3'-END CLEAVAGE AND POLYADENYLATION OF MESSENGER-RNA PRECURSORS

[31] ANALYSIS OF MESSENGER-RNA 3' END FORMATION BY MODIFICATION INTERFERENCE - THE ONLY MODIFICATIONS WHICH PREVENT PROCESSING LIE IN AAUAAA AND THE POLY(A) SITE [J]. EMBO JOURNAL, 1987, 6 (13) : 4177 - 4184

[32] THE HUMAN U1 SNRNA PROMOTER AND ENHANCER DO NOT DIRECT SYNTHESIS OF MESSENGER-RNA [J]. NUCLEIC ACIDS RESEARCH, 1988, 16 (13) : 5827 - 5840

[33] MECHANISMS OF MESSENGER-RNA DEGRADATION IN EUKARYOTES [J]. TRENDS IN BIOCHEMICAL SCIENCES, 1994, 19 (08) : 336 - 340

[34] DEVEGVAR HEN, 1986, CELL, V47, P259

[35] INVOLVEMENT OF LONG TERMINAL REPEAT U3 SEQUENCES OVERLAPPING THE TRANSCRIPTION CONTROL REGION IN HUMAN-IMMUNODEFICIENCY-VIRUS TYPE-1 MESSENGER-RNA 3'-END FORMATION [J]. MOLECULAR AND CELLULAR BIOLOGY, 1991, 11 (03) : 1624 - 1630

[36] RELATIVE ROLES OF SIGNALS UPSTREAM OF AAUAAA AND PROMOTER PROXIMITY IN REGULATION OF HUMAN-IMMUNODEFICIENCY-VIRUS TYPE-1 MESSENGER-RNA 3' END FORMATION [J]. MOLECULAR AND CELLULAR BIOLOGY, 1992, 12 (12) : 5555 - 5562

[37] HOW DO PROTEINS RECOGNIZE SPECIFIC RNA SITES - NEW CLUES FROM AUTOGENOUSLY REGULATED RIBOSOMAL-PROTEINS [J]. TRENDS IN BIOCHEMICAL SCIENCES, 1989, 14 (08) : 335 - 338

[38] 3' RNA PROCESSING EFFICIENCY PLAYS A PRIMARY ROLE IN GENERATING TERMINATION-COMPETENT RNA POLYMERASE-II ELONGATION COMPLEXES [J]. MOLECULAR AND CELLULAR BIOLOGY, 1993, 13 (06) : 3472 - 3480

[39] POLY(A) SIGNALS AND TRANSCRIPTIONAL PAUSE SITES COMBINE TO PREVENT INTERFERENCE BETWEEN RNA POLYMERASE-II PROMOTERS [J]. EMBO JOURNAL, 1993, 12 (06) : 2539 - 2548

[40] A PAUSE SITE FOR RNA POLYMERASE-II IS ASSOCIATED WITH TERMINATION OF TRANSCRIPTION [J]. EMBO JOURNAL, 1991, 10 (07) : 1833 - 1842

[31] ANALYSIS OF MESSENGER-RNA 3' END FORMATION BY MODIFICATION INTERFERENCE - THE ONLY MODIFICATIONS WHICH PREVENT PROCESSING LIE IN AAUAAA AND THE POLY(A) SITE [J]. EMBO JOURNAL, 1987, 6 (13) : 4177 - 4184

[32] THE HUMAN U1 SNRNA PROMOTER AND ENHANCER DO NOT DIRECT SYNTHESIS OF MESSENGER-RNA [J]. NUCLEIC ACIDS RESEARCH, 1988, 16 (13) : 5827 - 5840

[33] MECHANISMS OF MESSENGER-RNA DEGRADATION IN EUKARYOTES [J]. TRENDS IN BIOCHEMICAL SCIENCES, 1994, 19 (08) : 336 - 340

[34] DEVEGVAR HEN, 1986, CELL, V47, P259

[35] INVOLVEMENT OF LONG TERMINAL REPEAT U3 SEQUENCES OVERLAPPING THE TRANSCRIPTION CONTROL REGION IN HUMAN-IMMUNODEFICIENCY-VIRUS TYPE-1 MESSENGER-RNA 3'-END FORMATION [J]. MOLECULAR AND CELLULAR BIOLOGY, 1991, 11 (03) : 1624 - 1630

[36] RELATIVE ROLES OF SIGNALS UPSTREAM OF AAUAAA AND PROMOTER PROXIMITY IN REGULATION OF HUMAN-IMMUNODEFICIENCY-VIRUS TYPE-1 MESSENGER-RNA 3' END FORMATION [J]. MOLECULAR AND CELLULAR BIOLOGY, 1992, 12 (12) : 5555 - 5562

[37] HOW DO PROTEINS RECOGNIZE SPECIFIC RNA SITES - NEW CLUES FROM AUTOGENOUSLY REGULATED RIBOSOMAL-PROTEINS [J]. TRENDS IN BIOCHEMICAL SCIENCES, 1989, 14 (08) : 335 - 338

[38] 3' RNA PROCESSING EFFICIENCY PLAYS A PRIMARY ROLE IN GENERATING TERMINATION-COMPETENT RNA POLYMERASE-II ELONGATION COMPLEXES [J]. MOLECULAR AND CELLULAR BIOLOGY, 1993, 13 (06) : 3472 - 3480

[39] POLY(A) SIGNALS AND TRANSCRIPTIONAL PAUSE SITES COMBINE TO PREVENT INTERFERENCE BETWEEN RNA POLYMERASE-II PROMOTERS [J]. EMBO JOURNAL, 1993, 12 (06) : 2539 - 2548

[40] A PAUSE SITE FOR RNA POLYMERASE-II IS ASSOCIATED WITH TERMINATION OF TRANSCRIPTION [J]. EMBO JOURNAL, 1991, 10 (07) : 1833 - 1842