Could the solution be
found in a single gene, asks Bob Holmes
I think that the cure for schizophrenia can be
found in a single gene.
Not exact matches
In 1986 my research group at the Rockefeller University and another led by Jeffrey Hall of Brandeis University and Michael Rosbash of the Howard Hughes Medical Institute at Brandeis found that the three mutant flies had three different alterations in a single gene named period, or per, which each of our teams had independently isolated two years earlie
In 1986 my research group at the Rockefeller University and another led by Jeffrey Hall of Brandeis University and Michael Rosbash of the Howard Hughes Medical Institute at Brandeis
found that the three mutant flies had three different alterations
in a single gene named period, or per, which each of our teams had independently isolated two years earlie
in a
single gene named period, or per, which each of our teams had independently isolated two years earlier.
In yeast, for example, they've
found that increasing the activity of a
single gene, called Sir2, can significantly extend life span.
The researchers determined that CRISPR had successfully corrected a
gene that causes blindness, but Kellie Schaefer, a PhD student
in the lab of Vinit Mahajan, MD, PhD, associate professor of ophthalmology at Stanford University, and co-author of the study,
found that the genomes of two independent
gene therapy recipients had sustained more than 1,500
single - nucleotide mutations and more than 100 larger deletions and insertions.
Working with this hypothesis, the researchers conducted a statistical analysis of the CX3CR1
gene in over 7000 schizophrenia and autism patients and healthy subjects,
finding one mutant candidate, a
single amino acid switch from alanine to threonine, as a candidate marker for prediction.
After
gene - typing about 3,000 people, Sturm
found that how OCA2 is expressed — and how much pigment a person has — is strongly linked to three
single nucleotide polymorphisms (SNPs), or
single letter variations,
in a DNA sequence near the OCA2
gene.
The two studies together suggest that
single copies of inactivating ANGPTL3 mutations are
found in roughly one of every 250 people of European descent, whereas people with mutations
in both copies of the
gene — as
in the family studied by Musunuru and colleagues — are much rarer.
Reviewing thousands of genome wide associate studies (GWAS) to identify genetic variants
in single nucleotide polymorphisms (SNPs), investigators at Dartmouth's Norris Cotton Cancer Center
found that some alleles (one of a pair of
genes located on a specific chromosome) are more frequently risk - associated with disease than protective.
Mitochondria carry only a few
genes, but they are so plentiful that it's often easier to
find their DNA than the
single full human genome
in a cell's nucleus.
Harvard Medical School researcher Melina Claussnitzer and her team
found that a
single variation
in the FTO
gene caused fat cells that would normally become healthier beige to turn into white fat cells instead.
The team
found that a mutation
in a
single pair of nucleotides
in the
gene causes seed coat permeability — that is, a change
in one pair out of the approximately 1 billion base pairs that make up the soybean genome.
However, cancer cells may instead be coaxed to turn back into normal tissue simply by reactivating a
single gene, according to a study that
found that restoring normal levels of a human colorectal cancer
gene in mice stopped tumor growth and re-established normal intestinal function within only 4 days.
«It's important they've
found this
gene, but it took a sample of 20,000 people to
find it, precisely because the effect is so small,» says Robert Plomin at the Institute of Psychiatry
in London, and lead author of a groundbreaking study
in 2007 which failed to
find any
single genes of disproportionate importance
in intelligence.
The researchers
found that the blond hair commonly seen
in Northern Europeans is caused by a
single change
in the DNA that regulates the expression of a
gene that encodes a protein called KITLG, also known as stem cell factor.
Yet for years biologists could not
find a
single gene involved
in language.
Pinker says that the
findings are a first step
in demonstrating that intelligence relies on large numbers of
genes, each with a tiny effect, rather than on
single genes that have moderate or large effects, but which are so rare that none has yet been identified.
«
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.»
There is little dispute that genetics accounts for a large amount of the variation
in people's intelligence, but studies have consistently failed to
find any
single genes that have a substantial impact.
Although the
gene sequences were not identical to the Mikovits - Ruscetti XMRV
gene sequence reported
in Science, they were so close Lo believed he had
found genetic variants of a
single MLV - like virus species that likely included XMRV.
They
found a
single mutation
in the ADGRE2
gene shared by family members with vibratory urticaria but not present
in unaffected people.
The team
found that adding
in a
single extra copy of
gene that expresses Maf1 decreased stored lipids by 34 percent, while reducing Maf1 levels increased stored lipids by 94 percent.
With the completion of the first phase of the Human Genome Project
in 2000, and the advent of sequencing technologies that can detect
gene variations such as
single nucleotide polymorphisms (SNPs), for the first time scientists have the tools
in hand to
find the key immune
genes and genetic networks that play roles
in vaccine response.
The team
found that a
single polymorphism (a difference
in one «letter» of the sequence)
in the BDNF
gene accounted for significant differences
in intelligence among those with similar injuries and comparable intelligence before being injured.
«We report here a
gene therapy dose -
finding study
in a large animal model of a severe muscle disease where a
single treatment resulted
in dramatic rescue,» said Childers.
They
found up to seven variations of the
gene — some differing by as much as 25 % of their base pairs —
in a
single snail.
They
found a point mutation
in the
gene (a
single altered base pair)
in one of 91 randomly selected short individuals, and no such mutations
in 300 people of average height — suggesting that about 1 % of all short people may carry a SHOX mutation.
«The bad news about our
finding is that it shows that resistance can arise through
single mutations
in one
gene and pop up anywhere, at any time,» Dr. Fidock says.
An alteration
in the neuregulin - 1
gene — a
single change
in one letter of the DNA code for the protein — has been
found in families with schizophrenia and linked to late - onset Alzheimer's disease with psychosis.
The researchers, led by Dr Charles Wondji, used a wide range of methods to narrow down how the resistance works,
finding a
single mutation
in the GSTe2
gene, which makes insects break down DDT so it's no longer toxic.
Beyond offering further proof that
single genes can have dramatic influences on longevity, an idea that drew skepticism just a decade ago, the new
finding may help scientists explain how severely reducing calorie intake extends life span
in a variety of animals (SN: 11/25/00, p. 341: Low - cal diet may reduce cancer
in monkeys).
A recently published study from two Iowa State University scientists shows that a
gene found only
in a
single plant species can increase protein content when introduced into staple crops.
Now, a study led by a researcher at the Salk Institute has
found that variants of a
single gene can largely determine a plant's ability to thrive
in environments where iron is scarce.
A second major
finding of the new study, which analyzes the genomes of over 2,500 «simplex» families — those
in which a
single child but neither parent nor siblings, if any, have ASD — is that the pool of spontaneously mutated
genes contributing to ASD across the population totals about 400.
«This is an important
finding that will help future researchers, and eventually physicians, to maximize the effectiveness of
gene therapy for curtailing sensory deficits associated with USH3 syndrome and, perhaps,
in other disorders linked to defects
in single genes,» said Alagramam.
The team also compared the 7442
genes found as
single copies
in both the cobra and the python with the same
genes in all other land vertebrates sequenced so far.
In the years after finding the CFTR gene at the root of the disease, Collins, Tsui and others discovered the situation was far more complex than they had ever dreamed: Instead of just a single mutation in the gene, researchers found some 1,900 distinct mutation
In the years after
finding the CFTR
gene at the root of the disease, Collins, Tsui and others discovered the situation was far more complex than they had ever dreamed: Instead of just a
single mutation
in the gene, researchers found some 1,900 distinct mutation
in the
gene, researchers
found some 1,900 distinct mutations.
Nonetheless, not a
single life - extending
gene has been
found in the human genome yet.
Your feelings about brussels sprouts could come down to a
single gene: Researchers at the University of Connecticut
found that people missing the receptor for a bitter chemical called PROP tend to like veggies rich
in the compound.
Ruffled
genes Burke was part of a team that,
in 1995,
found that the different approaches of male ruffs were caused by a
single inherited factor.
The authors
find that evolved differences
in UV absorbance between the species could be explained by changes to a
single gene, MYB - FL.
In a study, published in Science, they investigated a gene region that contains a particular single nucleotide variant associated with increased risk for developing colorectal and prostate cancers — and found that removing this region caused dramatic resistance to tumor formatio
In a study, published
in Science, they investigated a gene region that contains a particular single nucleotide variant associated with increased risk for developing colorectal and prostate cancers — and found that removing this region caused dramatic resistance to tumor formatio
in Science, they investigated a
gene region that contains a particular
single nucleotide variant associated with increased risk for developing colorectal and prostate cancers — and
found that removing this region caused dramatic resistance to tumor formation.
The investigators
found that people who carry a
single copy of the KL - VS variant of the KLOTHO
gene, roughly 20 percent of the population, have more klotho protein
in their blood than non-carriers.
«Trying to
find a
single causative
gene for diseases with a complex genetic background is like looking for the proverbial needle
in a haystack,» says Lea Davis, PhD, of the section of Genetic Medicine at the University of Chicago, co-corresponding author of the PLOS Genetics report.
Two
genes critical to the immune system's adaptability
in battling viruses, bacteria and other invaders receive on and off signals from a
single DNA segment, HHMI researchers have
found.
In findings appearing online today in Cell Stem Cell, researchers in the laboratory of Gladstone Investigator Yadong Huang, MD, PhD, describe how they transferred a single gene called Sox2 into both mouse and human skin cell
In findings appearing online today
in Cell Stem Cell, researchers in the laboratory of Gladstone Investigator Yadong Huang, MD, PhD, describe how they transferred a single gene called Sox2 into both mouse and human skin cell
in Cell Stem Cell, researchers
in the laboratory of Gladstone Investigator Yadong Huang, MD, PhD, describe how they transferred a single gene called Sox2 into both mouse and human skin cell
in the laboratory of Gladstone Investigator Yadong Huang, MD, PhD, describe how they transferred a
single gene called Sox2 into both mouse and human skin cells.
For the 374 expressed
genes, we
find many regions with statistically significant association of
single nucleotide polymorphisms (SNPs) with expression variation
in lymphoblastoid cell lines after correcting for multiple tests.
July 3, 2013 New mechanism for human
gene expression discovered
In a study that could change the way scientists view the process of protein production in humans, University of Chicago researchers have found a single gene that encodes two separate proteins from the same sequence of messenger RN
In a study that could change the way scientists view the process of protein production
in humans, University of Chicago researchers have found a single gene that encodes two separate proteins from the same sequence of messenger RN
in humans, University of Chicago researchers have
found a
single gene that encodes two separate proteins from the same sequence of messenger RNA.
As an example, skeletal malformations and dysplasias, often detected through routine prenatal ultrasound examination, constitute a phenotypic
finding in more than 300 syndromic and non-syndromic disorders and their genetic etiology may be due to a wide variety of genetic aberrations, ranging from copy number variations to
single gene mutations.
A
single disabling change — an alteration of one nucleotide — was
found in the TRAPPC9
gene in all three girls.