Analysis of differentially expressed proteins revealed enrichment in cytoskeleton organization, mitochondrial activity and ROS management, while
gene expression analysis revealed enrichment in the epithelial - to - mesenchymal transition pathway.
Comparative
gene expression analysis revealed a significant overexpression of TRF2, β - catenin and hTERT genes (p < 0.01) in clonospheres at high Bleomycin concentration (80μM)(Fig 2f).
Single - cell differential
gene expression analysis revealed a spectrum of known transcripts, including several linked to cytotoxic and costimulatory function that are expressed at higher levels in the TEMRA (effector memory T cells expressing CD45RA) subset, which is highly enriched for CD4 - CTLs, compared with CD4 + T cells in the central memory (TCM) and effector memory (TEM) subsets.
Global
gene expression analyses reveal changes in biological processes after hyperthermia in a rat glioma model.
Not exact matches
The title of the paper is «Bioinformatic
analysis reveals a pattern of STAT3 - associated
gene expression specific to basal - like breast cancers in human tumors.»
Expression analyses revealed that these
genes are active almost exclusively in testicular germ cells, where, at a minimum, they likely contribute to sperm production.
«
Gene analysis adds layers to understanding how our livers function: Tracking gene expression patterns for 20,000 gene in 1,500 cells revealed a mosaic of activities.&ra
Gene analysis adds layers to understanding how our livers function: Tracking
gene expression patterns for 20,000 gene in 1,500 cells revealed a mosaic of activities.&ra
gene expression patterns for 20,000
gene in 1,500 cells revealed a mosaic of activities.&ra
gene in 1,500 cells
revealed a mosaic of activities.»
Erlich used a multitude of statistical genetic and integrative genomics
analyses to
reveal that STRs have a function: they act like springs or knobs that can expand and contract, and fine - tune the nearby
gene expression.
Methanosaeta were the dominant methane - producing microorganisms in the digesters and known to convert acetate to methane, but
analysis of the
gene expression in the digester
revealed that Methanosaeta were also highly expressing
genes for converting carbon dioxide to methane.
Analysis of the most aggressive of these cells
revealed a pattern of
gene expression distinct from that known to occur in breast - to - bone metastasis, as described in an earlier paper by Massagué.
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.
Genome - wide
analysis of variance (ANOVA)
revealed that germline SNPs / CNVs and somatic CNAs influenced > 39 % of
gene expression probes, roughly half acting in cis and half in trans.
Early in vitro
analyses of
gene expression revealed that the cell lines were germ - cells, our target cell type.
Calcification rate measurements and
gene expression analysis by microarray RNA transcriptional profiling at two time - points (midday and night - time)
revealed several
genes common within mammalian
gene regulatory networks.
The principal component
analysis revealed that aging explains ~ 16 % of protein
expression variability and is associated with
Gene Ontology terms transmembrane, integral / intrinsic membrane, endoplasmic reticulum and mitochondrion.
Analysis of
gene expression array in TSC2 - deficient AML cells
reveals IRF7 as a pivotal factor in the Rheb / mTOR pathway.
Deeper
analyses,
revealed that the RNA
expression pattern of a rare variant of the NCAN
gene was highly correlated with that of the previously suggested susceptibility
genes for developmental dyslexia.
Microarray
analysis revealed temperature - dependent
expression of distinct sets of
genes, as well as 700 A. fumigatus
genes not present or significantly diverged in the closely related sexual species Neosartorya fischeri, many of which may have roles in the pathogenicity phenotype.
Comparison of mRNA and protein
expression revealed distinct
expression profiles for many
genes and underscores the importance of multi-omic
analysis in single cells.
Proteomic
analysis to profile protein abundance resulted in the identification and relative quantification for 912 proteins with two or more unique peptides and 86 proteins with significant abundance changes after treatment with the neurotoxins, while microarray
analyses to profile
gene expression revealed 181
genes with significant changes in mRNA after treatment.
Analysis of synaptic
gene expression in the neocortex of primates
reveals evolutionary changes in glutamatergic neurotransmission.
These techniques and functional
analysis of the resulting data
revealed a number of up - and down - regulated proteins and mRNAs; i.e., up - regulated by a signal (originating internal or external to the cell) that results in increased
expression of one or more
genes and as a result the protein (s) encoded by those
genes, and down - regulated by a process resulting in decreased
gene and corresponding protein
expression.
MicroRNA
expression profile and functional
analysis reveal that miR - 382 is a critical novel
gene of alcohol addiction.
The present study shows that such a gradient is also seen at the level of single cell
analysis, but
reveals that there is considerable cell - to - cell variation within this gradient in the
expression of pluripotency
genes.
Transcriptomics
analysis of inguinal WAT showed a marked effect of cold on overall
gene expression, as
revealed by principle component
analysis and hierarchical clustering.
Transcriptomics
analysis revealed that, in POU5F1 - null cells,
gene expression was downregulated not only for extra-embryonic trophectoderm
genes, such as CDX2, but also for regulators of the pluripotent epiblast, including NANOG.
Unbiased clustering
analysis of P (+) neurons
revealed four different classes, each with distinct cell surface receptor
gene expression profiles.
Although many common
genes were expressed in the three tissues, cluster
analysis based on transcript levels
revealed distinct
gene expression profiles of the d - 18 EET (Fig. 2C and SI Appendix, Fig.