The copyright line for this article was changed on July 25, 2014 after original online publication.
Characterization of a population of neural progenitor cells in the infant hippocampus
Version of Record online: 1 JUL 2014
© 2013 The Authors. Neuropathology and Applied Neurobiology published by John Wiley & Sons Ltd on behalf of British Neuropathological Society.
This is an open access article under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
Neuropathology and Applied Neurobiology
Volume 40, Issue 5, pages 544–550, August 2014
How to Cite
Paine, S. M. L., Willsher, A. R., Nicholson, S. L., Sebire, N. J. and Jacques, T. S. (2014), Characterization of a population of neural progenitor cells in the infant hippocampus. Neuropathology and Applied Neurobiology, 40: 544–550. doi: 10.1111/nan.12065
- Issue online: 1 JUL 2014
- Version of Record online: 1 JUL 2014
- Accepted manuscript online: 6 JUN 2013 10:44PM EST
- Manuscript Accepted: 31 MAY 2013
- Manuscript Received: 22 JAN 2013
- Great Ormond Street Hospital Children's Charity
- HEFCE Clinical Senior Lecturer Awards
Figure S1. Positive controls were stained in parallel with the cases and each showed the expected pattern of immunoreactivity. CD31 (brain, A), CD34 (brain, B), CD45 (tonsil, C), CD68 (brain, D), CD133 (pancreas, E), DCX (brain, F), EMA (brain, G), GFAP (brain, H), HLA-DR (tonsil, I), Ki67 (small intestine, J), MAP2 (brain, K), nestin (brain, L), Oct3/4 (germinoma, M), SOX2 (focal cortical dysplasia, N), TUJ1 (small intestine, O), vimentin (brain, P). All images × 20 objective.
Figure S2. The rod cells (arrows) were negative for the immunostains CD31 (A), CD133 (B), EMA (C), GFAP (D), MAP2 (F), Oct3/4 (G), SOX2 (H) and vimentin (I). An occasional rod cell was positive for Ki67 (white arrow, E), an epitope that is particularly prone to post mortem degradation. All images × 20 objective.
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