ライフサイエンスコーパス: light microscope

1 or mappings of proteomes under the lens of a light microscope.

2 grams to beyond the diffraction limit of the light microscope.

3 ucleotides, well below the resolution of the light microscope.

4 loss was evaluated morphometrically under a light microscope.

5 oxin released, and the cell morphology under light microscope.

6 olarizer in the optical path of a wide-field light microscope.

7 ere drawn using a drawing tube attached to a light microscope.

8 typically convolved in an ordinary polarized light microscope.

9 VL were traced in serial sections under the light microscope.

10 rmined by counting foci of infection under a light microscope.

11 ctions and inspected optic nervous under the light microscope.

12 i) the integrity of the sarcolemma under the light microscope.

13 ed by the short optical penetration depth of light microscopes.

14 e instructions on how to build a modular low-light microscope (1-4 d) by coupling two microscope obje

15 rbing the mature biofilms was examined under light microscope and confocal laser scanning microscope.

16 say developed in Peru which uses an inverted light microscope and culture in Middlebrook 7H9 broth to

17 g a conventional wide-field epi-fluorescence light microscope and digital imaging with a low noise co

18 ramatically expanded the capabilities of the light microscope and its usefulness in microbiology rese

19 n were easily identified and counted under a light microscope and many more taste buds, patterned in

20 varicosities that could be identified in the light microscope, and each varicosity made a single syna

21 morphisms, large enough to be visible in the light microscope, and the single nucleotide polymorphism

22 sphine, labeled with ReAsH, monitored in the light microscope, and used to trigger the photoconversio

23 ed with standard light microscopes, confocal light microscopes, and electron microscopes.

24 been defined primarily at the resolution of light microscopes, and the relationship between gamma-H2

25 m and spatial resolution at the limit of the light microscope ( approximately 0.2 micro m).

26 ucleolinus, clearly visible with transmitted light microscopes at 10x magnification, is present in ea

27 n and Arp2/3 complex interact, we employed a light microscope-based assay to visualize actin polymeri

28 f the trapezoid body and documented with the light microscope before being studied with serial-sectio

29 rease the spatial resolution of a wide-field light microscope by a factor of two, with greater resolu

30 orms of microimaging performed with standard light microscopes, confocal light microscopes, and elect

31 f MSU crystals under a compensated polarized light microscope (CPLM) in synovial fluid aspirated from

32 Light microscope examination of stained sections showed

33 The median light microscope grade of SP mRNA expression in the earl

34 The inherent resolution limit of the light microscope has been a limiting factor in investiga

35 The light microscope has long been used to document the loca

36 Anyone who has used a light microscope has wished that its resolution could be

37 erally bellow the 300nm diffraction limit of light microscopes, has limited most imaging studies to e

38 ocalized to myelin by immunofluorescence and light microscope HRP immunocytochemistry.

39 hniques can also improve the resolution of a light microscope image beyond what is achievable with wi

40 human chromosomes 6 and 22 and then examined light microscope images of interphase tertiary chromatin

41 Thus, light microscope images of tertiary structure cannot dis

42 In these model systems, light microscope images reveal fibers or beaded fibers a

43 Live-cell liquid crystal polarized light microscope imaging showed nondisjunction was cause

44 eins phakosin, filensin, and vimentin, using light microscope immunocytochemical methodology.

45 tional thin-section electron microscopy, and light microscope immunocytochemistry to examine and char

46 oid was imaged within the chip using a white light microscope in either transmission or, due to the h

47 first using a cryogenically adapted confocal light microscope in which the specimen is coupled to a h

48 omatic cell counting in which a conventional light microscope is equipped with a web camera to obtain

49 The light microscope is traditionally an instrument of subst

50 no structural differences identified at the light microscope level in fascicular/non-fascicular tiss

51 neuropil, perikaryon, and dendrites) at the light microscope level using microdensitometry calibrate

52 c space and stria vascularis observed at the light microscope level were unchanged in either Cx null

53 logically identical to coiled bodies (at the light microscope level) formed in such coilin-depleted e

54 vessels in epoxy resin embedded specimens at light microscope level, and that there is an increase in

55 At the light microscope level, neurons of the SN pars reticulat

56 At the light microscope level, rich plexuses of NMDAR1-positive

57 At the light microscope level, we detect no difference between

58 ing identifiable only as small puncta at the light microscope level, we examined the area with electr

59 three-dimensional analysis techniques at the light microscope level, we quantified the number, length

60 and dfw2J mice was indistinguishable at the light microscope level.

61 obvious changes in lens architecture at the light microscope level.

62 le excrescences within these clusters at the light microscope level.

63 no morphological alterations detected at the light microscope level.

64 on on lens architecture was evaluated at the light-microscope level.

65 eptors (GluR5/6/7) in these laminae by using light microscope (LM) and electron microscope (EM) immun

66 tion, when grown in liquid and examined in a light microscope, lonS mutant cells were extremely long

67 hickness is near the resolution limit of the light microscope, making studies relating cortex thickne

68 uch shorter than the resolution limit of the light microscope, making visualization of this gradient

69 Under light microscope, predominant lamellar patterns were fou

70 Using a light microscope severing assay, cofilin's severing acti

71 hnologies plus the plethora of sophisticated light microscope techniques now available make studying

72 We report a light microscope that generates images with translationa

73 e growth cones using a new type of polarized light microscope (the Pol-Scope).

74 In a polarizing light microscope, these structures exhibit a "Maltese-cr

75 nmotile on motility agar plates, but under a light microscope they exhibited random movement and tumb

76 mals and the pontine nuclei examined under a light microscope to detect PHA-L-labeled fibers.

77 TV culture system, was examined daily with a light microscope to identify T. vaginalis.

78 FCS was restricted by the resolution of the light microscope to the micrometer scale.

79 semblies in water from the resolution of the light microscope to the nanometer resolution of the elec

80 olecules allows localization and tracking in light microscopes to a precision about an order of magni

81 n defined using the semiautomated, multimode light microscope, together with a fluorescent analogue o

82 bihelical motility as captured by high-speed light microscope videography.

83 Morphometry in the light microscope was used to measure loss of rod photore

84 Under examination with the light microscope, we found that both types of receptors

85 A light microscope with a micrometer inset into the eyepie

86 cted by eye or a video camera using a simple light microscope with a proper illuminating system.

87 trate the utility of integrating an inverted light microscope with an ambient ionization source, nano