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MOESM2 of Neuroplasticity pathways and protein-interaction networks are modulated by vortioxetine in rodents

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posted on 2017-08-04, 05:00 authored by Jessica Waller, Sara Nygaard, Yan Li, Kristian Jardin, Joseph Tamm, Aicha Abdourahman, Betina Elfving, Alan Pehrson, Connie SĂĄnchez, Rasmus Wernersson
Additional file 2: Figure S1. Merged mouse and rat network (mapped to human proteins) and summary of biological functions of each sub-network. Biological functions were manually extracted from the Function and Gene Ontology fields of the UniProt protein entries. The genes with dark, bold borders were used to build the network of protein–protein interaction partners. Squares with bold borders represent upregulated targets from the rat network, and circles with bold borders indicate differentially-regulated targets from the mouse network. The arrowheads indicate the common targets found in mouse and rat networks. This network of physically-interacting proteins containing clusters related to synaptic plasticity, synaptic transmission, neurodevelopment, cell growth, metabolism, and apoptosis, was significantly modulated in both mouse and rat.

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H. Lundbeck A/S

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