Figure - PMC

Skip to main content

An official website of the United States government

Here's how you know

Here's how you know

Official websites use .gov
A .gov website belongs to an official government organization in the United States.

Secure .gov websites use HTTPS
A lock ( ) or https:// means you've safely connected to the .gov website. Share sensitive information only on official, secure websites.

View full-text article in PMC

. 2018 Mar 5;9:58. doi: 10.3389/fgene.2018.00058

Search in PMC
Search in PubMed
View in NLM Catalog
Add to search

Copyright © 2018 Kovalchuk, Ilnytskyy, Rodriguez-Juarez, Katz, Sidransky, Kolb and Kovalchuk.

This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

PMC Copyright notice

Levels of NPAS4, NPAS4 targets and PCNA in the hippocampal tissues of control and TNBC and PR+BC TumorGraft mice. Schematic representation of the control of NPAS4 protein by AKT1 and ERK1/2 pathways. Expression levels of Npas4 gene and its target genes 9Fos, Npr3, and Pcsk1 in TNBC (red) and PR+BC (purple) animals are given in log2 fold change, as compared to controls. Western immunoblotting was performed to deternime the levels of NPAS4, BDNF, FOSB, and PCNA. The graph represents Western immunoblotting results. Data are shown as relative units/percent change from control. Due to protein size differences and scarcity of tissue, membranes were re-used several times. ^*p < 0.05; ^**p < 0.01.