ライフサイエンスコーパス: photometry

1 ts and earlier times, using coarsely sampled photometry.

2 ys during skill learning in mice using fiber photometry.

3 d MPOD by customized heterochromatic flicker photometry.

4 sing slit-lamp biomicroscopy and laser flare photometry.

5 y were assessed with heterochromatic flicker photometry.

6 ierarchical triple, identified in the Kepler photometry.

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

8 ical testing using electroretinogram flicker photometry.

9 s were measured with heterochromatic flicker photometry.

10 POD) was measured by heterochromatic flicker photometry.

11 transients recorded with fura-2 and digital photometry.

12 dichroism spectroscopy and light-scattering photometry.

13 uorescence microscopy, flow cytometry, or UV photometry.

14 ofiles measured with heterochromatic flicker photometry.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

29 Photometry and spectroscopy of these afterglows have pro

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

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

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

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

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

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

36 Using fiber photometry calcium imaging, we recorded calcium transien

37 asured by customized heterochromatic flicker photometry (cHFP).

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

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

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

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

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

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

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

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

46 ychophysically using heterochromatic flicker photometry (HFP).

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

63 Fiber photometry revealed that activity dynamics of a ventral

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

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

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

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

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

69 s is measured with a fluorescence microscope photometry system.

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

71 d using a customized heterochromatic flicker photometry technique.

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

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

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

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

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

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

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

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

80 -0.40; P = 0.0002), and maximum laser flare photometry value (r = -0.26; P = 0.020).

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

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

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

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

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

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

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

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

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

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

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

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

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