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

1 ard, single beam fluorescence recovery after photobleaching experiment.

2 id dynamics with fluorescence recovery after photobleaching experiments.

3 ere monitored by fluorescence recovery after photobleaching experiments.

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

5 pool with kinetics similar to those seen in 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 te, we performed fluorescence recovery after photobleaching experiments in living cells, which expres

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

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

31 Photobleaching experiments in vivo demonstrated that the

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

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

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

35 Photobleaching experiments indicate that actin and tubul

36 Photobleaching experiments indicate that both hypertonic

37 Immunolocalization and photobleaching experiments indicate that individual vesi

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

39 Photobleaching experiments indicated that co-assembly of

40 Photobleaching experiments indicated that different grou

41 Photobleaching experiments indicated that Golgi-to-ER pr

42 Finally, photobleaching experiments indicated that PIP2 binding i

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

44 Through fluorescence recovery after photobleaching experiments, many components of the AMR h

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

46 Fluorescence recovery after photobleaching experiments on green fluorescent protein

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

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

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

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

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

52 Photobleaching experiments provide direct evidence that

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

54 In vivo photobleaching experiments provided direct evidence that

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

56 Photobleaching experiments reveal that centrosome-bound

57 Fluorescence recovery after photobleaching experiments reveal that polar PBP3 molecu

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

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

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

61 Photobleaching experiments revealed that CD94/NKG2A-EGFP

62 RNAi depletion, genome editing, and photobleaching experiments revealed that DDR-2 signals t

63 Photobleaching experiments revealed that during initial

64 Photobleaching experiments revealed that during normal i

65 Fluorescence-recovery-after-photobleaching experiments revealed that Kv2.1, VAPA, an

66 Photobleaching experiments revealed that OSER-inducing p

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

68 Selective photobleaching experiments revealed that single BSEP-YFP

69 Photobleaching experiments revealed that SUMO-1 dynamics

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

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

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

73 Fluorescence loss in photobleaching experiments show subnuclear concentration

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

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

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

77 Photobleaching experiments show that the new Golgi is no

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

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

80 Photobleaching experiments showed that Sec13 shuttles be

81 Fluorescence recovery after photobleaching experiments showed that the effector prot

82 Fluorescence recovery after photobleaching experiments showed that, under conditions

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

84 Photobleaching experiments suggest that vesicles move by

85 4 as measured by fluorescence recovery after photobleaching experiments, the rapid sequestration of a

86 These data, together with photobleaching experiments to measure nucleolar protein

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

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

89 Using photobleaching experiments, we analyzed the dynamics of

90 scopy (cryo-EM) analysis and single-molecule photobleaching experiments, we uncover three major struc

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

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

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

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

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

96 In summary, any inference from photobleaching experiments with B > 0.1 is likely to be

97 Photobleaching experiments with live cells revealed that