Darnell's comprehensive history of RNA research will reward anyone
interested in gene expression.
Not exact matches
Sebat's team was especially
interested in the parts of noncoding DNA that regulate
gene expression.
Because this imprinting affects hundreds of
genes that are non-coding, including microRNAs and non-coding RNAs, it's a very
interesting fine - tuning mechanism for the dosage of
gene expression in the brain and elsewhere
in the body.»
Epiviz implements multiple visualization methods for location - based data (such as genomic regions of
interest) and feature - based data (such as
gene expression), using interactive data visualization techniques not available
in web - based genome browsers.
«The other thing I think is
interesting is that there are not that many cases where people have been able to use
gene expression, absent any genetics, to zoom
in so precisely on a genetic change that causes an obvious trait,» he added.
One especially
interesting area of inquiry, according to Greenberg, includes the regulatory elements that control the
expression of
genes in response to sensory experience.
This under -
expression was particularly
interesting because although hundreds of
genes have already been identified for their presumed roles
in autistic disorders, each one alone can at best only explain 1 % of cases.
«This technique will be useful for other studies
interested in characterising the link between
gene expression and physical, external traits.»
Easily accessible from nasal biopsies, these cells — which belong to nerve tissues and can differentiate into neurons — constitute an
interesting model to identify the
genes and proteins whose
expression is deregulated
in patients with ASD.
Understanding enhancer functions is of great
interest due to their importance
in gene expression as well as evolution and disease.
The characteristics
in which Cembrowski and his collaborators were
interested included connectivity (downstream brain targets),
gene expression, and electrophysiology (the science behind the spikes).
His lab is
interested in the regulation of
gene expression by mRNA processing
in C. elegans and human cells.
He group is also
interested in high throughput
gene expression data analysis, especially using Bayesian network (BN) approaches.
One
interesting hypothesis by the study authors looks at the role that thyroid hormone plays
in regulating the
expression of a
gene called the amyloid precursor protein (APP), which has a role
in Alzheimer's.
The Morris lab is specifically
interested in utilizing the recently described endogenous non-coding RNA pathway
in human cells to epigenetically modulate
gene expression in those
genes involved
in HIV, cystic fibrosis, and cancer.
There has been a rapidly increasing
interest in whether environmental factors modulate the establishment and maintenance of epigenetic modifications, and thereby affect
gene expression and phenotype
in humans and wildlife.
He is also
interested in genes induced by the interferon response, and his future plans include investigating
genes identified
in the
expression of genome - wide association screens for predisposition to cancers.
We hope our content will be of particular
interest to industrial or academic scientists active
in R&D
in molecular biotechnology,
gene transfer and
expression, applied microbiology, environmental biotechnology, biofuels and bioenergy, nanotechnology, bioprocessing, chemical biotechnology, tissue engineering and regenerative medicine, nucleic acid therapeutics and vaccines, plant biotechnology, and patenting and regulatory issues.
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.
We have a longstanding
interest in understanding
gene expression regulation, and
in our wetlab at the Sanger Institute use mouse T helper cells as a model of cell differentiation.
The
gene - of -
interest is first inspected on three aspects
in the BXD GRP, i.e. the existence of genetic variations, e (p) QTLs, and its
expression pattern across strains.
When bred to mice with a cre recombinase
gene under the control of a promoter of
interest, the STOP sequence of the targeted
gene is deleted
in the tissue of
interest, and EYFP
expression is observed.
Real rates of change can only be determined from actual transcript numbers, and this gives us the kinetics of
gene expression which we are
interested in.»
We are particularly
interested in how miRNAs can generate thresholds
in target
gene expression and mediate feedforward and feedback loops
in gene networks.
We are particularly
interested in how cells use
gene networks to make robust decisions even
in the presence of significant fluctuations
in gene expression.
High - throughput ChIP - Seq: One of the major questions for researchers
interested in understanding chromatin dynamics is to investigate how protein - DNA interactions alter Epigenetic profiles and subsequent
gene expression.
For instance, a researcher
interested in cardiovascular disease could access GTEx data to view all the genetic variants
in the human genome that affect
gene expression in the heart.
His research
interests are phenotypic plasticity,
gene expression and cell wall chemistry
in the freshwater green alga,
Besides information gathered to answer specific experimental questions, as determined by the
interests of individual partners [35]--[41], the collective data offered the opportunity to search for coordinated
gene expression patterns
in a systematic exploration of the mouse ES transcriptome under a battery of different experimental settings, thus minimizing possible site - specific artifacts.
Kennedy is
interested in understanding why reduced
gene expression in ribosomes enhances longevity
in yeast and worms — ribosomes are tiny organelles that occur within the cell and are involved
in the production of proteins.
The Bioinformatics group uses computational methods to analyse genome sequences, amino acid sequences, and
gene expression data, both to identify new
genes of
interest and to determine their structure, function and role
in the cell.
«We're
interested in identifying
genes that are up - or down - regulated compared to normal and how their
expression is regulated during tumor formation.
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.
His research
interests are phenotypic plasticity,
gene expression and cell wall chemistry
in the freshwater green alga, Desmodesmus.
These mice were created and deposited by The Pleiades Promoter Project (Centre for Molecular Medicine and Therapeutics, University of British Columbia); their goal is to generate 160 fully characterized, human DNA promoters of less than 4 kb (MiniPromoters) to drive
gene expression in defined brain regions of therapeutic
interest for studying disorders such as Alzheimer's disease, Parkinson's disease, Huntington's disease, Amyotrophic Lateral Sclerosis (Lou Gehrig's disease), Multiple Sclerosis, Spinocerebellar Ataxia, Depression, Autism, and Cancer.
To develop a better understanding of the preventative and therapeutic potentials of LA, much of the current
interest is focused on elucidating its molecular mechanisms
in redox dependent
gene expression.