| scholarly article | Q13442814 |
| P50 | author | Donald Ganem | Q66789604 |
| P2093 | author name string | J. Cherrington | |
| R. Russnak | |||
| P2860 | cites work | The human 64-kDa polyadenylylation factor contains a ribonucleoprotein-type RNA binding domain and unusual auxiliary motifs | Q24301982 |
| Cleavage and polyadenylation factor CPF specifically interacts with the pre-mRNA 3' processing signal AAUAAA | Q24564625 | ||
| Efficient polyadenylation within the human immunodeficiency virus type 1 long terminal repeat requires flanking U3-specific sequences | Q24645438 | ||
| 3' non-coding region sequences in eukaryotic messenger RNA | Q27860858 | ||
| Cloning and expression of the essential gene for poly(A) polymerase from S. cerevisiae | Q27934513 | ||
| Point mutations in AAUAAA and the poly (A) addition site: effects on the accuracy and efficiency of cleavage and polyadenylation in vitro | Q35880505 | ||
| The consensus sequence YGTGTTYY located downstream from the AATAAA signal is required for efficient formation of mRNA 3' termini | Q36136653 | ||
| Molecular analyses of two poly(A) site-processing factors that determine the recognition and efficiency of cleavage of the pre-mRNA. | Q36691462 | ||
| Efficiency of utilization of the simian virus 40 late polyadenylation site: effects of upstream sequences | Q36761958 | ||
| Mutations in poly(A) site downstream elements affect in vitro cleavage activity | Q36787633 | ||
| Sequences upstream of AAUAAA influence poly(A) site selection in a complex transcription unit | Q36795452 | ||
| Polyadenylation at correct sites in genome RNA is not required for retrovirus replication or genome encapsidation | Q36829761 | ||
| Identification of a sequence element on the 3' side of AAUAAA which is necessary for simian virus 40 late mRNA 3'-end processing. | Q36894844 | ||
| The AAUAAA sequence is required both for cleavage and for polyadenylation of simian virus 40 pre-mRNA in vitro | Q36916774 | ||
| Definition of essential sequences and functional equivalence of elements downstream of the adenovirus E2A and the early simian virus 40 polyadenylation sites | Q36951086 | ||
| Construction of a modular dihydrofolate reductase cDNA gene: analysis of signals utilized for efficient expression | Q36975957 | ||
| The human immunodeficiency virus type 1 polyadenylylation signal: a 3' long terminal repeat element upstream of the AAUAAA necessary for efficient polyadenylylation | Q37426718 | ||
| 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 | Q37691120 | ||
| Involvement of long terminal repeat U3 sequences overlapping the transcription control region in human immunodeficiency virus type 1 mRNA 3' end formation | Q40677805 | ||
| Poly(A) site efficiency reflects the stability of complex formation involving the downstream element | Q41079693 | ||
| Isolation and expression of cDNA clones encoding mammalian poly(A) polymerase | Q41083859 | ||
| A short cis-acting sequence is required for hepatitis B virus pregenome encapsidation and sufficient for packaging of foreign RNA. | Q41227891 | ||
| Analysis of mRNA 3' end formation by modification interference: the only modifications which prevent processing lie in AAUAAA and the poly(A) site | Q41360804 | ||
| Regulation of polyadenylation in human immunodeficiency virus (HIV): contributions of promoter proximity and upstream sequences | Q41521560 | ||
| The efficiency of RNA 3'-end formation is determined by the distance between the cap site and the poly(A) site in spleen necrosis virus | Q41713738 | ||
| Purification and characterization of a mammalian polyadenylate polymerase involved in the 3' end processing of messenger RNA precursors. | Q41767252 | ||
| Four factors are required for 3'-end cleavage of pre-mRNAs | Q43727383 | ||
| Purification of the cleavage and polyadenylation factor involved in the 3'-processing of messenger RNA precursors. | Q44234133 | ||
| A dissection of the cauliflower mosaic virus polyadenylation signal | Q45110213 | ||
| Proximity to the promoter inhibits recognition of cauliflower mosaic virus polyadenylation signal. | Q45849027 | ||
| Sequences 5' to the polyadenylation signal mediate differential poly(A) site use in hepatitis B viruses | Q46958551 | ||
| The sequence 5'-AAUAAA-3'forms parts of the recognition site for polyadenylation of late SV40 mRNAs | Q48410195 | ||
| An ordered pathway of assembly of components required for polyadenylation site recognition and processing. | Q51172966 | ||
| 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 | ||
| Primary structure and expression of bovine poly(A) polymerase | Q59097203 | ||
| Requirement of a downstream sequence for generation of a poly(A) addition site | Q64380598 | ||
| Occlusion of the HIV poly(A) site | Q68198316 | ||
| A functionally redundant downstream sequence in SV40 late pre-mRNA is required for mRNA 3'-end formation and for assembly of a precleavage complex in vitro | Q69823612 | ||
| 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 | microbiology | Q7193 |
| immunology | Q101929 | ||
| regulatory sequence | Q3238407 | ||
| TATA box | Q1413955 | ||
| P304 | page(s) | 7589-7596 | |
| P577 | publication date | 1992-12-01 | |
| P1433 | published in | Journal of Virology | Q1251128 |
| P1476 | title | Upstream sequences and cap proximity in the regulation of polyadenylation in ground squirrel hepatitis virus | |
| P478 | volume | 66 |
| Q35856603 | A common mechanism for the enhancement of mRNA 3' processing by U3 sequences in two distantly related lentiviruses |
| Q39876436 | A host factor that binds near the termini of hepatitis B virus pregenomic RNA |
| Q35896223 | A novel transcriptional element in circular DNA monomers of the duck hepatitis B virus |
| Q33854031 | Differential regulation of hepatitis B virus gene expression by the Sp1 transcription factor |
| Q35898446 | Effects of mutations within and adjacent to the terminal repeats of hepatitis B virus pregenomic RNA on viral DNA synthesis |
| Q35943827 | In vitro epsilon RNA-dependent protein priming activity of human hepatitis B virus polymerase. |
| Q35846709 | In vivo activity of the hepatitis B virus core promoter: tissue specificity and temporal regulation. |
| Q41288691 | Plant mRNA 3'-end formation |
| Q37628010 | Poly(A) site selection in the yeast Ty retroelement requires an upstream region and sequence-specific titratable factor(s) in vitro. |
| Q36567679 | Promoter-proximal poly(A) sites are processed efficiently, but the RNA products are unstable in the nucleus |
| Q39452015 | Recruitment of a basal polyadenylation factor by the upstream sequence element of the human lamin B2 polyadenylation signal. |
| Q41882662 | Sequence elements upstream of the 3' cleavage site confer substrate strength to the adenovirus L1 and L3 polyadenylation sites |
| Q36663019 | Sequences homologous to 5' splice sites are required for the inhibitory activity of papillomavirus late 3' untranslated regions |
| Q34801348 | Upstream and downstream cis-acting elements for cleavage at the L4 polyadenylation site of adenovirus-2. |
| Q36629024 | pet, a small sequence distal to the pregenome cap site, is required for expression of the duck hepatitis B virus pregenome. |
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