 ion design for high efficiency mid- and deep-UV device applications.

84 For a typical UV disinfection dose (400 J/m(2)), various extents of ph

85 Trusted decadal forecasts of UV dosage over the United States in summer require under

86 The UV emission generated by the NIR-activated UCNP effectiv

87 The bright, rapidly fading UV emission indicates a high mass ( approximately 0.03 s

88 Using UV-exposed human skin fibroblasts, we found that, at the

89 Consequently, moderate sun/UV exposure is strongly recommended.

90 aging and cutaneous carcinogenesis caused by UV exposure, to treatment-limiting radiation dermatitis

91 However, the increasing incidence of sun/UV exposure-related illness, such as skin cancer, is ser

92 t provide sufficient protection for extended UV exposure.

93 cally reduce CO2 with >90% selectivity under UV-filtered simulated solar light irradiation (AM 1.5G,

94 Seven UV filters (UV-Fs), including 3 hydroxy-metabolites of o

95 Bromoform was generated by all the reactive UV filters at different yields.

96 In the collected pool samples, all the UV filters except dioxybenzone were detected.

97 Little is known about the fate of UV filters in seawater swimming pools disinfected with c

98 ments were conducted in seawater spiked with UV filters to investigate the reactivity of UV filters.

99 the transformation pathways of the reactive UV filters were proposed for the first time.

100 for BP-3, a metabolite (BP-1), and six other UV filters.

101 UV filters to investigate the reactivity of UV filters.

102 romatography with ultraviolet detector (HPLC-UV) for the extraction and determination of organosulphu

103 rested in converting from the UV/H2O2 to the UV/free chlorine advanced oxidation process (AOP).

104 At pH 7.0-8.3, the UV/free chlorine AOP was less efficient.

105 Seven UV filters (UV-Fs), including 3 hydroxy-metabolites of oxybenzone (b

106 distribution (MWD) of Hf-bound polymers via UV-GPC analysis.

107 diated (253.7 nm, 310-410 nm), and oxidized (UV-H2O2, ozone) poultry litter extracts.

108 ewater are interested in converting from the UV/H2O2 to the UV/free chlorine advanced oxidation proce

109 xidation processes (AOPs) (i.e., O3/H2O2 and UV/H2O2) was investigated.

110 hemical reactions due to exposure to stress (UV, heat) or by hosts as a defense response.

111 Under 325 nm 2.30 mW cm(-2) UV illumination and at a -0.45% compressive strain, the

112 These results suggest that moderate UV illumination during growth may be used as a way to im

113 temporally modulated and spatially patterned UV illumination source to characterize both the temporal

114 f silver orthophosphate microparticles under UV illumination, in the presence of varying concentratio

115 ere infected intranasally with either RSV or UV-inactivated RSV.

116 GSTABP-G features a photoreactive moiety for UV-induced covalent binding to GSTs and GSH-binding enzy

117 UV-induced cross-linking suggested that F56Bpa interacts

118 on of the two methods revealed that, whereas UV-induced damage is virtually uniform throughout the ge

119 This research shows UV-induced damage to adenoviral proteins across the germ

120 ning ssDNA oligos generated during repair of UV-induced damage to study that process at both mechanis

121 rD helicase and Mfd translocase in repair of UV-induced damage.

122 ing to gain insight into factors that affect UV-induced DNA damage and repair and ultimately UV carci

123 site effects on transcription recovery after UV-induced DNA damage.

124 trated a C-->T mutation signature typical of UV-induced DNA damage.

125 known for translesion synthesis opposite the UV-induced DNA lesion cyclobutane pyrimidine dimer and w

126 roliferation but also for the suppression of UV-induced inflammation and DNA damage.

127 UV-induced PAF also activates cell cycle arrest and disr

128 nditions, were synthesized using thermo- and UV-initiated polymerization techniques.

129 as interfaced to a capillary electrophoresis-UV instrument using a polyimide coated fused silica capi

130 erived MCs (CBMCs) were infected with HRV or UV-irradiated HRV at increasing multiplicities of infect

131 When BM cells were harvested from UV-irradiated mice and transplanted into naive mice, the

132 In the presence of UV irradiation and ppm concentrations of copper(II) brom

133 ical products in the dark or under continued UV irradiation both resulted in nucleation and growth of

134 rapidly escorts it to the damaged DNA after UV irradiation in a DDB2-independent manner.

135 ed out to establish starch susceptibility to UV irradiation induced generation of free radicals.

136 a one-electron reduction of MV(2+) ions upon UV irradiation to form MV(+*) radical cations within the

137 Upon UV irradiation, a slowdown of transcript elongation and

138 n mouse skin are induced by short-term solar UV irradiation, and a long-term skin carcinogenesis stud

139 oactivable compounds/systems respond only to UV irradiation, but not near-infrared (NIR) light that o

140 t state of Mn2(CO)10, which, like under near-UV irradiation, led to complete release of carbonyls.

141 te of the catalyst, which, together with the UV irradiation, provides orthogonal means to control the

142 nd HSF1, protects against the development of UV irradiation-mediated cutaneous squamous cell carcinom

143 nt for damage bypass and cell survival after UV irradiation.

144 wafer, before the entire wafer is exposed to UV irradiation.

145 using this high quality AlN template: a deep UV-LED device fabricated and showed a strong single shar

146 , allowing for further re-growth of the deep UV-LED device.

147 efficiency (EQE) of about 0.03%, for a deep UV-LED grown on Si substrate.

148 zed a deep-ultraviolet light-emitting diode (UV-LED) device using this AlN/patterned Si.

149 Unexpectedly, its exposure to UV light affords, after reductive elimination of the ent

150 Exposure to UV light altered NOM, converting approximately 6 muM of

151 te shows high conductivity when treated with UV light and in the neutral state, and low conductivity

152 ganized gemini monomers were irradiated with UV light and monitored by FT-IR.

153 Short- and medium-wavelength UV light can cause photo-lesions in DNA origami.

154 (gammaSO4(2-),light) for GDD particles under UV light compared to the value (gammaSO4(2-),dark) under

155 c keratosis (AK) is a skin growth induced by UV light exposure that requires long-term management bec

156 The UV light generates free carriers in a photosensitive ZnO

157 licle melanocyte precursors are activated by UV light has not been extensively studied.

158 Under UV light irradiation, both at 273 and 298 K, JUC-62 show

159 UV light suppresses experimental autoimmune encephalomye

160 In brief, cells are irradiated with UV light to induce protein-RNA cross-links.

161 4% lower CO2 uptake, respectively, than when UV light was off.

162 of sample using brief, targeted exposure to UV light, uncaging the rhodamine and causing the particl

163 ut very little is known about the effects of UV light.

164 vioral and electrophysiological responses to UV light.

165 iverse chemicals, reactive oxygen species or UV light.

166 tomato consumption can mitigate ultraviolet (UV) light induced sunburn via unknown mechanisms.

167 leavable DNA capture probe with ultraviolet (UV) light.

168 We demonstrate that UV-light activation of polycrystalline ZnO films on flex

169 ins, are accumulated upon high temperatures, UV-light, drought, and nutrient deficiencies, and may co

170 orange Sc(3+) bridging dinitrogen complex to UV-light, photolysis to form the monomeric Sc(2+) comple

171 identified by corresponding low endocardial UV <3.7 mV.

172 UV-mediated photolysis of azF was then carried out to in

173 In UV method, the absorbance of chlorpyrifos and prophenofo

174 the fabrication and characterization of deep UV MgZnO semiconductor lasers.

175 A novel time-lapse synchrotron deep-UV microscopy methodology was developed that made use of

176 carpans (rPta), as characterized by RP-UHPLC-UV-MS.

177 ow field-flow fractionation (AF4) coupled to UV, multiangle light scattering (MALS) and differential

178 5, 95% CI 0.69-1.04; p=0.116), or bleach and UV (n=131; 45.6 cases per 10 000 exposure days; RR 0.91,

179 oll ultraviolet nanoimprint lithography (R2R UV-NIL) technique provides a solution for the continuous

180 g at an ultraviolet illumination wavelength (UV) of 266 nm.

181 m transistors (TFTs) with a simple, low-cost UV-ozone (UVO)-treated polymeric gate dielectric is repo

182 to the complex molecular networks underlying UV photobiological effects, which have important implica

183 s to pond seepage during wet periods, and to UV photodissociation during dry periods, mean that the s

184 arious spectroscopic tools, including vacuum UV photoionization mass spectrometry, absorption and act

185 nstable family of diazo compounds using flow UV photolysis and their first use in divergent protodebo

186 n with copper monochloride or triiodide, the UV-photolysis does not require chemicals and is not affe

187 nd elucidate the nanoshielding mechanism via UV plasmonic resonance and nanotailing effects.

188 se method based on combining an ultraviolet (UV) pre-ionization pulse (lambda = 266 nm) with an overl

189 for C difficile, for which bleach was used); UV (quaternary ammonium disinfectant and disinfecting ul

190 cell death when compared to cells exposed to UV radiation after 60 seconds of exposure.

191 were tested using WO3 coated surfaces under UV radiation and the efficiency of this degradation was

192 anine radicals, generated upon absorption of UV radiation directly by TEL21/Na(+).

193 re bromine consistent with increased surface UV radiation indicate that the eruptions led to stratosp

194 threats, including microbes, injuries, solar UV radiation, and allergens.

195 e map of DNA lesions induced by ultraviolet (UV) radiation, the ubiquitous carcinogen in sunlight tha

196 ) that e-liquids are most fluorescent in the UV range (between 350 and 405 nm) and (iii) fluorescence

197 nberry waste oil exhibited absorbance in the UV range at 100-400nm.

198 We show that this UV range can be used in conjunction with photoactive mol

199 ill remain exposed to reflected and indirect UV rays.

200 hysically shielding skin from direct harmful UV rays; however, skin may still remain exposed to refle

201 ins unchanged to an increase when changes in UV reflectance are at an upper bound.

202 e in population-weighted concentrations when UV reflectance remains unchanged to an increase when cha

203 could outweigh small air-quality penalties, UV reflectance standards for cool roofing materials coul

204 entrations depend on the potential change in UV reflectance, ranging from a decrease in population-we

205 We have developed a UV resonance Raman (UVRR) spectroscopy approach to quant

206 Deep UV resonance Raman spectroscopy is introduced as an anal

207 l color changes upon sun exposure due to its UV-responsive capabilities that are visually detectable

208 the realization of electrically driven deep UV semiconductor lasers to date.

209 time, we experimentally demonstrate the deep-UV SH generations (SHGs) by combined degenerate four-wav

210 , they serve as the secondary pump, and deep-UV SHs are generated within the wavelength range of 334.

211 t still remains challenging to generate deep-UV SHs especially in optical fibers.

212 UV spectra and high resolution product ion spectra of th

213 For each oligomer, the UV spectra exhibit distinct changes in the electronic en

214 The UV spectra of the tetra- and pentamer are superimposable

215 Five different parameters of difference-UV spectra were obtained by subtracting spectra of unhea

216 However, the study was limited to UV spectrophotometric analysis under acidic conditions,

217 novel approach in the analysis of difference-UV spectrophotometric data for determining the heat dena

218 The present work describes a novel HPLC and UV-spectrophotometric method for the simultaneous estima

219 UV spectroscopy showed the lowest limits of quantificati

220 effects of irradiation were also studied by UV spectroscopy.

221 to adenoviral proteins across the germicidal UV spectrum at wavelength intervals between 200 and 300

222 y and incident sunlight alter the ability of UV to inactivate waterborne pathogens.

223 atients was significantly lower after adding UV to standard cleaning strategies (n=76; 33.9 cases per

224 e component, we realized the first COF-based UV- to NIR-responsive photodetector.

225 Here, few-femtosecond extreme UV transient absorption spectroscopy (FXTAS) at the vana

226 pectroscopic determinations showed a typical UV-VIS absorption for furans during the storage of irrad

227 ctroscopy, X-ray photoelectron spectroscopy, UV-vis absorption spectra, and photoluminescence spectra

228 However, the inherent advantages of UV-vis absorption spectroelectrochemistry should overcom

229 UV-Vis absorption study of these solutes has also been c

230 lectron paramagnetic resonance (EPR), SQUID, UV-vis absorption, and X-ray absorption spectroscopy (XA

231 We report the synthesis, UV-vis absorption, electrochemical characterisation, and

232 es are demonstrated through a combination of UV-vis absorption, resonance Raman, (1)H NMR, EPR, and X

233 ples from different origins were analysed by UV-vis according to ISO 3632 (2011) and by HPLC-DAD.

234 UV-vis and (1)H NMR investigations of the photochemical

235 e(III)-peroxo complexes are characterized by UV-vis and mass spectrometry techniques, and their react

236 tigates the use of synchronous fluorescence, UV-Vis and near infrared (NIR) spectroscopy coupled with

237 In the present work, we used UV-vis and NMR spectroscopies to investigate the electro

238 Using UV-vis and surface-sensitive IR spectroelectrochemical t

239 UV-vis competition was performed on the Abeta peptide as

240 Therefore, HPLC-DAD might be preferable to UV-vis for determining the safranal content and the clas

241 principal component analysis applied to the UV-vis spectra of saffron aqueous extracts revealed a cl

242 rphology, photoluminescence (PL) spectra and UV-vis spectra of these nanostructures were studied.

243 traction technique combined with microvolume UV-Vis spectrophotometric detection was proposed for the

244 UV-Vis spectrophotometry reveals that DNA films with sur

245 donors was investigated by transient IR and UV-vis spectroscopies in the presence of 0.2 M p-toluene

246 of air, followed by HPLC, HPLC-MS, EPR, and UV-VIS spectroscopy analysis of the resulting mixtures.

247 th increasing concentrations quantifiable by UV-vis spectroscopy and obvious to the naked eye.

248 UV-vis spectroscopy and time-dependent density functiona

249 UV-vis spectroscopy defined that they exhibit the proper

250 We also report CD and UV-Vis spectroscopy studies of adducted human Hb that re

251 probe 1 selectively detected CN(-) under the UV-vis spectroscopy through the rapid appearance of deep

252 Using UV-Vis spectroscopy to monitor the assembly/disassembly

253 re electrochemistry and variable-temperature UV-vis spectroscopy were used to obtain thermodynamic me

254 ction was tracked using low temperature NMR, UV-vis spectroscopy, and isotopic ((18)O) labeling exper

255 and its optoelectronic properties studied by UV-vis spectroscopy, cyclic voltammetry, and DFT calcula

256 osilane solution was then characterized via, UV-Vis spectroscopy, FTIR spectroscopy, dynamic light sc

257 Using UV-vis spectroscopy, we could measure the amount of Fe(3

258 y (AFM), scanning electron microscopy (SEM), UV-Vis spectroscopy, X-ray diffraction (XRD) analysis an

259 High-throughput UV-vis titrations in combination with chemical double-mu

260 rent spectroscopic techniques (FT-IR, Raman, UV-vis), TGA and Kaiser test.

261 +) was demonstrated and characterized by IR, UV-vis, EPR, NMR, and single-crystal X-ray diffractions.

262 o-Gr flakes (po-Gr-NR) were characterized by UV-vis, FT-IR, and Raman spectroscopies and FE-SEM, whic

263 om reaction monitoring instrumentation (like UV-vis, FTIR, Raman, and 2D NMR benchtop spectrometers),

264 d peaks than any spectrum of any kind (e.g., UV-vis, infrared, microwave, magnetic resonance, etc.).

265 lic acids have been investigated by means of UV-vis, laser induced fluorescence and Raman spectroscop

266 nced spectroscopic techniques (EPR, IR, XAS, UV-vis, NMR, luminescence spectroscopies).

267 tration experiments and variable temperature UV-Vis-NIR and EPR spectroscopic data indicate that, rel

268 ential scanning calorimetry and (1)H NMR and UV-vis-NIR spectroscopies is presented, demonstrating th

269 rtical heterostructure studied using XPS and UV-Vis-NIR spectroscopy.

270 combined results of electron spin resonance, UV-vis-NIR, and ultraviolet photoelectron spectroscopy.

271 Based on the in situ-obtained UV/Vis absorption spectra during the reaction, we propos

272 The cage structures and UV/Vis spectra were independently confirmed by state-of-

273 erized by dynamic light scattering (DLS) and UV/Vis spectroscopy.

274 ), Analytical Ultracentrifugation (AUC), and UV/Vis spectroscopy.

275 s of photochemical and kinetic studies using UV/vis, CD, and (1)H NMR spectroscopy, it was establishe

276 terized by NMR ((1)H, (11)B, and (13)C), IR, UV/vis, fluorescence spectroscopy, and high-resolution m

277 final degradation products were analyzed by UV/vis, NMR, GC-MS, and EPR.

278 ultispectral imaging instrument spanning the UV, visible and NIR regions (19 wavelengths ranging from

279 Stopped-flow UV-visible absorption and freeze-quench Mossbauer experi

280 Browning was monitored by UV-visible absorption spectrophotometry and UHPLC-DAD.

281 ylamine, and tyramine was carried out, using UV-visible absorption spectroscopy.

282 We used UV-visible and EPR spectroscopy to characterize heme bin

283 ion of electrophysiological measurements and UV-visible and FTIR spectroscopy, we characterized the p

284 LC-UV-Visible and LC-MS analyses showed that the fast react

285 oluminescence, scanning electron microscopy, UV-Visible spectra and X-ray diffraction pattern.

286 dy on C-S bond formation was investigated by UV-visible spectrophotometry, cyclic voltammetry, mass s

287 diffraction, electron microscopy, Raman, and UV-visible spectroscopies).

288 cterized with SEM, XRD, TEM, SAED, EDX, XPS, UV-visible spectroscopy, and open-circuit potential vers

289 geographical classification of saffron using UV-visible spectroscopy, conventionally adopted for qual

290 The modifying composite was characterized by UV-visible spectroscopy, energy dispersive X-ray spectro

291 Combining UV-visible spectroscopy, heme quantification, and site-d

292 e polarized femtosecond XANES, combined with UV-visible spectroscopy, to reveal sequential structural

293 ignal enhancement under Ultraviolet-visible (UV-visible) light irradiation that allows the detection

294 central dithienylethene via irradiation with UV/visible light.

295 (AIMD) simulations and molecular beam vacuum-UV (VUV) photoionization mass spectrometry experiments w

296 When UV was applied at progressively more depolarized preopen

297 HPLC-UV was applied to the analysis and characterization of f

298 (25)Mg ions confined in a Paul trap, at deep-UV wavelengths.

299 ase-accessible euchromatin is protected from UV, while lamina-associated heterochromatin at the nucle

300 extreme temperature, salinity, pH, pressure, UV, X-ray and heavy metals as a result of DNA phophoroth