BY The Sensa Team
Fragile X syndrome (FXS), due to mutations of the FMR1 gene, is the most common known inherited cause of developmental disability. The cognitive, behavioral, and neurological phenotypes observed in affected individuals…
READ MOREIn 2019, the world saw significant advances in the sophistication and pervasive use of artificial intelligence (“AI”). For instance, we witnessed the emergence of next-generation AI-powered natural text generators like…
It remains a significant challenge to define individual protein associations within networks where an individual protein can directly interact with other proteins and/or be part of large complexes, which contain functional…
Aortic stenosis (AS) is the most common valvular lesion, with >1 in 8 individuals aged 75 years and older having moderate or severe AS. The disease starts as focal leaflet thickening with calcification and gradually…