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Editor’s summary HNRNPH1 and HNRNPH2 are closely related RNA binding proteins with similar roles in RNA processing and splicing during neurogenesis. De novo mutations in the HNRNPH2 gene cause a rare and severe neurodevelopmental disorder for which there is currently no treatment. Here, Korff et al. designed gapmer antisense oligonucleotides (ASOs) to target Hnrnph2 and show that a knockdown of Hnrnph2 mRNA up-regulated Hnrnph1 mRNA and protein.
Abstract Old World orthohantaviruses, including Hantaan virus (HTNV), cause hemorrhagic fever with renal syndrome (HFRS) in Eurasia. Available inactivated vaccines often induce low neutralizing antibodies and short-term protection. We evaluated nucleic acid vaccines expressing a prefusion-stabilized HTNV glycoprotein in female BALB/c mice.
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