According to the University of California San Francisco, Huntington’s disease affects one in every 10,000 to 20,000 people in ...
Acquired DNA mutations found in the SERPINA1 gene can protect liver cells from damage in patients with alpha-1 antitrypsin ...
SACRAMENTO, the United States -- Scientists are sounding the alarm about a concerning genetic mutation of the H5N1 bird flu ...
You may scarcely notice it, but much of what you do every day requires your brain to engage in perceptual learning. To safely ...
The Brighterside of News on MSN6d
Gene mutation linked to substantial risk of Parkinson’s diseaseParkinson’s disease (PD) affects nearly 2% of adults over 65, making it the second most common neurodegenerative disorder. It ...
News-Medical.Net on MSN4d
Ovarian cancer mutations across populations show similarities and unique differencesAn extensive tumor genomic analysis of individuals with ovarian cancer, led by researchers from Huntsman Cancer Institute at ...
An extensive tumor genomic analysis of individuals with ovarian cancer, led by researchers from Huntsman Cancer Institute at ...
News Nation on MSN4d
Luxembourg’s Prince Frederik dead from genetic disease at 22( NewsNation) — Prince Frederik of Luxembourg has died at 22 from POLG mitochondrial disease, a genetic disorder he has had since birth. The family announced his death one day after Rare Disease Day, ...
A drug originally developed for high blood pressure could find a new use in the treatment of Huntington's disease, thanks to an artificial intelligence-based drug discovery programme at Spain's ...
A novel mouse model offers definitive evidence that a single inhibitory receptor family governs the critical natural killer cell functions of licensing and missing-self.
R-708-5p is a stress-regulated microRNA and a potential biomarker for the differential diagnosis of human mood disorders.
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