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1 nfish can see their own, otherwise rare, red bioluminescence).
2 ng the possible role of ferritin in the worm bioluminescence.
3 phase when using a caliper as compared with bioluminescence.
4 nes to coordinate group behaviors, including bioluminescence.
5 ic slice cultures was monitored as PER2::LUC bioluminescence.
6 ently available luciferases that exhibit NIR bioluminescence.
7 tly oxidizes to oxyluciferin, the emitter of bioluminescence.
8 er cells; tumor growth was measured based on bioluminescence.
9 from luciferase to GAF-FP, resulting in NIR bioluminescence.
10 associated with host colonization, including bioluminescence.
11 py, tumors regressed and possessed decreased bioluminescence.
12 ve microbial behavior, such as virulence and bioluminescence.
13 onding mutants of NanoLuc that enable bright bioluminescence.
14 to entrain the circadian rhythm in PER2::LUC bioluminescence.
15 he spectrum of both downwelling sunlight and bioluminescence.
16 reverse engineer promoter activity from the bioluminescence.
17 and the D-luciferin substrate had levels of bioluminescence 11-fold greater than colons of mice give
18 regulation implies an adaptive function for bioluminescence, a controversial question for more than
20 ma cells with aequorin reporter gene and the bioluminescence activities of stable biosensor were meas
22 ppression of tumor size, but the decrease of bioluminescence after CR-PIT was not observed consistent
23 luciferases promises to expand the power of bioluminescence and allow multiple events to be imaged i
24 re oxygen [8] and energy (NADH or NADPH) for bioluminescence and are reported to emit green light (la
25 tastatic spreading by three-dimensional (3D) bioluminescence and cross-validated it with standard bio
28 acy tests (PET) using bacterial replication, bioluminescence and fluorescence in a three-way study.
29 lization of the position the tumor with MRI, bioluminescence and fluorescence reflectance imaging, an
30 However, Malcosteus niger produces far-red bioluminescence and its longwave retinal sensitivity is
31 Our study demonstrates that dual noninvasive bioluminescence and NIR fluorescence imaging of cancer x
32 S/AinR pheromone-signaling system to control bioluminescence and other symbiotic colonization factors
33 umor response to oncolysis sequentially with bioluminescence and positron emission tomography (PET),
34 ctivity of exposed airway samples using both bioluminescence and standard colony-forming unit assays.
35 al (metastatic) growth were quantified using bioluminescence and were then used to generate a mathema
36 uch as those of radioluminescence (1-1.5 h), bioluminescence ( approximately 30 min) and low-excitati
37 hat energy-consuming processes (motility and bioluminescence) are downregulated, and microarray-based
39 cycles suggests a mechanical stimulation of bioluminescence, as organisms carried by currents collid
40 rcadian rhythms in C elegans recorded with a bioluminescence assay in vivo and demonstrate the main f
45 by a green LED emitting light similar to the bioluminescence, attract staphilinid rove beetles (coleo
49 Here, we have developed a new multicolored bioluminescence-based reporter system that can specifica
51 can be visualized by bioluminescent imaging, bioluminescence being detected in the snout and lungs of
52 ul colonization of habitats ranging from the bioluminescence-biased but basically dark deep sea to cl
54 served as a marker of infection detected as bioluminescence (BLM) by in vivo and ex vivo imaging.
55 was quantified relative to a control using a bioluminescence camera system at day 7 after sonication.
57 occurs across diverse taxa, measurements of bioluminescence can be powerful to detect and quantify o
59 50,000 observations are classified for their bioluminescence capability based on literature descripti
61 acterial infection imaging for fluorescence, bioluminescence, chemiluminescence and photoacoustic ima
62 sing standard microscopy techniques, such as bioluminescence, chemiluminescence or radioluminescence.
69 n level can be distinguished in tissue-level bioluminescence data without the need for single-cell me
70 nd cut off, which results in the recovery of bioluminescence due to the release of luciferase from Au
72 ence detection (including chemiluminescence, bioluminescence, electrogenerated chemiluminescence, and
73 show that 5-HT2AR interacts with SAP97 using bioluminescence energy transfer and that overexpression
75 allows a direct comparison between in vitro bioluminescence experiments and in silico ordinary diffe
79 fold increase in pancreas-specific NF-kappaB bioluminescence following 12 h of caerulein compared wit
80 species or higher rates in lineages that use bioluminescence for defense, a function presumably not u
81 ibiotic treatment were assessed by recording bioluminescence for short-time periods and by recording
83 gle i.p. injections of g-E and g-EAR delayed bioluminescence from metastasizing ES-2-luc cells for 2
86 mit light of longer wavelength than standard bioluminescence-generating proteins, greatly enhance sen
87 r (IHF) is a key coactivator of the luxCDABE bioluminescence genes that is required together with Lux
91 e- and effector number-dependent increase in bioluminescence imaging (BLI) activity of the caspase-3
92 njected, and tumor growth was monitored with bioluminescence imaging (BLI) and magnetic resonance ima
93 wo iRFP chimeras enables combined multicolor bioluminescence imaging (BLI) and the respective multico
94 erefore, we investigated luciferase-mediated bioluminescence imaging (BLI) as a non-invasive techniqu
95 wo noninvasive imaging technologies, MRI and bioluminescence imaging (BLI), we can visualize both the
99 prachiasmatic nucleus (SCN) firing rate with bioluminescence imaging and locomotor activity monitorin
100 construct, lesions can be identified through bioluminescence imaging and single-photon emission compu
103 ility and left ventricular function, whereas bioluminescence imaging assessed stem cell engraftment d
109 e as exemplary reagents for greatly improved bioluminescence imaging in FAAH-expressing tissues such
110 of alphaSYN was monitored noninvasively with bioluminescence imaging in the mouse striatum and substa
116 ifically designed to allow simultaneous live bioluminescence imaging of the mouse brain, allowing rea
118 address this knowledge gap through real-time bioluminescence imaging of transgenic Nrf2-luciferase (N
123 e model system in combination with real-time bioluminescence imaging to demonstrate the relative impo
124 efficiency, we used nonlinear ultrasound and bioluminescence imaging to optimize the acoustic pressur
130 oped to monitor biofilm formation, utilizing bioluminescence imaging with equine P. aeruginosa isolat
133 luracil ((3)H-FEAU) cellular uptake, in vivo bioluminescence imaging, and 9-(4-(18)F-fluoro-3-hydroxy
134 ed carrying reporter genes for fluorescence, bioluminescence imaging, and human PET reporter genes.
135 eration in the major organs, two-dimensional bioluminescence imaging, and three-dimensional diffuse l
136 escence and cross-validated it with standard bioluminescence imaging, caliper measurement and necrops
156 Voltage-gated proton channels, HV1, trigger bioluminescence in dinoflagellates, enable calcification
159 lso suggests that the evolutionary origin of bioluminescence in nonphotosynthetic dinoflagellates may
160 to cover the major existing applications for bioluminescence in the context of the diversity of lucif
163 on of the invertebrate Daphnia magna and the bioluminescence inhibition of the marine bacteria Vibrio
166 ation of bioluminescent data is limited: the bioluminescence is different from gene expression becaus
167 ian control may optimize energy use for when bioluminescence is most visible, attracting insects that
168 capability of animals to emit light, called bioluminescence, is considered to be a major factor in e
171 rol of several cellular processes, including bioluminescence (luciferase), fluorescence (enhanced gre
172 applications in cancer imaging (fluorescence/bioluminescence, magnetic resonance (MR), positron emiss
175 oped a highly translational and quantitative bioluminescence microscopy method to measure single cell
177 pH dependent fluorescence spectra and emits bioluminescence of different colors with different engin
181 0.65 mm(3) +/- 0.15, P < .0001) and relative bioluminescence optical imaging photon signal (0.57 x 10
182 0.65 mm(3) +/- 0.15, P < .0001) and relative bioluminescence optical imaging photon signal (0.57 x 10
184 lation coefficients between CFU and relative bioluminescence; P. aeruginosa ATCC9027 tatH5-pMElux is
185 lia site, were used to characterize rhythmic bioluminescence patterns in June 2013, in response to wa
186 tinuously, implying a metabolic function for bioluminescence, perhaps as a byproduct of oxidative met
188 This mechanism may be a common feature of bioluminescence processes in which light is produced by
190 eness of the method by modeling experimental bioluminescence profiles of light-sensitive fibroblasts,
191 that for subcutaneously implanted cells, NIR bioluminescence provided a 10-fold increase in sensitivi
192 laces the BRD9 bromodomain from chromatin in bioluminescence proximity assays without affecting the B
193 ated ALL, successful MV treatment (judged by bioluminescence quantification and survival) was complet
195 ow that the damping rate of population-level bioluminescence recordings can serve as an accurate meas
196 pared with control (100% vs 0%), and in vivo bioluminescence recordings showed a similar rapid decrea
199 maximal information coefficient statistic to bioluminescence reporter data from individual neurons wh
202 each variant were tested individually using bioluminescence reporters and biofilm growth assays, and
204 ular kinetics were imaged with Fluc and Rluc bioluminescence reporters plus two 18F-labeled PET repor
209 ouple to dopamine D1R receptors by real-time bioluminescence resonance energy transfer (BRET) assays.
211 ditional signaling investigation approaches, bioluminescence resonance energy transfer (BRET) biosens
213 ular fluorescence complementation (BiFC) and bioluminescence resonance energy transfer (BRET) in live
216 ecular fluorescein arsenical hairpin (FlAsH) bioluminescence resonance energy transfer (BRET) reporte
217 salmeterol-mediated desensitization through bioluminescence resonance energy transfer (BRET) studies
218 sent a new sensor platform (LUMABS) based on bioluminescence resonance energy transfer (BRET) that al
220 e describe a broadly applicable method using bioluminescence resonance energy transfer (BRET) to reve
223 robing the receptor for ubiquitination using bioluminescence resonance energy transfer (BRET), we det
224 e of them for their functional efficacies in bioluminescence resonance energy transfer (BRET)-based a
226 operties and high affinity, as determined by bioluminescence resonance energy transfer (BRET)-based s
229 lphas, and beta-arrestin1 were studied using bioluminescence resonance energy transfer 2 (BRET(2)) in
231 odimers, as demonstrated by experiments with bioluminescence resonance energy transfer and bimolecula
232 e now use competitive inhibition of receptor bioluminescence resonance energy transfer and bimolecula
241 vator, to the Golgi apparatus, determined by bioluminescence resonance energy transfer between Ggamma
242 ous ligands with G protein subtypes by using bioluminescence resonance energy transfer biosensors mon
244 ing alanine-scanning mutagenesis, in cellulo bioluminescence resonance energy transfer experiments, a
245 of the Go protein by GluK1 was validated in bioluminescence resonance energy transfer experiments, w
247 arrestin2, Rab5, Rab7, and Rab11 proteins in bioluminescence resonance energy transfer measurements t
248 APJ mutants in TMD1 and TMD2 also decreased bioluminescence resonance energy transfer of APJ dimer.
252 n of the split HuR luciferase assay with the bioluminescence resonance energy transfer technique sugg
254 r fractionation, co-immunoprecipitation, and bioluminescence resonance energy transfer that combined
263 ocal microscopy or with a recently developed bioluminescence resonance energy transfer-based approach
266 ith measuring changes in the GAP activity by bioluminescence resonance energy transfer-based assay in
268 a large panel of G protein subtypes using a bioluminescence resonance energy transfer-based assay wi
272 eceptor signaling to NF-kappaB, we developed bioluminescence resonance energy transfer-based interact
273 to form a functional carrier as assessed by bioluminescence resonance energy transfer; 3) in MPC1 de
276 mine induced phase-advances of the PER2::LUC bioluminescence rhythm during the subjective day and pha
280 circadian and rapidly induced PER2-dependent bioluminescence rhythms in previously arrhythmic Cry1/2-
281 as more severe, as indicated by increases in bioluminescence, S. aureus CFU in tissue, and death with
284 ltrasonographic imaging were used to observe bioluminescence signal and changes in tumor size among t
285 bserved a significant increase (~15 fold) in bioluminescence signal compared to control after 8-h inc
286 ificant (p < 0.05) 20.5 h periodicity in the bioluminescence signal, corresponding to inertial fluctu
288 vein inoculation, most luciferase-generated bioluminescence signals were detected in the mouse abdom
289 g, wave guiding and lensing, camouflage, and bioluminescence, that are responsible for the unique opt
291 oxycycline was precisely evaluated utilizing bioluminescence to measure ATP efflux and fluorescence t
293 ession was measured in EPEC-infected mice by bioluminescence using an in vivo imaging system (IVIS).
294 ectrometry imaging, fluorescence tomography, bioluminescence, variations of OCT, and optoacoustic ima
296 gical iron and catalytic energy for the worm bioluminescence when coupled to a reduction process with
298 iRFPs, the chimeric luciferases exhibit NIR bioluminescence with maxima at 670 nm and 720 nm, respec
299 off of the promoter, or where an increase in bioluminescence would be better interpreted as a longer
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