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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