GoPubMed Proteins lists recent and important papers and reviews for
proteins. Page last changed on 19 Dec 2016.
Brain expressed myelocytomatosis oncogene
B-Myc, MYCB, B-Myc protein
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Top mentioned proteins:
c-Myc, ACID, MAX, PCNA, L-myc
Papers on
B-Myc
Differential expression of transcription factors and inflammation-, ROS-, and cell death-related genes in organotypic cultures in the modiolus, the organ of Corti and the stria vascularis of newborn rats.
Berlin, Germany. In Cell Mol Neurobiol, 2014
These clusters include the TF Jun, Bmyc, Nfyc, Foxd3, Hes1, the ROS-associated molecules Sod3, and Nos2, and the inflammatory chemokine Ccl20.
Gender-dependent histone deacetylases injury may contribute to differences in liver recovery rates of male and female mice.
Chengdu, China. In Transplant Proc, 2013
Additionally, the hepatocyte proliferation inhibitor B-myc was evaluated as an HDAC1 and HDAC2 target gene.
Loss of Bmyc results in increased apoptosis associated with upregulation of Myc expression in juvenile murine testis.
Turku, Finland. In Reproduction, 2012
The BMYC protein has been shown to function as a transcription factor in vitro and to inhibit MYC.
Impairment of liver regeneration by the histone deacetylase inhibitor valproic acid in mice.
Chengdu, China. In J Zhejiang Univ Sci B, 2012
We identified B-myc as a target gene of HDACs by complementary DNA (cDNA) microarray.
B-myc: N-terminal recognition of myc binding proteins.
GeneRIF
West Lafayette, United States. In Biochemistry, 2006
The results provide new insights into Myc N-terminal protein-protein interactions providing a model for Myc regulation through differential involvement of Myc homology boxes 1 and 2 (MBI and MBII) in the binding of Myc interacting proteins.
Characterization of tylM3/tylM2 and mydC/mycB pairs required for efficient glycosyltransfer in macrolide antibiotic biosynthesis.
Austin, United States. In J Am Chem Soc, 2005
The heterologous expression of tylM3 and mydC, two homologous genes of previously unknown function, along with genes encoding their respective partner glycosyltransferases, tylM2 and mycB, and the necessary sugar biosynthesis genes significantly enhances the glycosyltransferase activity in the engineered Streptomyces venezuelae host in which the native glycosyltransferase, desVII, has been inactivated.
Visualization of Myc/Max/Mad family dimers and the competition for dimerization in living cells.
Ann Arbor, United States. In Mol Cell Biol, 2004
Max formed heterodimers with the basic helix-loop-helix leucine zipper (bHLHZIP) domain of Myc (bMyc) more efficiently than it formed homodimers.
Immortalization of epididymal epithelium in transgenic mice expressing simian virus 40 T antigen: characterization of cell lines and regulation of the polyoma enhancer activator 3.
Turku, Finland. In Endocrinology, 2004
Epididymal tumorigenesis was associated with an increase in c-Myc expression, and a marked decrease in B-Myc expression, with a 500-fold lower level in the GPX5-Tag1 caput epididymis compared with wild-type caput.
Organization of the biosynthetic gene cluster for the polyketide macrolide mycinamicin in Micromonospora griseorubida.
Funabashi, Japan. In Fems Microbiol Lett, 2003
Immediately downstream of mycA, there is a set of genes for desosamine biosynthesis (mydA-G and mycB).
Fumonisin B(1)-induced alterations in cytokine expression and apoptosis signaling genes in mouse liver and kidney after an acute exposure.
Athens, United States. In Toxicology, 2002
Treatment of mice with FB(1) increased the expression of B-Myc, c-Myc and Max, oncogenic transcription factors in the kidney.
Modulation of selected cell signaling genes in mouse liver by fumonisin B1.
Athens, United States. In Chem Biol Interact, 2002
Expression of oncogenic transcription factors, c-Myc, B-Myc, Max and Mad, and apoptotic genes, namely Bcl-2, Bax and Bad, was increased after FB1 treatment.
Cloning, sequencing, and characterization of the iturin A operon.
Yokohama, Japan. In J Bacteriol, 2001
Comparison of the amino acid sequences encoded by the iturin A operon and the mycosubtilin operon revealed that ituD, ituA, and ituB have high levels of homology to the counterpart genes fenF (79%), mycA (79%), and mycB (79%), respectively.
B-Myc, a proximal caput epididymal protein, is dependent on androgens and testicular factors for expression.
Lubbock, United States. In Biol Reprod, 2001
Furthermore, in situ and immunohistochemical analyses show that within the epididymis B-myc mRNA and protein are specifically expressed by the epithelial cells and that B-Myc protein is localized to both the nuclear and cytosolic compartments.
Autonomously replicating sequences identified in transcriptional regulatory regions of human N-myc gene.
Sapporo, Japan. In Int J Oncol, 1994
Among the cell lines obtained, only the cells co-transfected with pN-mycP-B, the region of which contains enhancer activity described above, harboured the replicated pN-mycB-P in an episomal state.
The myc gene family proteins and their role in transformation and differentiation.
Review
Stockholm, Sweden. In Semin Cancer Biol, 1990
In normal tissues, expression of Nmyc and Lmyc is restricted to embryonic development and a few adult tissues whereas c-myc and Bmyc are very widely expressed.
