Not exact matches
To discover these
targets, the team determined
when and where each
gene is turned on or off in the cells and tissues of H. contortus to reveal new insights into the worm's lifecycle.
When a
target gene is unmethylated, the reporter is also unmethylated, triggering expression of a glowing protein that illuminates the cell.
If drugs could
target the corresponding
gene in people, it might allow dieters to keep burning calories at the same rate they do
when eating normally.
After moving to Berkeley, he arrived at a career crossroads in 1994,
when Spyros Artavanis - Tsakonas, then at Yale, discovered and subsequently patented the human relative of the fruit fly
gene notch, which plays a role in cell - to - cell interactions and could be an anti-cancer
target.
However, they determined the blood levels of SMN are not altered
when SMN levels are altered in motor neurons using a
gene therapy approach delivered directly into the cerebrospinal fluid to
target the central nervous system.
The researchers found a set of frequently mutated
genes in SBAs that could be helpful to clinicians
when they are looking to use
targeted therapies that work best in cancers with specifics mutations.
The proposed strategy reflects a continuing move toward combination therapies, particularly
when it comes to epigenetic approaches, which
target the mechanisms that control whether
genes are switched «on» or «off.»
Although that marker, called IL21, had not previously been associated with autoimmune diseases, the
gene that produces it sits right in the stretch of DNA known to make these mice vulnerable to diabetes, suggesting that IL21 might make a drug
target, says Sarvetnick.Furthermore, by giving the animals a shot of dead bacteria — similar to an immunization in humans —
when they were newborns, Sarvetnick and her colleagues prevented a surfeit of CD4 + and CD8 + cells.
Remarkably,
when the researchers manipulated the activity of these three
genes, almost all of the other
genes in the network were corrected, pointing to novel therapeutic
targets for CAVD.
When the researchers treated mice with JQ1, many of the abnormal activity levels of Brd4
target genes returned to normal.
«
When we deleted the
gene and were able to reconstitute the social deficits, that was the moment we realized we'd hit the right
target.
When Cas9 and the short guide RNA
targeting a disease
gene are delivered into cells, a specific cut is made in the genome, and the cells» DNA repair processes glue the cut back together, often deleting a small portion of the genome.
When SETDB1 is active, the expression levels of
target genes are repressed.
Whereas many researchers at the summit expressed confidence that off -
target effects could be considerably reduced, Rudolf Jaenisch of MIT stressed a less - appreciated worry:
When CRISPR repairs one copy of a disease
gene, it sometimes introduces mutations into the healthy copy.
They then measured the amount of messenger RNA of
genes that were
targeted by the dodder microRNAs and saw that the level of messenger RNA from the host was reduced
when the dodder microRNAs were present.
When they focused on
genes involved in drug resistance, the group found that C. krusei differs from C. albicans; many of the sites that are often mutated in the
target of azole drugs in resistant C. albicans are not mutated in C. krusei.
If so, it could make cell fate more resilient to random mutations in a plant's genetic code, even
when such changes keep some
gene - regulating proteins from binding their intended DNA
targets.
But now, with the finding that glioblastoma can be triggered
when two
genes fuse, a
targeted therapy to reverse the disease may be a step closer.
«Blood cancers develop
when immune cell DNA editing hits off -
target spots: Team urges consideration of cutting - and - pasting errors
when using enzymes for
gene modification.»
«
When targeting cancer
genes, home in on the one percent: Many cancer - related mRNAs bind a protein and uncover a hidden site that's a possible Achilles heel.»
Foltz realized that
when BEX1 is inhibited, cells grow uncontrollably and can form tumors — and researchers hope to develop treatments that
target the malfunctioning
gene.
from the University of Washington reported a surprising finding -
when delivered via AAV infection,
gene targeting vectors with relatively short (1 kb) homology arms underwent homologous recombination at a frequency three orders of magnitude higher than identical
targeting vectors delivered through transfection of naked DNA
In that year, Russell and Hirata from the University of Washington reported a surprising finding -
when delivered via AAV infection,
gene targeting vectors with relatively short (1 kb) homology arms underwent homologous recombination at a frequency three orders of magnitude higher than identical
targeting vectors delivered through transfection of naked DNA.
The double strand break then can be repaired by error - prone non-homologous end joining (NHEJ) often introducing insertions and deletions leading to a non-functional
gene product
when this break is placed within the coding region of the
targeted gene [27].
A quirk of the huntingtin
gene might be helpful
when it comes to avoiding these «off -
target effects».
Although CRISPR is incredibly useful for generating mutations by NHEJ and generating small mutations with HDR,
when it comes to larger scale genome editing, such as replacement of a mouse
gene with its human ortholog (greater than 5 kb), it remains to be seen whether CRISPR is as robust as conventional
gene targeting.
By studying these malignant cells in greater detail, they discovered that the virus,
when inserting its DNA into the genome of the patient's cells,
targets genes that are important in cell proliferation.
July 13, 2016 New technique
targets gene that causes neurodegenerative disease Neuroscientists at the University of Chicago studying a unique
gene that expresses two proteins, one that is necessary for life and another, that
when mutated causes a neurodegenerative disease called spinocerebellar ataxia type 6 (SCA6), have developed a technique to selectively block the disease - causing protein without affecting the other.
«Identification of
genes that contribute to Alzheimer's risk and that influence the progression of disease will help lead us to the cause of the disease, identify proteins and other new
targets for drug development, and provide genetic methods for determining which people are at greatest risk for Alzheimer's disease
when preventative measures become available,» said Dr. Schellenberg.
The Myriad Genetics patents on BRCA1 / BRCA2 testing, even
when enforceable, covered only the
targeted sequencing of those
genes in cancer patients.
When Cas9 arrives at its
target location on the DNA, it facilitates a change in the local genetic code, affecting the function of that
gene.
«
When we manipulated these master regulators, the
gene network returned back towards normal, suggesting that we might be able to therapeutically
target these regulators to delay or prevent the progression of CAVD.»
There are
genes that,
when mutated, cause disorders of language, speech and comprehension, and statistical analyses of our genomes show that these
genes were
targets of Darwinian natural selection.
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.
When multiplexing amplicons of different
gene targets it is important to use the appropriate sequencing chemistry.
T lymphocytes, or T cells, are removed from patients» peripheral blood and reprogrammed with a
gene, CAR, that
when expressed actually redirects all of the T cells against a single
target.
In the more immediate future, the team plans to use global approaches to identify all the
targets of Kdm6b.1 during regeneration, and to find out what gives the signal to turn these
genes off
when regeneration is complete.
The observation that the amount of HIF - 1 plummets
when cells are shifted to high - oxygen conditions squared with the factor's hallmark ability to activate
target genes only
when oxygen is limited.
They believe vitamin D can only effectively
target genes when its «partner receptor» is activated by vitamin A.