genetics

The effort will encompass a 100,000-person study to discover the causes of depression, a new treatment center and a community outreach program.

Using Broad Stem Cell Research Center’s cell isolation and genetic sequencing technologies and sophisticated bioinformatics, scientists identify elusive LncRNA genes.

A new UCLA program offers hope and potential answers for people who have undergone extensive medical testing but still don’t know what is causing their symptoms.

Other diagnostic tools may be more efficient and cost-effective for the general population, although genetic screening remains valuable for women in groups known to carry certain genetic mutations.

Soraya de Chadarevian, a professor in the UCLA Department of History and the Institute for Society and Genetics, has been awarded an NSF grant to explore the history of genetics research.

The DNA-based discovery means the biological family Canidae has 36 members, not 35.

Findings are the first to shed light on the genetic differences between DiGeorge syndrome patients with autism and those with psychosis.

New study focuses on rare DNA mutations that affect protein function.

Research by scientists at the Broad Stem Cell Research Center shows that the cells carrying parents’ genes to a child are unprotected during part of the prenatal stage of development.

The team, led by Dr. Joanne Weidhaas, found that acute estrogen withdrawal was associated with breast cancer in women with the KRAS-variant.

Two UCLA researchers are asking the public to help in their study of the online phenomenon.

Several new studies, one co-authored by a UCLA professor, show that transcription is in fact the most influential step in determining protein abundance.

Stem cell gene therapy technique leads to production of healthy blood cells, could be used for other genetic diseases.

Life scientists have created an accurate new method to identify markers for many diseases — a significant step toward a new era of personalized medicine, tailored to each person’s DNA and RNA.

Scientists found that removing a specific molecular switch from a mutant protein can trigger symptoms in mice that are similar to those found in people with the disease.

Genes relating to immune function and histone methylation — molecular changes that alter DNA expression — are risk factors.

Why do some people develop PTSD while others who suffered the same ordeal do not? A UCLA discovery may shed light on the answer.

People with a deficiency of the iron-regulating hormone hepcidin are especially vulnerable to Vibrio vulnificus, but research shows a medical form of the hormone can cure the infection.

The scientists resolved a dispute over whether a small population of black-headed squirrel monkeys, which are found only in an isolated part of Brazil, is a sub-species of another species or its own species.

Scientists from UCLA, Harvard, Mass General and Stanford present strong evidence that a chemical modification on RNA plays a key role in determining embryonic stem cells’ ability to adopt different cellular identities.

When adult mice with Noonan syndrome were treated with lovastatin, their memory and ability to remember objects and navigate mazes improved dramatically.

The disease may be more harmful than previously thought, say UCLA researchers, who found genetic damage is present not only in the lungs but also in circulating blood.

UCLA researchers have developed a standard to assess how closely stem cell culture conditions in the lab resemble a developing embryo.

UCLA research may lead to a simple saliva test to diagnose at an early stage diabetes and cancer, and perhaps neurological disorders and autoimmune diseases.

A landmark UCLA study makes a persuasive argument for the routine clinical use of DNA sequencing as a tool for diagnosing children with rare genetic disorders.