Ending the message is not so simple

[1] POLY(A) SITE SELECTION IN THE HIV-1 PROVIRUS - INHIBITION OF PROMOTER-PROXIMAL POLYADENYLATION BY THE DOWNSTREAM MAJOR SPLICE DONOR SITE [J]. GENES & DEVELOPMENT, 1995, 9 (23) : 3008 - 3025

[2] MULTIPLE FUNCTIONS FOR POLY(A)-BINDING PROTEIN IN MESSENGER-RNA DECAPPING AND DEADENYLATION IN YEAST [J]. GENES & DEVELOPMENT, 1995, 9 (19) : 2421 - 2432

[3] EDWALDSGILBERT G, 1995, MOL CELL BIOL, V15, P6420

[4] SEQUENCES HOMOLOGOUS TO 5' SPLICE SITES ARE REQUIRED FOR THE INHIBITORY ACTIVITY OF PAPILLOMAVIRUS LATE 3' UNTRANSLATED REGIONS [J]. MOLECULAR AND CELLULAR BIOLOGY, 1994, 14 (08) : 5278 - 5289

[5] THE HUMAN U1A SNRNP PROTEIN REGULATES POLYADENYLATION VIA A DIRECT INTERACTION WITH POLY(A) POLYMERASE [J]. CELL, 1994, 76 (03) : 531 - 541

[6] An intron enhancer recognized by splicing factors activates polyadenylation [J]. GENES & DEVELOPMENT, 1996, 10 (02) : 208 - 219

[7] Interaction between the U1 snRNP-A protein and the 160-kD subunit Of cleavage-polyadenylation specificity factor increases polyadenylation efficiency in vitro [J]. GENES & DEVELOPMENT, 1996, 10 (03) : 325 - 337

[8] ALTERNATIVE POLY(A) SITE UTILIZATION DURING ADENOVIRUS INFECTION COINCIDES WITH A DECREASE IN THE ACTIVITY OF A POLY(A) SITE PROCESSING FACTOR [J]. MOLECULAR AND CELLULAR BIOLOGY, 1993, 13 (04) : 2411 - 2419

[9] REGULATED IMMUNOGLOBULIN (IG) RNA PROCESSING DOES NOT REQUIRE SPECIFIC CIS-ACTING SEQUENCES - NON-IG RNA CAN BE ALTERNATIVELY PROCESSED IN B-CELLS AND PLASMA-CELLS [J]. MOLECULAR AND CELLULAR BIOLOGY, 1994, 14 (12) : 7891 - 7898

[10] THE REGULATED PRODUCTION OF MU-M AND MU-S MESSENGER-RNA IS DEPENDENT ON THE RELATIVE EFFICIENCIES OF MU-S POLY(A) SITE USAGE AND THE C-MU-4-TO-M1 SPLICE [J]. MOLECULAR AND CELLULAR BIOLOGY, 1989, 9 (02) : 726 - 738

[1] POLY(A) SITE SELECTION IN THE HIV-1 PROVIRUS - INHIBITION OF PROMOTER-PROXIMAL POLYADENYLATION BY THE DOWNSTREAM MAJOR SPLICE DONOR SITE [J]. GENES & DEVELOPMENT, 1995, 9 (23) : 3008 - 3025

[2] MULTIPLE FUNCTIONS FOR POLY(A)-BINDING PROTEIN IN MESSENGER-RNA DECAPPING AND DEADENYLATION IN YEAST [J]. GENES & DEVELOPMENT, 1995, 9 (19) : 2421 - 2432

[3] EDWALDSGILBERT G, 1995, MOL CELL BIOL, V15, P6420

[4] SEQUENCES HOMOLOGOUS TO 5' SPLICE SITES ARE REQUIRED FOR THE INHIBITORY ACTIVITY OF PAPILLOMAVIRUS LATE 3' UNTRANSLATED REGIONS [J]. MOLECULAR AND CELLULAR BIOLOGY, 1994, 14 (08) : 5278 - 5289

[5] THE HUMAN U1A SNRNP PROTEIN REGULATES POLYADENYLATION VIA A DIRECT INTERACTION WITH POLY(A) POLYMERASE [J]. CELL, 1994, 76 (03) : 531 - 541

[6] An intron enhancer recognized by splicing factors activates polyadenylation [J]. GENES & DEVELOPMENT, 1996, 10 (02) : 208 - 219

[7] Interaction between the U1 snRNP-A protein and the 160-kD subunit Of cleavage-polyadenylation specificity factor increases polyadenylation efficiency in vitro [J]. GENES & DEVELOPMENT, 1996, 10 (03) : 325 - 337

[8] ALTERNATIVE POLY(A) SITE UTILIZATION DURING ADENOVIRUS INFECTION COINCIDES WITH A DECREASE IN THE ACTIVITY OF A POLY(A) SITE PROCESSING FACTOR [J]. MOLECULAR AND CELLULAR BIOLOGY, 1993, 13 (04) : 2411 - 2419

[9] REGULATED IMMUNOGLOBULIN (IG) RNA PROCESSING DOES NOT REQUIRE SPECIFIC CIS-ACTING SEQUENCES - NON-IG RNA CAN BE ALTERNATIVELY PROCESSED IN B-CELLS AND PLASMA-CELLS [J]. MOLECULAR AND CELLULAR BIOLOGY, 1994, 14 (12) : 7891 - 7898

[10] THE REGULATED PRODUCTION OF MU-M AND MU-S MESSENGER-RNA IS DEPENDENT ON THE RELATIVE EFFICIENCIES OF MU-S POLY(A) SITE USAGE AND THE C-MU-4-TO-M1 SPLICE [J]. MOLECULAR AND CELLULAR BIOLOGY, 1989, 9 (02) : 726 - 738