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By means of surface plasmon resonance and atomic force microscopy we analyzed the formation and subsequently the structure of these solid-supported membranes.
Here, using immunofluorescence and electron microscopy, we analyzed sarcomere formation and myofibril organization after siRNA-mediated knockdown of skNAC or Smyd1 expression in murine C2C12 skeletal muscle cells.
Using intravital fluorescence microscopy we analyzed vascularization of the implants and venular leukocyte endothelial cell interaction in the surrounding host tissue over a 14 day period.
Using cryogenic electron microscopy, we analyzed the non-AAA structure of the p28-bound human RP at 4.5 Å resolution and determined seven distinct conformations of the Rpn1-p28-AAA subcomplex within the p28-bound RP at subnanometer resolutions.
Using in vivo near-infrared reflected-light oblique transillumination (RLOT) microscopy, we analyzed leukocyte adhesion, transmigration, and interstitial migration upon microinjection with relevant chemoattractants including MIP-1α, PAF, or fluorescent-labeled E. coli.
By laser confocal microscopy, we analyzed double immunolabeling of peroxisomes co-stained for phosphorylated tau.
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Using electron microscopy (EM), we analyzed micro-structural alterations in intracellular organelles focusing on mitochondria and the ER.
By confocal microscopy analysis, we analyzed the subcellular localization pattern of Numb transfected in HEK293 cells in the presence or absence of CA-PKC θ.
Using structured illumination super resolution microscopy (SR-SIM), we analyzed ATR and Nup153 colocalization in prophase cells.
"... Using electron microscopy and serial reconstructions, we analyzed the dendritic trees of four morphologically distinct neocortical interneuron subtypes to reveal two underlying organizational principles common to all.
Using light microscopy and electron tomography we analyzed the bundle organization of interphase microtubules in S. pombe.
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