ライフサイエンスコーパス: phase-contrast microscopy

1 imaging techniques such as fluorescence and phase contrast microscopy.

2 the IAS in the basal state was determined by phase contrast microscopy.

3 es were morphologically indistinguishable by phase contrast microscopy.

4 irochete morphogroup were also identified by phase contrast microscopy.

5 The spirochete morphogroup was identified by phase contrast microscopy.

6 py and the motion of the underlying cells by phase-contrast microscopy.

7 NK cells and FLS were studied by time-lapse phase-contrast microscopy.

8 by trypan blue staining, cell counting, and phase-contrast microscopy.

9 Cell morphology was documented by inverted phase-contrast microscopy.

10 On-going observations were by phase-contrast microscopy.

11 On-going observations were by phase-contrast microscopy.

12 ofilm formed by the wild type over 8 h using phase-contrast microscopy.

13 Observations were made by phase-contrast microscopy.

14 e ankyrin-3-positive vesicles appear dark on phase-contrast microscopy.

15 moval at 6 weeks by culture, DNA probes, and phase-contrast microscopy.

16 Cell shape change was determined by phase-contrast microscopy.

17 t scattering, as well as by fluorescence and phase-contrast microscopy.

18 ten requires the use of transmitted light or phase-contrast microscopy.

19 ollows: (1) by the morphologic appearance on phase-contrast microscopy; (2) by the levels of aldehyde

20 fixed for study by disseminated interference phase contrast microscopy and electron microscopy.

21 ic acid and Ca(2+) (CaDPA) were monitored by phase contrast microscopy and Raman spectroscopy, respec

22 r matrix protein type-I collagen by means of phase contrast microscopy and rotating disk rheometry.

23 Evaluations were performed by means of phase-contrast microscopy and [3H]thymidine uptake assay

24 logy and cell-cell networks were assessed by phase-contrast microscopy and a cell viability assay, re

25 Neurite outgrowth was assessed by phase-contrast microscopy and calcein AM staining and qu

26 erior vitreous detachment were examined with phase-contrast microscopy and confocal microscopy after

27 Apoptosis was measured by phase-contrast microscopy and flow cytometry.

28 e periods on the order of weeks by utilizing phase-contrast microscopy and show that these cells acqu

29 ellar motion, visualizing the cell bodies by phase-contrast microscopy and the flagellar filaments by

30 Time-lapse video phase-contrast microscopy and time-lapse digital confoca

31 Phase-contrast microscopy and Wright staining showed mor

32 The experiments were videorecorded (phase-contrast microscopy), and PMN adhesion/migration w

33 as observed by scanning electron microscopy, phase contrast microscopy, and confocal scanning laser m

34 ology that combines fluorescence microscopy, phase contrast microscopy, and laser tweezers Raman spec

35 opy with simultaneous patch-clamp recording, phase contrast microscopy, and traction force microscopy

36 as observed by scanning electron microscopy, phase-contrast microscopy, and fluorescence microscopy.

37 -), as demonstrated by annexin V positivity, phase-contrast microscopy, and in selected cases 4',6'-d

38 fewer attached bacteria, as determined using phase-contrast microscopy, and less biofilm (P < 0.0001)

39 rulent NAP1 strain using optical density and phase-contrast microscopy assays.

40 Phase contrast microscopy assesses changes in refractili

41 n vitro on purified type 1 collagen by video phase-contrast microscopy at 22 degrees C.

42 Phase-contrast microscopy consistently identified a crea

43 Phase contrast microscopy coupled to digital image proce

44 Phase-contrast microscopy demonstrated that freshly isol

45 specimens were processed as flat mounts for phase-contrast microscopy followed by immunolabeling for

46 sent a new approach for retrieving halo-free phase contrast microscopy (hfPC) images by upgrading the

47 pseudoholes (14 eyes) using interference and phase-contrast microscopy, immunocytochemistry, and tran

48 wth factor-beta1 (TGF-beta1) was analyzed by phase contrast microscopy, immunofluorescence, quantitat

49 at combines the automated image analysis for phase-contrast microscopy movies with an easy-to-use int

50 Phase contrast microscopy of vernix showed multiple cell

51 pted to use multi-trap Raman spectroscopy or phase-contrast microscopy of spores adhered on a cover s

52 Under phase contrast microscopy, PDL cells in non-mineralizing

53 d of the rapid drop in spore refractility by phase contrast microscopy, precisely corresponds to the

54 present a methodology that combines external phase contrast microscopy, Raman spectroscopy, and optic

55 Fluorescence and phase contrast microscopy revealed characteristic apopto

56 Phase contrast microscopy revealed identical sperm defec

57 Examination by phase-contrast microscopy revealed the lytic death of ma

58 ic and phenotypic changes were determined by phase-contrast microscopy, sensitivity to the oxidant te

59 of 3 s data segments of light intensity from phase-contrast microscopy showed no significant delay be

60 e-contrast microscopy, structural details in phase-contrast microscopy, structural details in direct

61 of pressure-sensitive, refractile bodies in phase-contrast microscopy, structural details in phase-c

62 Phase-contrast microscopy studies of the entire GBM syst

63 nveloping membranous structure identified on phase-contrast microscopy to show positive stain results

64 ation and vegetative outgrowth by time lapse phase contrast microscopy, transmission electron microsc

65 Phase-contrast microscopy was used to follow biofilm dev

66 ifferential interference contrast (DIC), and phase contrast microscopy, we tracked the movement of MT

67 Using phase-contrast microscopy, we found that a crc mutant on