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The antibiotic-resistant gene was removed from the genomic DNA of W303-1b/F using the Cre- loxP system, then W303-1b/F cells were further transformed with the linearized recombinant plasmid pGAPg-gshF to obtain engineered strain W303-1b/FF (Table 2)

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At the computational level, the structural differences between the enzyme-inhibitor binding sites of hTYR and mTYR were revealed

Emerging evidence VIP for allergic asthma has strong preclinical support but clinical application is limited by delivery challenges

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Lung function in men with and without HIV