Green fluorescent protein as a real time quantitative reporter of heterologous protein production
Albano CR, Randers-Eichhorn L, Bentley WE, Rao G. 1998. Green fluorescent protein as a real time quantitative reporter of heterologous protein production. Biotechnol Prog 14:351-354.
Tightly regulated tac promoter vectors useful for the expression of unfused and fused proteins in Escherichia coli
Amann E, Ochs B, Abel KJ. 1988. Tightly regulated tac promoter vectors useful for the expression of unfused and fused proteins in Escherichia coli. Gene 69:301-315.
Quantitative analysis of ribosome binding sites in E. coli
Barrick D, Villanueba K, Childs J, Kalil R, Schneider TD, Lawrence CE, Gold L, Stormo D. 1994. Quantitative analysis of ribosome binding sites in E. coli. Nucleic Acids Res 22:1287-1295.
Translational initiation on structured messengers. Another role for the Shine-Dalgarno interaction
de Smit MH, van Duin J. 1994. Translational initiation on structured messengers. Another role for the Shine-Dalgarno interaction. J Mol Biol 235:173-184.
Optimization of DsRed production in Escherichia coli: Effect of ribosome binding site sequestration on translation efficiency
Pfleger BF, Fawzi NJ, Keasling JD. 2005. Optimization of DsRed production in Escherichia coli: Effect of ribosome binding site sequestration on translation efficiency. Biotechnol Bioeng 92:553-558.
Control of cloned gene expression by promoter inversion in vivo: Construction of the heat-pulse-activated att-nutL-p-att-N module
Podhajska AJ, Hasan N, Szybalski W. 1985. Control of cloned gene expression by promoter inversion in vivo: Construction of the heat-pulse-activated att-nutL-p-att-N module. Gene 40:163-168.
Expression plasmid with a very tight two-step control: Int/att-mediated gene inversion with respect to the stationary promoter
Sektas M, Hasan N, Szybalski W. 2001. Expression plasmid with a very tight two-step control: Int/att-mediated gene inversion with respect to the stationary promoter. Gene 267:213-220.