As we visualize a future in which more of our tasks are left to machines — Google's driverless car, computer-guided surgery — we may be able to make our systems easier and safer without inducing complacency.
To test whether the end-on conversion roles of MCAK and CENP-E are restricted to monopolar spindles or are broadly relevant for bipolar spindles as well, we visualized KT-MT attachment status in bipolar spindles.
Although the luminal marker dsRed-HDEL confirms the presence of the ER at the cortex of the bud neck, Sec61 (Luedeke et al., 2005) and all the ER-membrane protein that we visualized, as well as the lipid dye DiOC6 are excluded from the ER in this area.
As we have visualized in Fig. 2 sustaining EE performance is based on having an open modular architecture in the firms involved, and the horizontal integration of these modules (BUs) (Mathews 2012) in the EE.
As an example, we visualized mapped reads to the fog-1 gene locus with the UCSC Genome Browser.
As a result, we visualized how EGCG, FIS, and ERI, modulated signal transduction and cytokine secretion in interrogated cells under basal conditions or following subsequent exposure to stimuli.
Using light microscopy as well as multiphoton confocal microscopy techniques, we visualized in detail the intricate colocalization of tumor and host cells in situ.
The regions were randomly chosen as long as we could visualize the cell body and follow the dendrite.
First, we visualized Syb1 as a GFP-fusion protein in Δrho3 cells.
In order to test this experimentally as suggested by the reviewers, we visualized inhibitory boutons with the markers VGAT, which labels pre-synaptically all inhibitory synapses, and with PV, since PV+ interneurons are the subpopulation in interneurons where ErbB4 is primarily expressed (Fazzari et al., 2010; Wen L et al., 2010).
