ライフサイエンスコーパス: photometry

1 ICP OES) to 60 mg kg(-1) (K and Na by flame photometry).

2 e light of the parent star, and in broadband photometry.

3 ical testing using electroretinogram flicker photometry.

4 s were measured with heterochromatic flicker photometry.

5 POD) was measured by heterochromatic flicker photometry.

6 transients recorded with fura-2 and digital photometry.

7 dichroism spectroscopy and light-scattering photometry.

8 uorescence microscopy, flow cytometry, or UV photometry.

9 ofiles measured with heterochromatic flicker photometry.

10 in the light curve obtained by low-precision photometry.

11 icrom of F-actin/microm(3)), via image-based photometry.

12 ans, basil, and mint using ICP OES and flame photometry.

13 red vHP activity during the task using fiber photometry.

14 pillary electrophoresis (CE-SDS), or by mass photometry.

15 BAergic interneurons in vivo via optic fibre photometry.

16 sing the calcium indicator jGCaMP7 and fiber photometry.

17 pproaches cannot be readily applied to fiber photometry.

18 aqueous flare measurement using laser flare photometry.

19 A based epitope binning experiments and mass photometry.

20 ty, confirmed by electrophysiology and fiber-photometry.

21 transients in real-time using in vivo fiber photometry.

22 ts and earlier times, using coarsely sampled photometry.

23 ys during skill learning in mice using fiber photometry.

24 d MPOD by customized heterochromatic flicker photometry.

25 sing slit-lamp biomicroscopy and laser flare photometry.

26 y were assessed with heterochromatic flicker photometry.

27 ierarchical triple, identified in the Kepler photometry.

28 Size-exclusion chromatography, mass photometry(13) and electron microscopy reveal that these

29 ies in juvenile zebra finches and used fibre photometry(3) to monitor concurrent dopamine activity in

30 Here, we demonstrate dynamic mass photometry, a method for label-free imaging, tracking an

31 on the surface is available through XPS and photometry, a novel method to quantitatively account for

32 ed by whole-cell patch clamp and indo-1 Ca2+ photometry after influx of Ca2+ through voltage-dependen

33 The use of laser flare photometry alone does not seem to be useful in detecting

34 extent of up to 2 mm of tissue and multisite photometry along the taper.

35 vo extracellular electrophysiology and fiber photometry, along with in vivo endoscopic one-photon and

36 Here, we present Guided Photometry Analysis in Python (GuPPy), a free and open-s

37 ve" samples were equal to 23.3% for indirect photometry and 10% for ion chromatography.

38 mesolimbic dopamine signaling, we used fiber photometry and a genetically encoded dopamine sensor to

39 ely using customized heterochromatic flicker photometry and blood samples genotyped for 440 single nu

40 Here, we use fiber photometry and chemogenetic tools to record and manipula

41 l Ca2+ transients were recorded with digital photometry and confocal microscopy using fura-2 and mag-

42 single-cell level using simultaneous indo-1 photometry and constant potential amperometry.

43 In vivo photometry and CRISPR-Cas9-mediated knockout of the GRP

44 Fiber photometry and electrophysiological results indicate tha

45 Next, in vivo fiber photometry and electrophysiology results show that H1R d

46 supramolecular complexes observable by mass photometry and EM.

47 ntral periaqueductal gray (vPAG) using fiber photometry and ex vivo whole-cell slice electrophysiolog

48 ubble making solution and laser transmission photometry and find that it agrees well with the geometr

49 imal apical dendrite using two-photon Ca(2+) photometry and focal TTX application.

50 Native mass spectrometry, mass photometry and glycopeptide profiling revealed significa

51 Recoveries obtained by photometry and HPLC-UV/VIS spectroscopy were within the

52 , along with solution studies including mass photometry and in vivo transcription assays, reveal that

53 in mice of both sexes we used in vivo fiber photometry and inhibitory optogenetics to identify a spe

54 s tested and for seafood when using indirect photometry and ion chromatography, respectively.

55 e on exoplanet theory and remote sensing via photometry and low-resolution spectroscopy.

56 r dLight1.3b together with multiregion fiber photometry and machine learning-based analysis to decode

57 he well-studied viral HK97 fold, we use mass photometry and native charge detection mass spectrometry

58 Here, we use mass photometry and negative stain electron microscopy to sho

59 cium and neurotransmitter sensors with fiber photometry and optogenetics in mice, we find that mesoli

60 hin 100 parsecs of the Sun, determined using photometry and parallax data from the Gaia satellite(4).

61 orimotor, dorsolateral striatum (DLS), fibre photometry and photo-identified electrophysiological rec

62 les inhaled) was determined by laser aerosol photometry and pneumotachometry at the mouth.

63 Using simultaneous fiber photometry and polysomnography, we observed time-delinea

64 Mass photometry and single-particle cryo-electron microscopy

65 We synthesize the optical to near-infrared photometry and spectroscopy of SSS17a collected by the O

66 Photometry and spectroscopy of these afterglows have pro

67 -step instructions for how to leverage fiber photometry and two-photon imaging to measure dLight1 tra

68 avior in adult male mice using in vivo fiber photometry and two-photon microscopy.

69 Fiber photometry and viral mapping reveal distinct activity pa

70 new fluorescence polymerization assay, mass photometry, and atomic force microscopy.

71 ific information on the IONP coating, simple photometry, and citrate-selective reversed-phase high-pe

72 luding various forms of chromatography, mass photometry, and different tiers of mass spectrometry, to

73 ngle-photon microscopy (miniscope) and fiber photometry, and how the application of these technologie

74 pectrometry (XLMS), AlphaFold modeling, mass photometry, and native mass spectrometry (MS), we obtain

75 Single-cell sequencing, fiber photometry, and optogenetic experiments revealed that st

76 rotein levels were determined by laser flare photometry, and outflow facility was determined by Schio

77 ulus at 460 nm using heterochromatic flicker photometry, and the results were compared with measureme

78 ion of a multimode BODIPY-type fluorescence, photometry, and X-ray photoelectron spectroscopy (XPS) l

79 s for research, the rapid expansion in fiber photometry applications has occurred without coordinatio

80 In this study, an intersectional fiber photometry approach was used in male Sprague Dawley rats

81 Using novel fiber photometry approaches to assess real-time activity of as

82 glycolipid content, the affinities from mass photometry are found to be, overall, in good agreement w

83 These results introduce mass photometry as a rapid, simple and label-free method for

84 These results introduce mass photometry as an accurate, rapid and label-free single m

85 K2-360 was first identified in K2 photometry as the host of an ultra-short-period (USP) pl

86 ces (redshifts, z), estimated from multiband photometry, as large as z ~ 16, far beyond pre-JWST limi

87 Here, we developed fluorescence lifetime photometry at high temporal resolution (FLIPR), which ut

88 ological recordings, optogenetics, and fiber-photometry-based calcium imaging applied to wild-type an

89 C2230 also decreased fiber photometry-based calcium responses in the parabrachial n

90 In vivo photometry-based detection of optogenetically-evoked DA

91 tional magnetic resonance imaging (fMRI) and photometry-based neuronal calcium recordings in the anes

92 The use of mMORp for in vivo fiber photometry, behavioral chemogenetics, and intersectional

93 e task, we monitored FSI activity with fiber photometry calcium imaging and manipulated FSI activity

94 Fiber photometry calcium imaging showed that opioid-naive CeLC

95 Using fiber photometry calcium imaging we define D1 MSNs as the spec

96 Using fiber photometry calcium imaging, we recorded calcium transien

97 hol reward and aversive memories using fiber photometry calcium imaging.

98 Here, we show that mass photometry can accurately count, distinguish by molecula

99 trate that native mass spectrometry and mass photometry can provide unique insights into the physical

100 Here we used fiber photometry, cell-type and pathway-specific optogenetic m

101 Here, we combine fiber photometry, chemo/optogenetics, virus-assisted retrograd

102 asured by customized heterochromatic flicker photometry (cHFP).

103 Here, using fiber-optic photometry combined with optogenetic and molecular techn

104 Functional imaging and fiber photometry confirmed activation in response to magnetic

105 In vivo fiber photometry confirmed behavior-associated increases in RT

106 sense dsRNA byproducts were measured by mass photometry, contributing directly to immunological react

107 To address this, we developed a fiber Photometry Coupled focused Ultrasound System (PhoCUS) fo

108 ng and recall for the first time using fiber photometry coupled to a serotonin biosensor.

109 ease was also demonstrated via in vivo fiber photometry coupled with calcium and 5-HT biosensors.

110 Rather, mass photometry, crosslinking mass spectrometry, single molec

111 open source hardware and software for fiber photometry data acquisition consisting of a compact, low

112 y to other bacterial RNA helicases, and mass photometry data confirmed that CrhR exists as a dimer in

113 Results from our photometry data include a lower limit of 0.44 kilometer

114 activity in freely behaving mice with GCaMP photometry demonstrated striking estradiol-dependent pla

115 aging, we determined that the striatal fiber photometry does not reflect spiking-related changes in c

116 Ac astrocytes were measured by in vivo fiber photometry during conditioned place preference (CPP) to

117 In vivo studies with fibre photometry enabled direct recording of NOPLight binding

118 Mass photometry enabled the determination of the number of nu

119 Fiber photometry enables recording of population neuronal calc

120 Mass photometry experiments showed that RADX forms multiple o

121 Measured ultraviolet-visible photometry favours models with low metallicity (Z approx

122 developed frame-projected independent-fiber photometry (FIP), which we used to record fluorescence a

123 a(2+)-activated K+ channels and using indo-1 photometry following depolarization-induced Ca2+ loading

124 Here, we integrate fiber photometry for in vivo monitoring of dopamine and dMSN/i

125 results demonstrate the capabilities of mass photometry for quantifying protein-protein interactions

126 Fiber photometry (FP) is an adaptable method for recording in

127 Despite the popularity of fiber photometry (FP), its integration with operant behavior p

128 In vivo photometry further showed that the motivational deficit

129 Fiber photometry has become a popular technique to measure neu

130 ly, the opportunity for discovery with fiber photometry has exploded with the development of an exten

131 the fovea using the heterochromatic flicker photometry (HFP) and the two-wavelength autofluorescence

132 was estimated with a heterochromatic flicker photometry (HFP) method in a large biracial population s

133 ) was measured using heterochromatic flicker photometry (HFP).

134 ychophysically using heterochromatic flicker photometry (HFP).

135 luorescence [AF] and heterochromatic flicker photometry [HFP]), and serum concentrations of L and Z,

136 D was measured using heterochromatic flicker photometry in 10 eyes (5 patients) with MacTel and compa

137 Next, we used fiber photometry in aIC and observed phasic increases in aIC a

138 A (VTA(DA->BA)) using two-photon imaging and photometry in behaving mice.

139 In the present study, we used in vivo fiber photometry in C57BL/6J male mice to record from amygdala

140 MPOD was measured using flicker photometry in free view at 458 nm with a 1 degrees stimu

141 -associated dynamics of OH cells using fiber photometry in free-feeding mice.

142 We recorded calcium activity using fiber photometry in freely behaving mice and found arousal-sta

143 inary phosphate and calcium were measured by photometry in gsk3(KI) and gsk3(WT) mice, before and aft

144 NAcC dopamine was measured using fiber photometry in male and female rats during cocaine self-a

145 In this study, we used fiber photometry in mice to examine how release of the arousal

146 al iGlucoSnFR in vivo when observed by fiber photometry in mouse brain and reports transient increase

147 arker for neuronal activity, was detected by photometry in the mPFC of males but not in females with

148 g operant responding, as assessed by GRAB-DA photometry in the nucleus accumbens, but not the dorsal

149 We used in vivo fiber photometry in the ventral tegmental area and measured ph

150 Fiber photometry is a key technique for characterizing brain-b

151 Mass photometry is a recently developed methodology capable o

152 In conclusion, the indirect photometry is a reliable method especially as "screening

153 Fiber photometry is increasingly utilized to monitor fluoresce

154 en the proposed method and traditional flame photometry is observed for animal blood samples that pos

155 Fiber photometry is the process of recording bulk neural activ

156 Overall, our findings indicate that dLight photometry is well suited to measuring dopamine dynamics

157 nical cell and flare grading and laser flare photometry (LFP).

158 tection by multiangle laser-light-scattering photometry (MALLS) and differential refractometry (RI).

159 ion chromatography analysis, while indirect photometry may cause "false positive" results (5% of ana

160 in complexes agreed well with that from mass photometry measurement.

161 In agreement with these results, fibre photometry measurements of an adenosine sensor(11) revea

162 However, mass photometry measurements show that these mutations do not

163 Fiber photometry method and chemogenetics were used to parse t

164 swer these questions, we utilize multi-fiber photometry (MFP) to simultaneously record Ca(2+) signals

165 elective pharmacology and in vivo time-lapse photometry monitoring of lipid metabolism, we find that

166 sal hypothalamic astrocytes, real-time fiber photometry monitoring of white adipose tissue norepineph

167 dodecamer assembly of GlnA(1) by using mass photometry (MP) and single particle cryo-electron micros

168 Here, we show that mass photometry (MP) can accurately characterize the heteroge

169 Mass photometry (MP) has emerged as a powerful approach to st

170 Mass photometry (MP) is a technology for the mass measurement

171 f the two proteins was studied by using mass photometry (MP) to determine equilibrium conditions and

172 n fluorescence microscopy (smTIRFM) and mass photometry (MP) with biophysical and biochemical analyse

173 Here, we benchmark mass photometry (MP), a recently introduced technology for ma

174 we used native mass spectrometry (MS), mass photometry (MP), and biochemical experiments that (i) va

175 Combining native MS with mass photometry (MP), we reveal that super-dimerization is se

176 0 cells), in vivo calcium imaging with fiber photometry (n = >=4 mice), and use of viral strategies i

177 Using in vivo fiber photometry, neonatal Agrp neurons showed a rapid increas

178 GCaMP fibre photometry of arcuate kisspeptin neurons revealed that t

179 Fiber photometry of calcium responses from calcitonin-gene-rel

180 elevated dopamine detected with optic-fiber photometry of dopamine sensor GRAB(DA2m) and promoted co

181 Here we report submillimeter photometry of eight x-ray-absorbed active galactic nucle

182 DNA level, as determined by quantitative DNA photometry of individual cells.

183 In vivo fiber photometry of SON neurons from hibernating squirrels, to

184 spectively, and calibrated by emission flame photometry of the micropunch brain samples.

185 port an analysis of dayside multi-wavelength photometry of the transiting hot-Jupiter WASP-12b that r

186 Then, using gCaMP fiber photometry of VTA TH neurons, we identified medial and l

187 mbination of microextraction with SUPRAS and photometry or HPLC-UV/VIS spectroscopy were developed fo

188 Here, we use fiber photometry paired with a genetically encoded dopamine se

189 Here, we employ mass photometry, phylogenetics, and structural biology to int

190 Here, we present a dual microfluidic-photometry platform that enables simultaneous intracrani

191 LC photometry predicted when CI subjects began responding t

192 Using fiber photometry recording and two-photon imaging, our ACh sen

193 Fiber-photometry recording indicated that the activities of rV

194 In addition, fiber photometry recording indicates that this neuron subtype

195 Fiber photometry recording of several wake-promoting neuromodu

196 Fiber photometry recordings during progressive ratio operant b

197 onal signal we performed projection-specific photometry recordings from several inputs to ACC during

198 Fiber photometry recordings of dopaminergic activity in the BL

199 nce in mouse surgery, enables repeated fiber photometry recordings or optogenetic manipulation during

200 Fiber photometry recordings reveal attenuation of responses to

201 Fiber photometry recordings reveal that Bar(Vglut2) neuron act

202 Fiber photometry recordings revealed that these patterns of ac

203 Our fiber photometry recordings showed DA neurons in medial and la

204 -light melatonin onset (DLMO) and wrist-worn photometry, respectively.

205 Patients with uveitis and laser flare photometry results (flare) more than 20 photon units/mse

206 Fiber photometry results corroborated these findings, showing

207 Remarkably, the mass photometry results indicate that glycolipids are distrib

208 is, analytical ultracentrifugation, and mass photometry reveal that, despite its distinct chemical st

209 Supporting this hypothesis, fiber photometry revealed selective activation of excitatory M

210 Fiber photometry revealed that acetylcholine release in mPFC n

211 Fiber photometry revealed that activity dynamics of a ventral

212 Fiber photometry revealed that cocaine-treated mice showed a s

213 Dual-color photometry revealed that dopamine release in the nucleus

214 ation using optogenetics, chemogenetics, and photometry revealed that glutamatergic projections from

215 Mass photometry revealed that sKLA can form a stable structur

216 Fiber photometry revealed that their activity is strongly incr

217 In vivo fiber photometry revealed that these neurons are selectively e

218 In vivo photometry revealed that while SCN(VIP) neurons are acut

219 for these clones using improved single-cell photometry (SCP) techniques.

220 -of-flight mass spectrometry (QTOF MS), mass photometry, SEC, and CE-SDS did not resolve partially or

221 s measured MPOD with heterochromatic flicker photometry, serum lutein and serum zeaxanthin by high pe

222 sly with in vivo calcium recording via fiber photometry, showcasing its compatibility with optical mo

223 , GCamp6f fluorescence recordings with fiber photometry showed that M2 cortex activity was engaged by

224 Fiber photometry showed that repeated optogenetic or sensory s

225 s such, it remains unclear whether the fiber photometry signal reflects changes in somatic calcium, c

226 rojections and observed phasic VTA-PFC fiber photometry signals after the delivery of rewards.

227 Fiber photometry studies show that activity of GABAergic and g

228 ecute, analyze, and suitably interpret fiber photometry studies.

229 nuous arterial glucose monitoring with fiber photometry, studies investigated whether neurons in the

230 atch the observed spectrum and the broadband photometry suggest that heat redistribution from the day

231 Here, we engineered a fiber photometry system [4] and monitored population-level Ca(

232 s is measured with a fluorescence microscope photometry system.

233 probe (fura-2) and a fluorescence microscope photometry system.

234 d using a customized heterochromatic flicker photometry technique.

235 d with fura 2 and studied using fluorescence photometry techniques.

236 Here we present optical photometry that shows moderate detections of light in th

237 Photometry, the measurement of the visual quantity of li

238 ex vivo electrophysiology and in vivo fiber photometry to assess changes in BNST plasticity, cell-sp

239 We employed fiber photometry to assess LTSI calcium activity in a range of

240 Here, we use mass photometry to comprehensively quantify all the key biomo

241 We use photometry to determine a mean, dust-free stellar age of

242 we use rapid local perfusion and single-cell photometry to examine the kinetics of calcium responses

243 ly encoded dopamine sensor dLight1 and fiber photometry to explore the ability of striatal dopamine r

244 ings, we used in vivo optogenetics and fiber photometry to further examine BNST(PKCdelta) cells in th

245 )(,)(15)(,)(16) In this study, we used fiber photometry to investigate the in vivo dynamics of these

246 mission tomography (PET), and spectral fiber photometry to investigate the selective neuromodulatory

247 Utilizing fiber photometry to measure circuit activity in vivo in conjun

248 Here we used fiber photometry to measure DA transients in the NAcc of male

249 We then used dLight fiber photometry to measure dopamine binding across the ventra

250 ule VII of the cerebellum, while using fiber photometry to measure sensor fluorescence during anxiety

251 We used photometry to measure the dynamics of cytosolic Ca(2+) (

252 isual cortex, revealed using dual-site fiber photometry to monitor noradrenergic Ca(2+) responses of

253 Using fiber photometry to monitor population neural activity, we dem

254 Here, we used calcium photometry to monitor the effect of CB(1) activation on

255 We use mass photometry to observe tubulin monomers and heterodimers

256 Here, we apply mass photometry to quantify a series of high-affinity interac

257 Here, we use mass photometry to quantify and monitor the full range of act

258 The recent advent of mass photometry to quantify mass distributions of unlabeled b

259 an intersectional viral approach with fiber photometry to record bulk calcium activity in VP GABAerg

260 IPN GABAergic neurons and used in vivo fiber photometry to record changes in fluorescence, as a proxy

261 Here we utilized fiber photometry to record from the dmPFC and its axonal proje

262 We used fiber photometry to record in vivo activity in vHIP-NAc affere

263 ncoded Ca(2+) indicator GCaMP and used fiber photometry to record population PVT Ca(2+) signals.

264 In this study, we used fiber photometry to record the temporal dynamics in the popula

265 Here, we use in vivo fiber photometry to show that ELA results in sex-specific chan

266 alanine-scanning mutagenesis and patch clamp photometry to study the role of the first transmembrane

267 Here we used electrophysiology and fibre photometry to test how dopamine signals associated with

268 and applied a new methodology, termed fiber photometry, to optically record natural neural activity

269 ve approach, called dye-overload patch-clamp photometry, to quantify the agonist-gated Ca(2+) flux of

270 ing single flash and heterochromatic flicker photometry under conditions of dark- or light-adaptation

271 -0.40; P = 0.0002), and maximum laser flare photometry value (r = -0.26; P = 0.020).

272 Fiber photometry was used to measure and compare neuronal acti

273 Heterochromatic flicker photometry was used to measure MPOD at 0.5 degrees eccen

274 Heterochromatic flicker photometry was used to measure the macular pigment (MP)

275 tch clamp recordings and fura-2 fluorescence photometry was used to study the membrane currents durin

276 -dry method, and [Na(+)] and [K(+)] by flame photometry, was guided by the observation of a subtle ch

277 Finally, using fiber photometry we were able to record calcium signals in viv

278 Using fiber photometry, we continuously imaged population calcium dy

279 plasma measurements and in vivo single-fiber photometry, we demonstrate that psilocybin induces robus

280 electrophysiology and intracellular chloride photometry, we demonstrated that visTRN dynamically cont

281 COLM, optogenetics, viral tracing, and fiber photometry, we explore the diversity of dopamine neurons

282 ime monitoring of neural activity with fiber photometry, we find that medial NAc shell projections to

283 Using GCaMP6 fiber photometry, we find that the ARN(KISS) neuron population

284 Using fiber photometry, we found elevated claustrum activity prior t

285 Using patch clamp photometry, we found that the fraction of the total curr

286 man functional neuroimaging and rodent fiber photometry, we identified a mOFC-BLA projection that mod

287 cording population calcium dynamics by fiber photometry, we observe that the neuronal response to con

288 tion behavior data paired with in-vivo fiber photometry, we show how similar levels of alcohol intake

289 gh anatomical, behavioral, and in vivo fiber photometry, we show that the PAG and dLS neurons are syn

290 Using in vivo fiber photometry, we simultaneously recorded activity in DA te

291 The flare values as obtained by laser flare photometry were consistent with the slit-lamp biomicrosc

292 tivity fluctuations were measured with fiber photometry while male and female rats learned to associa

293 of resistance arteries by performing Fura-2 photometry while recording and controlling V(m) of intac

294 In this study, we combined 2-site fiber photometry with electroencephalogram/electromyography re

295 Here, we combine fiber photometry with functional magnetic resonance imaging (f

296 cluding electrochemical recordings and fiber photometry with genetically encoded optical sensors for

297 the present study, we combined in vivo fiber photometry with nutrient-conditioned flavor in a rat mod

298 genetically encoded calcium indicator) fiber photometry with simultaneous videography to probe DMN fu

299 tography coupled with laser light-scattering photometry, yielding a mass distribution of YiiP homo-ol

300 Modeling of the spectra and photometry yields a luminosity (normalized by the lumino