«The Medaka experiment
finding of new genes affected by microgravity provides a good animal model to clarify this mechanism.»
Not exact matches
Collaboration based on
new findings from the Regeneron Genetics Center ® showing variant in HSD17B13
gene is associated with reduced risk
of chronic liver diseases
Mostly they are optimists, excited by the latest
findings: the newly isolated
gene variant that may help explain schizophrenia, the
new telescopic images that reveal the violent births
of distant....
On the contrary, he
finds it useful to ponder an array
of reductionist attempts to explain the existence
of religion, from that which seeks to pinpoint the area
of the human brain or the specific
genes connected to religiosity to that which sees religion as a malfunction
of the human mind or a vestigial remnant from a primitive stage
of human development suitable only for whimpering, immature dullards (a point
of view championed by the
new atheists).
«In two studies
of breast - fed infants involving more than 3,000 children in Britain and
New Zealand, breastfeeding was
found to raise intelligence an average
of nearly 7 IQ points if the children had a particular version
of a
gene called FADS2.
And researchers generally shied away from clinical research on any patented
genes — a 2003 survey
found that 53 percent
of genetics labs decided not to develop a
new genetic test because
of a patent or license.
«But the discovery
of this network
of genes linked to epilepsy opens avenues for
finding new treatments.
In the
new research, the UB scientists
found they could reverse those social deficits with a very low dose
of romidepsin, which, they
found, restores
gene expression and function using an epigenetic mechanism, where
gene changes are caused by influences other than DNA sequences.
As well as understanding the implications
of finding this
new variant
of the botulism
gene cluster in a non-clostridial species
of gut bacterium, the team are interested in exploring how it might help in developing
new treatments for diseases.
As CRISPR - Cas9 starts to move into clinical trials, a
new study published in Nature Methods has
found that the
gene - editing technology can introduce hundreds
of unintended mutations into the genome.
An apparently
new Variant
of human serum albumin, albumin Naskapi, has been
found in high frequency in the Naskapi Indians
of Quebec and, in lower frequency, in other North American Indians.The family and population data
of the albumin are consistent with its inheritance as a simple autosomal trait Controlled by a
gene designated Al Naskapi.
Virgin, an immunologist, said he thinks the
new findings will produce a more complicated but also much more insightful picture
of how human, bacterial and viral
genes influence human health.
«
Gene sequencing study reveals unusual mutations in endometriosis:
Findings advance search for
new ways to classify aggressive forms
of the disease.»
«Within the context
of our emerging appreciation
of polygenic risk, where
gene variations are implicated in several disorders, the
new findings point to only partial overlap in the risk mechanisms for these two forms
of bipolar disorder,» said Dr. Krystal.
The
findings by a team
of Massachusetts General Hospital (MGH) investigators, which will be published in the April 24 issue
of Cell and are receiving advance online release, support the importance
of epigenetics — processes controlling whether or not
genes are expressed — in cancer pathology and identify molecular circuits that may be targeted by
new therapeutic approaches.
A
new report by researchers in the Perelman School
of Medicine at the University
of Pennsylvania
found that loss -
of - function mutations to Filaggrin - 2 (FLG2), a
gene that creates a protein responsible for retaining moisture and protecting the skin from environmental irritants, were associated with atopic dermatitis in African American children.
John March
of Cornell University in Ithaca,
New York and his team took the bacterium Lactobacillus gasseri, which is
found in some probiotic yogurts, and equipped it with a human
gene for a hormone called glucagon - like peptide - 1.
Perhaps most significantly, in a study led by Frances Champagne — then a graduate student in Meaney's lab, now an associate professor with her own lab at Columbia University in
New York — they
found that inattentive mothering in rodents causes methylation
of the
genes for estrogen receptors in the brain.
These differentially expressed microRNAs point the way toward
finding more
genes associated with glaucoma, more clues about how these glaucoma types each go about damaging our optic nerve and potential
new points
of intervention, the scientists say.
New research presented here yesterday at the annual meeting
of the American Association for the Advancement
of Science (which publishes ScienceNOW)
finds that a
gene associated with increased risk
of asthma is also linked to resistance against a parasitic worm.
By examining
gene expression patterns, the
new study
found that parrot brains are structured differently than the brains
of songbirds and hummingbirds, which also exhibit vocal learning.
With the advent
of new gene editing techniques, some less common animal models such as octopuses may
find their way into scientists» toolkits.
More than 80 percent
of the viral
gene sequences he
found were
new to science.
The study
found several
genes that are associated with resistance to antibiotics, including
new genes that might point to previously unknown mechanisms
of drug resistance.
To
find out what BRCA2 does normally, the team reporting the
new results, which includes Allan Bradley
of Baylor College
of Medicine in Houston and Paul Hasty
of Lexicon Genetics Inc. in The Woodlands, Texas, created «knockout» mice in which the
gene was inactivated.
Scientists from the Biogerontology Research Foundation (BGRF), a UK - based charity
founded to support aging research and address the challenges
of a rapidly aging population, propose a
new concept for signalome - wide analysis
of changes in intracellular pathways, called OncoFinder, which allows for accurate and robust cross-platform analysis
of gene expression data.
The
new finding shows that «
gene flow across taxonomic boundaries happens,» observes geneticist Michael F. Hammer
of the University
of Arizona.
In a
new study, researchers are taking joint biopsy tissue from patients at the start
of a
new therapy and then six weeks later to see if they can
find a predictor
gene sequence that will clearly identify which patients respond to a particular therapy.
The unexpected
finding may also spark a
new avenue
of research on a type
of gene regulation known as imprinting.
They
found genes for five
new receptors, all
of which belong to a known family
of proteins called formyl peptide receptors (FPRs).
Another
found gene is linked to angiogenesis, the production
of new blood vessels to support a tumor.
Until now, de novo genetic mutations, alterations in a
gene found for the first time in one family member, were believed to be mainly the result
of new mutations in the sperm or eggs (germline)
of one
of the parents and passed on to their child.
Joint lead author Professor Manfred Kayser from Erasmus MC said: «Besides substantially increasing our understanding
of human pigmentation genetics in general,
finding these
new hair colour
genes is also important for further increasing the accuracy
of hair colour prediction from DNA traces in future forensic applications, which can help to
find unknown perpetrators
of crime.»
A parallel paper in the same journal by researchers from the University
of Liverpool shows that this same
gene also caused the peppered moth to turn black during the mid-19th century, when it evolved to
find new ways to camouflage itself; a side - effect
of industrial pollution at the time.
The
new findings suggest a way to stratify the wide range
of patients with MDD, which may boost the likelihood
of identifying culpable
genes.
They knew that they had
found a
new type
of genetic defect, because the DNA in cancer cells from people with the altered
gene was riddled with mutations.
«Single
gene encourages growth
of intestinal stem cells, supporting «niche» cells, and cancer:
Finding in mice could lead to
new therapies for damaged organs, cancer.»
First author Professor Martin Hrabe de Angelis, Director
of Institute
of Experimental Genetics at the Helmholtz Zentrum München, who invented the mouse clinic concept, said: «Our
findings with regard to the
genes examined are now available to the scientific community as a valid data set, which can be downloaded free
of charge from the IMPC (International Mouse Phenotyping Consortium) website, and form an excellent basis on which we and other research groups can develop and test
new hypotheses.»
The Grants had shown that
gene flow has occurred in the finches
of Daphne Major during the past 40 years, but the
new study
found extensive evidence for
gene flow throughout the roughly 1 million years that the birds have occupied the archipelago, which has helped the researchers update their understanding
of how the lineages diverged over time.
Researchers now suspect that this
finding will open up a whole
new area
of medical genetics, with DNA repair
genes becoming the prime suspects in causing other cancers and hereditary illnesses.
The three Ras
genes found in humans — H - Ras, K - Ras and N - Ras — were among the first to be linked to cancer development, and a
new study led by VCU Massey Cancer Center researcher Paul Dent, Ph.D., has shown the recently approved breast cancer drug neratinib can block the function
of Ras as well as several other oncogenes through an unexpected process.
Professor Peter Kraft at Harvard TH Chan School
of Public Health, USA, says: «Given the size
of these studies, we expected that we would
find a lot
of new breast cancer risk variants, but the studies tells us a lot more about which
genes are involved, revealing many previously unsuspected
genes and genetic mechanisms underlying breast carcinogenesis.
These
new findings appear in
Genes and Development, a leading journal in the field
of developmental biology.
Shaw reverses the process in a
new paper, taking what he
finds in humans back to the flies and gaining
new insight into humans as a result: identification
of a human
gene that is more active after sleep deprivation.
Now, Mitchum's team is trying to
find how this key
gene might work differently in other nematode types, like root - knot nematode as part
of a
new National Science Foundation grant.
The study, published in
New Phytologist, shows how a
gene found in the common fruit fly, Drosophila melanogaster, can be expressed in Arabidopsis, a member
of the cabbage family, to improve TNT removal from contaminated soil.
«We have already
found several
gene types that are dramatically expanded in the octopus relative to other vertebrates, and we think they play a critical role allowing a
new level
of neuronal complexity to be reached in invertebrates,» he said.
A
new study led by Boston Children's Hospital and the University
of Montreal raises a note
of caution,
finding that person - to - person genetic differences may undercut the efficacy
of the
gene editing process or, in more rare cases, cause a potentially dangerous «off target» effect.
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.
«The good news is that this
finding predicts that patients missing either
gene should be sensitive to
new therapies targeting focal adhesion enzymes, which are currently being tested in early - stage clinical trials,» says Shaw, who is also a member
of the Moores Cancer Center and an adjunct professor at the University
of California, San Diego.