ライフサイエンスコーパス: bright field

1 mic capillary diameter: 5.1 +/- 0.1 microns (bright field, 39 capillaries in 10 animals) and 5.1 +/-

2 on the human expert analysis of conventional bright-field and birefringence images were performed.

3 Bright-field and dark-field illumination techniques for

4 havior are identified for further study from bright-field and dark-field light-microscopy modes, resp

5 ce expressing only human HbC were studied by bright-field and differential interference contrast vide

6 alized proteins using immunofluorescence and bright-field and electron microscopy.

7 Bright-field and epifluorescence microscopy and CLSM sho

8 opically as follows: (i) in wet mounts (with bright-field and epifluorescence microscopy), (ii) in mo

9 and protobiofilm in the feedwater stream by bright-field and epifluorescence microscopy.

10 The instrument has bright-field and fluorescence microscopy capabilities in

11 Bright-field and fluorescence microscopy provided simila

12 images collected from the same sample using bright-field and fluorescence microscopy.

13 lls were measured blinded to diagnosis using bright-field and fluorescent microscopy.

14 gh-spatial-resolution ex vivo MR imaging and bright-field and immunofluorescent histologic examinatio

15 as a function of mesogen concentration using bright-field and polarized optical microscopy.

16 Bright-field and scanning electron microscopy establishe

17 lt microscope to record large field-of-view, bright-field, and fluorescence images of samples that ar

18 the cost of targeting the N-terminus, while bright field APP C-terminus studies were performed for 1

19 ual label immunofluorescent and single label bright-field approaches.

20 Validation of a bright-field assay for assessment of HER-2/neu gene ampl

21 in situ hybridization represents a promising bright-field assay for the assessment of HER-2/neu gene

22 Bright field (BF) optical microscopy is regarded as a po

23 Streamers can be visualized in bright field by phase imaging, and fluorescence-staining

24 ic information theoretic approach to segment bright field defocused images.

25 e in extracting information from microscopic bright field defocused images.

26 lysis of cellular processes with microscopic bright field defocused imaging has the advantage of low

27 We present an integrative method combining bright-field dual-colour chromogenic and silver ISH assa

28 We used axial (bright-field) electron tomography in the scanning transm

29 e is successfully applied to phase contrast, bright field, fluorescence microscopy and binary images.

30 irmed using 3 different types of microscopy (bright-field, fluorescence, and electron), 2 additional

31 Streptavidin-Nanogold was used to generate bright-field gene copy signals using GoldEnhance gold-ba

32 th high-angle annular dark-field and annular bright-field (HAADF and ABF) imaging and nanoscale compo

33 whose tumors were resected with traditional bright-field illumination only.

34 ., intrinsic UV fluorescence, birefringence, bright-field image analysis, etc.) is often complicated

35 Bright-field image retinal maps and fluorescent images w

36 However bright field images lack the contrast and nuclei reporti

37 Bright field images of the splitting processes at the ju

38 sistent with those of Bragg fringe widths in bright-field images obtained at lower magnification.

39 D archives multi-wavelength fluorescence and bright-field images of tissue microarrays for scoring an

40 subdermal blood vessels by using intravital bright-field images, hyperspectral imaging, fluorescence

41 Bright field imaging of biological samples stained with

42 Simultaneous high-speed bright field imaging of cavitation and measurements of t

43 ble automated identification of particles by bright field imaging, followed by classification by SHG.

44 entification of the head of the animal under bright field imaging.

45 Here, we report a time-lapse-based bright-field imaging analysis system that allows us to i

46 Specifically, we performed high-throughput bright-field imaging of numerous drug-treated and -untre

47 Via bright-field imaging with an ultrafast electron microsco

48 lular drug responses only by high-throughput bright-field imaging with the aid of machine learning al

49 of the immobilized cell were monitored using bright-field imaging.

50 ted in rat-tendon cryosections using SHG and bright-field imaging.

51 mple experimental setup, based on a standard bright-field inverted microscope (no fluorescence requir

52 nt also altered the pattern of mu-ORi at the bright-field light microscopic level.

53 e molecular binding events under an ordinary bright-field microscope and serve as a diffraction grati

54 This technique uses an unmodified bright-field microscope, an array of microlenses, and a

55 n can expand the functionality of commercial bright field microscopes, provide easy field detection o

56 severe to mild lymphocytic infiltrations by bright field microscopy were examined in parallel with i

57 ion, (e) distorted posterior suture lines by bright field microscopy, and (f) development of a mild a

58 l immunofluorescent microscopy, single label bright field microscopy, and electron microscopy (EM).

59 In bright field microscopy, each cell contains a bright yel

60 small angle neutron scattering, rheology and bright field microscopy, we identify the coexistence of

61 Cell growth and viability were evaluated by bright field microscopy.

62 traps and analyzed for > 30 mold taxa using bright field microscopy.

63 Diameter was observed using bright field microscopy.

64 For phenotypic analysis, we performed bright-field microscopy and Aliziran Red S staining to a

65 -positive cells were counted by conventional bright-field microscopy and confirmed by confocal micros

66 This method is based on fluorescence and bright-field microscopy and on a custom MATLAB program t

67 methods to trace impregnated dendrites from bright-field microscopy images that enabled accurate 3-d

68 Bright-field microscopy provides a blurred visualization

69 om an aqueous stream into plugs, (iii) using bright-field microscopy to detect the formation of a fib

70 ective under different recording conditions (bright-field microscopy with simultaneous patch-clamp re

71 bserving wound closure with fluorescence and bright-field microscopy, (2) histology to quantify infla

72 Gram staining, bright-field microscopy, hematoxylin and eosin, periodic

73 vide a means of locating single molecules by bright-field microscopy, prior to single-molecule detect

74 ycine were counted in a masked fashion under bright-field microscopy.

75 f chromosomal translocations by conventional bright-field microscopy.

76 llows switching between epifluorescence/TIRF/bright field modes without adjustments or objective repl

77 sample debris, previously not possible with bright-field or scanning ion imaging.

78 a task that has not been routine with either bright-field or TOF-SIMS.

79 ening drug discovery platforms, for example, bright-field, phase contrast, and fluorescence microscop

80 introduce quantitative image restoration in bright field (QRBF), a digital image processing method t

81 d magnetite by employing a strain-sensitive, bright-field scanning transmission electron microscopy a

82 The combination of bright-field, scanning ion, and fluorescence microscopy

83 improvement of SIM, compared to conventional bright field system is a factor of 2.

84 animals studied using vertical illumination (bright-field) techniques.

85 The images can be bright fields that display position-dependent quantum no

86 We used bright-field, time-lapse video, cross-polarized, phase-c

87 rganization of the crystals were examined by bright-field transmission electron microscopy and electr

88 a much higher contrast than that achieved in bright-field transmission electron microscopy imaging of

89 icroscope, allowing the analysis with simple bright field visualization.