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. 2010 Feb 1;25(7):2107–2119. doi: 10.1093/ndt/gfq006

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© The Author 2010. Published by Oxford University Press [on behalf of the ERA-EDTA]. All rights reserved. This is an Open Access article of the Creative Commons Attribution License (http://creativecommons.org/licenses?by-nc/2.0/uk) which permits unres distribution, and reproduction in any medium, provided the original work is properly cited.

This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/2.5),which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.

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Fig. 2 — Localization of claudin-2, -10 and -11: photomicrographs showing serial sections of human renal cortical tissue stained for N-cadherin (A), E-cadherin (B), claudin-2 (C), L. tetragonolobus (D), claudin-10 (E), D. biflorus (F) and claudin-11 (G); representative negative control (H) [N-cadherin and claudin-2 stained strongly positive in L. tetragonolobus positive proximal tubules which showed faint discrete junctional staining for claudin-10 and E-cadherin, faint cytoplasmic staining for claudin-11 and negative for D. biflorus (asterisks, A–G); in addition, strongly positive claudin-10 and -11 staining coincided with strong E-cadherin staining in tubules with a subpopulation of cells intensely stained with D. biflorus suggestive of TAL (arrows); scale bar 100 µm].