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Chemical polysialylation and in vivo tetramerization improve pharmacokinetic characteristics of recombinant human butyrylcholinesterase-based bioscavengers, we examine two approaches for long-acting rhBChE production: I) chemical polysialylation and II) in-vivo
Chemical polysialylation and in vivo tetramerization improve pharmacokinetic characteristics of recombinant human butyrylcholinesterase-based bioscavengers, we examine two approaches for long-acting rhBChE production: I) chemical polysialylation and II) in-vivo
Application of Tetrameric Recombinant Human Butyrylcholinesterase as a Biopharmaceutical for Amelioration of Symptoms of Acute Organophosphate Poisoning of recombinant tetrameric butyrylcholinesterase that enables large-scale production with the yield > 30 mg
Application of Tetrameric Recombinant Human Butyrylcholinesterase as a Biopharmaceutical for Amelioration of Symptoms of Acute Organophosphate Poisoning of recombinant tetrameric butyrylcholinesterase that enables large-scale production with the yield > 30 mg
The DFT-DVM theoretical study of the differences of quadrupole splitting and the iron electronic structure for the rough heme models for alpha- and beta-subunits in deoxyhemoglobin and for deoxymyoglobinTETRAMERIC DEOXYHEMOGLOBIN
Compounds identified by virtual docking to a tetrameric EGFR extracellular domain can modulate Grb2 internalization studies have identified a novel prone extracellular tetrameric EGFR configuration, which we identify as a
Compounds identified by virtual docking to a tetrameric EGFR extracellular domain can modulate Grb2 internalization studies have identified a novel prone extracellular tetrameric EGFR configuration, which we identify as a
Определение полулетальной дозы гидрохлортиазида в экспериментах in vivoЦель данного исследования – определение полулетальной дозы гидрохлортиазида в экспериментах in vivo
3D structure of the natural tetrameric form of human butyrylcholinesterase as revealed by cryoEM, SAXS and MD-length glycosylated tetrameric human BChE have been unsuccessful so far. Here, a combination of three complementary
Compounds identified by virtual docking to a tetrameric EGFR extracellular domain can modulate Grb2 internalization studies have identified a novel prone extracellular tetrameric EGFR configuration, which we identify as a
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