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Fig 7. Structural and Functional Characterization of NS3-IRS1 Interaction and Its Impact on GLUT4 Expression. (A) GRAMM platform generated protein interaction overview and surface model based on docking of IRS1 and NS3-HD12 structure, highlighting key residues within the NS3 helicase domain (HD12; amino acids 180-481) involved in the interaction with IRS1.
Abstract Vinyl ethyl ether (VEE) is a key intermediate in the synthesis of pharmaceutical compounds, making accurate determination of arsenic (As) levels in VEE essential for pharmaceutical quality control. However, highly accurate analysis of VEE is challenging owing to its high volatility and potential loss of volatile arsenic compounds.
Introduction Cardiovascular diseases (CVD) pose a significant threat to human health and represent the primary cause of non-communicable disease-related deaths worldwide [1]. In 2015, out of 39.8 million deaths attributed to non-communicable diseases, 17.9 million were due to CVD [1]. The high fatality rate associated with CVD has raised concern globally, emphasizing the urgency of prevention and control.
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