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Molecular mechanisms for somatostatin inhibition of c-fos gene expression
American Journal of Physiology-Gastrointestinal and Liver Physiology, 1997We reported previously that somatostatin inhibits the expression of the immediate early gene c-fos. Accordingly, we characterized the molecular mechanisms by which somatostatin inhibits c-fos gene expression. Because growth factors activate c-fos through a region of its promoter known as the serum response element [SRE; base pairs (bp) -357 to -276 ...
A, Todisco +4 more
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The c-fos gene and early-onset familial Alzheimer's disease
Neuroscience Letters, 1993A gene for early-onset familial Alzheimer's disease (FAD) is located on chromosome 14q24.3. The c-fos gene (FOS) is also located in the same band of this chromosome and is thus a candidate for the FAD locus. A yeast artificial chromosome (YAC) clone was identified which contains FOS.
Lori L.C. Bonnycastle +13 more
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Cell, 1983
The complete nucleotide sequence of the FBJ-MuSV proviral DNA and the cellular homolog (c-fos) of its oncogene (v-fos) have been determined. The 4026 nucleotide long FBJ-MuSV proviral DNA contains two long terminal repeats, a substitution of 1639 nucleotides of mouse cellular DNA (v-fos) and the 3' end of the env gene derived from FBJ-MuLV.
C, Van Beveren +4 more
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The complete nucleotide sequence of the FBJ-MuSV proviral DNA and the cellular homolog (c-fos) of its oncogene (v-fos) have been determined. The 4026 nucleotide long FBJ-MuSV proviral DNA contains two long terminal repeats, a substitution of 1639 nucleotides of mouse cellular DNA (v-fos) and the 3' end of the env gene derived from FBJ-MuLV.
C, Van Beveren +4 more
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Gene, 2008
We present herein a new model for the structure of the Drosophila kayak gene as well as preliminary data on the functional differences of its various isoforms. kayak is a homolog of the human proto-oncogene, c-fos. kayak has three different starts of transcription, and therefore promoters (P)kay-alpha, (P)kay-beta and (P)kay-gamma.
Stephanie Gidget, Hudson +1 more
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We present herein a new model for the structure of the Drosophila kayak gene as well as preliminary data on the functional differences of its various isoforms. kayak is a homolog of the human proto-oncogene, c-fos. kayak has three different starts of transcription, and therefore promoters (P)kay-alpha, (P)kay-beta and (P)kay-gamma.
Stephanie Gidget, Hudson +1 more
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Proto-oncogene fos: an inducible multifaceted gene.
Symposium on Fundamental Cancer Research, 1988Proto-oncogene fos, which is expressed during cell growth and cell differentiation and development, is a multifaceted gene. The viral homolog, v-fos, was identified as the resident transforming gene of FBJ-murine osteosarcoma virus, which induces bone tumors in mice. Owing to an in-frame deletion during the biogenesis of the v-fos gene, the products of
R L, Mitchell, S K, Hanks, I M, Verma
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Gene, 1998
In contrast to c-jun and junB, the junD gene is constitutively expressed in quiescent cells. The junD promoter, therefore, may provide a paradigm for promoters mostly active in growth arrested cells. We report here that the human junD promoter is repressed by serum and TPA.
I, Berger, Y, Shaul
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In contrast to c-jun and junB, the junD gene is constitutively expressed in quiescent cells. The junD promoter, therefore, may provide a paradigm for promoters mostly active in growth arrested cells. We report here that the human junD promoter is repressed by serum and TPA.
I, Berger, Y, Shaul
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A Fos-Jun element in the first intron of an α2u-globulin gene
Molecular and Cellular Biochemistry, 1993The hepatic expression of the alpha-2u-globulin gene family is controlled by a variety of hormones including steroids, growth hormone and insulin. The mechanisms by which these hormones affect alpha 2u-globulin expression are only partially understood. Recently we isolated and characterized clone RAP 01, an alpha 2u-globulin gene expressed in the liver.
P, van Dijck +4 more
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Fos-transformation activates genes associated with invasion.
Oncogene, 1994Fos oncoproteins transform cells by functioning as transcription factors. Over-expression of c-fos results in minimal morphological transformation while the two viral isolates, FBJ and FBR v-fos, result in full morphological transformation. Fos-transformed cells are serum dependent for proliferation but not for morphological transformation. To identify
R F, Hennigan, K L, Hawker, B W, Ozanne
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The immediate early genes Fos and Egr1 become STAT1 transcriptional targets in the absence of STAT3
FEBS Letters, 2011D. Schiavone +3 more
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Progress in Neuro-psychopharmacology and Biological Psychiatry, 2004
S. Kyosseva
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S. Kyosseva
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