Myocyte enhancer factor 2C, an osteoblast
transcription factor identified by dimethyl sulfoxide (DMSO)- enhanced mineralization.
Not exact matches
To see how the mutation affects alpha - synuclein production, the researchers
identified two
transcription factors that bind to the enhancer that carries this mutation.
Currently, enhancers can be
identified through chromatin - based assays, such as ChIP - seq, which predict enhancer elements indirectly based on the enhancer's association with specific epigenomic marks, such as
transcription factors or molecular tags on DNA - associated histone proteins.
In a series of experiments, the researchers first
identified a set of 19
transcription factors that were expressed at significantly greater levels in cultured human glioblastoma stem cells capable of tumor propagation than in differentiated tumor cells.
«
Transcription factors distinguishing glioblastoma stem cells
identified.»
A screen for mouse genes dependent on dHAND, a
transcription factor implicated in neural crest development,
identified Ufd1, which maps to human 22q11 and encodes a protein involved in degradation of ubiquitinated proteins.
In addition, using methods for the analysis of regulatory networks developed by the Califano lab in the Center for Computational Biology and Bioinformatics, Department of Systems Biology, the researchers
identified a number of
transcription factors (gene regulators) that have the potential to mimic the environmental signals that trigger papillae to induce new hair growth.
The key regulator they
identified were the RFX
transcription factors.
The researchers used an example to demonstrate the mechanism: They
identified the
transcription factor STAT3, which regulates inflammatory processes and can promote tumor development, as a prominent target protein of one peroxiredoxin.
To understand defective disease process, investigators need to track where and how
transcription factors bind to DNA to
identify the differences between healthy and diseased cells.
The current study
identified a new role for a particular group of proteins, known as RFX
transcription factors, in the development and survival of the hair cells.
Under the supervision of Professor Jussi Taipale, researchers at Karolinska Institutet have previously
identified most of the DNA words recognised by individual
transcription factors.
A neuro - oncology research team at Dartmouth's Norris Cotton Cancer Center, led by the Director Mark A. Israel, MD with first author Gilbert J. Rahme, PhD, recently
identified the
transcription factor Id4 as a suppressor of tumor cell invasion in glioblastoma.
By studying Arabidopsis plants for which the genes for these
transcription factors had been selectively knocked out, the group
identified a single
transcription factor that when inactive resulted in longer roots.
Some
transcription factors already have been
identified as playing a role in melanoma development.
The team
identified a lncRNA, called NANCI, that regulates the critical
transcription factor Nkx2.1.
An international consortium under the leadership of Prof. Dr. Thomas Laux, a biologist from the University of Freiburg, has
identified the
transcription factor WUSCHEL HOMEOBOX (WOX) 5 as the signal molecule, showing that it moves through pores from the cells inside the quiescent centre into the stem cells.
Using the recently completed tomato genome sequence they then
identified the gene as SlGLK2 — a so - called
transcription factor, which controls when and where other genes are switched on or off.
To start, the scientists examined previous experiments and
identified several
transcription factors — managerial proteins that switch on the activity of large sets of genes — that seemed crucial to the ability of immature neurons to develop into adult sensory neurons.
The researchers
identified a
transcription factor called POU6F2, which is found in developing nerve cells in the retina and corneal cells in mice.
We
identified a protective mechanism that is controlled by the
transcription factor ARNT, which effectively inhibits progression of chronic kidney injury by transcriptional induction of ALK3, the principal mediator of anti-fibrotic and pro-regenerative BMP signaling responses.
A few years ago, Singh and colleagues
identified a
transcription factor called PU.1 that acts as the primary signal, a central genetic switch to initiate development of myeloid progenitor cells.
Researchers
identify a network of a dozen
transcription factors needed to maintain the pluripotent state of mouse embryonic stem cells.
Of 17 regulatory variants
identified in the two genes with regulatory variant burden, we show that at least six alter
transcription factor - DNA binding in human neuroblastoma cells.
One way is to
identify transcription factors, and one way to
identify transcription factors in microRNAs that can be used for reprogramming, is to screen for them through microarrays or RNA sequencing within the embryonic brain tissue.
We have
identified a number of key
transcription factors that are deregulated during this process, and we are using this information to investigate mechanisms by which differentiation can be reprogrammed in tumour cells.
In this publication, Mergoud et al.
identify UNC - 120 / SRF as the first conserved
transcription factor that regulates the pace of muscle aging in a cell autonomous manner, downstream of the insulin / IGF1 receptor.
«This study
identifies how the modification of the DNA structure affects the binding of
transcription factors, and this increases our understanding of how genes are regulated in cells and further aids us in deciphering the grammar written into DNA,» study co-author Jussi Taipale from Karolinska Institutet in Sweden said in a statement.
Through these studies he has
identified a new
transcription factor and associated pathway that could yield new avenues for therapeutic intervention in SMA.
In this study, Mergoud et al.
identify UNC - 120 / SRF as the first conserved
transcription factor that regulates the pace of muscle aging in a cell autonomous manner, downstream of the insulin / IGF1 receptor.
For example, a research team last year used LINCS data to
identify the role of a critical
transcription regulator, heat shock
factor 1 (HSF1), in cancer.
The GDDS laboratory was responsible for first
identifying the
transcription factor SOX10 as a key lineage - specific regulatory
factor in melanocytes that is mutated congenitally in individuals with Waardenburg syndrome IV.
Evidence from mouse knockout models and human mendelian disorders suggest that these
transcription factors have a function in determining cell
identify in the developing breast.
ChIP - Seq is a powerful tool to study genetic regulation, because it enables one to accurately
identify regions of DNA bound by specific proteins, such as
transcription factors or RNA Polymerase II components.
Here, we
identify three additional novel mutant alleles of the SHELL gene, which encode a type II MADS - box
transcription factor, and determine oil yield via control of shell fruit form phenotype in a manner similar to two previously
identified mutant SHELL alleles.
In addition, well - characterized expression profiles for melanoma cells have been
identified that correlate highly proliferative cell states with increased expression for pathways regulated by the lineage - specific
transcription factors SOX10 and MITF; conversely, migratory / invasive cell states have been correlated with TGFβ1 signaling pathways.
Other researchers had
identified a
transcription factor called C / EBPα as another development trigger.
Approximately 50 % of PTCL are unclassifiable and categorized as PTCL, not otherwise specified (PTCL - NOS).1 Using gene expression profiling, PTCL - NOS lymphocytes can be distinguished from normal T lymphocytes, with deregulation of genes involved in apoptosis, proliferation, cell adhesion, and
transcription regulation.2 Two subgroups of PTCL - NOS have been
identified, which are characterized by high expression of either GATA3 or TBX21 / T - bet
transcription factors and downstream target genes.3 However, actionable biomarkers closely related to the pathogenic mechanism need to be further investigated and may become potential therapeutic targets of PTCL - NOS. 4, 5
We used a bioninformatics analysis to
identify that miR - 181a targets components of the bone morphogenetic protein (BMP) signalling pathway, including the
transcription factors Smad1 and Smad5, which we find are expressed by rat mDA neurons and are required for BMP - induced neurite growth.
Their system was based on earlier studies in which Singh and his colleagues
identified a
transcription factor called PU.1 as a central genetic switch that triggers development of myeloid progenitor cells.
In last years, the «Stress and Cancer» laboratory has
identified two new molecular players of the oxidative stress response, the miR - 200 family of microRNA and the
transcription factor JunD.
Using our own data and publically available data from array comparative genomic hybridization (aCGH), we
identified a minimal deletion for the cardiomyopathy associated with del1p36 that included only the terminal 14 exons of the
transcription factor PRDM16 (PR domain containing 16), a gene that had previously been shown to direct brown fat determination and differentiation.
For example, our studies
identified transcription factors, RNA binding proteins, and signaling genes as critical miRNA targets during contexts such as development of peripheral sensory organs, wing, eye, and CNS, or during behavioral contexts such as egg - laying, rhythmic behavior, and locomotor activity (Figure 2).
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Identifying the
transcription factors mediating enhancer — target gene regulation in the human genome.
Measurements that are increasingly available range from those that
identify transcription factor occupancy and initiation of
transcription to long - lasting and heritable epigenetic marks such as DNA methylation.
Exploiting
transcription factor binding site clustering to
identify cis - regulatory modules involved in pattern formation in the Drosophila genome B.P. Berman, Y. Nibu, B.D. Pfeiffer, P. Tomancak, S.E. Celniker, M. Levine, G.M. Rubin, M.B. Eisen Proc Natl Acad Sci U S A (2002) 99:757 - 762
The first is
identifying relevant
transcription factors to reprogram stem cells, and the second is finding potential drugs with off - label benefits or adverse effects.
IRF8, a crucial
transcription factor for pDC development and activation, was
identified as a target of miR - 618.
Here we show that the
transcription factor Gata6 controls the identity of the previously uncharacterized sebaceous duct (SD) lineage and
identify the Gata6 downstream
transcription factor network that specifies a lineage switch between sebocytes and SD cells.
Scientists from Massachusetts Eye and Ear have
identified a new
transcription factor involved in retinal neovascularization: Runt - related
transcription factor 1 (RUNX1).