Fryland, Tue Christensen, Jane Pallesen, Jonatan Mattheisen, Manuel Palmfeldt, Johan Bak, Mads Grove, Jakob Demontis, Ditte Blechingberg, Jenny Ooi, Hong Nyegaard, Mette Hauberg, Mads Tommerup, Niels Gregersen, Niels Mors, Ole Corydon, Thomas Nielsen, Anders Børglum, Anders Additional file 10: of Identification of the BRD1 interaction network and its impact on mental disorder risk Upregulation of BRD1-S and BRD1-L. A QPCR measurement of BRD1 mRNA in BRD1-S and BRD1-L cells showed a ~24-fold higher BRD1 mRNA levels compared to HEK293T controls (*P <0.0001). Error bars indicate the standard error of the mean from n = 2 independent RNA samples. B Western blotting analysis using an antibody against endogenous BRD1 (BRD1 S/L) showed high levels of BRD1-S and BRD1-L in the stable cell lines compared to the expression level of BRD1 in HEK293T cells (293 T). D Expression array data showing log2 fold change values for probes that target BRD1 and seven housekeeping genes: Glyceraldehyde 3-phosphate dehydrogenase (GAPDH), Ubiquitin C (UBC), TATA box binding protein (TBP), hypoxanthine phosphoribosyltransferase 1 (HPRT1), Beta Actin (ACTB), Beta-2 microglobulin (B2M), and glucuronidase beta (GUSB). (PDF 76 kb) Functional genomics;Mental disorders;Schizophrenia;Interactome;Regulome;Proteomics;Chip-seq 2016-05-03
    https://springernature.figshare.com/articles/journal_contribution/Additional_file_10_of_Identification_of_the_BRD1_interaction_network_and_its_impact_on_mental_disorder_risk/4383374
10.6084/m9.figshare.c.3617657_D10.v1