Jihong Hao

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Dear Editor, MYH9 disorders are autosomal dominant disorders, characterized by macrothrombocytopenia and granulocyte inclusion bodies, and include May–Hegglin anomaly (MHA), Sebastian syndrome (SBS), Fechtner syndrome (FTNS), and Epstein syndrome (EPTS). These disorders are caused by mutations in MYH9, which codes for the nonmuscle myosin heavy chain IIA(More)
Metals are vital toxic components of fine particulate matter (PM2.5). Cellular responses to exposure to PM2.5 or PM metal components remain unknown. Post-transcriptional profiling and subsequent cell- and individual-based assays implied that the metal ion-binding miR-4516/RPL37/autophagy pathway could play a critical role in cellular responses to PM2.5 and(More)
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