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Here, we used reflectance confocal microscopy (RCM) imaging in humans and in mice to visualize tumor architecture in vivo.
Here, we generated knock-in mice to visualize SPIG1-expressing cells with green fluorescent protein.
In a few instances, we used Pax2-GFP transgenic mice to visualize GABAergic interneurons [51].
We recently generated knock-in mice to visualize SPIG1-expressing cells with green fluorescent protein (GFP) [31].
Recordings were made from adult Atoh1/nGFP transgenic mice to visualize Merkel cells within the intact skin.
Murphy and colleagues utilized Ephrin- B2-H2BGFP mice to visualize the nuclei of arterial ECs to examine the dynamics of cells during formation and regression of arterial venous malformations [ 145].
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In summary, our anatomical studies made use of a Dab1 lacZ reporter mouse to visualize all cells potentially responsive to reelin signalling.
Taketani et al. applied a miniaturized Raman endoscope (mRE) system as a noninvasive in situ method for monitoring the advancement of colorectal tumors in model mice and to visualize and measure the Raman spectra of any targeted point within the colorectal tumor without damaging the tissues [107].
Multiphoton Imaging of Rac-FRET Mouse Intestine, Related to Figure 5 Ex vivo multiphoton z stack imaging of Rac-FRET mouse intestine to visualize the 3D space investigated from the base of the crypts towards the villi (0 150 μm).
After different times, cells were fixed with 3% paraformaldehyde (PF), permeabilized with 0.1% Triton X-100, and stained with FITC-labelled goat-anti-mouse IgG to visualize antibodies bound to and internalized in the cells.
Next, we applied another widely used angiogenesis model, postnatal mouse retina, to visualize postnatal angiogenesis and vessel network patterning.
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