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. 2019 Sep 28;1(1):vdz029. doi: 10.1093/noajnl/vdz029

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© The Author(s) 2019. Published by Oxford University Press, the Society for Neuro-Oncology and the European Association of Neuro-Oncology.

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

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Figure 3. — DNM1 and PLP1 are more expressed in invasive areas of patient-derived xenografts and in patients. (A) Immunostaining of Nestin (red) and DNM1 or PLP1 (green) in the tumor core (upper panels) and in the invasive area (middle panels) of P3 tumors. DAPI was used for nuclear staining (blue). Scale bars: 100 µm. Lower panels represent magnified images as delineated by dashed line squares, with plot profiles defined using Fiji software (defined by white lines). Both DNM1 and PLP1 are cytoplasmic. (B) The graphs represent DNM1 and PLP1 staining intensity of 10 different images from P3 core and invasive areas (Student t-test, ** P < .01; ***P < .001). (C) Immunostaining of DNM1 or PLP1 (green) in the tumor core (upper panels) and in the invasive area (lower panels) of P3 tumors. DAPI was used for nuclear staining (blue). Scale bars: 100 µm. The graphs represent DNM1 and PLP1 staining intensity of 10 different images of core and invasive areas from several patient sections (Student t-test, ***P < .001; ****P < .0001).