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One hundred and forty-one treatment-nave patients were classified into hepatitis B e antigen-negative chronic infection (HBeAg - CInf, n=44), HBeAg-negative chronic hepatitis (HBeAg - CHep, n=20), HBeAg + CInf (n=36), and HBeAg + CHep (n=41) based on an issued clinical practice guideline (4)
Most rare missense alleles are deleterious in humans: implications for complex disease and association studies
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Small molecule oral GLP-1 receptor agonists are currently in development, and we introduce how these chemicals have addressed the challenge posed by interactions with the large extracellular ligand binding domain of the GLP-1 receptor
