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Alphavirus-based vectors have been engineered for in vitro and in vivo expression of heterelogous genes.
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Since SAR did not cross-react with mouse RAGE, transgenic C57Bl6 mice expressing human RAGE were engineered for in vivo testing.
To this end, the α-, β-, and ω-oxidation pathways have been engineered for use in various hosts.
Glycosylation of pharmaceutical erythropoietin has been engineered for improved in vivo stability and erythropoetic activity [10].
In the past, many feature descriptors have been engineered for more robust matching in certain cases.
Gelatin/Alginate hydrogels were engineered for bioplotting in tissue engineering.
ZFNs (Sangamo) were engineered for expression in P. falciparum as described in the Supporting Information experimental section.
The orf18 gene was engineered for overexpression in Escherichia coli, and the recombinant ArdA protein was purified to homogeneity.
The new NDDS was engineered for use in photodynamic therapy (PDT) combined with hyperthermia (HPT) to address cancer treatment.
The micelle core was engineered for disintegration in early endosomal pH of tumor cells, quickly releasing DOX.
Low-defect potassium poly(heptazine imide) (PHIK-BM) was engineered for application in photocatalytic oxidation of organic substrates.
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