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cell analysis reveals that endogenous retrotransposons generate somatic mosaicism in neuronal and non-neuronal cells.
Zena Werb, University of California, San Francisco, USA Single -
cell analysis reveals a stem - cell program in human metastatic breast cancer cells.
«Nature, meet nurture: Single -
cell analysis reveals diverse landscape of genetic changes in the brain after a sensory experience.»
Not exact matches
I won't
reveal yet who my favorites are, but I will say that these young scientist - founders came up with very creative solutions for preventing infections in some common surgeries, tackling resistance in targeted antibody drugs, improving gene vectors for
cell therapies, helping the vision - impaired «see» faces and better read their environments, imaging hard - to - see spots in the lungs and other organs, improving genetic risk
analysis, and expediting the logistical operations of hospitals.
An in - depth genetic
analysis, performed with the participation of graduate students Tal Lupo and Lihee Asaf, pointed to a gene called WNT5B, which was
revealed to be the factor prompting stem
cells to differentiate into lymphatic
cells.
The
analysis revealed that the human genome is organized into large pieces of low or high epigenetic stochasticity, and that these regions correspond to areas of chromosomes that are structurally different in the
cell nucleus.
An
analysis of the HPV16 genome from 5,570 human
cell and tissue samples
revealed that the virus actually consists of thousands of unique genomes, such that infected women living in the same region often have different HPV16 sequences and variable risks to cancer.
«Our
analysis revealed that the differences between tame and aggressive foxes may lie in
cells in the anterior pituitary gland, which can change their shapes to communicate with one another about when it's time to release stress hormones,» Hekman said.
Information theory
analysis of
cell signaling
reveals mechanisms for reliable cellular responses despite signal variability.
Further
analysis of the genes that had been stimulated in the responders
revealed that they were involved in immune
cell function relevant to the inflammatory disease process in RA.
Additional
analysis revealed that ChABC gene therapy changed the way that inflammatory
cells in the region respond following injury.
A separate
analysis of 3BNC117 by Ching - Lan Lu et al.
reveals that the antibody not only blocks infection of new
cells, but accelerates the clearance of infected
cells as well.
This
analysis, done on separate samples from the same patient,
revealed that many of the affected genes confer advantages to cancer
cells by, for example, enhancing
cell migration or resistance to chemotherapy.
Expression
analyses revealed that these genes are active almost exclusively in testicular germ
cells, where, at a minimum, they likely contribute to sperm production.
Chromatin immunoprecipitation sequencing
analysis revealed enrichment of H3K27me3 at specific loci in KDM6A - null
cells, including PRC2 / EZH2 and their downstream targets.
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.
Simultaneous T
cell antigen receptor (TCR)
analysis in single
cells and bulk subsets
revealed that CD4 - TEMRA
cells show marked clonal expansion compared with TCM and TEM
cells and that most of CD4 - TEMRA were dengue virus (DENV)-- specific in donors with previous DENV infection.
«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.»
Recent advances in our understanding of cancer have
revealed that the disease can not be understood through simple
analysis of genetic mutations within the cancerous
cells.
Recent advances in our understanding of cancer have
revealed that the disease can not be understood through simple
analysis of genetic mutations within cancerous
cells.
Analyses of RV144 volunteers
revealed that particular vaccine - induced immune responses, including production of certain antiviral antibodies and CD4 + T
cell responses to HIV's outer shell, or envelope, correlate with reduced HIV infection.
The
analysis performed
revealed that many variations in immune
cell function triggered by chronic HIV infection are associated with high levels of bNAbs.
«Single -
cell analysis of embryos
reveals mis - segregation of parental genomes.»
New genetic
analyses of tropical marine microorganisms have
revealed that some species of single -
celled plankton are converting significant amounts of nitrogen from the air into nutrients, helping to fortify the base of the ocean's food pyramid.
An
analysis revealed three distinct types of
cell phone users: low - use extroverts, low - use introverts and a high - use group.
«Our
analysis revealed that terminal acid shock was not completely lethal to the yeast's
cells, although nearly a third of the yeast died in some experiments,» Bochman said.
Targeting the labeled
cells for
analysis, they
revealed that their organoids contained a population of sensory
cells that have the same functional signature as
cells that detect gravity and motion in the human inner ear.
Analysis of the trajectories of people carrying
cell phones
reveals that human mobility patterns are highly predictable.
Additional
analyses revealed that stem
cells were also smaller, had a higher nucleus - to - cytoplasm ratio, and were less viscous than mature
cells.
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.
A major component of the study was a comprehensive
analysis of the «phosphoproteome» of prostate cancer tumors and
cells,
revealing changes in the phosphorylation states of cellular proteins.
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.
Individual profiles based on the
analysis of each patient's tumor
cells revealed clinically relevant information that could be used to prioritize the drugs most likely to be effective in these cases.
The treatment induced changes in the synthesis of 101 proteins and ELISA
analysis revealed a sixfold higher secretion of type II collagen compared to control
cells.
X-ray studies at the Department of Energy's SLAC National Accelerator Laboratory, combined with Stanford biological studies and computational
analysis,
revealed remarkable similarities in the structure of binding sites, which allow a given T
cell to recognize many different invaders that provoke an immune response.
Further
analysis revealed that the mice in Tg / Tg group, which developed severe hyperglycemia, lost > 75 % of their β
cells compared with WT mice of the same strain and similar age.
The results of our microRNA (miRNA) profile
analysis for these
cells revealed that CSCs that are highly metastatic to bone and brain expressed significantly lower level of miR - 7 and that this miRNA was capable of modulating one of the essential genes for induced pluripotent stem
cell, KLF4.
A proteomics
analysis revealed expression changes of 56 proteins, and a further protein pathway
analysis suggested their association with the
cell morphology, the organization, and the increased cellular movement and the proliferation.
Immunohistochemical
analysis of perigonadal, perirenal, mesenteric, and subcutaneous adipose tissue
revealed that the percentage of
cells expressing the macrophage marker F4 / 80 (F4 / 80 +) was significantly and positively correlated with both adipocyte size and body mass.
Proteomic
analysis of arginine methylation sites in human
cells reveals dynamic regulation during transcriptional arrest.
Molecular
analyses revealed that some of the former regulatory T
cells had become follicular helper T
cells (Tfh).
A deep - sequencing
analysis reveals that non-malignant skin
cells harbor many more cancer - driving mutations than previously expected.
Global
analysis of genome, transcriptome and proteome
reveals the response to aneuploidy in human
cells.
Flow cytometric
analysis revealed that anti-Thy 1.2 antibody plus complement depleted > 97 % of the Thy 1.2 +
cells (data not shown).
St. Jude Children's Research Hospital
analysis reveals how the protein p53, which triggers cancer
cells to commit suicide, attaches to its regulatory molecule; findings could lead to drugs to unleash p53 to battle a range of cancers.
Analysis of mEPSC properties in SPNs
revealed a significant decrease in mEPSC frequency only in iSPNs from 6 - month old Q175 mice, with no genotypic differences in mEPSC amplitude in either
cell type.
Additional cellular
analysis revealed a subset of these bacterial proteins that were secreted into the host cytoplasm independent of the known Salmonella mechanisms for transporting virulence proteins into host
cells
Early in vitro
analyses of gene expression
revealed that the
cell lines were germ -
cells, our target
cell type.
Analysis of gene expression array in TSC2 - deficient AML
cells reveals IRF7 as a pivotal factor in the Rheb / mTOR pathway.
Mats Nilsson demonstrated a unique technology to
reveal cells harboring specific mutations in tissue sections, while Ruedi Aebersold held an impressive lecture, illustrating about how powerful mass spectrometry provides a basis for for computational
analyses, commented moderator Ulf Landegren.