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. 2012 Sep 24;6:65. doi: 10.3389/fncir.2012.00065

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Copyright © 2012 Magno, Oliveira, Mucha, Rubin and Kessaris.

This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in other forums, provided the original authors and source are credited and subject to any copyright notices concerning any third-party graphics etc.

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Embryonic origin of type I and type II nNOS cortical interneurons. (A) Coexpression of nNOS and GFP/YFP/Venus/β-gal in type I cells in different transgenic mouse lines. Arrows and arrowheads point to double and single-labeled type I cells, respectively. (B) Contribution of different progenitor pools to type I cortical interneurons. The extent of co-localization between nNOS and GFP/YFP/Venus/β-gal in type I cells is shown as a percentage of the total nNOS type I cells (B) or as a percentage of the total GFP/YFP/Venus/ β-gal-expressing interneurons (C). (D) Coexpression of nNOS and GFP/YFP/Venus/β-gal in type II cells in different transgenic mouse lines. Arrows and arrowheads point to double and single-labeled type II cells, respectively. (E) Contribution of different progenitor pools to type II cells. The extent of co-localization between nNOS and GFP/YFP/Venus/β-gal in type II cells is shown as a percentage of the total nNOS type II cells (E) or as a percentage of the total GFP/YFP/Venus/β-gal-expressing interneurons (F). Error bars indicate SEM. Scale bar: 20 μm.