| P2093 | author name string | G. G. Carmichael | |
| | D. B. Batt | |
| P2860 | cites work | BioTechniques | Q4914664 |
| | Proceedings of the National Academy of Sciences of the United States of America | Q1146531 |
| | 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 |
| | Isolation of biologically active ribonucleic acid from sources enriched in ribonuclease | Q26778460 |
| | A multicomponent complex is required for the AAUAAA-dependent cross-linking of a 64-kilodalton protein to polyadenylation substrates | Q28776198 |
| | Polyomavirus early-late switch is not regulated at the level of transcription initiation and is associated with changes in RNA processing | Q33678489 |
| | Polyomavirus tumor induction in mice: influences of viral coding and noncoding sequences on tumor profiles | Q33720764 |
| | The biochemistry of 3'-end cleavage and polyadenylation of messenger RNA precursors. | Q34243656 |
| | Polyadenylation and transcription termination in gene constructs containing multiple tandem polyadenylation signals | Q34859580 |
| | Targeted nuclear antisense RNA mimics natural antisense-induced degradation of polyoma virus early RNA. | Q35223801 |
| | Efficiency of processing of viral RNA during the early and late phases of productive infection by polyoma virus | Q35235817 |
| | The consensus sequence YGTGTTYY located downstream from the AATAAA signal is required for efficient formation of mRNA 3' termini | Q36136653 |
| | Polyoma virus early-late switch: regulation of late RNA accumulation by DNA replication | Q36536249 |
| | The 64-kilodalton subunit of the CstF polyadenylation factor binds to pre-mRNAs downstream of the cleavage site and influences cleavage site location | Q36667262 |
| | Molecular analyses of two poly(A) site-processing factors that determine the recognition and efficiency of cleavage of the pre-mRNA. | Q36691462 |
| | Definition of the upstream efficiency element of the simian virus 40 late polyadenylation signal by using in vitro analyses | Q36706227 |
| | Splice site choice in a complex transcription unit containing multiple inefficient polyadenylation signals | Q36738496 |
| | Efficiency of utilization of the simian virus 40 late polyadenylation site: effects of upstream sequences | Q36761958 |
| | Leader-to-leader splicing is required for efficient production and accumulation of polyomavirus late mRNAs | Q36779971 |
| | Sequences upstream of AAUAAA influence poly(A) site selection in a complex transcription unit | Q36795452 |
| | Polyomavirus late pre-mRNA processing: DNA replication-associated changes in leader exon multiplicity suggest a role for leader-to-leader splicing in the early-late switch | Q36795859 |
| | Deletion analysis of the polyomavirus late promoter: evidence for both positive and negative elements in the absence of early proteins. | Q36830178 |
| | Polyomavirus late leader region serves an essential spacer function necessary for viability and late gene expression | Q36862385 |
| | Duplication of functional polyadenylation signals in polyomavirus DNA does not alter efficiency of polyadenylation or transcription termination | Q36863412 |
| | 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 | Q36902305 |
| | Kinetics and Efficiency of Polyadenylation of Late Polyomavirus Nuclear RNA: Generation of Oligomeric Polyadenylated RNAs and Their Processing into mRNA | Q36943662 |
| | Sequences on the 3' side of hexanucleotide AAUAAA affect efficiency of cleavage at the polyadenylation site. | Q36946265 |
| | Definition of essential sequences and functional equivalence of elements downstream of the adenovirus E2A and the early simian virus 40 polyadenylation sites | Q36951086 |
| | ATTAAA as well as downstream sequences are required for RNA 3'-end formation in the E3 complex transcription unit of adenovirus | Q36951615 |
| | 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 |
| | Regulation of poly(A) site selection in adenovirus. | Q40100264 |
| | Regulation of polyadenylation in hepatitis B viruses: stimulation by the upstream activating signal PS1 is orientation-dependent, distance-independent, and additive | Q40508994 |
| | An RNA-binding protein specifically interacts with a functionally important domain of the downstream element of the simian virus 40 late polyadenylation signal | Q40641554 |
| | Involvement of long terminal repeat U3 sequences overlapping the transcription control region in human immunodeficiency virus type 1 mRNA 3' end formation | Q40677805 |
| | A complex secondary structure in U1A pre-mRNA that binds two molecules of U1A protein is required for regulation of polyadenylation | Q40874579 |
| | Poly(A) site efficiency reflects the stability of complex formation involving the downstream element | Q41079693 |
| | Double-stranded RNA triggers generalized translational arrest in Xenopus oocytes | Q43600096 |
| | Four factors are required for 3'-end cleavage of pre-mRNAs | Q43727383 |
| | Preparation of mammalian extracts active in polyadenylation | Q44545552 |
| | A dissection of the cauliflower mosaic virus polyadenylation signal | Q45110213 |
| | Sequences 5' to the polyadenylation signal mediate differential poly(A) site use in hepatitis B viruses | Q46958551 |
| | An ordered pathway of assembly of components required for polyadenylation site recognition and processing. | Q51172966 |
| | 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 |
| | Simple, inexpensive preparation of T1/T2 ribonuclease suitable for use in RNase protection experiments | Q67897677 |
| | A multisubunit factor, CstF, is required for polyadenylation of mammalian pre-mRNAs | Q68164668 |
| | CPSF recognition of an HIV-1 mRNA 3'-processing enhancer: multiple sequence contacts involved in poly(A) site definition | Q72427107 |
| | Direct interaction of the U1 snRNP-A protein with the upstream efficiency element of the SV40 late polyadenylation signal | Q72718794 |
| P433 | issue | 9 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | post-transcriptional modification | Q417379 |
| P304 | page(s) | 4783-4790 | |
| P577 | publication date | 1995-09-01 | |
| P1433 | published in | Molecular and Cellular Biology | Q3319478 |
| P1476 | title | Characterization of the polyomavirus late polyadenylation signal | |
| | Characterization of the Polyomavirus Late Polyadenylation Signal | |
| P478 | volume | 15 | |