Datasets for the four remaining complexes were collected by a conventional cryo-TEM on a Thermo Fisher Scientific Glacios microscope operated at an accelerating voltage of 200 kV with a 50 m C2 aperture and a 100-m objective aperture, at an indicated magnification of 120 k in nanoprobe TEM mode
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We study molecule mechanisms of such plasticity and aim to modulate the scar response by coaxing scar forming cells to adopt alternative cell fates
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