News-Medical.Net on MSN
Single-cell technique maps pre-malignant gene mutations in solid tissues
A new single-cell profiling technique has mapped pre-malignant gene mutations and their effects in solid tissues for the ...
Mutations in the tumor suppressor TP53 are a common cause of cancer, making the altered protein an attractive target for ...
9don MSN
Childhood deafness: Researchers identify over 200 mutations, including previously unknown variants
Deafness, the most common sensorineural hearing loss at all stages of life, occurs either independently or as part of ...
Live Science on MSN
These genes were thought to lead to blindness 100% of the time. They don't.
Genetic variants believed to cause blindness in nearly everyone who carries them actually lead to vision loss less than 30% ...
A new study headed by teams at the Wellcome Sanger Institute, EMBL’s European Bioinformatics Institute (EMBL-EBI), and Open Targets has indicated how mutations that cause cancer drug resistance fall ...
A rare form of diabetes affecting newborn babies and caused by a genetic disorder has been discovered by scientists in the UK ...
New York, NY [December 15, 2025] —Scientists at the Icahn School of Medicine at Mount Sinai have developed a novel artificial intelligence tool that not only identifies disease-causing genetic ...
Many people are familiar with histamine, a biological molecule that serves as a key driver of allergic reactions and other ...
Researchers have discovered a rare new type of diabetes that affects babies early in life. The condition is caused by changes ...
A lung cancer diagnosis can feel frightening. And when a family member is diagnosed, you might wonder about your own risk, prompting you to ask if lung cancer is hereditary. Smoking tobacco accounts ...
Some results have been hidden because they may be inaccessible to you
Show inaccessible results