This important study introduces a new biology-informed strategy for deep learning models aiming to predict mutational effects in antibody sequences. It provides solid evidence that separating ...

The acquisition of mutations conferring a high level of resistance to sotrovimab and the dynamics of the viral load of severe acute respiratory syndrome coronavirus 2 ...

The most common genetic cause of hereditary deafness in humans are mutations in the GJB2 gene, especially the 35delG and 235delC mutations. At the recent ARO meeting, researchers from Ear Nose and ...

In a recent study posted to PLOS Pathogens, researchers analyzed the structural function of the genetic background of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) in the appearance and ...

Inhibition of emerging polyclonal on-target acquired resistance mutations remains a critical unmet need in the treatment of fibroblast growth factor receptor 2 (FGFR2)-driven tumors. In the current ...