These genetic discoveries reinforce
earlier gene studies implicating abnormal inflammation and fat metabolism in the disease.
Not exact matches
«Strategic alliances are definitely becoming crucial in building businesses of all kinds and at an
earlier stage than ever before,» says
Gene Slowinski, director of strategic - alliance
studies at Rutgers University's Graduate School of Management.
Abeona Therapeutics (ABEO)- Data for ABO - 102 in MPS IIIA appears encouraging to me (decreases in heparan sulfate, neurocognitive benefits), initial data for ABO - 101 in MPS IIIB showed
early promise, EB - 101 in RDEB could see an expedited path to market if the pivotal
study yields fruit, and other
gene therapy candidates are soon to enter the clinic.
Waddington says that it was his
early studies of Whitehead which got him out of a view of single strands of linear causation (e.g., one
gene - one trait), to a view of multiple interactions sustaining a «concrescence.»
As of the
early 2000s, the
study of
gene structure and function, molecular genetics, has been amongst the most prominent sub-field of molecular biology.
Earlier efforts to hunt down disease - causing
genes — so - called genomewide association
studies — frequently came up empty - handed because medical researchers had to take cost - saving shortcuts.
Armed with the both the king cobra and Burmese python genome the team was able to show that, despite previous hypotheses that venom
genes evolve «
early» in the lineage leading to snakes, venom
gene families do not duplicate
early, in fact the
study shows that the rapid and extensive expansion of functionally important venom toxin families is restricted to the venomous «advanced» snake lineage.
Note added in proof: Additional evidence for CA1 - CA3 differences is provided by a recent
study measuring immediate
early gene activation in two different novel rooms (36).
This
study took a different approach — targeting a drug to a protein that controls how
genes are turned on and off,
early in the viral replication process.
The
study found that zebrafish that failed to inherit specific genetic instructions from mom developed fatal defects
earlier in development, even if the fish could make their own version of the
gene.
To more accurately reflect the mechanisms driving oligodendrogliomas, the researchers used RNA sequencing to
study directly, on a single - cell level,
gene expression in samples from six
early - stage human tumors.
A
gene associated with the risk of schizophrenia regulates critical components of
early brain development, according to a new
study led by researchers from Penn State University.
Korenberg was the
early pioneer of
studying these individuals with partial
gene deletions as a way of gathering clues to the specific function of those
genes and
gene networks.
Genetic tests for mutations in the so - called breast cancer
genes, BRCA1 and BRCA2, may not reveal as much about cancer risk as
earlier reports have estimated, according to two
studies published in tomorrow's New England Journal of Medicine.
Now, in a provocative
study that raises unsettling questions about the widespread use of vitamin supplements, Swedish researchers have showed that relatively low doses of antioxidants spur the growth of
early lung tumors in cancer - prone mice, perhaps by hindering a well - known tumor suppressor
gene.
Not long after the HD
gene was isolated,
studies led by MacDonald, also a co-author of the current investigation, found that a variation in the number of CAG trinucleotide repeats within the HD
gene, which codes for a protein called huntingtin, is the primary determinant of the age at which HD symptoms appear, with a greater number of CAG repeats associated with an
earlier symptom onset.
The researchers discovered the actions of multiple independent meiotic drivers in fission yeasts in an
earlier study, reported in 2014 in eLife, but didn't know which
genes were responsible, or how they destroyed gametes that didn't inherit the
genes.
In
earlier studies, Wang and his colleagues had revealed that a
gene in mice called Pad4 (peptidylarginine deiminase 4) produces an enzyme that plays an important role in protecting the body from infection.
One
study, known as DIAN TU, will administer experimental drugs to more than 160 people in the U.S., the U.K., and Australia who have one of three mutant
genes that cause an
early - onset version of the disease.
In a
study published
earlier this year, Jiang and other collaborators at Duke described a mouse model of autism in which they deleted a prominent autism
gene called SHANK3, which is mutated in 1 percent of people with the disorder.
First, looking at a
study of 185 cases of childhood epilepsy, Wittkowski's team found that mutations in
genes that control axonal guidance and calcium signaling — both of which are important
early in the developing brain when neurons are forming the appropriate connections — led to increased chances of having the disorder.
Earlier studies looked at many
genes from a few animals or a few
genes from many animals, but Brown University biologist Casey Dunn and his team cast a wider net, sampling DNA from all across the genomes of 71 different animals.
Earlier, smaller
studies had associated the three
gene variants with type 2 diabetes.
«Using innovative data normalization and
gene selection approaches, we combined the statistical power of multiple genomic
studies and masked their variability and batch effects to identify robust
early diagnostic biomarkers of pancreatic cancer,» said first author Manoj Bhasin, PhD, Co-Director of BIDMC's Genomics, Proteomics, Bioinformatics and Systems Biology Center and Assistant Professor of Medicine at HMS.
The
study found that, on average, Bifidobacterium were established
earlier and more frequently in infants fed by women with an active copy of the
gene, the secretors, than without one, the non-secretors.
Booij and her colleagues hope that this
study will shed more light on the specific role of
early environmental influences on brain development,
gene expression and emotional regulation.
The Penn
study did not examine why no statistically significant relationships between smoking, the
gene variants under investigation, and
earlier menopause were observed in African Americans.
In the new
study, the team genetically inactivated HIV - 1 in transgenic mice, reducing the RNA expression of viral
genes by roughly 60 to 95 percent, confirming their
earlier findings.
Lead author Johan den Boon, associate scientist with the Morgridge Institute for Research at the University of Wisconsin - Madison, says the research team used
gene expression profiling on 128 specimens from the
Study to Understand Cervical Cancer
Early Endpoints and Determinants, or SUCCEED.
Earlier mouse
studies by Li and his collaborators had indicated that the expression of several imprinted
genes changes as hematopoietic stem cells embark on their journey from quiescent reserve cells to multi-lineage progenitor cells, which form the many highly specialized cell types that circulate within the blood stream.
Earlier studies had linked several
genes to small increases in asthma risk.
The variant lies near a
gene called telomerase RNA component, or TERC, and
earlier studies in animals have shown that low TERC expression is associated with shorter telomeres, and faster biological aging.
Two
studies presented at the Biology of Genomes meeting in Cold Spring Harbor, New York, last week show how human genomes have changed over centuries or decades, charting how since Roman times the British have evolved to be taller and fairer, and how just in the last generation a
gene that favors cigarette smoking led to
early death in some groups.
A follow - up
study of 96 other patients with Alzheimer's disease confirmed that this HLA variant is associated with
earlier onset of Alzheimer's, although Payami cautions that another
gene very close to HLA - A2, and not HLA - A2 itself, could be at fault.
Early comparative
studies threw conserved regulatory regions, RNA
genes, and other features into relief, bringing meaning to much of our genome, including the 98 % that lies outside protein - coding regions.
A
study done by researchers at Fox Chase Cancer Center shows that many relatives of patients who undergo testing for a
gene linked to breast and ovarian cancers misinterpret the results, and less than half of those who could benefit from genetic testing say they plan to get tested themselves — despite the fact that knowing your genetic status may help catch the disease in its
earliest stages.
«These findings raise the possibility that by determining the
gene expression profile of a patient's tumor, physicians may be able to identify aggressive disease at the outset of diagnosis and start treatment
earlier,» said Sungyong You, PhD, an instructor in the Cedars - Sinai Department of Surgery and the first author of the
study.
Preclinical
studies suggest that Cdk5 is a
gene that is important for the normal wiring of the brain during
early development and may be involved in some neurodegenerative disorders, including ALS, Parkinson's and Alzheimer's disease.
However, the new, larger
study found that the effect of viral replication capacity was very
early after infection, and was independent of both initial viral load and whether individuals carried certain protective variants of immune
genes called HLA that positively influence immune responses to HIV.
They hope to
study APOBEC's importance in fighting off mutations
early in the development of embryonic life, and in the development of the eggs and sperm that carry our
genes to the next generation.
Geneticists usually prefer to
study genes that are easy to mutate so that work can be replicated or varied, but only one lin - 4 mutation had ever been observed, in Brenner's Cambridge lab a few years
earlier.
The introduction of CRISPR, which is simpler and more efficient than other techniques, will probably accelerate the race to get
gene - edited cells into the clinic across the world, says Carl June, who specializes in immunotherapy at the University of Pennsylvania in Philadelphia and led one of the
earlier studies.
A
study carried out by the Laboratoire Neurobiologie des Interactions Cellulaires et Neurophysiopathologie (CNRS / Aix - Marseille Université), in collaboration with clinicians from Marseilles Public Hospitals (AP - HM) and scientists from the Salk Institute in San Diego (US), has revealed a new
gene that plays a crucial role during
early development in humans and whose under - expression may induce certain autistic traits.
The
study, published today, confirms that if patients with this disease are given
gene therapy
early in life, the results can be dramatic.
«Our present
study shows examination of the
gene expression profiles at the very
early age of initial clinical detection reveals both strong evidence of
early biological processes in ASD and abnormal signals with the potential to serve as an
early, practical biomarker of risk for the disorder in general pediatric settings.»
«We observed that a large number of
genes were involved in pathways related to wound healing, immunity, and metabolism, and this is consistent with the idea that the
earliest stages of domestication may involve adapting to highly crowded conditions,» said Mark Christie, lead author of the
study.
Carmichael and his team began by determining which molecules become more prevalent in the brain during the recovery period after a stroke, and listing all of the
genes that are up - or down - regulated, which the researchers had previously identified during an
earlier study.
IN THE BEGINNING
Early embryos (a four - cell embryo shown) from mice and humans look the same on the outside, but
gene activity
studies show some big differences under the hood.
«Therefore — says the expert — , the results of our
study with planarians describes one of the first
genes of these animals that is necessary for
early brain regeneration and anterior regeneration.»
In an
earlier study, Spector's team knocked out the Malat1
gene in mice and curiously, these mice had no apparent abnormalities, a fact that would seem improbable if Malat1 did in fact have an important function.