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. 2015 Feb 6;10(2):e0117370. doi: 10.1371/journal.pone.0117370

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© 2015 Bougerol et al

This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.

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Fig 10 — Visualization of spinal GFP⁺ neurons at x40 in fluorescence condition (A1) and infrared condition (A2) in a whole-mount isolated in vitro preparation of brainstem-spinal cord with dorsal-side opened. Patch-clamp intracellular recordings (bottom traces) of spinal GFP⁺ neurons (Intra.) either with a persisting (B1), a non-persisting firing pattern (B2), or a slow-delayed firing pattern (B3) during spontaneous fictive swimming episodes (f. sw.). The upper trace in B1–B3 represents the extracellular fictive swimming activity recorded simultaneously in a ventral motor root (Vr). DIC, differential interference contrast. The white arrowhead points to the GFP⁺ neuron targeted for patch clamp recording.