ライフサイエンスコーパス: fluorescent speckle microscopy

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1 al and contrast relative to classic (random) fluorescent speckle microscopy.

2 ellae of migrating cells, using quantitative Fluorescent Speckle Microscopy.

3 ion of rhodamine-conjugated (rh)-tubulin and fluorescent speckle microscopy.

4 omparable to results in two dimensions using fluorescent speckle microscopy.

5 this dynamic interface using high resolution fluorescent speckle microscopy and direct labeling of ki

6 Methods such as fluorescent speckle microscopy and spatial temporal imag

7 We have used multimode fluorescent speckle microscopy (FSM) and correlative dif

8 Fluorescent speckle microscopy (FSM) is a method for mea

9 Fluorescent speckle microscopy (FSM) is a new technique

10 Fluorescent Speckle Microscopy (FSM) is a technology for

11 lapse dual-wavelength spinning-disk confocal fluorescent speckle microscopy (FSM) of MTs and f-actin

12 We report here a method called fluorescent speckle microscopy (FSM) that uses a very lo

13 ent issue of the Journal of Cell Biology use fluorescent speckle microscopy (FSM) to analyze the rela

14 Using fluorescent speckle microscopy (FSM) to assess actin dyn

15 Here we use fluorescent speckle microscopy (FSM) to demonstrate that

16 We have used multimode fluorescent speckle microscopy (FSM) to directly address

17 Using fluorescent speckle microscopy (FSM), differential inter

18 nce recovery after photobleaching (FRAP) and fluorescent speckle microscopy (FSM).

19 Using quantitative fluorescent speckle microscopy, immunofluorescence, and

20 Fluorescent speckle microscopy is a new and simplified m

21 otubule dynamics and translocation using the fluorescent speckle microscopy microtubule marking techn

22 Computational analysis of fluorescent speckle microscopy movies of migrating epith

23 In addition, as determined by fluorescent speckle microscopy, MT polymerization rarely

24 Time-lapse fluorescent speckle microscopy of fluorescently labeled

25 cells with fluorescently labeled tubulin for fluorescent speckle microscopy on kinetochore microtubul

26 We performed fluorescent speckle microscopy on spreading Drosophila S

27 Using quantitative fluorescent speckle microscopy (qFSM) of migrating epith

28 Furthermore, fluorescent speckle microscopy revealed that detached ki

29 Fluorescent speckle microscopy revealed that rates of ac

30 Fluorescent speckle microscopy reveals that dynactin or

31 sed dual-wavelength digital fluorescence and fluorescent speckle microscopy to analyze microtubules a

32 Here we used fluorescent speckle microscopy to evaluate the influence

33 We use quantitative fluorescent speckle microscopy to map with high resoluti

34 We developed correlational fluorescent speckle microscopy to measure the coupling o

35 We used fluorescent speckle microscopy to probe the dynamics of

36 ad to enhance the resolution of quantitative Fluorescent Speckle Microscopy to the submicron level.

37 nsfected keratocytes with GFP-actin and used fluorescent speckle microscopy, to observe speckle flow.

38 s article, we describe the basic concepts of fluorescent speckle microscopy, total internal reflectio

39 Using combined traction force and fluorescent speckle microscopy, we observed a robust bip

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