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The Ebola epidemic that tore through West Africa in 2014 claimed 11,310 lives, far more than any previous outbreak. A combination of factors contributed to its savagery, among them a mobile population, crumbling public health systems, official neglect and hazardous burial practices. But new research suggests another impetus: The virus may have evolved a new weapon against its human hosts. In studies published on Thursday in the journal Cell, two teams of scientists report that a genetic mutation may have made Ebola more deadly by improving the virus's ability to enter human cells.

The advent of increasingly powerful and inexpensive DNA sequencing methods is changing many aspects of genetics research. In particular, human genome sequencing is transforming our understanding of many aspects of human biology and medicine. However, we must be careful to remember that genes alone do not determine our futures-environmental factors and chance also play important roles.

Dean Ornish shares new research that shows how adopting healthy lifestyle habits can affect a person at a genetic level. For instance, he says, when you live healthier, eat better, exercise, and love more, your brain cells actually increase.

A stride to understand the cancer and move towards its prevention, this time experts from around the world involved in searching the genome of cancer have analyzed the mutational signatures, the processes of mutation in the DNA of cells (which are always in the origin of cancer) and they follow a fixed pattern.

Of two genetically identical mice, how can one be small and another fat? Research on epigenetic changes resulting from the environment can give us clues into obesity in mice--and humans.

The UK's leading cancer charity yesterday welcomed work by British scientists who created a breed of genetically modified hens that can produce cancer-fighting medicines in their eggs. The research could slash the cost of producing drugs and potentially save the NHS millions of pounds.

Using a patient's own stem cells, researchers have corrected the genetic alteration that causes sickle cell disease, a painful, disabling inherited blood disorder that affects mostly African-Americans. The corrected stem cells were coaxed into immature red blood cells in a test tube that then turned on a normal version of the gene

Huntington disease is caused by a mutation in the HTT gene. Understanding how the mutation causes neurodegeneration might help researchers develop treatments that protect brain function. This animation describes the genetic defect that underlies Huntington disease. Created by the editors at Nature Reviews Disease Primers.

WEDNESDAY, April 22, 2015 (HealthDay News) -- In a step toward personalized vaccines against cancer, scientists report they have developed an immune-system therapy that knocks out several types of aggressive tumors in mice. German researchers said the findings, reported April 22 in the journal Nature, could lead to a "blueprint" for developing tailored vaccines for a range of cancers. Such vaccines would be designed for individual patients, based on the specific genetic mutations in their tumors.

By then, researchers had identified three genetic mutations that can be inherited and, if they are, cause a form of Alzheimer's called early onset because it strikes before age 65 and sometimes far earlier. Since 2004, Hornstein and all five of her siblings have been tested. Hornstein is the only one who doesn't carry PSEN1, one of the mutations.

This video excerpt from NOVA examines the promise and realities of developing drugs designed to treat genetic disorders. The video presents the story of one patient, Michael McCarrick, whose lungs were devastated from years of suffering from cystic fibrosis. After researchers identified the gene involved in cystic fibrosis, it took decades to find ways to fortify the faulty protein responsible for the serious illness. While two drugs, including one called Kalydeco, offer a small number of patients hope that they will not have to endure a lung transplant, it may be years and several hundred million more development dollars before effective drugs are available for a wider population.

A decade ago, an international research team completed an ambitious effort to read the 3 billion letters of genetic information found in every human cell. The program, known as the Human Genome Project, provided the blueprint for human life, an achievement that has been compared to landing a man on the moon.

A decade-old technique that allows researchers to control brain function in lab animals could partially restore sight to the blind. In a trial sponsored by RetroSense Therapeutics, a startup company in Ann Arbor, Michigan, doctors will inject a harmless virus loaded with DNA from photoreceptive algae into the eyes of 15 patients suffering from retinitis pigmentosa. The experimental procedure represents the first human test of optogenetics, which is a technique that genetically modifies neurons to make them responsive to light. Doctors from the Retina Foundation of the Southwest will perform the procedure, and attempt to transfer the job duties of photoreceptor cells to different cells in the eye to restore sight.

Biologists have long puzzled about how evolutionary selection, known for its ruthless requirement for efficiency, allows the existence of males - when in so many species their only contribution to reproduction are spermatozoa. But research published today in Nature shows that sexual selection - when males compete and females choose over reproduction - improves population health and protects against extinction, even in the face of genetic stress from high levels of inbreeding.

Similar to humans who have obsessive compulsive disorder, dogs exhibit compulsive behaviors, in which they might repetitively spin around, chase their tail, bark, chew, or suck on a toy or a part of their body for an excessive amount of time. In the latest study from Tufts University, researchers identified genetic pathways that increase the severity of canine compulsive disorders in Doberman pinschers. This discovery may lead to the development of improved treatments and therapies for obsessive compulsive disorder (OCD) in people. 

The researchers concluded that genetics - or perhaps other factors, such as environmental influences - play a larger role than practice in certain aspects of musical talent such as recognizing pitch and rhythms. Mosey and her colleagues made another interesting finding: Genes may determine a person's motivation to practice. The majority of participants who reported practicing a lot also shared a high percentage of the same genes. "The association between practice and skill was largely due to the same genes, suggesting that practice will not necessarily make you perfect, but it certainly will enhance your skills," Mosey said.

Medical researchers have discovered a gene that increases the risk of schizophrenia, a mental illness that affects more than 2 million Americans, sometimes causing delusions and hallucinations. The finding was first reported this week in the scientific journal "Nature".

A genetic "crystal ball" can predict whether certain people will respond effectively to the flu vaccine. Nine genes are associated with a strong immune response to the flu vaccine in those aged 35 and under, a new study finds. If these genes were highly active before vaccination, an individual would generate a high level of antibodies after vaccination, no matter the flu strain in the vaccine, researchers report online August 25 in Science Immunology. This response can help a person avoid getting the flu.

This case study centers on symbiotic relationships between insects and bacteria using Drosophila melanogaster, the common fruit fly, and the recently discovered bacterial species Sodalis praecaptivus. Until recently, the only known Sodalis species of bacteria were symbiotically associated with several different species of insects. However, free-living non-symbiont Sodalis species are being tested in several different insect species to determine if they can transition into symbiotic relationships. A pre-class assignment (see Supplemental Materials) directs students to read an open access research journal article providing a comprehensive review of S. praecaptivus and describing an experimental weevil model that parallels that of the fruit fly. A PowerPoint presentation shown in class (see Supplemental Materials) provides further background before students work in small groups to complete the case study focusing on results from D. melanogaster and S. praecaptivus model experiments.  Although developed for a genetics course, this interrupted case is appropriate for an upper-level biology course. It can be completed within a 75-minute class meeting, or adapted for shorter time periods.

A zebrafish model of a rare genetic disease has revealed an unexpected regulatory pathway for cholesterol absorption and processing. The findings, reported in the Journal of Molecular Medicine, were "quite surprising and have the potential to teach us about the basic physiology of cholesterol management," said Ela Knapik, M.D., associate professor of Medicine and Cell and Developmental Biology.