ライフサイエンスコーパス: photobleaching experiment

1 ard, single beam fluorescence recovery after photobleaching experiment.

2 ere monitored by fluorescence recovery after photobleaching experiments.

3 pool with kinetics similar to those seen in photobleaching experiments.

4 imately 45 s) in fluorescence recovery after photobleaching experiments.

5 id dynamics with fluorescence recovery after photobleaching experiments.

6 In simulated spot photobleaching experiments, a approximately 25% decrease

7 e microscopy and fluorescence recovery after photobleaching experiments and found that mycomembrane f

8 Fluorescence recovery after photobleaching experiments and particle tracking by tota

9 mework for quantitatively analyzing stepwise photobleaching experiments and shed light on the localiz

10 and vesicular transport; thus, we performed photobleaching experiments and showed that proteasomes a

11 n dynamics using fluorescence recovery after photobleaching experiments and single-molecule imaging.

12 t the outcome of fluorescence recovery after photobleaching experiments and the behavior of a functio

13 ions detected in fluorescence recovery after photobleaching experiments and the temperatures at which

14 ns that simulate fluorescence recovery after photobleaching experiments, and indicate how such data m

15 In simulated photobleaching experiments, apparent diffusive transport

16 tive measurements, along with nocodazole and photobleaching experiments, are consistent with a redist

17 Recently, FM1-43 photobleaching experiments carried out a frog motor end-

18 Photobleaching experiments confirmed that the bilayer se

19 Fluorescence recovery after photobleaching experiments confirmed that the GJIC remai

20 Fluorescence recovery after photobleaching experiments demonstrate that in this muta

21 Surprisingly, photobleaching experiments demonstrate that, although Sp

22 Fluorescence recovery after photobleaching experiments demonstrated that subunit exc

23 Fluorescence recovery after photobleaching experiments demonstrated the bilayers' fl

24 the contact area fluorescence recovery after photobleaching experiment enables in situ measurements o

25 s used to uncage Ca(2)(+) or IP3 and conduct photobleaching experiments from multiple geometrically c

26 Photobleaching experiments identified dynamic (60%) and

27 Photobleaching experiments in living cells indicate that

28 cle tracking and fluorescence recovery after photobleaching experiments in primary neurons, in differ

29 Moreover, fluorescence recovery after photobleaching experiments in the nucleoplasm show a dec

30 Photobleaching experiments in vivo demonstrated that the

31 Fluorescence recovery after photobleaching experiments in yeast show a very dynamic

32 in reporters and fluorescence recovery after photobleaching experiments in zebrafish embryos identifi

33 roach of in vivo fluorescence recovery after photobleaching experiments, in vitro permeabilized cell

34 Photobleaching experiments indicate that actin and tubul

35 Photobleaching experiments indicate that both hypertonic

36 Immunolocalization and photobleaching experiments indicate that individual vesi

37 ELISA and fluorescence recovery after photobleaching experiments indicate that NoxA1ds, but no

38 Photobleaching experiments indicated that co-assembly of

39 Photobleaching experiments indicated that different grou

40 Photobleaching experiments indicated that Golgi-to-ER pr

41 Finally, photobleaching experiments indicated that PIP2 binding i

42 In fluorescence recovery after photobleaching experiments, KLP61F-GFP displays dynamic

43 ation with FRAP (fluorescence recovery after photobleaching) experiments of GFP-tubulin to examine th

44 Fluorescence recovery after photobleaching experiments on green fluorescent protein

45 To this aim, we have carried out photobleaching experiments on nerve terminals of hippoca

46 ver, measured by fluorescence recovery after photobleaching experiments, only CaMKII increases the dy

47 Mechanistically, fluorescence-recovery-after-photobleaching experiments point for the upstream role o

48 In photobleaching experiments, PR in the presence of the ag

49 on model for the fluorescence recovery after photobleaching experiment previously used to demonstrate

50 Photobleaching experiments provide direct evidence that

51 Fluorescence-recovery-after-photobleaching experiments provided data suggesting that

52 In vivo photobleaching experiments provided direct evidence that

53 ent accumulation at the mitotic poles and by photobleaching experiments remains continuous through th

54 Photobleaching experiments reveal that centrosome-bound

55 Fluorescence recovery after photobleaching experiments reveal that polar PBP3 molecu

56 rtins-beta is essential for cell growth, and photobleaching experiments revealed a critical role for

57 In contrast, photobleaching experiments revealed a GFP-tagged variant

58 Fluorescence recovery after photobleaching experiments revealed a high mobility of t

59 Photobleaching experiments revealed that CD94/NKG2A-EGFP

60 Photobleaching experiments revealed that during initial

61 Photobleaching experiments revealed that during normal i

62 Photobleaching experiments revealed that OSER-inducing p

63 Single-molecule fluorescence photobleaching experiments revealed that PopD formed mos

64 Selective photobleaching experiments revealed that single BSEP-YFP

65 Photobleaching experiments revealed that SUMO-1 dynamics

66 d-associated cables and fluorescence loss in photobleaching experiments revealed that this apparent e

67 combination with fluorescence-recovery-after-photobleaching experiments, revealed that nicotine, acti

68 gth control, but fluorescence recovery after photobleaching experiments rule out the initial bolus mo

69 Fluorescence loss in photobleaching experiments show subnuclear concentration

70 of RI-occupancy as single-molecule pull-down photobleaching experiments show that 41 +/- 10% of SKIP

71 Fluorescence recovery after photobleaching experiments show that approximately 60% o

72 Fluorescence recovery after photobleaching experiments show that myosin II is stabil

73 Photobleaching experiments show that the new Golgi is no

74 istinguishable at all stages of mitosis, and photobleaching experiments showed that diffusion of the

75 Furthermore, fluorescence photobleaching experiments showed that protein in the im

76 Photobleaching experiments showed that Sec13 shuttles be

77 Fluorescence recovery after photobleaching experiments showed that the effector prot

78 Fluorescence recovery after photobleaching experiments showed that, under conditions

79 Fluorescence anisotropy imaging and photobleaching experiments suggest that TCs are function

80 Photobleaching experiments suggest that vesicles move by

81 4 as measured by fluorescence recovery after photobleaching experiments, the rapid sequestration of a

82 diffusion of Ku was measured by fluorescence photobleaching experiments using cells expressing green

83 Fluorescence recovery after photobleaching experiments was used to assess the rate o

84 Using photobleaching experiments, we analyzed the dynamics of

85 Previously, fluorescence recovery after photobleaching experiments were performed in HEK cells e

86 To address this question, fluorescence photobleaching experiments were performed using HeLa cel

87 the rate of Pten nuclear import detected by photobleaching experiments, whereas Ndfip1(-/-) fibrobla

88 complemented by fluorescence recovery after photobleaching experiments, which reveal an inverse corr

89 sing a two-photon standing wave fluorescence photobleaching experiment with 100 nm spatial resolution

90 Photobleaching experiments with live cells revealed that