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GoPubMed Proteins lists recent and important papers and reviews for proteins. Page last changed on 19 Aug 2016.

FBJ osteosarcoma oncogene

Fos, c-Fos
an immediate early gene encoding a nuclear protein involved in signal transduction [RGD, Feb 2006] (from NCBI)
Top mentioned proteins: AP-1, CAN, V1a, HAD, ACID
Papers using Fos antibodies
Maintenance of the Foxp3-dependent developmental program in mature regulatory T cells requires continued expression of Foxp3
Baumgrass Ria et al., In Frontiers in Immunology, 2006
... IL-2-APC (BD), IL-4-PE (BD), IL-17-PE (eBioscience), IFN-γ-Pacific orange (own in-house antibody), NFATc2-FITC (own antibody, BD), c-Fos-A488 (Santa Cruz Biotechnology), phospho-c-Jun-A488 (Santa Cruz Biotechnology), ...
Photobleaching correction in fluorescence microscopy images.
Dryer Stuart E., In PLoS ONE, 2006
... The specific antibody against rat c-Fos was raised in rabbit (Sigma Aldrich) and used in a dilution ...
Kalanchosides A-C, new cytotoxic bufadienolides from the aerial parts of Kalanchoe gracilis
Bharti Alok C et al., In BMC Complementary and Alternative Medicine, 2005
... actin, c-Jun, JunB, JunD, and c-Fos were purchased from Santa Cruz Biotechnology (Santa Cruz, CA) ...
History and new insights into host defense against vaginal candidiasis.
Brand Alexandra Carolyn, In PLoS ONE, 2003
... Antibodies to phospho-p38, phospho-ERK1/2, phospho-JNK, phospho-MKP1, phospho-IκBα, IκBα and c-Fos were purchased from Cell Signalling Technologies (New England Biolabs, UK) ...
Regulation of Ras–MAPK pathway mitogenic activity by restricting nuclear entry of activated MAPK in endoderm differentiation of embryonic carcinoma and stem cells
Xu Xiang-Xi et al., In The Journal of Cell Biology, 1998
... Dab2/p96 monoclonal, clathrin heavy chain monoclonal, and Erk1 monoclonal (BD Biosciences); Elk-1 polyclonal, phospho-Elk-1 monoclonal, c-Fos polyclonal, and PEA-15 polyclonal (Santa Cruz Biotechnology, Inc.); phospho-Erk2/1 monoclonal and ...
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Papers on Fos
Signaling Network Controlling Androgenic Repression of c-Fos in Prostate Adenocarcinoma Cells.
Danielpour et al., United States. In J Biol Chem, Feb 2016
UNASSIGNED: The transcription factor c-Fos controls many important cellular processes including cell growth and apoptosis.
Lactobacillus plantarum L67 glycoprotein protects against cadmium chloride toxicity in RAW 264.7 cells.
Lim et al., Kwangyang, South Korea. In J Dairy Sci, Feb 2016
It also significantly suppressed inflammatory factors such as AP-1 (c-Jun and c-Fos), mitogen-activated protein kinases (ERK, JNK, and p38), and inducible nitric oxide synthase.
Retrograde Melanopsin Signaling Increases With Age in Retinal Degenerate Mice Lacking Rods and the Majority of Cones.
Vugler et al., London, United Kingdom. In Invest Ophthalmol Vis Sci, Feb 2016
METHODS: We used functional anatomy for c-fos (Fos) and tyrosine hydroxylase (TH) to measure light-driven activation of dopamine neurons along a dorsal-ventral transect in C3H/He wild-type and rodless-coneless rd/rd cl (rdcl) mice aged 3, 5, and >14 months.
Alcohol consumption increases locomotion in an open field and induces Fos-immunoreactivity in reward and approach/withdrawal-related neurocircuitries.
Céspedes et al., Santos, Brazil. In Alcohol, Jan 2016
Additionally, alcohol intake increased Fos-immunoreactivity (Fos-ir) in the prefrontal cortex, in the shell region of the nucleus accumbens, in the medial and central amygdala, in the bed nucleus of the stria terminalis, in the septal region, and in the paraventricular and dorsomedial hypothalamus, structures that have been linked to reward and to approach/withdrawal behavior.
Activation of the hypothalamic-pituitary-adrenal axis in lithium-induced conditioned taste aversion learning.
Lee et al., Seoul, South Korea. In Eur J Pharmacol, Jan 2016
Intraperitoneal injections (ip) of lithium chloride at large doses induce c-Fos expression in the brain regions implicated in conditioned taste aversion (CTA) learning, and also activate the hypothalamic-pituitary-adrenal (HPA) axis and increase the plasma corticosterone levels in rats.
Ethanol-induced anxiolysis and neuronal activation in the amygdala and bed nucleus of the stria terminalis.
Wilson et al., Columbia, United States. In Alcohol, Dec 2015
Rats were then tested for anxiety-like behavior in the light-dark box (LD box) following acute ethanol treatment (1 g/kg; intraperitoneally [i.p.]), and neuronal activation in the amygdala and bed nucleus of the stria terminalis (BNST) was assessed using Fos immunohistochemistry. EPM exposure increased plasma CORT levels without altering plasma NPY levels.
Gut Commensal E. coli Proteins Activate Host Satiety Pathways following Nutrient-Induced Bacterial Growth.
Fetissov et al., Rouen, France. In Cell Metab, Dec 2015
Indeed, intestinal infusions of E. coli stationary phase proteins increased plasma PYY and their intraperitoneal injections suppressed acutely food intake and activated c-Fos in hypothalamic POMC neurons, while their repeated administrations reduced meal size.
Physiological role of aquaporin 5 in salivary glands.
Hosoi, Tokushima, Japan. In Pflugers Arch, Dec 2015
Elevated NF-κB and AP-1 (c-Fos/c-Jun) form a complex that can bind to the NF-κB-responsive element on the AQP5 promoter and thus potentially downregulate AQP5 transcription.
Genome-wide association between YAP/TAZ/TEAD and AP-1 at enhancers drives oncogenic growth.
Piccolo et al., Padova, Italy. In Nat Cell Biol, Sep 2015
By ChIP-seq analyses in breast cancer cells, we discovered that the YAP/TAZ transcriptional response is pervasively mediated by a dual element: TEAD factors, through which YAP/TAZ bind to DNA, co-occupying chromatin with activator protein-1 (AP-1, dimer of JUN and FOS proteins) at composite cis-regulatory elements harbouring both TEAD and AP-1 motifs.
Signalling in inflammatory skin disease by AP-1 (Fos/Jun).
Wagner et al., Madrid, Spain. In Clin Exp Rheumatol, Jul 2015
The sequential recruitment and activation of immune cells is modulated by a combination of cytokines and chemokines, which are regulated by transcription factors, such as AP-1 (Fos/Jun), NF-κB, NFATs, and STATs.
Activity-Induced DNA Breaks Govern the Expression of Neuronal Early-Response Genes.
Tsai et al., Cambridge, United States. In Cell, Jul 2015
Here, using both molecular and genome-wide next-generation sequencing methods, we report that neuronal activity stimulation triggers the formation of DNA double strand breaks (DSBs) in the promoters of a subset of early-response genes, including Fos, Npas4, and Egr1.
A temporal shift in the circuits mediating retrieval of fear memory.
Quirk et al., San Juan, Puerto Rico. In Nature, Apr 2015
Consistent with this, the paraventricular nucleus of the thalamus (PVT), a subregion of the dorsal midline thalamus, showed increased c-Fos expression only at late time points, indicating that the PVT is gradually recruited for fear retrieval.
Function through synthesis-informed design.
Stevens et al., Stanford, United States. In Acc Chem Res, Apr 2015
In this Account, we address studies in our laboratory on function-oriented synthesis (FOS), a strategy to achieve function by design and with synthetic economy.
Neurologic Regulation and Orthodontic Tooth Movement.
Faber et al., In Front Oral Biol, 2014
Tooth movement activates peripheral sensory nerve endings, which transmit painful signals to the brain after being processed at the trigeminal spinal nucleus, resulting in local expression of pain related genes, such as c-Fos.
Fosfomycin: Uses and potentialities in veterinary medicine.
Soraci et al., Tandil, Argentina. In Open Vet J, 2013
Fosfomycin (FOS) is a natural bactericidal broad-spectrum antibiotic which acts on proliferating bacteria by inhibiting cell wall and early murein/peptidoglycan synthesis.
Ghrelin-deficient mice have fewer orexin cells and reduced cFOS expression in the mesolimbic dopamine pathway under a restricted feeding paradigm.
Abizaid et al., Ottawa, Canada. In Neuroscience, 2012
expression of cFOS in the ventral tegmental area (VTA) was reduced after 7 days of restricted feeding in GHSR knock-out animals
Differentiation-induced skin cancer suppression by FOS, p53, and TACE/ADAM17.
Wagner et al., Madrid, Spain. In J Clin Invest, 2012
Epidermal Fos deletion in tumor models induced p53 expression. Epidermal cell differentiation and skin tumor suppression were caused by a p53-dependent transcriptional activation of the metalloprotease TACE.
Forced expression of stabilized c-Fos in dendritic cells reduces cytokine production and immune responses in vivo.
Yoshimura et al., Tokyo, Japan. In Biochem Biophys Res Commun, 2012
These data suggest that c-Fos in dendritic cells plays a suppressive role in certain innate and adaptive immune responses.
[Inhomogeneous hippocampal activation along the rostrocaudal axis in mice after exploration of novel environment].
Anokhin et al., In Zh Vyssh Nerv Deiat Im I P Pavlova, 2012
In mice trained in 8-arm maze C-Fos expression was increased, mainly, in the caudal parts of CA1, CA3 and dentate gyrus as compared to the control group trained to enter the home cage through an isolated arm.
Individual variations in maternal care early in life correlate with later life decision-making and c-fos expression in prefrontal subregions of rats.
Joëls et al., Amsterdam, Netherlands. In Plos One, 2011
maternal care early in life correlate with later life decision-making and c-fos expression in prefrontal subregions
More papers using Fos antibodies
Central poststroke pain and Wallenberg's lateral medullary infarction: Frequency, character, and determinants in 63 patients.
Premkumar Louis S., In PLoS ONE, 1996
... ) with anti-Fos (rabbit polyclonal IgG for c-fos p62; 1∶20,000; Santa Cruz Biotechnology, Santa Cruz, CA, USA), ...
c-fos gene expression in postnatal rat retinas with light/dark cycle
Park Jong Seok et al., In Korean Journal of Ophthalmology : KJO, 1995
... As the primary antibody, the anti-c-Fos antibody (rabbit-polyclonal; Santa Cruz Biotechnology Inc., Santa Cruz, CA, ...
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