| scholarly article | Q13442814 |
| P819 | ADS bibcode | 1985PNAS...82.3949C |
| P356 | DOI | 10.1073/PNAS.82.12.3949 |
| P932 | PMC publication ID | 397911 |
| P698 | PubMed publication ID | 2987956 |
| P5875 | ResearchGate publication ID | 20168234 |
| P2093 | author name string | Wickens M | |
| Conway L | |||
| P2860 | cites work | 57 Sequencing end-labeled DNA with base-specific chemical cleavages | Q27860479 |
| 3' non-coding region sequences in eukaryotic messenger RNA | Q27860858 | ||
| Most kappa immunoglobulin mRNA in human lymphocytes is homologous to a small family of germ-line V genes | Q28854607 | ||
| Steps in the processing of Ad2 mRNA: poly(A)+ nuclear sequences are conserved and poly(A) addition precedes splicing | Q34057240 | ||
| Requirement for the 3' flanking region of the bovine growth hormone gene for accurate polyadenylylation | Q36263836 | ||
| Simian Virus 40 Mutants with Deletions at the 3′ End of the Early Region Are Defective in Adenovirus Helper Function | Q36498657 | ||
| Analysis in Cos-1 Cells of Processing and Polyadenylation Signals by Using Derivatives of the Herpes Simplex Virus Type 1 Thymidine Kinase Gene | Q36936614 | ||
| Sequences on the 3' side of hexanucleotide AAUAAA affect efficiency of cleavage at the polyadenylation site. | Q36946265 | ||
| Variety in the level of gene control in eukaryotic cells | Q40103370 | ||
| The pathway of eukaryotic mRNA formation | Q40107733 | ||
| Post-transcriptional processing of simian virus 40 late transcripts in injected frog oocytes | Q45794821 | ||
| Generation of authentic 3′ termini of an H2A mRNA in vivo is dependent on a short inverted DNA repeat and on spacer sequences | Q48405245 | ||
| The sequence 5'-AAUAAA-3'forms parts of the recognition site for polyadenylation of late SV40 mRNAs | Q48410195 | ||
| Alpha-thalassaemia caused by a polyadenylation signal mutation. | Q55062701 | ||
| Inhibition of RNA cleavage but not polyadenylation by a point mutation in mRNA 3′ consensus sequence AAUAAA | Q58451156 | ||
| A sequence downstream of AAUAAA is required for rabbit β-globin mRNA 3′-end formation | Q59058833 | ||
| Are U4 small nuclear ribonucleoproteins involved in polyadenylation? | Q59062270 | ||
| Requirement of a downstream sequence for generation of a poly(A) addition site | Q64380598 | ||
| The terminal RNA stem-loop structure and 80 bp of spacer DNA are required for the formation of 3′ termini of sea urchin H2A mRNA | Q70179284 | ||
| Role of the Conserved AAUAAA Sequence: Four AAUAAA Point Mutants Prevent Messenger RNA 3′ End Formation | Q72749074 | ||
| P433 | issue | 12 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | SV40 | Q734305 |
| virus | Q808 | ||
| Anura | Q53636 | ||
| P304 | page(s) | 3949-3953 | |
| P577 | publication date | 1985-06-01 | |
| P1433 | published in | Proceedings of the National Academy of Sciences of the United States of America | Q1146531 |
| P1476 | title | A sequence downstream of A-A-U-A-A-A is required for formation of simian virus 40 late mRNA 3' termini in frog oocytes | |
| P478 | volume | 82 |
| Q45110213 | A dissection of the cauliflower mosaic virus polyadenylation signal |
| Q28776198 | A multicomponent complex is required for the AAUAAA-dependent cross-linking of a 64-kilodalton protein to polyadenylation substrates |
| Q36774538 | A uridylate tract mediates efficient heterogeneous nuclear ribonucleoprotein C protein-RNA cross-linking and functionally substitutes for the downstream element of the polyadenylation signal |
| Q36860194 | Adenovirus mutants with splice-enhancing mutations in the E3 complex transcription unit are also defective in E3A RNA 3'-end formation |
| Q35071007 | Alternative 3' processing ofXenopusα-tubulin mRNAs; efficient use of a CAUAAA polyadenylation signal |
| Q41864496 | Alternative poly(A) site utilization during adenovirus infection coincides with a decrease in the activity of a poly(A) site processing factor |
| Q24798039 | Alternative polyadenylation of cyclooxygenase-2. |
| Q40641554 | An RNA-binding protein specifically interacts with a functionally important domain of the downstream element of the simian virus 40 late polyadenylation signal |
| Q36866486 | Analysis of adenovirus type 2 L1 RNA 3'-end formation in vivo and in vitro |
| Q41360804 | Analysis of mRNA 3' end formation by modification interference: the only modifications which prevent processing lie in AAUAAA and the poly(A) site |
| Q36788795 | Assembly of a polyadenylation-specific 25S ribonucleoprotein complex in vitro |
| Q35070406 | Bipartite structure of the downstream element of the mouse beta globin (major) poly(A) signal |
| Q34282553 | Characterization of specific protein-RNA complexes associated with the coupling of polyadenylation and last-intron removal |
| Q36554283 | Characterization of the Polyomavirus Late Polyadenylation Signal |
| Q33930140 | Cleavage and polyadenylation of messenger RNA precursors in vitro occurs within large and specific 3' processing complexes. |
| Q36009672 | Components required for in vitro cleavage and polyadenylation of eukaryotic mRNA. |
| Q36706227 | Definition of the upstream efficiency element of the simian virus 40 late polyadenylation signal by using in vitro analyses |
| Q40555654 | Deletions in the SV40 late polyadenylation region downstream of the AATAAA mediate similar effects on expression in various mammalian cell lines |
| Q36695876 | Different classes of polyadenylation sites in the yeast Saccharomyces cerevisiae |
| Q36815370 | Different sequence elements are required for function of the cauliflower mosaic virus polyadenylation site in Saccharomyces cerevisiae compared with in plants |
| Q35938476 | Differential utilization of poly (A) signals between DHFR alleles in CHL cells |
| Q40416987 | Discrimination among multiple AATAAA sequences correlates with interspecies conservation of select 3' untranslated nucleotides |
| Q36843844 | Effects of intron length on differential processing of mouse mu heavy-chain mRNA |
| Q36761958 | Efficiency of utilization of the simian virus 40 late polyadenylation site: effects of upstream sequences |
| Q24601682 | Elements upstream of the AAUAAA within the human immunodeficiency virus polyadenylation signal are required for efficient polyadenylation in vitro |
| Q34607301 | Evidence for altered DNA conformations in the simian virus 40 genome: site-specific DNA cleavage by the chiral complex lambda-tris(4,7-diphenyl-1,10-phenanthroline)cobalt(III). |
| Q36902305 | Fine-structure analysis of the processing and polyadenylation region of the herpes simplex virus type 1 thymidine kinase gene by using linker scanning, internal deletion, and insertion mutations |
| Q41330964 | Formation of mRNA 3' termini: stability and dissociation of a complex involving the AAUAAA sequence |
| Q35228128 | Functional analysis of point mutations in the AAUAAA motif of the SV40 late polyadenylation signal |
| Q39452272 | Functionally significant secondary structure of the simian virus 40 late polyadenylation signal |
| Q33879922 | Generation of histone mRNA 3' ends by endonucleolytic cleavage of the pre-mRNA in a snRNP-dependent in vitro reaction |
| Q29618259 | High frequency retrotransposition in cultured mammalian cells |
| Q36921323 | Identification of a complex associated with processing and polyadenylation in vitro of herpes simplex virus type 1 thymidine kinase precursor RNA |
| Q34723405 | Identification of a novel sequence that governs both polyadenylation and alternative splicing in region E3 of adenovirus |
| Q36894844 | Identification of a sequence element on the 3' side of AAUAAA which is necessary for simian virus 40 late mRNA 3'-end processing. |
| Q40668071 | In vitro cleavage of the simian virus 40 early polyadenylation site adjacent to a required downstream TG sequence |
| Q33687217 | Isolation and characterization of a Xenopus laevis C protein cDNA: structure and expression of a heterogeneous nuclear ribonucleoprotein core protein |
| Q48971845 | Masking and unmasking maternal mRNA. The role of polyadenylation, transcription, splicing, and nuclear history |
| Q36691462 | Molecular analyses of two poly(A) site-processing factors that determine the recognition and efficiency of cleavage of the pre-mRNA. |
| Q45878857 | Multiple sequence elements are involved in RNA 3' end formation in spleen necrosis virus |
| Q33866547 | Mutational analysis of a yeast transcriptional terminator |
| Q36849107 | Patterns of polyadenylation site selection in gene constructs containing multiple polyadenylation signals |
| Q40644140 | Poly(A) polymerase purified from HeLa cell nuclear extract is required for both cleavage and polyadenylation of pre-mRNA in vitro |
| Q34053472 | Poly(A) signals and transcriptional pause sites combine to prevent interference between RNA polymerase II promoters. |
| Q36114829 | Polyadenylation at a cryptic site in the pBR322 portion of pSV2-neo: prevention of its utilization by the SV40 late poly(A) signal |
| Q33621282 | Potentiation of a polyadenylylation site by a downstream protein-DNA interaction |
| Q36095276 | Processing at immunoglobulin polyadenylation sites in lymphoid cell extracts. |
| Q36838958 | Products of in vitro cleavage and polyadenylation of simian virus 40 late pre-mRNAs |
| Q34726725 | Putative polyadenylation signals in nuclear genes of higher plants: a compilation and analysis |
| Q36710092 | RNA processing in vitro produces mature 3' ends of a variety of Saccharomyces cerevisiae mRNAs |
| Q40100264 | Regulation of poly(A) site selection in adenovirus. |
| Q41521560 | Regulation of polyadenylation in human immunodeficiency virus (HIV): contributions of promoter proximity and upstream sequences |
| Q35045330 | Requirement of A-A-U-A-A-A and adjacent downstream sequences for SV40 early polyadenylation |
| Q36834250 | Requirements for accurate and efficient mRNA 3' end cleavage and polyadenylation of a simian virus 40 early pre-RNA in vitro |
| Q36763488 | Role of poly(A) polymerase in the cleavage and polyadenylation of mRNA precursor |
| Q24599827 | Secondary structure as a functional feature in the downstream region of mammalian polyadenylation signals |
| Q36780246 | Sedimentation analysis of polyadenylation-specific complexes |
| Q35564243 | Selection of sequence elements that substitute for the standard AATAAA motif which signals 3' processing and polyadenylation of late simian virus 40 mRNAs |
| Q42574256 | Sequences capable of restoring poly(A) site function define two distinct downstream elements. |
| Q36764593 | Sequences downstream of AAUAAA signals affect pre-mRNA cleavage and polyadenylation in vitro both directly and indirectly |
| Q36914137 | Sequences near the 3' secretion-specific polyadenylation site influence levels of secretion-specific and membrane-specific IgG2b mRNA in myeloma cells |
| Q36795452 | Sequences upstream of AAUAAA influence poly(A) site selection in a complex transcription unit |
| Q37533985 | Site-specific cleavage of left-handed DNA in pBR322 by lambda-tris(diphenylphenanthroline)cobalt(III). |
| Q41360882 | Specific pre-cleavage and post-cleavage complexes involved in the formation of SV40 late mRNA 3' termini in vitro |
| Q36667262 | The 64-kilodalton subunit of the CstF polyadenylation factor binds to pre-mRNAs downstream of the cleavage site and influences cleavage site location |
| Q36916774 | The AAUAAA sequence is required both for cleavage and for polyadenylation of simian virus 40 pre-mRNA in vitro |
| Q36847550 | The C proteins of heterogeneous nuclear ribonucleoprotein complexes interact with RNA sequences downstream of polyadenylation cleavage sites |
| Q36559866 | The cap and the 3' splice site similarly affect polyadenylation efficiency |
| Q42857570 | The complete sequence of a frog alpha-tubulin gene and its regulated expression in mouse L-cells |
| Q37426718 | The human immunodeficiency virus type 1 polyadenylylation signal: a 3' long terminal repeat element upstream of the AAUAAA necessary for efficient polyadenylylation |
| Q39720399 | Transcription and polyadenylation in a short human intergenic region. |
| Q40667653 | Tripartite sequences within and 3' to the sea urchin H2A histone gene display properties associated with a transcriptional termination process |
| Q30452170 | Two distant upstream regions containing cis-acting signals regulating splicing facilitate 3'-end processing of avian sarcoma virus RNA |
| Q40640624 | UV cross-linking of polypeptides associated with 3'-terminal exons |
| Q40062402 | Upstream sequences and cap proximity in the regulation of polyadenylation in ground squirrel hepatitis virus |
| Q33958705 | Utilization of splicing elements and polyadenylation signal elements in the coupling of polyadenylation and last-intron removal |
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