SEQUENCES REQUIRED FOR ANTITERMINATION BY PHAGE-82 Q-PROTEIN

[1] VECTORS BEARING A HYBRID TRP-LAC PROMOTER USEFUL FOR REGULATED EXPRESSION OF CLONED GENES IN ESCHERICHIA-COLI [J]. GENE, 1983, 25 (2-3) : 167 - 178

[2] IDENTIFICATION AND CHARACTERIZATION OF A NEW TRANSCRIPTIONAL TERMINATION FACTOR FROM ESCHERICHIA-COLI [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES, 1984, 81 (23): : 7373 - 7377

[3] PROCEDURE FOR RAPID, LARGE-SCALE PURIFICATION OF ESCHERICHIA-COLI DNA-DEPENDENT RNA-POLYMERASE INVOLVING POLYMIN-P PRECIPITATION AND DNA-CELLULOSE CHROMATOGRAPHY [J]. BIOCHEMISTRY, 1975, 14 (21) : 4634 - 4638

[4] INTERACTION OF RNA-POLYMERASE WITH LACUV5 PROMOTER DNA DURING MESSENGER-RNA INITIATION AND ELONGATION - FOOTPRINTING, METHYLATION, AND RIFAMPICIN-SENSITIVITY CHANGES ACCOMPANYING TRANSCRIPTION INITIATION [J]. JOURNAL OF MOLECULAR BIOLOGY, 1985, 183 (02) : 165 - 177

[5] SPECIFICITY OF THE BACTERIOPHAGE LAMBDA-N GENE-PRODUCT (PN) - NUT SEQUENCES ARE NECESSARY AND SUFFICIENT FOR ANTI-TERMINATION BY PN [J]. CELL, 1979, 18 (04) : 1145 - 1151

[6] TRANSCRIPTION ANTITERMINATION INVITRO BY LAMBDA-N-GENE PRODUCT - REQUIREMENT FOR A PHAGE NUT SITE AND THE PRODUCTS OF HOST NUSA-GENE, NUSB-GENE, AND NUSE-GENE [J]. CELL, 1984, 38 (01) : 165 - 173

[7] Friedman DI., 1983, LAMBDA, P21

[8] GOLIGER JA, 1987, J BIOL CHEM, V262, P11721

[9] EARLY TRANSCRIBED SEQUENCES AFFECT TERMINATION EFFICIENCY OF ESCHERICHIA-COLI RNA-POLYMERASE [J]. JOURNAL OF MOLECULAR BIOLOGY, 1989, 205 (02) : 331 - 341

[10] THE PHAGE-LAMBDA Q GENE-PRODUCT - ACTIVITY OF A TRANSCRIPTION ANTI-TERMINATOR INVITRO [J]. CELL, 1982, 30 (02) : 637 - 648

[1] VECTORS BEARING A HYBRID TRP-LAC PROMOTER USEFUL FOR REGULATED EXPRESSION OF CLONED GENES IN ESCHERICHIA-COLI [J]. GENE, 1983, 25 (2-3) : 167 - 178

[2] IDENTIFICATION AND CHARACTERIZATION OF A NEW TRANSCRIPTIONAL TERMINATION FACTOR FROM ESCHERICHIA-COLI [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES, 1984, 81 (23): : 7373 - 7377

[3] PROCEDURE FOR RAPID, LARGE-SCALE PURIFICATION OF ESCHERICHIA-COLI DNA-DEPENDENT RNA-POLYMERASE INVOLVING POLYMIN-P PRECIPITATION AND DNA-CELLULOSE CHROMATOGRAPHY [J]. BIOCHEMISTRY, 1975, 14 (21) : 4634 - 4638

[4] INTERACTION OF RNA-POLYMERASE WITH LACUV5 PROMOTER DNA DURING MESSENGER-RNA INITIATION AND ELONGATION - FOOTPRINTING, METHYLATION, AND RIFAMPICIN-SENSITIVITY CHANGES ACCOMPANYING TRANSCRIPTION INITIATION [J]. JOURNAL OF MOLECULAR BIOLOGY, 1985, 183 (02) : 165 - 177

[5] SPECIFICITY OF THE BACTERIOPHAGE LAMBDA-N GENE-PRODUCT (PN) - NUT SEQUENCES ARE NECESSARY AND SUFFICIENT FOR ANTI-TERMINATION BY PN [J]. CELL, 1979, 18 (04) : 1145 - 1151

[6] TRANSCRIPTION ANTITERMINATION INVITRO BY LAMBDA-N-GENE PRODUCT - REQUIREMENT FOR A PHAGE NUT SITE AND THE PRODUCTS OF HOST NUSA-GENE, NUSB-GENE, AND NUSE-GENE [J]. CELL, 1984, 38 (01) : 165 - 173

[7] Friedman DI., 1983, LAMBDA, P21

[8] GOLIGER JA, 1987, J BIOL CHEM, V262, P11721

[9] EARLY TRANSCRIBED SEQUENCES AFFECT TERMINATION EFFICIENCY OF ESCHERICHIA-COLI RNA-POLYMERASE [J]. JOURNAL OF MOLECULAR BIOLOGY, 1989, 205 (02) : 331 - 341

[10] THE PHAGE-LAMBDA Q GENE-PRODUCT - ACTIVITY OF A TRANSCRIPTION ANTI-TERMINATOR INVITRO [J]. CELL, 1982, 30 (02) : 637 - 648