Acute cocaine - A-FOS mouse vs. Littermate control
Description:
Acute cocaine - A-FOS mouse vs. Littermate control DNA microarray Change in gene expression Animals received a single injection of cocaine (30 mg / kg intraperitoneal) and the striatum harvested at 24 hours. Avadis Microarray analysis software; standard unpaired T-test. A p < 0.001 was used as a cutoff for the selection of genes. Genes are considered up or down regulated if their expression changed 1.4 fold relative to basal conditions. (NIF Table ID 334 [184])
Authors:
Paletzki RF, Myakishev MV, Polesskaya O, Orosz A, Hyman SE, Vinson C
Cellular DNA-binding proteins encoded by the c-fos genes (GENES, FOS). They are involved in growth-related transcriptional control. c-fos combines with c-jun (PROTO-ONCOGENE PROTEINS C-JUN) to form a c-fos/c-jun heterodimer (TRANSCRIPTION FACTOR AP-1) that binds to the TRE (TPA-responsive element) in promoters of certain genes.
Generated by gene2mesh v. 1.1.1
Retrovirus-associated DNA sequences (fos) originally isolated from the Finkel-Biskis-Jinkins (FBJ-MSV) and Finkel-Biskis-Reilly (FBR-MSV) murine sarcoma viruses. The proto-oncogene protein c-fos codes for a nuclear protein which is involved in growth-related transcriptional control. The insertion of c-fos into FBJ-MSV or FBR-MSV induces osteogenic sarcomas in mice. The human c-fos gene is located at 14q21-31 on the long arm of chromosome 14.
Generated by gene2mesh v. 1.1.1
Transforming proteins coded by fos oncogenes. These proteins have been found in the Finkel-Biskis-Jinkins (FBJ-MSV) and Finkel-Biskis-Reilly (FBR-MSV) murine sarcoma viruses which induce osteogenic sarcomas in mice. The FBJ-MSV v-fos gene encodes a p55-kDa protein and the FBR-MSV v-fos gene encodes a p75-kDa fusion protein.
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A basic-leucine zipper transcription factor that is closely related to C-FOS PROTEINS. It forms heterodimeric complexes with C-JUN PROTEINS to regulate GENE transcription.
Generated by gene2mesh v. 1.1.1
Acute cocaine - Cocaine vs. Saline Quantitative real-time PCR Change in gene expression Animals received a single injection of saline or cocaine (30 mg / kg intraperitoneal) and the striatum harvested at either 4 hours or 24 hours (time tissue harvested confirmed by author). Prism 4 software used to perform standard T-tests p < 0.05. A negative number indicates an increase in expression in the cocaine treated animal. (NIF Table ID 336 [186])
Authors:
Paletzki RF, Myakishev MV, Polesskaya O, Orosz A, Hyman SE, Vinson C
To identify genetic differences in the EWcp of inbred mouse strains that differ in behaviors relevant to EWcp function, we used publicly available tools from the Allen Brain Atlas to identify 68 tran- scripts that were selectively expressed in the EWcp, and examined their expression within tissue punch microdissection samples containing the EWcp of adult male C57BL/6J (B6) and DBA/2J (D2) mice. Using 96-well quantitative real-time PCR (qPCR) arrays that included the EWcp-specific genes, several other genes of interest, and five housekeeping genes, we identified strain differences in expression of 11 EWcp-specific genes (BC023892, Btg3, Bves, Cart, Cck, Ghsr, Neto1, Postn, Ptprn, Rcn1, and Ucn), two immediate early genes (Egr1 and Fos), and one dopamine-related gene (Drd5). Statistics reported as p-value.
Acute cocaine - A-FOS mouse vs. Littermate control
Description:
Acute cocaine - A-FOS mouse vs. Littermate control DNA microarray Change in gene expression Animals received a single injection of cocaine (30 mg / kg intraperitoneal) and the striatum harvested at 24 hours. Avadis Microarray analysis software; standard unpaired T-test. A p < 0.001 was used as a cutoff for the selection of genes. Genes are considered up or down regulated if their expression changed 1.4 fold relative to basal conditions. (NIF Table ID 334 [184])
Gene expression following traumatic brain injury in humans: Differential expression of genes related to transcriptional control, signal transduction, and cell cycle regulation and apoptosis
Gene expression following traumatic brain injury in humans: Differential expression of genes related to development, differentiation, intracellular interactions, general physiology and pathology, non-transcriptional cellular function, transcriptional control signal transcription, cell cycle regulations and apoptosis.
Gene Ontology (GO) gene set. This set contains genes that have been annotated to the GO term "transcription factor AP-1 complex", which is defined as "A heterodimeric transcription factor complex composed of proteins from the c-Fos, c-Jun, activating transcription factor (ATF) or JDP families. The subunits contain a basic leucine zipper (bZIP) domain that is essential for dimerization and DNA binding. Jun-Fos heterodimers bind preferentially to a heptamer consensus sequence (TPA responsive element (TRE)), whereas Jun-ATF dimers bind the cyclic AMP responsive element (CRE) to regulate transcription of target genes." This gene set was automatically constructed using annotation and ontology data provided by GO and only includes annotations with experimental and curatorial evidence codes (EXP, IDA, IPI, IMP, IGI, IEP, TAS, IC). The transitive closure of this term is taken into account using is_a and part_of relationships. For more information: The Gene Ontology Consortium (GOC), http://geneontology.org This gene set was generated using the GeneWeaver GO loader v. 0.2.8.
Authors:
M Ashburner, CA Ball, JA Blake, D Botstein, H Butler, JM Cherry, AP Davis, K Dolinski, SS Dwight, JT Eppig, MA Harris, DP Hill, L Issel-Tarver, A Kasarskis, S Lewis, JC Matese, JE Richardson, M Ringwald, GM Rubin, G Sherlock
Differentially expressed in the Nucleus accumbens following 24 hr continuous 9.5g/kg/day alcohol drinking vs. water drinking in alcohol preferring rats. Estimated BAC in the alcohol exposed group was > 85mg%. The 406 significanlty different probe sets represent 374 uniquely named genes, with most gene expression differences in the range of 1.1-1.3 fold.
Piechota M, Korostynski M, Solecki W, Gieryk A, Slezak M, Bilecki W, Ziolkowska B, Kostrzewa E, Cymerman I, Swiech L, Jaworski J, Przewlocki R
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