Figure 3
From: Diverse species-specific phenotypic consequences of loss of function sorting nexin 14 mutations
Homozygous Snx14 mutation causes placental abnormalities in mice. (A, B) Placentas from E10.5 mice were examined with hematoxylin and eosin (H&E) stain to examine tissue structure. (C, D) Monocarboxylate transporter 4 (MCT4, green) is expressed in syncitiotrophoblasts of the labyrinthine zone. (E, F) E-Cadherin (CDH1, magenta). (C–F) Sections were counterstained with DAPI (Blue). Maternal decidua (M), giant cells (G), spongiotrophoblasts (S) and labyrinth (L).
