Because the pathophysiology of cancer is linked to alteration of
cellular gene expression, the bioinformatics toolbox promises to offer countless molecular insights into mechanisms, diagnostics, and new medical interventions for cancer.
On the other hand, using near - term nanotechnology to deliver into cancer cells siRNA or miRNA to alter
cellular gene expression might also make it possible to «repair cancerous cells».
Not exact matches
This so - called microRNA disrupts the
expression of two key
cellular genes called TGF - β and SMAD3, in a process known as RNA interference (RNAi).
«Because many broadly expressed
genes that play key roles in essential
cellular functions are under the control of cell - specific enhancers, the ability to affect enhancer function by knocking down eRNAs could potentially provide a new strategy for altering
gene expression in vivo in a cell - specific manner,» said Glass, noting that in his research, anti-sense oligonucleotides were developed in conjunction with Isis Pharmaceuticals, which suppressed enhancer activity and reduced
expression in nearby
genes.
«TIA - 1 is known for its ability to regulate
gene expression during
cellular stress,» says Hewett, who studies the processes that suppress the severe electrical storms in the brain, leading to seizures.
Understanding the best ways to work with RNA and the various RNA detection methods can help scientists advance our understanding of
gene expression patterns and elucidate the roles of different genomic elements in
cellular function and dysfunction.
By comparing the
gene expression patterns of normal beta cells and insulin - producing cells derived from alpha cells, the researchers confirmed nearly complete
cellular reprogramming.
At the
cellular level, although they share canonical types of inhibitory interneurons (INs) and excitatory principal neurons (PNs), it remains largely unknown to what extent a single type in different brain regions displays similarity in
gene expression, axonal shape, connectivity, and developmental origins.
The goal of the NIH program, as described on its website, is «to understand the principles behind the three - dimensional organization of the nucleus in space and time (the fourth dimension), the role nuclear organization plays in
gene expression and
cellular function, and how changes in the nuclear organization affect normal development as well as various diseases.»
«What George's team has accomplished is a technological tour de force,» said Wyss Institute Founding Director Don Ingber, M.D., Ph.D. «By spotting incredibly subtle but incredibly important changes in
gene expression and precisely defining their position inside the cell, they have helped open the door to a new age of
cellular diagnostics.»
Crucially, the team also showed that a serotonergic neuron's
gene expression and function depend not only on its location in the adult brain stem, but also on its
cellular ancestor in the developing brain.
«We found dysregulated
expression in a suspect
gene complex which adds to evidence that PMDD is a disorder of
cellular response to estrogen and progesterone,» explained Peter Schmidt, M.D. of the NIH's National Institute of Mental Health, Behavioral Endocrinology Branch.
A diamond - based thermometer could be a useful tool in basic biology, Maurer says, noting that a number of biological processes, ranging from
gene expression to
cellular metabolism, are strongly affected by temperature.
Rho - kinase inhibitor Y - 27632 (ROCKi) is a potential drug molecule, which has been reported to support the
gene expressions typical for the chondrocytes, thus restricting their phenotypic conversion to fibroblastic cells upon the
cellular expansion.
With these tools, Verma is revealing how the aberrant
expression of normal
cellular genes can causes tumors.
To begin to explore the
cellular mechanisms that might be responsible for this response, histological analysis revealed less severe disruption of spermatogenesis and
gene expression studies suggested that an interplay of ATP - binding cassette (ABC) efflux transporters and solute carrier (SLC) influx transporters in the testicular cells might be involved.
In situ hybridization on sections of gustatory ganglia (geniculate, petrosal / nodose) and a somatosensory ganglion (trigeminal) were performed to reveal serotonin receptor
gene expression at the
cellular level.
The researchers then developed a new type of single - strand RNA interference (RNAi) agent, the proline - modified short hairpin RNA (PshRNA), which suppresses
gene expression by utilizing the
cellular system.
However, this
cellular intervention alters the normal
expression of hypophosphorylated retinoblastoma (RB) protein needed for the
expression of
genes involved in cell functions [3] and, therefore, results in an abnormal cell.
The NIH Common Fund's Library of Integrated Network - based
Cellular Signatures (LINCS) program aims to create a network - based understanding of biology by cataloging changes in
gene expression and other
cellular processes that occur when cells are exposed to a variety of perturbing agents.
The work has led him to explore the role of protein phosphorylation in a diverse array of
cellular functions, including transformation, cell communication, cell adhesion, cell - cycle regulation, the control of
gene expression, and protein degradation.
The lab focuses on clarifying the mechanisms of brain plasticity,
gene expression, and responses of
cellular elements to different psychotropic drugs, and have identified several novel brain sites and pathways that constitute attractive targets for new drug development.
In studying the human placenta, researchers looked at
gene expression: the process by which a
gene's DNA sequence is converted into
cellular proteins.
Along with the
cellular genes emphasized from the microarray analysis, two
genes that are suspected to be involved in the scleractinian coral calcification process were tested for
expression (Figs. 5A and 5B).
She has pioneered the intergration of large - scale genome and transcriptome sequencing data to understand how genetic variation affects
gene expression, providing insight to
cellular mechanisms underlying genetic risk for disease.
We also identified a «meditation effect» within the regular meditator group, characterized by a distinct network of
genes with
cellular functions that may be relevant to healthy aging, and this network was associated with increased
expression of a number of telomere maintenance pathway
genes and an increase in measured telomerase enzymatic activity.
In these mouse lines,
gene knockout can be induced by Cre recombinase
expression while proteins needed for later experiments (
cellular tracking for instance) can be controlled with FLP - FRT.
We work across disciplines and use a variety of techniques including microfluidics, standard microscopies (electron, optical, fluorescence, confocal), spectroscopies (fluorescence, UV, CD), scattering techniques (X-ray, light), protein
expression and characterization and cell - free
gene expression to investigate the utility of coacervate microdroplets as robust reaction compartments and
cellular mimics.
The isoforms of this histone play complex regulatory roles in several
cellular processes — epigenetic regulation of
gene expression, selective regulation of developmental
genes, and telomere maintenance — that could contributed to tumor growth and progression if dysregulated.
Closer examination of this
gene variant suggested it may regulate the
expression of a neighboring
gene, SLC39A8, which is known to help protect the airways and lungs from inflammation and
cellular damage.
Others were unanticipated, including significant differences in
expression levels among
genes involved in fundamental
cellular processes such as ribosomal biogenesis, transfer RNA processing, and Notch - signaling — part of a complex system of communication that governs basic
cellular activities and coordinates cell actions.
10x Genomics» Chromium Solutions are the industry standard for single cell digital
gene expression and
cellular heterogeneity analysis.
The scope of the journal encompasses all of «traditional» molecular biology (including DNA replication, recombination and repair,
gene expression, RNA processing, translation, and protein folding, modification, and degradation) as well as studies of the molecular interactions and mechanisms that underlie basic
cellular processes.
To further characterize HPP - 4382, we screened a selection of alternative
genes for
expression: two markers of endoplasmic - or general
cellular stress, HSPA6 and GADD45A, and ICAM1, a target of NF - B.
The Sarma laboratory is interested in the mechanisms of epigenetic
gene regulation, or how the dynamic modifications of the architecture of chromatin, the complex of DNA and proteins within the nucleus of our cells, impacts
gene expression and
cellular function.
Dr. Loftus» research is aimed at understanding how the human genome regulates
gene expression, with a focus on how this controls the
cellular processes governing mammalian development.
ATF2 is a protein that can regulate a vast array of
gene expression and therefore can contribute to many
cellular behaviors and processes.
With DriverMap, Cellecta offers a novel, comprehensive end - to - end service portfolio for identifying differential
gene expression, mapping of clinically actionable mutations in RNA, detecting
cellular composition, and profiling immunotherapy targets.
According to the researchers, when
expression of the
gene that codes for this protein — phosphoglycerate dehydrogenase or PHGDH — is suppressed in tumors and cell lines with an overabundance of the protein, the rate of
cellular growth declines markedly.
A number of recent articles, however, have reported that hiPSCs are, in fact, notably distinct from human embryonic stem cells in terms of their
gene expression, epigenetic profile, proliferative capacity and the susceptibility of their differentiated progeny to
cellular senescence and apoptosis [3 — 6].
The model will describe
cellular pathways that contribute to tumor formation and explain in detail how the genetic disposition of an individual can activate
expression of
genes that drive uncontrolled cell growth and lead to cancer.
In a general sense, FP timers can be used in any situation where one wants to understand the relationship between the age of a cell, protein, or
cellular structure and a particular biological event (trafficking to a subcellular location, start of
gene expression, development of a cell structure, etc).
A new
cellular signal discovered by a team of scientists at the University of Chicago and Tel Aviv University provides a promising new lever in the control of
gene expression.
Sirtuins are enzymes regulating the
expression of
genes that control the function of cells through key
cellular signalling pathways.
«Vertical integration of
gene function» describes how
gene expression initiates a series of biochemical,
cellular, and physiological changes that ultimately culminate in an observable behavior.
«This suggests that two different
gene expression programs may exist; one for normal
cellular activity and one for regeneration,» explains Stewart.
Now researchers at the Salk Institute for Biological Studies have identified an essential
cellular pathway in zebrafish that paves the way for limb regeneration by unlocking
gene expression patterns last seen during embryonic development.
This models depicts the ES cell as a highly plastic but nevertheless discrete and stable
cellular entity, one that in turn gives rise through a massive switch in
gene expression to discrete progenitor populations with more limited developmental potential.
Selection for
expression of the
gene requires transcription from a
cellular promoter, and consequently a mutation in a
cellular gene, and the activity of the tagged
gene can be followed by staining for beta galactosidase activity.
In certain cancers, low - complexity domains are improperly attached to other proteins that may then incorrectly form droplets in
cellular locations, leading to mis - regulated
expression of
genes, Fawzi said.