Scientists have discovered an on-and-off “switch” in cells that may hold the key to...
The DNA of every organism on Earth is a right-handed double helix, but why that would be...
On this episode of Bioscience Technology This Week, Christina Jakubowski focuses on a new...
Spontaneous mutations in the brain gene TBR1 disrupt the function of the encoded protein in children with severe autism. In addition, there is a direct link between TBR1 and FOXP2, a well-known language-related protein, according to a new study.
By comparing nine ancient genomes to those of modern humans, scientists have shown that previously unrecognized groups contributed to the genetic mix now present in most modern-day Europeans.
On this episode of Bioscience Technology This Week, Christina Jakubowski reports on new research seeking to prove how life on Earth began, by tracking the ancestors of RNA and DNA. Our second story focuses on the possibility of developing high-quality computed tomography scans from a lower radiation dose.
Researchers have identified clues to explain how breast implants may, on very rare occasions, contribute to the development of lymphoma. There have been 71 known cases worldwide of a type of blood cancer called anaplastic large cell lymphoma (ALCL) that the researchers suggest were associated with the patient's breast implants.
Researchers have identified a highly sensitive means of analyzing very tiny amounts of DNA. The discovery, they say, could increase the ability of forensic scientists to match genetic material in some criminal investigations.
Neuroscientists have found that a gene mutation that arose more than half a million years ago may be key to humans’ unique ability to produce and understand speech.
Researchers have identified nine genetic variants that dramatically increase the risk of developing type 2 diabetes, adding to our knowledge of the disease’s underpinnings and providing a glimpse of its vast genetic diversity.
A rare genetic disorder known as Jacobsen syndrome has been linked with autism, according to a recent joint investigation by researchers. In addition to suggesting better treatment options for people with Jacobsen syndrome, the finding also offers more clues into the genetic underpinnings of autism.
The story of cancer care seems so simple: find the mutated gene that causes cancer and turn it off or fix it. But rarely does a single gene cause cancer. More often, many genes are altered together to drive the disease. So the challenge becomes sorting out which altered genes are the most to blame in which cancers. A new study takes an important step toward answering this question in bladder cancer.
Researchers have discovered how two genes– Period and Cryptochrome– keep the circadian clocks in all human cells in time and in proper rhythm with the 24-hour day, as well as the seasons.
New research shows that schizophrenia isn’t a single disease but a group of eight genetically distinct disorders, each with its own set of symptoms.
Researchers have found that the genetic mutation BRAFV600E , frequently found in metastatic melanoma, not only secretes a protein that promotes the growth of melanoma tumor cells, but can also modify the network of normal cells around the tumor to support the disease's progression.
A new study has identified a pathological process that takes place in both mice and humans towards one of the most common diseases that people face in the industrialized world: type 2 diabetes.
Last November, the Food and Drug Administration ordered the company to stop marketing its personalized health reports, which purported to tell customers if they were genetically predisposed to more than 250 diseases and medical conditions. Now, 23andMe is working to win FDA clearance for its health tests one at a time.
Over the years researchers have made tremendous strides in the understanding and treatment of cancer by searching genomes for links between genetic alterations and disease. Now, a team of researchers has mined "junk DNA" sequences to identify a non-protein-coding RNA whose expression is linked to ovarian cancer.
New research published in the Proceedings of the National Academy of Science (PNAS) shows three genetic variants in humans that can account for a couple of IQ points– but before you get excited, these are only three variants out of likely thousands.
Life can be so intricate and novel that even a single cell can pack a few surprises, according to a new study. The pond-dwelling, single-celled organism Oxytricha trifallax has the remarkable ability to break its own DNA into nearly a quarter-million pieces and rapidly reassemble those pieces when it's time to mate, the study says.
Biologists have identified a gene that can slow the aging process throughout the entire body when activated remotely in key organ systems.
Were Albert Einstein and Leonardo da Vinci born brilliant or did they acquire their intelligence through effort? No one knows for sure, but telling people the latter– that hard work trumps genes– causes instant changes in the brain and may make them more willing to strive for success, indicates a new study.
The way in which some cells alter their behavior at the onset of osteoarthritis has been identified for the first time. Researchers found that changes in the rate at which molecules in joint cartilage called mRNA are created and destroyed are fundamental to causing this change in behavior.
An international team of researchers has identified a new inherited neuromuscular disorder. The rare condition is the result of a genetic mutation that interferes with the communication between nerves and muscles, resulting in impaired muscle control.
Researchers report that cells taken from the nasal septum are able to adapt to the environment of the knee joint and can thus repair articular cartilage defects. Read more...
In response to an ongoing, unprecedented outbreak of Ebola virus disease (EVD) in West Africa, a team of researchers has rapidly sequenced and analyzed more than 99 Ebola virus genomes.
Scientists have solved the mystery of why a specific signaling pathway can be associated with alcohol dependence. This signaling pathway is regulated by a gene, called neurofibromatosis type 1 (Nf1), which is linked with excessive drinking in mice.
A multi-institution research network has published three major papers that map and compare the genomes and epigenomes of humans and two model organisms, the fly, Drosophila melanogaster, and the worm, Caenorhabditis elegans, in unprecedented detail.
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