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. 2019 Aug 13;12(8):dmm040238. doi: 10.1242/dmm.040238

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© 2019. Published by The Company of Biologists Ltd

This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution and reproduction in any medium provided that the original work is properly attributed.

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Fig. 3. — No differences in diameter identified when analysing ASMA⁺ blood vessels. (A) Representative images from the ventral horn area of lumbar spinal cord tissue from WT (left) and FUS (1-359) (right) transgenic mice obtained at P50 (top) and at P90 (bottom). Insets show magnified view of boxed areas; arrows indicate pericyte cell bodies; n indicates nuclei. (B) Scatter-plot graphs showing the quantified diameter of ASMA⁺ blood vessels per lumbar ventral horn at P50 [left; WT n=6, FUS (1-359) n=8] and P90 [right; WT n=7, FUS (1-359) n=9]. Each datapoint represents mean diameter from six non-consecutive tissue slices along the lumbar spinal cord, dark grey lines represent mean±s.e.m. t-test between FUS (1-359) and WT groups non-significant in all cases.