Willoughby DS and Rosene J.M. Effects of oral creatine and resistance training on myogenic
regulatory factor expression.
Not exact matches
Transcription
factors are responsible for either inhibiting or promoting the
expression of genes, and master
regulatory transcription
factors are like transcription
factors on steroids: their actions regulate thousands of genes in different kinds of cells.
Hockemeyer says that it's unlikely to be another mutation, but rather an epigenetic change that affects
expression of the telomerase gene, or a change in the
expression of a transcription
factor or other
regulatory proteins that binds to the promoter upstream of the telomerase gene.
The MyD88 - independent pathway required Inferon
regulatory factor 3 — dependent
expression of TNFα to activate NF - κB, and the time required for TNFα synthesis established the delay.
A common haplotype of interferon
regulatory factor 5 (IRF5) regulates splicing and
expression and is associated with increased risk of systemic lupus erythematosus.
Regulated
expression of a gene encoding a nuclear
factor, IRF - 1, that specifically binds to IFN - β gene
regulatory elements.
Lipopolysaccharide stimulates the MyD88 - independent pathway and results in activation of IFN -
regulatory factor 3 and the
expression of a subset of lipopolysaccharide - inducible genes.
Dr. Loftus» current research integrates the identification of these types of epigenetic modifications that mark the melanocyte
regulatory genomic landscape with
regulatory protein and transcription
factor chromatin - binding domains, thus defining groups of non-coding DNA sequences utilized in the control of melanocyte gene
expression.
We are currently testing the hypothesis that these transcription
factors form a genomic
regulatory network, and disruption of that network by mutation destabilizes gene
expression programs, contributing to malignancy.
A short stretch of DNA that regulates gene
expression by acting as a landing platform for
regulatory proteins, e.g. transcription
factors.
Our results reveal the
regulatory mechanisms that interplay to drive transcription
factor occupancy, chromatin state, and gene
expression in complex mammalian cell states.
Specifically, we have generated clusters of transcripts that behave the same way under the entire spectrum of the sixty - seven experimental conditions; we have assembled genes in groups according to their time of
expression during successive days of ES cell differentiation; we have included expression profiles of specific gene classes such as transcription regulatory factors and Expressed Sequence Tags; transcripts have been arranged in «Expression Waves» and juxtaposed to genes with opposite or complementary expression patterns; we have designed search engines to display the expression profile of any transcript during ES cell differentiation; gene expression data have been organized in animated graphs of KEGG signaling and metabolic pathways; and finally, we have incorporated advanced functional annotations for individual genes or gene clusters of interest and links to microarray and genomic
expression during successive days of ES cell differentiation; we have included
expression profiles of specific gene classes such as transcription regulatory factors and Expressed Sequence Tags; transcripts have been arranged in «Expression Waves» and juxtaposed to genes with opposite or complementary expression patterns; we have designed search engines to display the expression profile of any transcript during ES cell differentiation; gene expression data have been organized in animated graphs of KEGG signaling and metabolic pathways; and finally, we have incorporated advanced functional annotations for individual genes or gene clusters of interest and links to microarray and genomic
expression profiles of specific gene classes such as transcription
regulatory factors and Expressed Sequence Tags; transcripts have been arranged in «
Expression Waves» and juxtaposed to genes with opposite or complementary expression patterns; we have designed search engines to display the expression profile of any transcript during ES cell differentiation; gene expression data have been organized in animated graphs of KEGG signaling and metabolic pathways; and finally, we have incorporated advanced functional annotations for individual genes or gene clusters of interest and links to microarray and genomic
Expression Waves» and juxtaposed to genes with opposite or complementary
expression patterns; we have designed search engines to display the expression profile of any transcript during ES cell differentiation; gene expression data have been organized in animated graphs of KEGG signaling and metabolic pathways; and finally, we have incorporated advanced functional annotations for individual genes or gene clusters of interest and links to microarray and genomic
expression patterns; we have designed search engines to display the
expression profile of any transcript during ES cell differentiation; gene expression data have been organized in animated graphs of KEGG signaling and metabolic pathways; and finally, we have incorporated advanced functional annotations for individual genes or gene clusters of interest and links to microarray and genomic
expression profile of any transcript during ES cell differentiation; gene
expression data have been organized in animated graphs of KEGG signaling and metabolic pathways; and finally, we have incorporated advanced functional annotations for individual genes or gene clusters of interest and links to microarray and genomic
expression data have been organized in animated graphs of KEGG signaling and metabolic pathways; and finally, we have incorporated advanced functional annotations for individual genes or gene clusters of interest and links to microarray and genomic resources.
Cell identity is specified by the coordinated action of transcription
factors, which bind to specific DNA
regulatory sequences and turn gene
expression on.
Duntas (2015) articulates, «In susceptible individuals, iodine excess increases intra-thyroid infiltrating Th17 cells and inhibits T
regulatory (Treg) cells development, while it triggers an abnormal
expression of tumor necrosis
factor - related apoptosis - inducing ligand (TRAIL) in thyrocytes, thus inducing apoptosis and parenchymal destruction» (31, p. 721).
The recent recognition that de novo lipogenesis might have relevance for lipid homeostasis in skeletal muscle stems from the realization that Sterol
regulatory element binding protein - 1c (SREBP - 1c), a member of the family of transcription
factors that regulate the
expression of genes involved in lipid storage in liver and adipose tissue, is also present in skeletal muscle at a level close to that observed in the liver, 41,42... [M] ost fascinating are the very recent demonstrations that glucose alone (in the absence of insulin) can stimulate de novo lipogenesis in skeletal muscle cells....