A multi-institutional team of researchers has created a new and improved genetic map for the laboratory rat, a cornerstone in medical and scientific research. Known as GRCr8, this updated genome assembly enhances the ability to study human diseases, behaviors and genetic traits more precisely.
Dietetics professor explains who should and should not embrace the latest weight-loss drugs
Holiday weight gain hits home for many come January. These days, folks making resolutions to slim down and get fit have an increasingly popular option to consider: GLP-1s.
Jointly active when it matters: Nerve cells in the eye work together to recognize contrast and movements
The processing of optical information in the retina of the eye, where the light-sensitive photoreceptors and the first nerve cells are located, is one of the most energy-intensive processes in the organism, especially in view of the low relative weight of the retina.
Machine learning helps predict ADHD in kindergarten students
A University of Alberta research team has successfully used machine learning as a tool for earlier detection of attention deficit hyperactivity disorder (ADHD) in kindergarten students.
Small antibody offers broad protection against influenza
Researchers at the University of Gothenburg, Sweden, in collaboration with colleagues in China, have discovered an antibody-like molecule that can protect mice from various influenza viruses. The findings could pave the way for new treatments and the development of broader influenza vaccines. The work is published in Nature Communications.
Genetic changes in brain cells link aging and Alzheimer’s
Genetic differences that contribute to how long a person will live and their risk of Alzheimer’s disease have been identified by researchers at UCL and the UK Dementia Research Institute (UK DRI).
Antiviral protein causes genetic changes implicated in Huntington’s disease progression
People genetically susceptible to Huntington’s disease often see their movement, mood, and cognition decline slowly over time. The cause is related to expansion of repeating DNA units, in which specific strings of genetic code—in this case, a series of cytosine-adenine-guanine nucleotides, or CAG, on one strand of the DNA and cytosine-thymine-guanine, or CTG, on the complementary strand—begin to repeat over and over, expanding to as many as 40 to 120 copies.
Science behind genetic testing for identifying risk of opioid misuse remains unproven, says study
Opioid misuse and specifically opioid use disorder (OUD), continues to represent a significant U.S. public health threat, with more than 6 million Americans aged 12 and older meeting the criteria for OUD in 2022. Efforts to ease the crisis have included the development of genetic testing to identify individuals most at risk for OUD.
Researchers enhance automated method to detect common sleep disorder affecting millions
A Mount Sinai-led team of researchers has enhanced an artificial intelligence (AI)-powered algorithm to analyze video recordings of clinical sleep tests, ultimately improving accurate diagnosis of a common sleep disorder affecting more than 80 million people worldwide.
Stimulant users are caught in fatal ‘fourth wave’ of opioid epidemic
In Pawtucket, Rhode Island, near a storefront advertising “free” cellphones, J.R. sat in an empty back stairwell and showed a reporter how he tries to avoid overdosing when he smokes crack cocaine. KFF Health News is identifying him by his initials because he fears being arrested for using illegal drugs.