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. 2017 Aug 28;27(11):5353–5368. doi: 10.1093/cercor/bhx220

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© The Author 2017. Published by Oxford University Press.

This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com

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Figure 1. — Light microscopic characterization of YFP-immunolabeled cells in the barrel cortex of the VIPcre-YFP mouse. (A) Distribution of the population of VIP cells in mouse barrel field shown in a 50 μm-thick, osmium-intensified and resin-embedded section. Most cells are located in superficial layers I–IV whereas much fewer are found in deep layers Va, Vb and VI. (B) Morphology of a cluster of bipolar VIP cells in layer II/III (left inset in A). (C) Multipolar VIP cell in layer Va (right inset in A). Arrows indicate primary dendrites. Scale bars = 100 μm in A; 10 μm in B, C.